期刊
ACS CATALYSIS
卷 8, 期 3, 页码 2615-+出版社
AMER CHEMICAL SOC
DOI: 10.1021/acscatal.7b04410
关键词
acidic OER; core-shell particle; density functional theory; electrocatalysis; X-ray absorption spectroscopy
资金
- U.S. Department of Energy [DE-FG02-13ER16381]
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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