铱
质子
催化作用
钌
质子化
质子交换膜燃料电池
膜
无机化学
氧化钌
氧化物
材料科学
Atom(片上系统)
光化学
化学工程
化学
离子
有机化学
生物化学
物理
冶金
量子力学
计算机科学
工程类
嵌入式系统
作者
Jialin Tang,Xinyan Liu,Xiaoxia Xiong,Qisheng Zeng,Yuan Ji,Chunxiao Liu,Jiawei Li,Hongliang Zeng,Yizhou Dai,Xinyan Zhang,Chengbo Li,Hong‐Jie Peng,Qiu Jiang,Tingting Zheng,Chih‐Wen Pao,Chuan Xia
标识
DOI:10.1002/adma.202407394
摘要
Abstract Proton exchange membrane water electrolysers promise to usher in a new era of clean energy, but they remain a formidable obstacle in designing active and durable electrocatalysts for the acidic oxygen evolution reaction (OER). In this study, a protonated iridium oxide embedded with single‐atom dispersed ruthenium atoms (H 3.8 Ir 1− x Ru x O 4 ) that demonstrates exceptional activity and stability in acidic water oxidation is introduced. The single Ru dopants favorably induce localized oxygen vacancies in the Ir─O lattice, synergistically strengthening the adsorption of OOH* intermediates and enhancing the intrinsic OER activity. In addition, the preferential oxidation of Ru and the electronegativity of the oxygen vacancies significantly stabilize the Ir─O active sites, improving the OER stability. Consequently, the H 3.8 Ir 1─ x Ru x O 4 catalyst shows an overpotential of 255 mV at 10 mA cm −2 and displays exceptional catalytic endurance in acidic electrolytes, surpassing 1100 h, representing a remarkable one‐order‐of‐magnitude increase in stability compared to that of pristine H 3.8 IrO 4 . A proton exchange membrane electrolyser utilizing the H 3.8 Ir 1− x Ru x O 4 catalyst as an anode exhibits stable performance for more than 1280 h under a high current density of 2 A cm −2 .
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