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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.
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