Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript. Nature Communications , Article number: (2026) Cite this article We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply. The photochemistry of UV-irradiated liquid water underlies many physical, chemical, and biological processes, with the formation of the hydrated electron as a central event. Despite extensive experimental and theoretical efforts, its microscopic origin remains incompletely understood. Using excited state molecular dynamics simulations of photoexcited liquid water, we resolve the sequence of chemical events leading to hydrated electron formation on the excited state. The excitation localizes on specific hydrogen-bond network defects, followed by two competing pathways. The first produces a hydrogen atom and undergoes ultrafast non-radiative decay to the ground state within 100 femtoseconds. The other proceeds via proton-coupled electron transfer, generating hydronium ions, hydroxyl radicals, and an excited state hydrated electron. This mechanism is driven by ultrafast coupled rotational and translational motions of water molecules, forming water-mediated ion-radical pairs that persist on picosecond timescales and influence visible emission. These results provide a unified framework for interpreting time-resolved spectroscopic observations and guide future experimental and theoretical investigations. All data generated in this study, including ESMD trajectories, cube files for representative pathways, geometries for the water dimer, input files for all calculations, and scripts for the analysis of spin density, have been deposited in the Zenodo database (https://doi.org/10.5281/zenodo.17714130). Source data are provided with this paper. Hart, E. J. & Boag, J. W. Absorption spectrum of the hydrated electron in water and in aqueous solutions. Am. Soc. Google Scholar Garrett, B. C. et al. Role of water in electron-initiated processes and radical chemistry: Issues and scientific advances. Google Scholar Young, R. M. & Neumark, D. M. Dynamics of solvated electrons in clusters. Google Scholar Wang, C.-R., Nguyen, J. Bond breaks of nucleotides by dissociative electron transfer of nonequilibrium prehydrated electrons: a new molecular mechanism for reductive DNA damage. Am. Soc. Google Scholar Boudaıffa, B., Cloutier, P., Hunting, D., Huels, M. A. & Sanche, L. Resonant formation of DNA strand breaks by low-energy (3 to 20 eV) electrons. Google Scholar Clarke, C. J., Michi Burrow, E. & Verlet, J. R. The role of water molecules in the dissociation of an electron-molecule contact pair. Nat. Google Scholar Jortner, J., Ottolenghi, M. & Stein, G. On the photochemistry of aqueous solutions of chloride, bromide, and iodide ions. Google Scholar Loh, Z.-H. et al. Observation of the fastest chemical processes in the radiolysis of water. Google Scholar Sunaryo, G. R., Katsumura, Y., Shirai, I., Hiroishi, D. & Ishigure, K. Radiolysis of water at elevated temperatures-i. irradiation with gamma-rays and fast neutrons at room temperature. Google Scholar Coons, M. P., You, Z.-Q. & Herbert, J. M. The hydrated electron at the surface of neat liquid water appears to be indistinguishable from the bulk species. Am. Soc. Google Scholar Sagar, D., Bain, C. D. & Verlet, J. R. Hydrated electrons at the water/air interface. Am. Soc. Google Scholar Liu, H.T. et al. Ultrafast photo-excitation dynamics in isolated, neutral water clusters. Bragg, A., Verlet, J., Kammrath, A., Cheshnovsky, O. & Neumark, D. Hydrated electron dynamics: from clusters to bulk. Google Scholar Verlet, J., Bragg, A., Kammrath, A., Cheshnovsky, O. & Neumark, D. Observation of large water-cluster anions with surface-bound excess electrons. Google Scholar Matsuzaki, K. et al. Partially hydrated electrons at the air/water interface observed by UV-excited time-resolved heterodyne-detected vibrational sum frequency generation spectroscopy. Am. Soc. Google Scholar LaForge, A. C. et al. Real-time dynamics of the formation of hydrated electrons upon irradiation of water clusters with extreme ultraviolet light. Google Scholar Elles, C. G., Shkrob, I. A., Crowell, R. A. & Bradforth, S. E.: Excited state dynamics of liquid water: insight from the dissociation reaction following two-photon excitation. Yamamoto, Y. -i & Suzuki, T. Ultrafast dynamics of water radiolysis: Hydrated electron formation, solvation, recombination, and scavenging. Google Scholar Elles, C. G., Rivera, C. A., Zhang, Y., Pieniazek, P. A. : Electronic structure of liquid water from polarization-dependent two-photon absorption spectroscopy. Sander, M. U., Luther, K. & Troe, J. Excitation energy dependence of the photoionization of liquid water. Google Scholar Nikogosyan, D. N., Oraevsky, A. & Rupasov, V. I. Two-photon ionization and dissociation of liquid water by powerful laser UV radiation. Google Scholar Goulet, T., Bernas, A., Ferradini, C. & Jay-Gerin, J.-P. On the electronic structure of liquid water: Conduction-band tail revealed by photoionization data. Google Scholar Engel, V. et al. Photodissociation of water in the first absorption band: a prototype for dissociation on a repulsive potential energy surface. Google Scholar Andresen, P., Ondrey, G., Titze, B. & Rothe, E. W. Nuclear and electron dynamics in the photodissociation of water. Google Scholar Novelli, F. et al. The birth and evolution of solvated electrons in the water. Proc. Natl. Acad. Sci. USA 120, 2216480120 (2023). Google Scholar Signorell, R. & Winter, B. Photoionization of the aqueous phase: clusters, droplets and liquid jets. Google Scholar Svoboda, V. et al. Real-time observation of water radiolysis and hydrated electron formation induced by extreme-ultraviolet pulses. Sci. Adv. Google Scholar Herbert, J. M. Structure of the aqueous electron. Google Scholar Couto, P. & Chipman, D. M.: Insights into the ultraviolet spectrum of liquid water from model calculations. Ziaei, V. & Bredow, T.: Red and blue shift of liquid water's excited states: a many body perturbation study. Couto, P. & Chipman, D. M.: Insights into the ultraviolet spectrum of liquid water from model calculations: The different roles of donor and acceptor hydrogen bonds in water pentamers. Svoboda, O., Ončák, M. & Slavíček, P.: Simulations of light induced processes in water based on ab initio path integrals molecular dynamics. Monti, M. et al. Defects at Play: Shaping the Photophysics and Photochemistry of Ice. Proc. Natl. Acad. Sci. Savolainen, J., Uhlig, F., Ahmed, S., Hamm, P. & Jungwirth, P. Direct observation of the collapse of the delocalized excess electron in water. Nat. Google Scholar Lin, M.-F. et al. Imaging the short-lived hydroxyl-hydronium pair in ionized liquid water. Google Scholar Kimura, Y., Alfano, J. C., Walhout, P. & Barbara, P. F. Ultrafast transient absorption spectroscopy of the solvated electron in water. Google Scholar Jacobson, L. D. & Herbert, J. M.: A one-electron model for the aqueous electron that includes many-body electron-water polarization: Bulk equilibrium structure, vertical electron binding energy, and optical absorption spectrum. Schnitker, J. & Rossky, P. J. An electron–water pseudopotential for condensed phase simulation. Google Scholar Turi, L. & Borgis, D. Analytical investigations of an electron–water molecule pseudopotential. development of a new pair potential and molecular dynamics simulations. Google Scholar Larsen, R. E., Glover, W. J. & Schwartz, B. J. Does the hydrated electron occupy a cavity?. Google Scholar Casey, J. R., Kahros, A. & Schwartz, B. J. To be or not to be in a cavity: the hydrated electron dilemma. Google Scholar Kumar, A., Walker, J. A., Bartels, D. M. & Sevilla, M. D. A simple ab initio model for the hydrated electron that matches experiment. Google Scholar Lee, S. et al. Ab initio study of water hexamer anions. Google Scholar Williams, C. F. & Herbert, J. M. Influence of structure on electron correlation effects and electron- water dispersion interactions in anionic water clusters. Google Scholar Lan, J. et al. Simulating the ghost: quantum dynamics of the solvated electron. Nat. Google Scholar Frank, I., Hutter, J., Marx, D. & Parrinello, M. Molecular dynamics in low-spin excited states. Google Scholar Odelius, M., Laikov, D. & Hutter, J. Excited state geometries within time-dependent and restricted open-shell density functional theories. Structure: THEOCHEM 630, 163–175 (2003). Google Scholar Kowalczyk, T., Tsuchimochi, T., Chen, P.-T., Top, L. & Van Voorhis, T.: Excitation energies and Stokes shifts from a restricted open-shell Kohn-Sham approach. Hait, D., Zhu, T., McMahon, D. P. & Van Voorhis, T. Prediction of excited-state energies and singlet–triplet gaps of charge-transfer states using a restricted open-shell Kohn–Sham approach. theory Comput. Google Scholar Fedorov, I. D. & Stegailov, V. V. Exciton nature of plasma phase transition in warm dense fluid hydrogen: Roks simulation. Google Scholar Carter-Fenk, K., Johnson, B. A., Herbert, J. M., Schenter, G. K. & Mundy, C. J. Birth of the hydrated electron via charge-transfer-to-solvent excitation of aqueous iodide. Google Scholar Wegner, F. Inverse participation ratio in 2+ ε dimensions. B Condens. Matter 36, 209–214 (1980). Google Scholar Liu, Y., Sierant, P., Stornati, P., Lewenstein, M. & Płodzień, M. Quantum algorithms for inverse participation ratio estimation in multiqubit and multiqudit systems. Google Scholar Giannini, S. et al. Exciton transport in molecular organic semiconductors boosted by transient quantum delocalization. Google Scholar Gasparotto, P., Hassanali, A. & Ceriotti, M. Probing defects and correlations in the hydrogen-bond network of ab initio water. theory Comput. Google Scholar & Robinson, G. W. Energetics and formation of the “hydrated electron”within an itinerant radical model. AIP Conf. Neumann, S., Eisfeld, W., Sobolewski, A. & Domcke, W. Simulation of the resonance raman spectrum of the hydrated electron in the hydrated-hydronium cluster model. Google Scholar Tauber, M. J. & Mathies, R. A. Fluorescence and resonance Raman spectra of the aqueous solvated electron. Google Scholar Calixto, M. & Romera, E. Inverse participation ratio and localization in topological insulator phase transitions. : Theory Exp. Google Scholar Kratochvil, H. T. et al. Transient water wires mediate selective proton transport in designed channel proteins. Google Scholar Hassanali, A., Prakash, M. K., Eshet, H. & Parrinello, M. On the recombination of hydronium and hydroxide ions in water. Google Scholar Freier, E., Wolf, S. & Gerwert, K. Proton transfer via a transient linear water-molecule chain in a membrane protein. Google Scholar Tang, F., Qiu, D. Y. & Wu, X. Optical absorption spectroscopy probes water wire and its ordering in a hydrogen-bond network. X 15, 011048 (2025). Google Scholar Plasser, F. et al. Surface hopping dynamics with correlated single-reference methods: 9h-adenine as a case study. theory Comput. Google Scholar Ibele, L. M., Sanchez-Murcia, P. A., Mai, S., Nogueira, J. J. & González, L. Excimer intermediates en route to long-lived charge-transfer states in single-stranded adenine DNA as revealed by nonadiabatic dynamics. Google Scholar Harrevelt, R. & Hemert, M. C. Photodissociation of water. i. electronic structure calculations for the excited states. Google Scholar Novelli, F. et al. High-mobility electrons in aqueous iodide solutions. ACS Omega 10, 5097–5104(2025). Sokolov, U. & Stein, G. Photolysis of liquid water at 1470 å. J. Chem. Google Scholar Sokolov, U. & Stein, G. Photolysis of liquid water at 1849 å. J. Chem. Google Scholar Siefermann, K. R. & Abel, B. The hydrated electron: A seemingly familiar chemical and biological transient. Google Scholar Segarra-Marti, J., Roca-Sanjuan, D., Merchan, M. & Lindh, R.: On the photophysics and photochemistry of the water dimer. Kumar, A., Kołaski, M., Lee, H. M. & Kim, K. S. Photoexcitation and photoionization dynamics of water photolysis. Google Scholar Borrelli, W. R., Liu, X. & Schwartz, B. J.: How the choice of exchange–correlation functional affects dft-based simulations of the hydrated electron. Coe, J. V., Williams, S. M. & Bowen, K. H. Photoelectron spectra of hydrated electron clusters vs. cluster size: connecting to bulk. Google Scholar Kar, R. & Nair, N. N. Nature of hydrated electron in varied solvation environments. Low, P. J. et al. Observation of a transient intermediate in the ultrafast relaxation dynamics of the excess electron in strong-field-ionized liquid water. Google Scholar Rybkin, V. V. Mechanism of aqueous carbon dioxide reduction by the solvated electron. Google Scholar Neupane, P., Bartels, D. M. & Thompson, W. H. Exploring the unusual reactivity of the hydrated electron with co2. Google Scholar Marsalek, O. et al. Chasing charge localization and chemical reactivity following photoionization in liquid water. Pieniazek, P. A., VandeVondele, J., Jungwirth, P., Krylov, A. I. & Bradforth, S. E. Electronic structure of the water dimer cation. Google Scholar Kamarchik, E., Kostko, O., Bowman, J. M., Ahmed, M. & Krylov, A. I.: Spectroscopic signatures of proton transfer dynamics in the water dimer cation. Schwartz, B. J. & Rossky, P. J. An exploration of the relationship between solvation dynamics and spectrally determined solvent response functions by computer simulation. Google Scholar Farr, E. P., Zho, C.-C., Challa, J. R. & Schwartz, B. J.: Temperature dependence of the hydrated electron's excited-state relaxation. elucidating the relaxation mechanism through ultrafast transient absorption and stimulated emission spectroscopy. Yanai, T., Tew, D. P. & Handy, N. C. A new hybrid exchange–correlation functional using the coulomb-attenuating method (cam-b3lyp). Google Scholar VandeVondele, J. & Hutter, J.: Gaussian basis sets for accurate calculations on molecular systems in gas and condensed phases. Villa, A. M. et al. Anomalous water fluorescence induced by solutes. Google Scholar Villa, A. M., Doglia, S. M., De Gioia, L., Bertini, L. & Natalello, A. Anomalous intrinsic fluorescence of HCl and NaOH aqueous solutions. Google Scholar Villa, A. M., Doglia, S. M., De Gioia, L., Natalello, A. & Bertini, L. Fluorescence of KCl aqueous solution: a possible spectroscopic signature of nucleation. Google Scholar Jordan, C. J. C., Coons, M. P., Herbert, J. M. & Verlet, J. R. R. Spectroscopy and dynamics of the hydrated electron at the water/air interface. Google Scholar Behler, J., Parrinello, M.: Generalized neural-network representation of high-dimensional potential-energy surfaces. Bartók, A. P., Payne, M. C., Kondor, R. & Csányi, G.: Gaussian approximation potentials: The accuracy of quantum mechanics, without the electrons. Zhang, L. et al. End-to-end Symmetry Preserving Inter-atomic Potential Energy Model For Finite And Extended Systems. In: Proceedings of the 32nd International Conference on Neural Information Processing Systems. (Curran Associates Inc., Red Hook, NY, USA, 2018). Batatia, I., Kovacs, D. P., Simm, G., Ortner, C. & Csanyi, G.: Mace: Higher order equivariant message passing neural networks for fast and accurate force fields. In: Koyejo, S. et al. Neural Inf. Process Syst. Pozdnyakov, S. & Ceriotti, M.: Smooth, exact rotational symmetrization for deep learning on point clouds. In: Oh, A. et al. Neural Inf. Berendsen, H. J., Grigera, J.-R. & Straatsma, T. P. The missing term in effective pair potentials. Google Scholar Abraham, M. J. et al. Gromacs: high performance molecular simulations through multi-level parallelism from laptops to supercomputers. Google Scholar Bussi, G., Donadio, D. & Parrinello, M.: Canonical sampling through velocity rescaling. Zeng, J. et al. DeePMD-kit v2: a software package for deep potential models. Google Scholar Zhang, C. et al. Modeling liquid water by climbing up Jacob's ladder in density functional theory facilitated by using deep neural network potentials. Google Scholar Chen, M. et al. Ab initio theory and modeling of water. Google Scholar Zhang, L., Wang, H., Car, R. & E, W. Phase diagram of a deep potential water model. Google Scholar Thompson, A. P. et al. Lammps - a flexible simulation tool for particle-based materials modeling at the atomic, meso, and continuum scales. Google Scholar Filatov, M. & Shaik, S. Application of spin-restricted open-shell Kohn–Sham method to atomic and molecular multiplet states. Google Scholar Hait, D. & Head-Gordon, M. Excited state orbital optimization via minimizing the square of the gradient: General approach and application to singly and doubly excited states via density functional theory. theory Comput. Google Scholar Larsen, A. H. et al. The atomic simulation environment-a python library for working with atoms. Google Scholar Kühne, T. D. et al. Cp2k: An electronic structure and molecular dynamics software package-quickstep: Efficient and accurate electronic structure calculations. Vydrov, O. & Van Voorhis, T.: Nonlocal van der Waals density functional: The simpler the better. Ambrosio, F., Miceli, G. & Pasquarello, A. Electronic levels of excess electrons in liquid water. Google Scholar Ambrosio, F., Guo, Z. & Pasquarello, A. Absolute energy levels of liquid water. Google Scholar Ambrosio, F., Miceli, G. & Pasquarello, A.: Redox levels in aqueous solution: Effect of van der Waals interactions and hybrid functionals. Lan, J., Chergui, M. & Pasquarello, A. Dynamics of the charge transfer to solvent process in aqueous iodide. Google Scholar Stetina, T. F., Sun, S., Lingerfelt, D. B., Clark, A. & Li, X. The role of excited-state proton relays in the photochemical dynamics of water nanodroplets. Google Scholar Crespo-Otero, R. & Barbatti, M. Recent advances and perspectives on nonadiabatic mixed quantum–classical dynamics. Google Scholar Prlj, A. et al. Best practices for nonadiabatic molecular dynamics simulations. arXiv preprint arXiv:2508.05263 (2025). Tokić, N., Piteša, T., Prlj, A., Sapunar, M. & Došlić, N. Advantages and limitations of Landau-Zener surface hopping dynamics. Croatica Chem. Google Scholar Suchan, J., Janoš, J. & Slavicek, P. Pragmatic approach to photodynamics: mixed Landau–Zener surface hopping with intersystem crossing. Theory Comput. Google Scholar Xie, W. & Domcke, W. Accuracy of trajectory surface-hopping methods: Test for a two-dimensional model of the photodissociation of phenol. Díaz Mirón, G. et al. Exploring the mechanisms behind non-aromatic fluorescence with the density functional tight binding method. Theory Comput. Google Scholar Martinka, J. et al. A descriptor is all you need: Accurate machine learning of nonadiabatic coupling vectors. Google Scholar Sprik, M. Coordination numbers as reaction coordinates in constrained molecular dynamics. Faraday Discuss. Google Scholar Sprik, M. Computation of the pk of liquid water using coordination constraints. Google Scholar Sirkin, Y. A. P., Hassanali, A. & Scherlis, D. A. One-dimensional confinement inhibits water dissociation in carbon nanotubes. Google Scholar Di Pino, S. et al. Water self-dissociation is insensitive to nanoscale environments. Google Scholar Kumar, R., Schmidt, J. & Skinner, J. Hydrogen bonding definitions and dynamics in liquid water. Download references and A.H. acknowledge funding from the European Research Council (ERC) under the European Union's Horizon 2020 research and innovation program (grant agreement No. The views and opinions expressed are those of the authors only and do not necessarily reflect those of the European Union or the European Research Council Executive Agency. Neither the European Union nor the granting authority can be held responsible for them. and A.H. also acknowledge MareNostrum5 (project EHPC-EXT-2023E01-029) for computational resources. was supported by the U.S. Department of Energy (DOE), Office of Science, Basic Energy Sciences (BES), the Chemical Sciences, Geosciences, and Biosciences Division, Chemical Physics and Interfacial Sciences Program, FWP 16249. Condensed Matter and Statistical Physics, The Abdus Salam International Center for Theoretical Physics, Trieste, Italy Gonzalo Díaz Mirón, Solana Di Pino, Diganta Dasgupta & Ali Hassanali SISSA – Scuola Internazionale Superiore di Studi Avanzati, Trieste, Italy Cesare Malosso & Diganta Dasgupta Laboratory of Computational Science and Modeling, IMX, École Polytechnique Fédérale de Lausanne, Lausanne, Switzerland Cesare Malosso Initiative for Computational Catalysis, Flatiron Institute, New York, USA Colin K. Egan Physical and Computational Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, USA Christopher J. Mundy Department of Chemical Engineering, University of Washington, Seattle, WA, USA Christopher J. Mundy Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar and A.H. conceived and designed the research. performed the ground state MLIP simulations, and G.D.M. carried out the ESMD simulations. G.D.M., S.D.P., C.K.E., and D.D. performed the data analysis. G.D.M., C.J.M., and A.H. contributed to the interpretation and discussion of the results. and A.H. wrote the original manuscript with input from all authors. All authors discussed the findings and contributed to the final version of the manuscript. Correspondence to Gonzalo Díaz Mirón or Ali Hassanali. The authors declare no competing interests. Nature Communications thanks Jinggang Lan, who co-reviewed with Yifan Li, and the other, anonymous, reviewer(s) for their contribution to the peer review of this work. A peer review file is available. Publisher's note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. Reprints and permissions Díaz Mirón, G., Malosso, C., Di Pino, S. et al. Simulating the Photochemical Birth of the Hydrated Electron in Liquid Water. Nat Commun (2026). Download citation Received: 04 September 2025 Accepted: 16 February 2026 Published: 10 March 2026 DOI: https://doi.org/10.1038/s41467-026-70045-7 Anyone you share the following link with will be able to read this content: Sorry, a shareable link is not currently available for this article. Provided by the Springer Nature SharedIt content-sharing initiative Nature Communications (Nat Commun) ISSN 2041-1723 (online) © 2026 Springer Nature Limited Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.
Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript. Nature Communications , Article number: (2026) Cite this article We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply. Solar-driven interfacial evaporation is a promising solution to address global freshwater scarcity, with woody biomass-based evaporators standing out for their sustainability and cost-effectiveness. However, current woody biomass-based systems often suffer from inefficient water management and suboptimal photothermal performance. Herein, we develop a dual-function lignin-engineered reconstituted wood framework strategy, achieving both compositional and structural optimization of woody biomass to enhance its evaporation performance via water management and thermal management. By partially retaining and reconfiguring lignin within the woody biomass framework, a higher fraction of loosely bound “intermediate water” with reduced evaporation enthalpy is generated while preserving the water-pumping capability. Concurrently, the extracted lignin is upcycled via laser-induced graphitization into a broadband photothermal layer composed of hierarchical graphene/graphitic carbon structures with solar absorptivity exceeding 95%. This synergistic design results in the E-150 solar evaporator, which achieves an evaporation rate of 2.24 kg m⁻² h⁻¹ and a photothermal conversion efficiency of 91.52% under one-sun irradiation, surpassing most reported wood-based evaporators. Moreover, the retained lignin sustains multiscale channel integrity, imparting strong salt resistance, high recyclability, and robust purification capabilities. This integrated biomass valorization strategy provides a scalable, low-cost, and eco-friendly route for high-performance solar desalination and sustainable water-energy applications. All data needed to evaluate the conclusions in the paper are present in the paper, the Supplementary Information, or from the corresponding author upon request. Source data are provided with this paper. Shannon, M. A. et al. Science and technology for water purification in the coming decades. Kim, Y. & Lee, W.-G. Seawater and its resources. in Seawater Batteries: Principles, Materials and Technology (Singapore, Springer Nature Singapore, 2022). Chaule, S. et al. Rational design of a high performance and robust solar evaporator via 3D-printing technology. Chen, C., Kuang, Y. & Hu, L. Challenges and opportunities for solar evaporation. Google Scholar Tao, P. et al. Solar-driven interfacial evaporation. Google Scholar Wu, X. et al. Interfacial solar evaporation: from fundamental research to applications. He, S. et al. Nature-inspired salt resistant bimodal porous solar evaporator for efficient and stable water desalination. Energy Environ. Google Scholar Chen, L. et al. 3D-printed tripodal porous wood-mimetic cellulosic composite evaporator for salt-free water desalination. Google Scholar Chao, W. et al. Enhanced wood-derived photothermal evaporation system by in-situ incorporated lignin carbon quantum dots. Google Scholar Xu, N., Song, Y., Wei, T. & Zhu, J. Flatband λ-Ti3O5 boosts solar evaporation. Google Scholar Li, L. et al. Polyelectrolyte ydrogel-functionalized photothermal sponge enables simultaneously continuous solar desalination and electricity generation without salt accumulation. Zhao, F. et al. Highly efficient solar vapour generation via hierarchically nanostructured gels. Google Scholar Ma, X. et al. Wood-based solar-driven interfacial evaporators: design and application. Chen, L. et al. Biomass waste-assisted micro (nano) plastics capture, utilization, and storage for sustainable water remediation. Google Scholar Qin, Q. et al. Bottom-up” and “top-down” strategies toward strong cellulose-based materials. Google Scholar Gu, Y. et al. Solar-powered high-performance lignin-wood evaporator for solar steam generation. Google Scholar Petridis, L. & Smith, J. C. Molecular-level driving forces in lignocellulosic biomass deconstruction for bioenergy. Google Scholar Thybring, E., Fredriksson, M., Zelinka, S. & Glass, S. Water in wood: a review of current understanding and knowledge gaps. Dong, Y. et al. Reviewing wood-based solar-driven interfacial evaporators for desalination. Water Res. Google Scholar Gnanasekaran, A. & Rajaram, K. Flake-like CuO nanostructure coated on flame treated eucalyptus wood evaporator for efficient solar steam generation at outdoor conditions. Google Scholar Gu, Y. et al. All wood-based evaporator via cell wall regulating for integrated water and energy generation. Wu, W. et al. Cellulose-based Interfacial solar evaporators: structural regulation and performance manipulation. Google Scholar Li, X. P. et al. Reshapable MXene/graphene oxide/polyaniline plastic hybrids with patternable surfaces for highly efficient solar-driven water purification. Google Scholar Wang, B. et al. Harnessing renewable lignocellulosic potential for sustainable wastewater purification. Google Scholar Tran, C. D. et al. Sustainable energy-storage materials from lignin–graphene nanocomposite-derived porous carbon film. Energy Technol. Google Scholar Okamoto, S. et al. Additive effect of graphene and lignin-derived graphene on radical polymerization behaviors of methacrylate monomers. Google Scholar Lin, J. et al. Laser-induced porous graphene films from commercial polymers. Google Scholar Yang, Z. et al. One-step sustainable preparation of laser induced S-doped graphene for assembly of high-performance Naturesupercapacitors. Google Scholar Zhao, F. et al. Materials for solar-powered water evaporation. Google Scholar Wei, D. et al. Water activation in solar-powered vapor generation. Google Scholar Gnanasekaran, A. & Rajaram, K. Rational design of different interfacial evaporators for solar steam generation: recent development, fabrication, challenges and applications. Energy Rev. Google Scholar Zhang, C. et al. Unveiling the structural characteristics of lignin and lignin–carbohydrate complexes in fibers and parenchyma cells of moso bamboo during different growing years. Google Scholar Tarasov, D., Leitch, M. & Fatehi, P. Lignin–carbohydrate complexes: properties, applications, analyses, and methods of extraction: a review. Google Scholar Yang, Z. et al. One-pot lignocellulose fractionation towards efficient whole sugar conversion and aromatic monomer production using a mild alkaline oxidation system. Green Chem. Google Scholar Wang, J., Qian, Y., Li, L. & Qiu, X. Atomic force microscopy and molecular dynamics simulations for study of lignin solution self-assembly mechanisms in organic–aqueous solvent mixtures. Google Scholar Bregado, J. L., Secchi, A. R. & Tavares, F. W. A density functional theory study on interactions in water-bridged dimeric complexes of lignin. Google Scholar Hackenstrass, K., Hasani, M. & Wohlert, M. Structure, flexibility and hydration properties of lignin dimers studied with molecular dynamics simulations. Google Scholar Cesari, L., Canabady-Rochelle, L. & Mutelet, F. Computational study of phenolic compounds-water clusters. Google Scholar Xuemin, G., Peng, Y. & Yanfen, W. How to reduce enthalpy in the interfacial solar water generation system for enhancing efficiency? Nano Energy 123, 109434 (2024). Jing, S. et al. The critical roles of water in the processing, structure, and properties of nanocellulose. Google Scholar Jia, L. et al. Crystal Nonlinearity. Google Scholar Engelund, E. T., Thygesen, L. G., Svensson, S. & Hill, C. A. A critical discussion of the physics of wood–water interactions. Google Scholar Bonnet, M. et al. NMR determination of sorption isotherms in earlywood and latewood of Douglas fir. Identification of bound water components related to their local environment. Google Scholar Li, J. & Ma, E. Characterization of water in wood by time-domain nuclear magnetic resonance spectroscopy (TD-NMR): a review. Google Scholar Kuang, Y. et al. A high-performance self-regenerating solar evaporator for continuous water desalination. Google Scholar Zhang, W. et al. Lignin laser lithography: a direct-write method for fabricating 3D graphene electrodes for microsupercapacitors. Energy Mater. Zhang, C. et al. An integrated and robust plant pulse monitoring system based on biomimetic wearable sensor. npj Flexible Electron. Shen, F. et al. A closed-loop strategy for ciprofloxacin adsorption and degradation by acetic acid/H2O2 modified biochar. et al. Raman spectroscopy of graphene-based materials and its applications in related devices. Xie, Z. et al. The rise of 2D photothermal materials beyond graphene for clean water production. Mohan, V. B., Lau, K. -t, Hui, D. & Bhattacharyya, D. Graphene-based materials and their composites: a review on production, applications and product limitations. Part B-Eng. Zhang, H. et al. Probing laser-induced structural transformation of lignin into few-layer graphene. Le, T. S. D. et al. Ultrafast laser pulses enable one-step graphene patterning on woods and leaves for green electronics. Chyan, Y. et al. Laser-induced graphene by multiple lasing: toward electronics on cloth, paper, and food. Pang, B. et al. Molecular-scale design of cellulose-based functional materials for flexible electronic devices. Du, C. et al. Heat-localized solar evaporation: transport processes and applications. Nano Energy 107, 108086 (2023). Lin, X. et al. Fully lignocellulosic biomass-based double-layered porous hydrogel for efficient solar steam generation. Sluiter, A. et al. Determination of structural carbohydrates and lignin in biomass. This work was supported by the National Natural Science Foundation of China (22308029) (X. S.), the Knowledge Innovation Program of Wuhan-Basi Research (2023020201010072) (C. C.), the Fundamental Research Funds for the Central Universities (691000003) (C. C.), and the 5·5 Engineering Research & Innovation Team Project of Beijing Forestry University (No. BLRC 2023B05) (T. Additionally, the authors appreciate the assistance of the Innovation Platform for High-Value Utilization of Forest Resources at Beijing Forestry University. We thank Insight Vision for their professional assistance in creating the three-dimensional rendering for Fig. These authors contributed equally: Bin Wang, Yanrong He, Zhihao Yang. State Key Laboratory of Efficient Production of Forest Resources, Beijing Key Laboratory of Lignocellulosic Chemistry, Beijing Forestry University, Beijing, China Bin Wang, Yanrong He, Zhihao Yang, Qian Sun, Xipeng Zhang, Xiaojun Shen, Jia-Long Wen & Tong-Qi Yuan Hubei Biomass-Resource Chemistry and Environmental Biotechnology Key Laboratory, School of Resource and Environmental Sciences, Wuhan University, Wuhan, China Chaoji Chen Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar conceived the concept, processing, and structure details. performed the design and preparation of the evaporator. carried out the evaporation test. co-wrote the manuscript. supervised the work and revised the manuscript. provided guidance on the structural analysis of lignocellulose. provided assistance in the enthalpy of the evaporation test of water. participated in large-scale sample preparation and outdoor evaporation tests. All authors commented on the submitted version of the manuscript. Correspondence to Xiaojun Shen, Chaoji Chen or Tong-Qi Yuan. The authors declare no competing interests. Nature Communications thanks the anonymous reviewers for their contribution to the peer review of this work. A peer review file is available. Publisher's note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations. Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/. Reprints and permissions Wang, B., He, Y., Yang, Z. et al. Reconstitution of woody biomass framework via dual-functional lignin engineering toward efficient and salt-resistant solar desalination. Nat Commun (2026). Received: 17 August 2025 Accepted: 23 February 2026 Published: 10 March 2026 Anyone you share the following link with will be able to read this content: Sorry, a shareable link is not currently available for this article. Provided by the Springer Nature SharedIt content-sharing initiative Nature Communications (Nat Commun) ISSN 2041-1723 (online) © 2026 Springer Nature Limited Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.
You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). Gemma Conroy is a freelance science journalist in Mexico City. Although social-media influencers often show elaborate skincare routines, dermatologists recommend simple steps for most people. Over the past five years, dermatologist Rajani Katta has noticed a change in the people who come into her office. Their skincare routines have been getting more complicated — some stretching to 12 steps — and often involve products that they found through social media, many of which don't have a lot of scientific backing. The science influencers going viral on TikTok to fight misinformation The science influencers going viral on TikTok to fight misinformation They didn't realize that some of those products were doing damage to their skin, says Katta, who specializes in sensitive skin and allergies at the University of Texas Health Science Center at Houston. “People are much more likely to experiment on themselves” than they have been in the past, she says. Globally, there seems to be more interest in skincare than ever before, with the industry expected to generate more than US$200 billion worldwide in 2026. Social-media platforms such as TikTok seem to be a main driver of the hot pursuit of youthful, glowing skin, with hashtags such as #SkinTok generating more than one billion views per month. They're also rife with harmful misinformation, such as the false claim that sunscreens cause skin cancer and vitamin-D deficiency. There's plenty of evidence that lifestyle factors are important — arguably more important — than products and daily rituals for keeping skin healthy. Often, the recommendations from physicians about skin run counter to what is circulating on social media. What's more, new research is elucidating the connections between the skin and other organ systems, and it has become clear that keeping skin healthy has effects far beyond one's outward appearance, says Mao-Qing Man, a dermatologist at Hebei Medical University in Shijiazhuang, China. “It has a lot of different dimensions,” says Daniel Kaplan, a dermatologist who focuses on immunology at the University of Pittsburgh in Pennsylvania. Skin is made up of three main layers: the hypodermis (bottom), dermis (middle) and epidermis (top). This waterproof shield is made of corneocytes — flat, dead cells filled with the protein keratin. These tough cells are surrounded by lipids called ceramides, which lock in moisture and keep invaders out of the skin. Although biology textbooks often compare the skin barrier to a brick wall, it's more like a thriving ecosystem of physical, chemical, microbial and immune functions, says Peter Lio, a dermatologist who specializes in eczema at Northwestern University in Evanston, Illinois. “Our skin barrier is incredibly dynamic and complex,” he says. For instance, some popular cosmetic procedures, such as chemical peels — which temporarily remove the outer layers of the skin to reduce wrinkles and acne scars — can cause lasting harm to the skin barrier and result in chronic sensitivity if done incorrectly or too frequently. “The skin does have powerful abilities to regenerate”, but some treatments can override that, says Katta. The surprisingly big health benefits of just a little exercise The surprisingly big health benefits of just a little exercise This damage can increase a person's risk of developing more chronic skin conditions, such as atopic dermatitis, psoriasis and even allergies, says Katta. It can also make it easier for pathogens such as Staphylococcus aureus, a bacterium that can cause abscesses and, in more severe cases, blood infections, to slip past the barrier. A common mistake that many people make at home is overusing harsh soaps, detergents and astringents — liquids that shrink body tissues by drawing water out of them, says Kaplan. The barrier also has an acid mantle — a thin, filmy layer of oils, fatty acids and amino acids — which helps to keep the skin stable and creates the conditions needed for a healthy microbiome to flourish (see ‘A home for beneficial bacteria'). Wiping out lipids with harsh products raises pH levels. This, in turn, weakens the community of beneficial microorganisms and enables pathogenic types to flourish. Taking scalding hot showers is another way to damage the skin barrier, says Tamia Harris-Tryon, a physician scientist who studies the skin microbiome at the University of Texas Southwestern Medical Center in Dallas. “If it's hot enough to clean your pots and pans of oil, it will clean your body of natural oils,” she says. Whereas gentle cleansers, moisturizers and sunscreen are generally safe for kids, potent serums and anti-ageing products for mature skin can wreak havoc on younger skin, he says. Over the long term, few things are worse for the skin than overexposure to UV radiation, either through natural sunlight or tanning beds, says Elsemieke Plasmeijer, a dermatologist and epidemiologist at the Netherlands Cancer Institute in Amsterdam. In 2022, almost 60,000 people died from melanoma, according to the World Health Organization's (WHO) International Agency for Research on Cancer. Meanwhile, UVB only reaches the epidermis, but causes sunburn and DNA damage that can lead to skin cancer. A 2019 study found that both types of UV radiation disrupt a protein that helps cells to stick together in the skin barrier1. This resulted in weaker bonds between corneocytes, leading to a less resilient skin barrier. Stress is wrecking your health: how can science help? Stress is wrecking your health: how can science help? In December, Pedram Gerami, a dermatologist who specializes in skin cancer at Northwestern University, and his colleagues reported that people who use indoor tanning beds were three times more likely to get melanoma than those who don't use them2. They were more likely to have multiple melanomas, even in parts of the body that usually have low levels of Sun damage, such as the thighs. The indoor tanning industry often argues that tanning beds are safer than natural sunlight because they emit more UVA than they do DNA-damaging UVB light. But this claim is often false, says Gerami. The science influencers going viral on TikTok to fight misinformation The surprisingly big health benefits of just a little exercise Stress is wrecking your health: how can science help? Do smartphones and social media really harm teens' mental health? These brain cells clear proteins that contribute to Alzheimer's Mechanism of co-transcriptional cap snatching by influenza polymerase Microbiota-mediated induction of beige adipocytes in response to dietary cues What my cave stay taught me about sensors Recruiting an Academic Lead in Computational Biomedical Imaging to build a vibrant research community engaged in imaging and its clinical translation. UMass Chan Medical School (FBGao Lab) Post Doc Position to study pathogenic mechanisms of Frontotemporal Dementia using patient iPSC-derived neurons No.1 Shizishan Street, Hongshan District, Wuhan, Hubei Province, China The science influencers going viral on TikTok to fight misinformation The surprisingly big health benefits of just a little exercise Stress is wrecking your health: how can science help? Do smartphones and social media really harm teens' mental health? An essential round-up of science news, opinion and analysis, delivered to your inbox every weekday. Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.
Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript. Nature Communications , Article number: (2026) Cite this article We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply. The development of stable Ru-based anodes for acidic proton exchange membrane water electrolysis is promising, but strictly limited by Ru over-oxidation and structural collapse due to lattice oxygen participation under high current densities. Rational design of competitive Ru-based catalyst is, thereby, highly desired. Here, by exploring a customized self-assembly route, we report a type of mesoporous Ru-Ti-O solid solution catalyst delivering competitive performance (1 A cm-2 for over 450 h at 0.4mgRucm-2). Mechanistic investigations reveal that the enhanced performance arises from the integration of atomic-scale electronic structure tuning and mesoscopic triple phase interface engineering. The electron delocalization forms a conductive network and suppresses Ru overoxidation through electron donation. Atomically dispersed Ru-O-Ti motifs favor the oxygen pathway mechanism over the lattice oxygen mechanism, suppressing lattice oxygen release and enhancing structural stability. Simultaneously, the ordered mesoporous architecture and radially aligned nanorod bundles establish a robust, super-hydrophilic triple phase interface, enabling effective water and gas exchange and mitigating concentration overpotentials. This cross-scale design strategy offers a possible route to non-Ir catalysts with measurable activity and long-term durability for scalable acidic water electrolysis. The source data generated in this study are provided in the Source Data file. Source data are provided with this paper. Li, A. et al. Atomically dispersed hexavalent iridium oxide from MnO2 reduction for oxygen evolution catalysis. Google Scholar Zhang, J. et al. Tantalum-stabilized ruthenium oxide electrocatalysts for industrial water electrolysis. Google Scholar Chen, Y. et al. Support-free iridium hydroxide for high-efficiency proton-exchange membrane water electrolysis. Google Scholar Feng, W. et al. Proton exchange membrane water splitting: advances in electrode structure and mass-charge transport optimization. Google Scholar Jo, S. et al. Nonprecious high-entropy chalcogenide glasses-based electrocatalysts for efficient and stable acidic oxygen evolution reaction in proton exchange membrane water electrolysis. Energy Mater. Google Scholar Lin, C. et al. In-situ reconstructed Ru atom array on α-MnO2 with superior performance for acidic water oxidation. Google Scholar Sun, K. et al. Enhancing heterointerface coupling for durable industrial-Level proton exchange membrane water electrolysis. Google Scholar Hu, S. et al. Low-dimensional electrocatalysts for acidic oxygen evolution: intrinsic activity, High current density operation, and Long-term stability. Google Scholar Liu, S. et al. Ultrathin perovskite derived Ir-based nanosheets for high-performance electrocatalytic water splitting. Energy Environ. Google Scholar Nong, H. N. et al. Key role of chemistry versus bias in electrocatalytic oxygen evolution. Google Scholar Wang, Q. et al. Long-term stability challenges and opportunities in acidic oxygen evolution electrocatalysis. Google Scholar et al. Boosting the durability of RuO2 via confinement effect for proton exchange membrane water electrolyzer. Google Scholar Ke, J. et al. Optimizing acidic oxygen evolution reaction via modulation doping in van der Waals layered iridium oxide. Google Scholar Liao, F. et al. Iridium oxide nanoribbons with metastable monoclinic phase for highly efficient electrocatalytic oxygen evolution. Google Scholar Song, Y. et al. Engineering Ir-based catalysts for high current density applications in proton exchange membrane water electrolyzers. Energy Environ. Google Scholar Huo, M. et al. Tailoring octahedron-tetrahedron synergism in spinel catalysts for acidic water electrolysis. Google Scholar Chen, J. et al. Cobalt-doped Ru@RuO2 core–shell heterostructure for efficient acidic water oxidation in low-Ru-loading proton exchange membrane water electrolyzers. Google Scholar et al. Non-iridium-based electrocatalyst for durable acidic oxygen evolution reaction in proton exchange membrane water electrolysis. Google Scholar Deng, L. et al. Accelerated proton transfer in asymmetric active units for sustainable acidic oxygen evolution reaction. Google Scholar Li, W. et al. Designing Ru-B-Cr moieties to activate the Ru site for acidic water electrolysis under industrial-level current density. Nano Lett. Google Scholar Wang, J. et al. Single-site Pt-doped RuO2 hollow nanospheres with interstitial C for high-performance acidic overall water splitting. Google Scholar Ping, X. et al. Locking the lattice oxygen in RuO2 to stabilize highly active Ru sites in acidic water oxidation. Google Scholar Xia, W. et al. Enhancing acidic water electrolysis via local electronic regulation of Ru/TiOx catalyst with oxygen coordination unsaturated Ti sites. ACS Catal. Google Scholar Xue, Y. et al. Stabilizing ruthenium dioxide with cation-anchored sulfate for durable oxygen evolution in proton-exchange membrane water electrolyzers. Google Scholar Chen, S. et al. Mn-doped RuO2 nanocrystals as highly active electrocatalysts for enhanced oxygen evolution in acidic media. ACS Catal. Google Scholar Liu, Z. et al. Synergistic Sr activation and Cr buffering effect on RuO2 electronic structures for enhancing the acidic oxygen evolution reaction. Nano Lett. Google Scholar Lee, K. et al. Modulating the valence electronic structure using earth-abundant aluminum for high-performance acidic oxygen evolution reaction. Google Scholar Shi, Z. et al. Customized reaction route for ruthenium oxide towards stabilized water oxidation in high-performance PEM electrolyzers. Google Scholar Zhu, W. et al. Direct dioxygen radical coupling driven by octahedral ruthenium-oxygen-cobalt collaborative coordination for acidic oxygen evolution reaction. Google Scholar Wang, Y. et al. Breaking the Ru-O-Ru symmetry of a RuO2 catalyst for sustainable acidic water oxidation. Google Scholar Cao, X. et al. Strain heterogeneity in RuO2 for efficient acidic oxygen evolution reaction in proton exchange membrane water electrolysis. Google Scholar Liu, H. et al. Cost-efficient and stable electrolysis of reverse osmosis water using a Co-RuO2-enabled PEM electrolyser. Google Scholar Han, X. et al. Defect engineering of RuO2 aerogel for efficient acidic water oxidation. ACS Mater. Google Scholar Li, Z. et al. Anchoring Ru clusters to highly defective N-doped carbon nanotubes via a thermal-shock strategy for stable industrial hydrogen evolution. Nano Res. Google Scholar Wang, X. et al. Electronic structure modulation of RuO2 by TiO2 enriched with oxygen vacancies to boost acidic O2 evolution. ACS Catal. Google Scholar Song, Y. et al. Sub-4 nm Ru-RuO2 schottky nanojunction as a catalyst for durable acidic water oxidation. Google Scholar Du, K. et al. Interface engineering breaks both stability and activity limits of RuO2 for sustainable water oxidation. Google Scholar Deng, L. et al. Valence oscillation of Ru active sites for efficient and robust acidic water oxidation. Google Scholar Deng, L. et al. Activity-stability balance: the role of electron supply effect of support in acidic oxygen evolution. Google Scholar Hao, Y. et al. Polarized ultrathin BN induced dynamic electron interactions for enhancing acidic oxygen evolution. Google Scholar Li, J. et al. Breathing-mimicking electrocatalysis for oxygen evolution and reduction. Google Scholar Ren, G. et al. Bubble-water/catalyst triphase interface microenvironment accelerates photocatalytic OER via optimizing semi-hydrophobic OH radical. Google Scholar Lan, K. et al. Versatile synthesis of mesoporous crystalline TiO2 materials by monomicelle assembly. Google Scholar Zhang, J. et al. Facile synthesis of mesoporous TiO2 architectures with tunable configurations and nanometer precision. Google Scholar Lan, K. et al. Precisely designed mesoscopic titania for high-volumetric-density pseudocapacitance. Google Scholar Varghese, S. wamy et al. Size-dependent modifications of the Raman spectrum of rutile TiO2. Google Scholar Zhao, G. et al. Metallic Ru-Ru interaction in Ruthenium oxide enabling durable proton exchange membrane water electrolysis. Google Scholar Zhou, C. et al. Pinning effect of lattice Pb suppressing lattice oxygen reactivity of Pb-RuO2 enables stable industrial-level electrolysis. Google Scholar Park, Y. et al. Atomic-level Ru-Ir mixing in rutile-type (RuIr)O2 for efficient and durable oxygen evolution catalysis. Google Scholar Li, X. et al. Optimal selection of RuO2 for durable oxygen evolution reactions in acidic media by continuous regulation of Ru–O covalency. Energy Environ. Google Scholar Liu, H. et al. Eliminating over-oxidation of ruthenium oxides by niobium for highly stable electrocatalytic oxygen evolution in acidic media. Google Scholar He, W. et al. Grain-boundary-rich RuO2 porous nanosheet for efficient and stable acidic water oxidation. Wang, Y. et al. Nano-metal diborides-supported anode catalyst with strongly coupled TaOx/IrO2 catalytic layer for low-iridium-loading proton exchange membrane electrolyzer. Lee, C. et al. Catalyst-support interactions in Zr2ON2-supported IrOx electrocatalysts to break the trade-off relationship between the activity and stability in the acidic oxygen evolution reaction. Hao, S. et al. Torsion strained iridium oxide for efficient acidic water oxidation in proton exchange membrane electrolyzers. Wang, Y. et al. Mesoporous single-crystalline particles as robust and efficient acidic oxygen evolution catalysts. Xue, Z.-H. et al. Simple and scalable introduction of single-atom Mn on RuO2 electrocatalysts for oxygen evolution reaction with long-term activity and stability. Cao, X. et al. Regulation of oxide pathway mechanism for sustainable acidic water oxidation. Lu, Q. et al. Breaking the activity-stability trade-off of RuO2 via metallic Ru bilateral regulation for acidic oxygen evolution reaction. Download references This work was supported by the National Key R&D Program of China (2021YFB4000202), National Natural Science Foundation of China (22375108), Technology Breakthrough Engineering Hydrogen Energy Field “Unveiling and Leading” Project (2024KJTW0018), Young Top-notch Talents Program of Inner Mongolia (Q202501), Natural Science Foundation of Inner Mongolia (2026JQYX06), Junma Program of Inner Mongolia University. acknowledges the support from the Chinese Academy of Sciences, China. We also thank the BL17B1 and BL05U station at Shanghai Synchrotron Radiation Facility (SSRF) for the help in characterizations, and staff members of the BL01B beamline at National Facility for Protein Science in Shanghai (https://cstr.cn/31129.02.NFPS) for technical support in data collection and analysis. These authors contributed equally: Jun-Ye Zhang, Kaihang Yue, Yuqi Zhao. College of Energy Materials and Chemistry, College of Chemistry and Chemical Engineering, Inner Mongolia University, Hohhot, PR China Jun-Ye Zhang, Yuqi Zhao, Rongyao Li, Wendi Wang, Lu Liu, Jialong Li, Kun Lan & Dongyuan Zhao Laboratory of Advanced Materials, Department of Chemistry, College of Chemistry and Materials, Fudan University, Shanghai, PR China Jun-Ye Zhang, Kaihang Yue, Yanjie Hu, Lu Liu & Dongyuan Zhao Key Laboratory of Materials for Energy Conversion, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai, PR China Kaihang Yue & Ya Yan Shanghai Advanced Research Institute, Chinese Academy of Sciences, Shanghai, PR China Yuqi Zhao, Qixuan Li, Hao Zhao, Lianhai Zu & Hui Yang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing, PR China Zhe Xu Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar contributed equally to this work. conceived and supervised this project. performed the material synthesis and most of the structural characterizations. carried out and analyzed electrochemical experiments. performed and analyzed in-situ characterizations and simulations. assisted with some structural characterizations and analyses. J.Z., L.Z., and K. L. cowrote the paper. All authors discussed and commented on the manuscript. Correspondence to Lianhai Zu, Kun Lan or Dongyuan Zhao. The authors declare no competing interests. Nature Communications thanks Lifang Jiao and the other anonymous reviewer(s) for their contribution to the peer review of this work. A peer review file is available. Publisher's note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations. Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/. Reprints and permissions Zhang, JY., Yue, K., Zhao, Y. et al. Mesoporous ruthenium titanium oxide solid solution with efficient three phase reaction interface for water electrolysis. Nat Commun (2026). Download citation Received: 06 November 2025 Accepted: 25 February 2026 Published: 10 March 2026 DOI: https://doi.org/10.1038/s41467-026-70502-3 Anyone you share the following link with will be able to read this content: Sorry, a shareable link is not currently available for this article. Provided by the Springer Nature SharedIt content-sharing initiative Nature Communications (Nat Commun) ISSN 2041-1723 (online) © 2026 Springer Nature Limited Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.
The discovery was led by University of Minnesota Twin Cities scientist Peter Makovicky along with Argentine paleontologist Sebastian Apesteguía. Their findings, published in the peer reviewed journal Nature, describe a nearly complete skeleton of Alnashetri cerropoliciensis. This dinosaur belonged to a peculiar group of bird like theropods called alvarezsaurs. These animals are known for their tiny teeth and unusually short arms that end in a single enlarged thumb claw. For decades, scientists struggled to understand this group because most well preserved fossils had been discovered in Asia. Fossils from South America were often incomplete, leaving major gaps in the evolutionary story. The almost complete Alnashetri fossil was uncovered in 2014 in northern Patagonia, Argentina, at a fossil rich site famous for exceptionally preserved Cretaceous animals. Preparing the specimen was a slow and careful process. "Going from fragmentary skeletons that are hard to interpret, to having a near complete and articulated animal is like finding a paleontological Rosetta Stone," said Peter Makovicky, lead author of the study and a professor in the University of Minnesota Department of Earth and Environmental Sciences. "We now have a reference point that allows us to accurately identify more scrappy finds and map out evolutionary transitions in anatomy and body size." The fossil is providing scientists with valuable insight into how this lineage of dinosaurs evolved, became smaller, and spread across ancient continents. The skeleton reveals that Alnashetri differed from its later relatives in several ways. It had longer arms and larger teeth, showing that some alvarezsaurs had already evolved very small body sizes before developing the specialized features that later species used for what scientists believe was an "ant-eating" diet. Alnashetri itself weighed less than 2 lbs, making it one of the smallest dinosaurs discovered in South America. By studying additional alvarezsaur fossils preserved in museum collections across North America and Europe, the team also found evidence that these animals appeared much earlier than scientists previously believed. Previous finds from the site include early snakes and small saber toothed mammals. "After more than 20 years of work, the La Buitrera fossil area has given us a unique insight into small dinosaurs and other vertebrates like no other site in South America," said Apesteguía, a researcher at Universidad Maimónides in Buenos Aires, Argentina. Scientists are still actively studying fossils from the same region, and more discoveries may soon add to the story of these unusual dinosaurs. The Moon Was Hit Again: NASA Scientists Discover a Newly Formed Crater Weight Loss Drugs Like Ozempic and Wegovy Show Surprising Heart Health Benefits Stay informed with ScienceDaily's free email newsletter, updated daily and weekly. Keep up to date with the latest news from ScienceDaily via social networks: Tell us what you think of ScienceDaily -- we welcome both positive and negative comments.
Imagine removing everything from the deepest regions of cosmic voids. What remains appears to be nothing but empty space. It may sound contradictory, but these enormous voids are filled with the vacuum of spacetime. In quantum field theory, the particles that make up our world such as electrons, top quarks, neutrinos, and even dark matter are not independent objects in the usual sense. These fields permeate every cubic centimeter of space and time. When we observe a particle, such as an electron moving through space, we are really detecting a ripple or vibration in its underlying field. The particle is a traveling excitation of that field. Even if all particles were removed, the fields would still remain. When physicists attempt to calculate how much energy exists in empty space, the results can range from extremely large values to theoretically infinite ones…which is also another episode. What matters is that this vacuum energy produces a measurable effect. In most environments across the universe, its influence is negligible. Regions filled with matter completely dominate the local behavior of space. Here on Earth, for example, matter is so dense that dark energy has no noticeable impact. If dark energy suddenly vanished, everyday physics would remain unchanged. The path of a thrown baseball would be identical. Galaxies, galaxy clusters, filaments, and walls of the cosmic web are all regions packed with matter. In these environments, dark energy plays almost no role. Voids are enormous regions where matter is largely absent. In fact, voids are where dark energy carries out its most important work. Instead, it takes place within the vast empty voids. Cosmic voids are not just empty gaps between structures in the universe. Over immense spans of time, this process gradually pulls the universe's large-scale structure apart. The intricate network of galaxies, clusters, and filaments that astronomers see today will not last forever. In that sense, cosmic voids are far from empty. They are filled with the subtle energy of quantum fields. That energy influences the entire universe by driving its accelerating expansion. Voids are the only regions where this effect becomes dominant, precisely because they contain almost nothing else. But their lack of matter means they are filled with dark energy. Note: Content may be edited for style and length. These Tiny Teeth Could Change What We Know About Human Origins Hormone Therapy May Supercharge Popular Weight-Loss Drugs After Menopause Nearly Half of Americans Don't Know This Popular Food Increases Colon Cancer Risk Stay informed with ScienceDaily's free email newsletter, updated daily and weekly. Or view our many newsfeeds in your RSS reader: Keep up to date with the latest news from ScienceDaily via social networks: Tell us what you think of ScienceDaily -- we welcome both positive and negative comments.
Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript. (2026)Cite this article Hard masks with high etch selectivity are essential for fabricating high-aspect-ratio nanostructures via deep and anisotropic plasma etching. While most two-dimensional materials are susceptible to plasma damage, we report that van der Waals metal oxyhalides, specifically CrOCl and FeOCl, exhibit extraordinary resistance to aggressive SF6/O2 plasma, far surpassing conventional hard mask materials. CrOCl achieves etch rates as low as ~2.4 nm min−1 and an etch selectivity >200:1 relative to silicon, representing improvements of ~30× over Si3N4, ~2.3× over Al2O3 and ~20× over TiN under identical conditions. CrOCl maintains subnanometre surface roughness after etching, even exhibiting plasma-induced surface smoothening. Beyond its inherent etch resistance, CrOCl can be chemically patterned using Cl2 plasma and mechanically transferred onto a broad range of substrates, including perovskite oxides, polymers, glasses and monolayer two-dimensional semiconductors, enabling patterning on materials that are typically incompatible with conventional hard masks. Using CrOCl masks, we demonstrate deep silicon etching with aspect ratios exceeding 39:1 and minimal feature distortion. These findings establish van der Waals metal oxyhalides as a versatile and scalable platform for next-generation nanofabrication, combining extreme plasma robustness, high-resolution patternability and broad substrate compatibility in one material system. This is a preview of subscription content, access via your institution Access Nature and 54 other Nature Portfolio journals Get Nature+, our best-value online-access subscription cancel any time Subscribe to this journal Receive 12 print issues and online access $259.00 per year only $21.58 per issue Buy this article Prices may be subject to local taxes which are calculated during checkout Source data are provided with this paper. The codes used to plot the data are available from the corresponding author upon reasonable request. Huff, M. Recent advances in reactive ion etching and applications of high-aspect-ratio microfabrication. Kumar, D. et al. Highly efficient back-end-of-line compatible flexible Si-based optical memristive crossbar array for edge neuromorphic physiological signal processing and bionic machine vision. Google Scholar Hsieh, A. C. & Hwang, T. TSV redundancy: architecture and design issues in 3-D IC. VLSI Syst. Google Scholar Yuvaraja, S. et al. Enhancement-mode ambipolar thin-film transistors and CMOS logic circuits using bilayer Ga2O3/NiO semiconductors. ACS Appl. Raman, S. & Sindhuja, M. Advances in silicon nanowire applications in energy generation, storage, sensing, and electronics: a review. Nela, L. et al. Multi-channel nanowire devices for efficient power conversion. Hazra, S. et al. A novel hardmask-to-substrate pattern transfer method for creating 3D, multi-level, hierarchical, high aspect-ratio structures for applications in microfluidics and cooling technologies. Shulaker, M. M., Saraswat, K., Wong, H. S. P. & Mitra, S. Monolithic three-dimensional integration of carbon nanotube FETs with silicon CMOS. In 2014 Symposium on VLSI Technology: Digest of Technical Papers https://doi.org/10.1109/VLSIT.2014.6894422 (IEEE, 2014). Lee, C., Kim, S., Kim, G. & Choi, C. Heterogeneous monolithic 3D integration for hybrid vertical CMOS inverter using n-type IGTO TFT on p-type Si FET. Reda, S. 3D integration advances computing. Jayachandran, D. et al. Three-dimensional integration of two-dimensional field-effect transistors. Sadaf, M. U. K. et al. Enabling static random-access memory cell scaling with monolithic 3D integration of 2D field-effect transistors. Pendurthi, R. et al. Monolithic three-dimensional integration of complementary two-dimensional field-effect transistors. Ghosh, S. et al. Monolithic and heterogeneous three-dimensional integration of two-dimensional materials with high-density vias. Yang, S. & Cheng, B. in Precision Machining Process and Technology (ed. Yang, S.) 1–43 (Springer Nature Singapore, 2025). Wu, B., Kumar, A. & Pamarthy, S. High aspect ratio silicon etch: a review. Lee, D. H. et al. Low-loss silicon waveguides with sidewall roughness reduction using a SiO2 hard mask and fluorine-based dry etching. Darnon, M. et al. Etching characteristics of TiN used as hard mask in dielectric etch process. Mechanical response of atomic layer deposition alumina coatings on stiff and compliant substrates. Jansen, H., de Boer, M., Burger, J., Legtenberg, R. & Elwenspoek, M. The black silicon method II: the effect of mask material and loading on the reactive ion etching of deep silicon trenches. Honjo, H. et al. Influence of hard mask materials on the magnetic properties of perpendicular MTJs with double CoFeB/MgO interface. Donaton, R. et al. Integration of Cu and low-k dielectrics: effect of hard mask and dry etch on electrical performance of damascene structures. Tang, Y. et al. A hard mask process and alignment device aims to achieve high consistency and mass-scale production of gas sensors based on spraying hydrothermal gas sensing material. Li, Z. et al. Spin-on metal oxide hard mask as underlayer for EUV lithography with chemically amplified resist. Padmanaban, M. et al. Progress in spin-on hard mask materials for advanced lithography. Lee, S. et al. Preparation and analysis of amorphous carbon films deposited from (C6H12)/Ar/He chemistry for application as the dry etch hard mask in the semiconductor manufacturing process. Thin Solid Films 519, 6737–6740 (2011). Schwierz, F., Granzner, R. & Pezoldt, J. Two-dimensional materials and their prospects in transistor electronics. Huang, Y. et al. An innovative way of etching MoS2: characterization and mechanistic investigation. Nano Res. Son, J. et al. Atomically precise graphene etch stops for three dimensional integrated systems from two dimensional material heterostructures. Wood, J. Koepke, and J. Lyding, "Graphene as an etch mask for silicon,". Master's thesis, University of Illinois at Urbana-Champaign. Stehle, Y. Y. et al. Anisotropic etching of hexagonal boron nitride and graphene: question of edge terminations. (in eng). Danielsen, D. R. et al. Super-resolution nanolithography of two-dimensional materials by anisotropic etching. ACS Appl. Söll, A. et al. High-κ wide-gap layered dielectric for two-dimensional van Der Waals heterostructures. ACS Nano 18, 10397–10406 (2024). Abdelwahab, I. et al. Highly efficient sum-frequency generation in niobium oxydichloride NbOCl2 nanosheets. Zeng, Y. et al. 2D FeOCl: a highly in-plane anisotropic antiferromagnetic semiconductor synthesized via temperature-oscillation chemical vapor transport. Zhang, L. et al. Bias voltage driven tunneling magnetoresistance polarity reversal in 2D stripy antiferromagnet CrOCl. Gu, P. et al. Multi-state data storage in a two-dimensional stripy antiferromagnet implemented by magnetoelectric effect. Momma, K. & Izumi, F. VESTA 3 for three-dimensional visualization of crystal, volumetric and morphology data. Ekinci, H., Jahed, N. M. S., Soltani, M. & Cui, B. The role of oxygen on anisotropy in chromium oxide hard mask etching for sub-micron fabrication. Goodwin, M. J., Harteveld, C. A. M., de Boer, M. J. & Vos, W. L. Deep reactive ion etching of cylindrical nanopores in silicon for photonic crystals. Tegen, S. & Moll, P. Etch characteristics of Al2O3 in ICP and MERIE plasma etchers. Gottscho, R. A., Jurgensen, C. W. & Vitkavage, D. J. Microscopic uniformity in plasma etching. Chang, B., Leussink, P., Jensen, F., Hübner, J. & Jansen, H. DREM: infinite etch selectivity and optimized scallop size distribution with conventional photoresists in an adapted multiplexed Bosch DRIE process. Azarnouche, L. et al. Unbiased line width roughness measurements with critical dimension scanning electron microscopy and critical dimension atomic force microscopy. Bunday, B. D. et al. Determination of optimal parameters for CD-SEM measurement of line-edge roughness. Manley, R. G. et al. P-40: glass substrate charging in flat panel display manufacturing. Nimbalkar, P. et al. A review of glass substrate technologies. Banerjee, R. et al. Controllable synthesis of environmentally stable vdW antiferromagnetic oxyhalide CrOCl. Pawbake, A. et al. Magnetic phases and zone-folded phonons in a frustrated van der Waals magnet. ACS Nano 19, 23693–23702 (2025). Giza, M. et al. Contact resistance engineering in WS2-based FET with MoS2 under-contact interlayer: a statistical approach. ACS Appl. Seah, M. P. Summary of ISO/TC 201 Standard: VII ISO 15472: 2001—surface chemical analysis—X-ray photoelectron spectrometers—calibration of energy scales. Interface Anal. We thank S. Miller and G. Lavallee for their discussions and insights on this study. We thank B. Liu for providing valuable suggestions regarding the SEM images taken for this Article. We acknowledge funding support from the NSF under NSF Career (grant no. ECCS-2042154), NSF Fuse (grant no. ECCS-2328741), the ONR (grant no. N00014-24-1-2565) and the ARO (grant no. W911NF-23-1-0279) (all four to S.D.). was supported by ERC-CZ programme (project LL2101) from the Ministry of Education Youth and Sports (MEYS) and by the project Advanced Functional Nanorobots (reg. CZ.02.1.01/0.0/0.0/15_003/0000444 financed by the ERDF). was supported by project LUAUS23049 from MEYS. was supported by project LUAUS23049 from Ministry of Education Youth and Sports (MEYS). acknowledges the assistance provided by the Advanced Multiscale Materials for Key Enabling Technologies project, supported by the Ministry of Education, Youth, and Sports of the Czech Republic, project no. CZ.02.01.01/00/22_008/0004558, co-funded by the European Union. and Y. Y. acknowledge support from the NSF CAREER award (DMR-2145455). These authors contributed equally: Pranavram Venkatram, Ziheng Chen. Engineering Science and Mechanics, Penn State University, University Park, PA, USA Pranavram Venkatram, Ziheng Chen, Krishnendu Mukhopadhyay, Lei Ding, Yang Yang & Saptarshi Das Materials Characterization Lab, Penn State University, University Park, PA, USA Department of Inorganic Chemistry, University of Chemistry and Technology Prague, Prague, Czech Republic Vlastimil Mazanek & Zdenek Sofer Nuclear Engineering, Penn State University, University Park, PA, USA Electrical Engineering, Penn State University, University Park, PA, USA Materials Science and Engineering, Penn State University, University Park, PA, USA Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar Search author on:PubMed Google Scholar conceived the idea. designed the experiments, analysed the data, discussed the results and agreed on their implications. helped with the AFM measurements. grew the CrOCl crystals. performed the STEM characterization and analysis under the supervision of Y.Y. helped with the XPS measurements and analysis. All authors contributed to the preparation of the manuscript. Correspondence to Saptarshi Das. The authors declare no competing interests. Nature Materials thanks Ralu Divan, Aaron Stein and the other, anonymous reviewer(s) for their contribution to the peer review of this work. Peer reviewer reports are available. Publisher's note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations. (a) Optical images of three representative CrOCl flakes selectively etched by masking specific regions to compare surface roughness between protected and exposed areas. (b) Corresponding roughness distributions showing a consistent decrease in surface roughness after etching relative to the pre-etch state. (c) Grouped bar plots of the median roughness for each flake further confirm that surface roughness decreases systematically post-etch, supporting the correlation between etching and surface morphology evolution in CrOCl. (a) Overview of the CrOCl hard mask structure, highlighting both the etched and unetched regions. The vertical yellow dashed line denotes the interface between the two regions, with the unetched region on the left and the etched region on the right. The two horizontal markers indicate the respective heights of the CrOCl hard mask before and after etching. (b-c) High-resolution STEM images of the unetched and etched regions of the CrOCl hard mask, respectively, corresponding to the areas outlined by the two boxes in (a). (d-e) Corresponding STEM-EDX maps acquired from the unetched and etched regions for CrOCl, respectively. (a) Raman spectroscopy, along with corresponding optical microscopy images, was conducted on a FeOCl flake before and after plasma exposure. The results exhibit negligible spectral changes, indicating minimal structural modification. (b) Shows the high-resolution XPS analysis of the Fe 2p and O 1 s core levels, evaluate chemical alterations induced by the plasma process. Additionally, XPS measurements of the F 1 s core level revealed the incorporation of fluorine species, suggesting the formation of non-volatile fluorinated by-products on the flake surface. (c) RMS surface roughness of the FeOCl flake pre- and post-plasma treatment measured by AFM. In contrast to CrOCl, a noticeable increase in surface roughness was observed following plasma exposure. (d) Optical images of three representative FeOCl flakes selectively etched by masking specific regions to compare surface roughness between protected and exposed areas. (e) Corresponding roughness distributions showing a consistent increase in surface roughness after etching relative to the pre-etch state. (f) Grouped bar plots of the median roughness for each flake further confirm that surface roughness increases systematically post-etch, supporting the correlation between etching and surface morphology evolution in FeOCl. (a) Overview of the FeOCl hard-mask structure, highlighting both the etched and unetched regions. The vertical yellow dashed line denotes the interface between the two regions, with the etched region on the left and the unetched region on the right. (b-c) High-resolution STEM images of the etched and unetched regions of the FeOCl hard mask, respectively, corresponding to the areas outlined by the two boxes in (a). (d-e) Corresponding STEM-EDX maps acquired from the etched and unetched regions for FeOCl, respectively. (a–c) demonstrates optical images overlaid with EDX elemental maps (F, O, and Cl for FeOCl; Ti, O, and Cl for TiOCl; Nb, O, and Cl for NbOCl). Corresponding high-resolution AFM measurement reveals the height profile to quantify the etch rates, underscoring FeOCl's comparable plasma resistance to CrOCl and the relatively faster etching of TiOCl and NbOCl. EDX mapping confirms uniform elemental distribution confirming the presence of the respective elements. (a) Cross-sectional STEM images of three representative Si pillars with a depth of ~1.5 μm patterned with CrOCl hard mask. (b–d) Shows the corresponding edges of the boxed regions in (a), across which LER values were extracted. The edge profiles are indicated by the yellow solid lines. (a) SEM image of a representative array of Si pillars capped with the CrOCl hard mask, with the corresponding EDX mapping confirming the presence of Cr and Cl on the pillar tops. (b) After exposure to a Cl2/O2 plasma (plasma process 3) etch for 1 min, the CrOCl mask is completely removed without any visible surface damage or measurable reduction in pillar height, confirming clean mask removal and preservation of the underlying Si structure. Optical and SEM images of the CrOCl mask on a standard 285 nm SiO2/p++-Si substrate with predefined line trench patterns, followed by corresponding optical and SEM images of the same CrOCl mask pattern transferred onto a silicon substrate. (a) Etch rates of CrOCl flakes measured under various industry-relevant chemistries. Roughness distributions corresponding to (b), BCl3/Cl2; (c), CF4/Ar; (d), CHF3/O2; and (e), Cl2/O2 are shown. Overall, CrOCl exhibits greater resistance to fluorine-based plasmas, underscoring its broad applicability as a robust hard mask, while its higher etch rates in chlorine-based chemistries highlight its suitability for precise pattern transfer. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. Reprints and permissions Venkatram, P., Chen, Z., Mukhopadhyay, K. et al. Two-dimensional crystalline hard masks for high-aspect-ratio nanofabrication. Accepted: 30 January 2026 Published: 10 March 2026 Version of record: 10 March 2026 DOI: https://doi.org/10.1038/s41563-026-02524-7 Anyone you share the following link with will be able to read this content: Sorry, a shareable link is not currently available for this article. Provided by the Springer Nature SharedIt content-sharing initiative © 2026 Springer Nature Limited Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.
For many people, noticing this symptom prompts a medical visit that can lead to an early diagnosis of bladder cancer. However, for people with colorblindness, detecting that warning sign may be far more difficult. Because many forms of color vision deficiency make it hard to perceive red tones, blood in urine can go unnoticed. Researchers from Stanford Medicine and collaborating institutions report that missing this early symptom may have serious consequences. After analyzing health records, the team found that people who had both bladder cancer and colorblindness faced a 52% higher mortality rate over 20 years compared with bladder cancer patients who have normal vision. The researchers believe that people with colorblindness may delay seeking care because they fail to recognize blood in their urine. "I'm hopeful that this study raises some awareness, not only for patients with colorblindness, but for our colleagues who see these patients," said Ehsan Rahimy, MD, adjunct clinical associate professor of ophthalmology and senior author of the study published in Nature Health. The study's lead author is Mustafa Fattah, a medical student at Columbia University Vagelos College of Physicians and Surgeons. Colorblindness, also known as color vision deficiency, is more common than many people realize. The most widespread types interfere with distinguishing between red and green shades. This can create everyday challenges such as interpreting traffic lights, coordinating clothing, or judging whether meat is fully cooked. In 2025, roughly 85,000 Americans were expected to receive a bladder cancer diagnosis. Earlier reports and smaller studies had already suggested that colorblindness might delay the diagnosis of certain diseases. Another experiment conducted in 2001 asked participants to identify which images of saliva, urine, and stool contained blood. These earlier findings prompted Rahimy and his colleagues to investigate whether colorblindness might ultimately affect survival in people diagnosed with bladder cancer or colorectal cancer. To explore the question, researchers used a large research platform called TriNetX. "The power in this type of study is the ability to curate a particular population of interest -- in this case, patients who are colorblind who develop bladder cancer or colorectal cancer," Rahimy said. From roughly 100 million U.S. patient records, the researchers identified 135 people diagnosed with both colorblindness and bladder cancer, along with 187 patients who had both colorblindness and colorectal cancer. For each group, the team created a comparable control group of patients with the same cancer diagnosis and similar demographic and health characteristics but with normal vision. "That was our working hypothesis, based on the previous studies," Rahimy said. The researchers expected to observe a similar pattern among people with colorectal cancer. Instead, they found no statistically significant difference in survival between patients with and without colorblindness. One reason may be that colorectal cancer typically presents with several early symptoms. Studies show that nearly two thirds of colorectal cancer patients first report abdominal pain, and more than half notice changes in bowel habits. By contrast, between 80% and 90% of bladder cancer patients initially notice blood in their urine without any pain. Colorectal cancer screening is widely recommended for most people between the ages of 45 and 75, which reduces reliance on noticing blood in stool as the first sign of trouble. Many people with colorblindness never receive a formal diagnosis, which means they would be classified as having normal vision in the database. "Most people with color vision deficiency are typically functioning fine. Many affected individuals may not even know they have it," Rahimy said. When we're seeing certain trends and things that warrant further investigation, they deserve their own more in-depth analyses or studies," Rahimy said. Rahimy said urologists and gastroenterologists, including a colleague who is colorblind, told him they had never considered colorblindness as a possible factor in cancer diagnosis. Some clinicians said they might start including questions about colorblindness in screening questionnaires. Doctors recommend getting a urine test during annual checkups, and some individuals may want to ask a partner or family member for help monitoring changes. "If you don't trust yourself to know that there's a change in the color of your urine, it could be worth having a partner or somebody you live with periodically checking it for blood, just to make sure," Rahimy said. These Tiny Teeth Could Change What We Know About Human Origins Nearly Half of Americans Don't Know This Popular Food Increases Colon Cancer Risk Stay informed with ScienceDaily's free email newsletter, updated daily and weekly. Keep up to date with the latest news from ScienceDaily via social networks: Tell us what you think of ScienceDaily -- we welcome both positive and negative comments.
Dimorphos and its larger partner Didymos are bound together by gravity. "This is a tiny change to the orbit, but given enough time, even a tiny change can grow to a significant deflection," said Thomas Statler, lead scientist for solar system small bodies at NASA Headquarters in Washington. "The team's amazingly precise measurement again validates kinetic impact as a technique for defending Earth against asteroid hazards and shows how a binary asteroid might be deflected by impacting just one member of the pair." When the DART spacecraft struck Dimorphos, it blasted a massive plume of rocky debris into space and reshaped the asteroid, which is about 560 feet (170 meters) wide. Scientists refer to this effect as the momentum enhancement factor. Earlier studies had already shown that the collision shortened Dimorphos' orbit around the larger asteroid Didymos, which measures nearly half a mile across (805 meters), by 33 minutes from its original 12-hour period. Specifically, the system's orbital period changed by about 0.15 seconds. "Over time, such a small change in an asteroid's motion can make the difference between a hazardous object hitting or missing our planet." However, the small shift in orbital speed demonstrates how spacecraft could be used to redirect a threatening asteroid if scientists detect it early enough. In that scenario, a spacecraft would strike the object and slightly alter its velocity. To improve early detection of such threats, NASA is developing the Near-Earth Object (NEO) Surveyor mission. Managed by NASA's Jet Propulsion Laboratory in Southern California, the mission will deploy the first space telescope specifically designed for planetary defense. The telescope will search for difficult to detect near-Earth objects, including dark asteroids and comets that reflect very little visible light. In addition to radar and other ground based observations, they relied on stellar occultations. Observing that momentary disappearance allows scientists to calculate the asteroid's position, speed, and shape with remarkable precision. This often requires multiple observation stations spread miles apart. Researchers depended on volunteer astronomers around the world who recorded 22 stellar occultations between October 2022 and March 2025. "When combined with years of existing ground-based observations, these stellar occultation observations became key in helping us calculate how DART had changed Didymos' orbit," said study co-lead Steve Chesley, a senior research scientist at JPL. "This work is highly weather dependent and often requires travel to remote regions with no guarantee of success. The results suggest that Dimorphos is slightly less dense than previously believed. This finding supports the idea that Dimorphos formed from debris shed by a rapidly spinning Didymos. Over time, the loose rocky material likely gathered together under gravity, creating what scientists call a "rubble pile" asteroid. The DART spacecraft was designed, built, and operated by the Johns Hopkins Applied Physics Laboratory in Laurel, Maryland, for NASA's Planetary Defense Coordination Office. This office leads NASA's work to protect Earth from potential asteroid threats. Note: Content may be edited for style and length. These Tiny Teeth Could Change What We Know About Human Origins Hormone Therapy May Supercharge Popular Weight-Loss Drugs After Menopause Nearly Half of Americans Don't Know This Popular Food Increases Colon Cancer Risk Stay informed with ScienceDaily's free email newsletter, updated daily and weekly. Or view our many newsfeeds in your RSS reader: Keep up to date with the latest news from ScienceDaily via social networks: Tell us what you think of ScienceDaily -- we welcome both positive and negative comments.