High-Entropy Metal Sulfide Nanoparticles Promise High-Performance Oxygen Evolution Reaction

被引:343
|
作者
Cui, Mingjin [1 ]
Yang, Chunpeng [1 ]
Li, Boyang [2 ]
Dong, Qi [1 ]
Wu, Meiling [1 ]
Hwang, Sooyeon [3 ]
Xie, Hua [1 ]
Wang, Xizheng [1 ]
Wang, Guofeng [2 ]
Hu, Liangbing [1 ]
机构
[1] Univ Maryland, Dept Mat Sci & Engn, College Pk, MD 20742 USA
[2] Univ Pittsburgh, Dept Mech Engn & Mat Sci, Pittsburgh, PA 15261 USA
[3] Brookhaven Natl Lab, Ctr Funct Nanomat, Upton, NY 11973 USA
基金
美国国家科学基金会;
关键词
catalytic stability; high‐ entropy; oxygen evolution reaction; synergistic effect; transition‐ metal sulfide nanoparticles; BIFUNCTIONAL ELECTROCATALYST; WATER OXIDATION; EFFICIENT; HYDROGEN; CATALYST; NANOSHEETS;
D O I
10.1002/aenm.202002887
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Transition metal sulfides with a multi-elemental nature represent a class of promising catalysts for oxygen evolution reaction (OER) owing to their good catalytic activity. However, their synthesis remains a challenge due to the thermodynamic immiscibility of the constituent multimetallic elements in a sulfide structure. Herein, for the first time the synthesis of high-entropy metal sulfide (HEMS, i.e., (CrMnFeCoNi)S-x) solid solution nanoparticles is reported. Computational and X-ray photoelectron spectroscopy analysis suggest that the (CrMnFeCoNi)S-x exhibits a synergistic effect among metal atoms that leads to desired electronic states to enhance OER activity. The (CrMnFeCoNi)S-x nanoparticles show one of the best activities (low overpotential 295 mV at 100 mA cm(-2) in 1 m KOH solution) and good durability (only slight polarization after 10 h by chronopotentiometry) compared with their unary, binary, ternary, and quaternary sulfide counterparts. This work opens up a new synthesis paradigm for high-entropy compound nanoparticles for highly efficient electrocatalysis applications.
引用
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页数:8
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