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硫介导的从锇纳米晶体到单原子的转变用于高效碱性析氢反应。

Sulfur-mediated transformation from osmium nanocrystals to single atoms for efficient alkaline hydrogen evolution reaction.

作者信息

Xue Wendan, Zhou Qixing, Wang Pengfei, Zuo Sijin, Li Fengxiang, Jiang Jiwei, Mo Fan, Yin Chuan, Liu Gaolei, Ban Zhan, Wei Yuanyuan, An Wen, Huang Xiulin, Wang Hui, Zhan Sihui

机构信息

Key Laboratory of Pollution Processes and Environmental Criteria (Ministry of Education), Carbon Neutrality Interdisciplinary Science Centre/College of Environmental Science and Engineering, Nankai University, Tianjin 300071, China.

State of Key Laboratory of Natural Medicines School of Engineering, China Pharmaceutical University, Nanjing 210009, China.

出版信息

Proc Natl Acad Sci U S A. 2025 Jul 8;122(27):e2426207122. doi: 10.1073/pnas.2426207122. Epub 2025 Jul 2.

Abstract

Osmium (Os)-based catalysts, recognized for their unique chemical and electronic properties along with cost-effectiveness, hold great potential for the hydrogen evolution reaction (HER). However, their practical application has long been limited because pure Os exhibits excessively strong adsorption of intermediates and suffers from stability issues. Herein, we report the development of a highly stable catalyst achieved by implanting the sulfur (S) atom into the matrix, facilitating the transformation of Os nanocrystals into Os single atoms. The prepared atomically dispersed Os catalyst (Os-SA@SNC) demonstrates outstanding catalytic activity, requiring only a 13 mV overpotential to achieve a current density of 10 mA cm in 1.0 M potassium hydroxide (KOH) solution, as well as the excellent durability. This performance surpasses that of commercial Pt/C and outperforms most of the reported state-of-the-art electrocatalysts. Theoretical simulations clarify the important role of S atoms in promoting the dispersion and diffusion of Os atoms. Moreover, density functional theory calculations indicate that S atoms adjust the local electronic structure of Os active sites, further facilitating the adsorption/dissociation of HO and optimizing the hydrogen adsorption free energy (ΔG), thereby accelerating the kinetics of both the Volmer and Heyrovsky steps in alkaline HER. This work revitalizes Os-based catalysts for energy conversion and paves the way for innovative HER catalyst design and application to contaminated soil/water remediation.

摘要

锇(Os)基催化剂因其独特的化学和电子性质以及成本效益而受到认可,在析氢反应(HER)中具有巨大潜力。然而,由于纯Os对中间体表现出过强的吸附作用且存在稳定性问题,其实际应用长期以来受到限制。在此,我们报道了一种通过将硫(S)原子植入基体而制备的高稳定性催化剂,该催化剂促使Os纳米晶体转变为Os单原子。所制备的原子分散的Os催化剂(Os-SA@SNC)表现出出色的催化活性,在1.0 M氢氧化钾(KOH)溶液中,仅需13 mV的过电位就能达到10 mA cm的电流密度,并且具有优异的耐久性。这一性能超过了商业Pt/C,优于大多数已报道的先进电催化剂。理论模拟阐明了S原子在促进Os原子分散和扩散方面的重要作用。此外,密度泛函理论计算表明,S原子调整了Os活性位点的局部电子结构,进一步促进了HO的吸附/解离并优化了氢吸附自由能(ΔG),从而加速了碱性HER中Volmer和Heyrovsky步骤的动力学。这项工作为基于Os的能量转换催化剂注入了新活力,并为创新的HER催化剂设计以及应用于污染土壤/水修复铺平了道路。

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本文引用的文献

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