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表面硫掺杂的纳米结构RuO及其对高效全海水分解的阴离子钝化作用

Surface S-Doped Nanostructured RuO and Its Anion Passivating Effect for Efficient Overall Seawater Splitting.

作者信息

Liu Yu, Wu Lu, Wang Yong, Shen Le-Wei, Tian Ge, Cui Lianmeng, Qin Ling, Zhou Liang, Zhang Yuexing, Rosei Federico, Yang Xiao-Yu

机构信息

State Key Laboratory of Silicate Materials for Architectures & State Key Laboratory of Advanced Technology for Materials Synthesis and Processing & School of Chemistry, Chemical Engineering and Life Sciences & Laoshan Laboratory & School of Materials Science and Engineering & International School of Materials Science and Engineering, Wuhan University of Technology, Wuhan 430070, China.

National energy key laboratory for new hydrogen-ammonia energy technologies, Foshan Xianhu Laboratory, Foshan 528200, China.

出版信息

ACS Nano. 2025 Jan 21;19(2):2715-2725. doi: 10.1021/acsnano.4c14851. Epub 2025 Jan 9.

Abstract

Electrolysis of seawater for hydrogen (H) production to harvest clean energy is an appealing approach. In this context, there is an urgent need for catalysts with high activity and durability. RuO electrocatalysts have shown efficient activity in the hydrogen and oxygen evolution reactions (HER and OER), but they still suffer from poor stability. Herein, surface S-doped nanostructured RuO (S-RuO) is rationally fabricated for efficient overall seawater splitting. Doping with S enhances the activity (overpotentials of 25 mV for the HER and 243 mV for the OER), long-term durability (1000 h at 100 mA cm), and achieves nearly 100% Faraday efficiency (FE). Moreover, the S-RuO-based anion exchange membrane seawater electrolyzer requires 2.01 V to reach 1.0 A cm under demanding industrial conditions. Experimental analysis and theoretical calculations indicate that surface S introduction could lower the valence state of Ru, thereby conferring enhanced activity and stability. Furthermore, the nanostructured S-RuO electrocatalyst is highly protected by the S-doped surface, which repels Cl in alkaline seawater. This investigation presents a feasible strategy for designing RuO-based seawater splitting catalysts with both high performance and good resistance to anodic corrosion.

摘要

通过电解海水制氢以获取清洁能源是一种很有吸引力的方法。在此背景下,迫切需要具有高活性和耐久性的催化剂。RuO 电催化剂在析氢反应(HER)和析氧反应(OER)中表现出高效活性,但稳定性仍然较差。在此,通过合理制备表面 S 掺杂的纳米结构 RuO(S-RuO)来实现高效的全海水分解。S 掺杂提高了活性(HER 的过电位为 25 mV,OER 的过电位为 243 mV)、长期耐久性(在 100 mA cm²下可达 1000 h),并实现了近 100%的法拉第效率(FE)。此外,基于 S-RuO 的阴离子交换膜海水电解槽在苛刻的工业条件下达到 1.0 A cm²需要 2.01 V。实验分析和理论计算表明,表面引入 S 可以降低 Ru 的价态,从而赋予增强的活性和稳定性。此外,纳米结构的 S-RuO 电催化剂受到 S 掺杂表面的高度保护,该表面可排斥碱性海水中的 Cl⁻。本研究提出了一种设计兼具高性能和良好抗阳极腐蚀性能的基于 RuO 的海水分解催化剂的可行策略。

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