铱
析氧
密度泛函理论
催化作用
氮化物
材料科学
电解质
电催化剂
过渡金属
电化学
化学工程
金属
无机化学
化学
化学物理
纳米技术
物理化学
计算化学
电极
冶金
生物化学
图层(电子)
工程类
作者
Brian M. Tackett,Wenchao Sheng,Shyam Kattel,Siyu Yao,Binhang Yan,Kurian A. Kuttiyiel,Qiyuan Wu,Jingguang G. Chen
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2018-02-16
卷期号:8 (3): 2615-2621
被引量:140
标识
DOI:10.1021/acscatal.7b04410
摘要
The oxygen evolution reaction (OER) has broad applications in electrochemical devices, but it often requires expensive and scarce Ir-based catalysts in acid electrolyte. Presented here is a framework to reduce Ir loading by combining core–shell iridium/metal nitride morphologies using in situ experiments and density functional theory (DFT) calculations. Several group VIII transition metal (Fe, Co, and Ni) nitrides are studied as core materials, with Ir/Fe4N core–shell particles showing enhancement in both OER activity and stability. In situ X-ray absorption fine structure measurements are used to determine the structure and stability of the core–shell catalysts under OER conditions. DFT calculations are used to demonstrate adsorbate binding energies as descriptors of the observed activity trends.
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