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作 者:Xueting Cao Yikun Kang Tao Jiang Zhe Chen Yaming Hao Shuangshuang Cha Wei Du Yefei Li Ming Gong
出 处:《Nano Research》2025年第4期601-609,共9页纳米研究(英文版)
基 金:supported by the National Natural Science Foundation of China(No.22172036);the Fundamental Research Funds for the Central Universities(No.20720220011).
摘 要:Stable oxygen evolution reaction(OER)catalyst alternatives to the precious IrO_(2) catalysts are of great importance to the next-generation proton-exchange membrane(PEM)electrolyzers.RuO_(2)-based materials are promising candidates but suffer from low stability under highly anodic potentials.Here,we reported a facet-selective etching strategy to improve the stability of polycrystalline RuO_(2) without significantly affecting the activity.The selective etching was enabled by the specific chemisorption of pyridazine(pyd)with contingent N atoms onto the RuO_(2) surface.The pyd-RuO_(2) catalyst,after etching,exhibited a low overpotential 247 mV at 100 mA·cm^(-2) and obvious stability improvement of over 200 h at 100 mA·cm^(-2) with only 0.63% Ru loss in acidic conditions.Combining various characterization techniques and theoretical calculations,we revealed that the crystalline RuO_(2)(110)facet is favorably etched by the coordination of pyridazine while protecting other surfaces,which significantly enriches the RuO_(2)(110)facets toward higher OER stability via the dynamic dissolution and repair mechanism in the ordered manner.This study offers alternative perspectives on the dissolution and stability mechanism of RuO_(2) and the facet-selective modulation of nanocrystals by ligand-driven etching.
关 键 词:ruthenium dioxide oxygen evolution reaction stability PYRIDAZINE facet-selective etching
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