铱
析氧
过电位
催化作用
分解水
交换电流密度
密度泛函理论
无机化学
电解
电催化剂
材料科学
化学
电解质
物理化学
电化学
电极
计算化学
光催化
有机化学
塔菲尔方程
作者
Hongyan Hu,Shilong Liu,Hongfei Sun,Wenli Sun,Jian Tang,Lingzhi Wei,Xiaowei Chen,Qianwang Chen,Yichao Lin,Ziqi Tian,Jianwei Su
出处
期刊:Small
[Wiley]
日期:2025-04-03
卷期号:21 (21): e2412096-e2412096
被引量:11
标识
DOI:10.1002/smll.202412096
摘要
Iridium (Ir)-based materials are the most widely used oxygen evolution reaction (OER) electrocatalysts in proton exchange membrane water electrolysis (PEMWE). However, their commercial application suffers from high cost and insufficient activity. To optimize the atom utilization efficiency of Ir, the aim is to engineer and develop a rutile-structured solid solution catalyst with minimal Ir content, which is identified through a phase boundary. Here, Ir0.10Mn0.90O2 represents the lowest Ir content in the desired IrO2-MnO2 solid solution. The Ir0.10Mn0.90O2 catalyst exhibits outstanding OER performance in acidic electrolytes, reaching a remarkable mass activity of 1135 A g-1 Ir at an overpotential of 300 mV, which is ≈50 times higher than that of a commercial IrO2 catalyst. Additionally, it demonstrates excellent stability at a current density of 200 mA cm-2 over 120 h during PEMWE operations. Density functional theory (DFT) calculations indicate that the hydroxylation process can be efficiently promoted by the electron-withdrawing on Ir sites in Ir0.10Mn0.90O2, contributing to the enhancement of OER activity.
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