环境友好型
电催化剂
材料科学
自愈
分解水
纳米技术
化学工程
催化作用
有机化学
电化学
光催化
电极
化学
生态学
工程类
生物
医学
替代医学
物理化学
病理
作者
Xuan Minh Chau Ta,Thành Trần‐Phú,Thi Kim Anh Nguyen,Qi Wang,Antonio Tricoli
标识
DOI:10.1021/acsami.5c01637
摘要
Electrochemical water splitting under acidic conditions is an efficient route for green hydrogen production from renewable electricity. Its implementation on a globally relevant scale is hindered by the lack of abundant and low-cost electrocatalysts for the oxygen evolution reaction that can operate stably and efficiently under highly acidic anodic conditions. Here, we report the design of stable and efficient acidic OER electrocatalysts consisting of a self-healing bismuth (Bi)-based matrix hosting transition metal active sites. Comprehensive structural performance investigation of Co- and Ni-BiOx electrodes provides insights into the role of the electrolyte composition and pH in the self-healing mechanism under anodic conditions. Our best-performing [Co-Bi]Ox and [Ni-Bi]Ox anodes achieve over 200 h of continuous electrolysis at a catalytic current of 10 mA cm-2 with an overpotential of 590 and 670 mV at a pH of 1 in a 0.1 M H2SO4 electrolyte. Notably, while the [Bi]Ox matrix did not contribute to the catalytic activity, it was essential to stabilize the active Co and Ni sites during the acidic OER. Our findings provide a promising strategy for the engineering of earth-abundant materials for efficient acidic water splitting, as an alternative to the use of poorly scalable and expensive noble metal catalysts.
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