过电位
析氧
电催化剂
催化作用
电解水
电解
无机化学
氧气
材料科学
化学
分解水
化学工程
离子
降级(电信)
反应机理
离子交换
碳纤维
动力学
碱度
兴奋剂
反应中间体
八面体
化学动力学
过渡金属
电极
质子交换膜燃料电池
碱性水电解
作者
Zhiang Hu,Jingkun Yu,Jiangwei Chang,Jiangwei Chang,Han Wu,Hongxiang Wei,G A Waterhouse,Xue Yong,Zhiyong Tang,Junbiao Chang,Junbiao Chang,Siyu Lu
摘要
ABSTRACT The sluggish kinetics of alkaline oxygen evolution reaction (OER), together with the highly polarizing conditions at industrial‐level ampere‐scale current densities, which cause catalyst instability, motivate the search for new approaches to break the challenging activity‐stability trade‐off. Herein, we demonstrate that atomic carbon doping into the octahedral voids of Fe 2 O 3 ultrathin nanosheets (C‐Fe 2 O 3 UNSs) with constructed Fe oh III– O–Fe oh III synergistic centers can modify the coverage of * OH intermediates and allow direct * O– * O radical coupling. This enables both structural and catalytic stabilization, as confirmed by operando spectroscopic measurements and density‐functional theory calculations, with an overpotential of 227 mV to achieve 500 mA cm −2 along with 4500‐h durability. When applying C‐Fe 2 O 3 UNSs in an anion exchange membrane water electrolyzer, it delivers a cell voltage of 1.72 V at 1.5 A cm −2 while operating for 2800 h from 1 to 5 A cm −2 , with a degradation rate of 3.05 mV kh −1 at 3 A cm −2 .
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