ZnCoNiS nanoflowers electrodes with rich heterointerface as efficient bifunctional electrocatalyst for overall water splitting

被引:7
|
作者
Li, Peiyan [1 ]
Zhang, Li [1 ,2 ]
Yao, Yong [1 ]
Xie, Tao [1 ]
Du, Wene [1 ]
Zhao, Ting [1 ]
Jiang, Jiahui [1 ]
机构
[1] Xinjiang Univ, Coll Chem, State Key Lab Chem & Utilizat Carbon Based Energy, Urumqi 830017, Xinjiang, Peoples R China
[2] Xinjiang Univ, Coll Chem Engn, State Key Lab Chem & Utilizat Carbon Based Energy, Urumqi 830017, Xinjiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Multiphase heterostructure; ZnCoNiS nanoflowers; MOF; Overall water splitting; METAL-ORGANIC FRAMEWORKS; NICKEL FOAM; HIGHLY EFFICIENT; SULFIDE NANOSHEETS; OXYGEN REDUCTION; ENERGY-STORAGE; IRON SULFIDE; HETEROSTRUCTURES; NANOSTRUCTURES;
D O I
10.1016/j.ijhydene.2023.07.353
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
Constructing heterojunction nanocomposites is promising for overall water splitting. Herein, the metal-organic frameworks (MOFs) derived multiphasic transition metal sulfide nanoflowers heterostructure electrode (ZnCoNiS) was synthesized by the hydrothermal and sulfuration methods. The nanoflowers structure can provide a large electrochemical active surface area and the abundant heterogeneous interfaces are beneficial to increase the synergy between different components to improve the kinetic energy of the reaction. The obtained ZnCoNiS shows outstanding electrocatalytic performance with low over -potentials of 134 mV for the oxygen evolution reaction (OER) and 146 mV for hydrogen evolution reaction (HER) at 10 mA cm-2. Impressively, the ZnCoNiS catalyst exhibits remarkable overall water-splitting performances with a cell voltage of 1.52 Vat 10 mA cm-2 and excellent stability in catalysis for over 100 h. This study demonstrates an approach for the design of rich heterogeneous junctions with high activity and stability, which can be used in the fields of solar energy to drive water splitting for hydrogen production.(c) 2023 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1521 / 1533
页数:13
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