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用于碱性氢氧化电催化的RuS活性位点的激活与识别

Activating and Identifying the Active Site of RuS for Alkaline Hydrogen Oxidation Electrocatalysis.

作者信息

Yang Chaoyi, Yue Jianchao, Wang Guangqin, Luo Wei

机构信息

College of Chemistry and Molecular Sciences, Wuhan University, 430072, Wuhan, Hubei, P. R. China.

出版信息

Angew Chem Int Ed Engl. 2024 Apr 22;63(17):e202401453. doi: 10.1002/anie.202401453. Epub 2024 Feb 29.

DOI:10.1002/anie.202401453
PMID:38366202
Abstract

Searching for highly efficient and economical electrocatalysts for alkaline hydrogen oxidation reaction (HOR) is crucial for the development of alkaline polymer membrane fuel cells. Here, we report a valid strategy to active pyrite-type RuS for alkaline HOR electrocatalysis by introducing sulfur vacancies. The obtained S-vacancies modified RuS exhibits outperformed HOR activity with a current density of 0.676 mA cm and mass activity of 1.43 mA μg, which are 15-fold and 40-fold improvement than those of Ru catalyst. In situ Raman spectra demonstrate the formation of S-H bond during the HOR process, identifying the S atom of RuS is the real active site for HOR catalysis. Density functional theory calculations and experimental results including in situ surface-enhanced infrared absorption spectroscopy suggest the introduction of S vacancies can rationally modify the p orbital of S atoms, leading to enhanced binding strength between the S sites and H atoms on the surface of RuS, together with the promoted connectivity of hydrogen-bonding network and lowered water formation energy, contributes to the enhanced HOR performance.

摘要

寻找用于碱性氢氧化反应(HOR)的高效且经济的电催化剂对于碱性聚合物膜燃料电池的发展至关重要。在此,我们报告了一种通过引入硫空位来活化黄铁矿型RuS用于碱性HOR电催化的有效策略。所获得的硫空位修饰的RuS表现出优异的HOR活性,电流密度为0.676 mA cm,质量活性为1.43 mA μg,分别比Ru催化剂提高了15倍和40倍。原位拉曼光谱表明在HOR过程中形成了S-H键,确定RuS的S原子是HOR催化的真正活性位点。密度泛函理论计算以及包括原位表面增强红外吸收光谱在内的实验结果表明,硫空位的引入可以合理地修饰S原子的p轨道,导致RuS表面S位点与H原子之间的结合强度增强,同时氢键网络的连通性得到促进且水生成能降低,这有助于提高HOR性能。

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