过电位
析氧
分解水
碳纤维
化学
化学工程
材料科学
催化作用
纳米技术
物理化学
电极
光催化
电化学
有机化学
复合材料
复合数
工程类
作者
Juan Wang,Chen Cheng,Qi Yuan,Hao Yang,Fanqi Meng,Qinghua Zhang,Lin Gu,Jianlei Cao,Leigang Li,Shu‐Chih Haw,Qi Shao,Liang Zhang,Tao Cheng,Feng Jiao,Xiaoqing Huang
出处
期刊:Chem
[Elsevier]
日期:2022-06-01
卷期号:8 (6): 1673-1687
被引量:76
标识
DOI:10.1016/j.chempr.2022.02.003
摘要
Summary
Oxygen evolution reaction (OER) plays a critical role in energy conversion technologies. Significant progress has been made in alkaline conditions. In contrast, it remains a challenge to develop stable OER electrocatalysts in acidic conditions. Herein, we report a new strategy to stabilize RuO2 by introducing interstitial carbon (C-RuO2-RuSe), where the optimized C-RuO2-RuSe-5 exhibits a low overpotential of 212, 259, and 294 mV to reach a current density of 10, 50, and 100 mA cm−2, respectively. More importantly, C-RuO2-RuSe-10 has long-term stability of up to 50 h, representing one of the most stable OER electrocatalysts. X-ray absorption spectroscopy reveals that the Ru–O bonds have been elongated due to the formation of interstitial C. Theoretical calculations show that the elongated Ru–O bonds in RuO2 enhance its stability and reduce energy barriers for OER. This work provides a new perspective for designing and constructing efficient Ru-based electrocatalysts for water splitting.
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