Sputter-Deposited High Entropy Alloy Thin Film Electrocatalyst for Enhanced Oxygen Evolution Reaction Performance

被引:34
作者
Li, Siang-Yun [1 ]
Nguyen, Thi Xuyen [2 ]
Su, Yen-Hsun [2 ]
Lin, Chia-Chun [2 ]
Huang, Yan-Jia [2 ]
Shen, Yun-Hwei [1 ]
Liu, Chuan-Pu [2 ]
Ruan, Jr-Jeng [2 ]
Chang, Kao-Shuo [2 ]
Ting, Jyh-Ming [2 ,3 ]
机构
[1] Natl Cheng Kung Univ, Dept Resources Engn, 1 Univ Rd, Tainan 70101, Taiwan
[2] Natl Cheng Kung Univ, Dept Mat Sci & Engn, 1 Univ Rd, Tainan 70101, Taiwan
[3] Natl Cheng Kung Univ, Hierarch Green Energy Mat Res Ctr, Tainan 70101, Taiwan
关键词
high entropy alloys; oxygen evolution reaction; surface electronic structure; thin films; EFFICIENT ELECTROCATALYSTS; XPS SPECTRA; OXIDE; METAL; NANOPARTICLES; SPINEL; CARBON; SITES; OER;
D O I
10.1002/smll.202106127
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Thin film catalysts, giving a different morphology, provide a significant advantage over catalyst particles for the gas evolution reaction. Taking the advantages of sputter deposition, a high entropy alloy (HEA) thin film electrocatalyst is hereby reported for the oxygen evolution reaction (OER). The catalyst characteristics are investigated not only in its as-deposited state, but also during and after the OER. For comparison, unary, binary, ternary, and quaternary thin film catalysts are prepared and characterized. The surface electronic structure modification due to the addition of a metal is studied experimentally and theoretically using density functional theory calculation. It is demonstrated that sputtered FeNiMoCrAl HEA thin film exhibits OER performance superior to all the reported HEA catalysts with robust electrocatalytic activity having a low overpotential of 220 mV at 10 mA cm(-2), and excellent electrochemical stability at different constant current densities of 10 and 100 mA cm(-2) for 50 h. Furthermore, the microstructure transformation is investigated during the OER, which is important for the understanding of the OER mechanism provided by HEA electrocatalyst. Such a finding will contribute to future catalyst design.
引用
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页数:11
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