Electrodeposited crystalline-amorphous Ni-Ni(OH)2 electrocatalysts for efficient hydrogen evolution via alkaline water splitting

被引:11
|
作者
Zhang, Weiying [1 ]
Yin, Qing [1 ]
Zhang, Yizhe [1 ]
Peng, Shaoqin [1 ]
Li, Yuexiang [1 ]
机构
[1] Nanchang Univ, Sch Chem & Chem Engn, Nanchang 330031, Peoples R China
基金
中国国家自然科学基金;
关键词
Electrodeposition; Crystalline-amorphous; Ni-Ni(OH) 2 heterostructure; Synergistic effect; Hydrogen evolution reaction; NICKEL FOAM; NI(OH)(2); NANOSHEETS; CATALYSTS; ARRAYS; CU;
D O I
10.1016/j.jallcom.2023.169727
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 electrocatalysts with crystalline-amorphous heterostructures have garnered particular attention owing to the pronounced synergistic effect between a crystalline phase with high electrical conductivity and an amorphous phase with abundant catalytic active sites. Herein, we construct crystallineamorphous Ni-Ni(OH)2 hybrids via a facile electrodeposition approach for efficient alkaline hydrogen evolution reaction (HER). The Ni-Ni(OH)2 heterostructures are directly electrodeposited on the surface of Cu nanowires (NWs) in-situ grown on Cu foam with a well-maintained nanowire morphology. The Cu NWs on Cu foam substrate provide a three-dimensional structure, and enable efficient electron transportation to the Ni-Ni(OH)2 sites. Moreover, in the crystalline-amorphous Ni-Ni(OH)2 heterostructures, amorphous Ni(OH)2 nanosheets accelerate the water dissociation, while crystalline Ni active sites promote the formation and combination of adsorbed hydrogen atoms. Such a promising synergistic effect leads to the enhanced HER performance with low overpotentials of 73 and 336 mV at the current densities of 10 and 100 mA cm-2, respectively, and a small Tafel slope of 33 mV dec-1. In addition, the integrated structure enables the Ni-Ni (OH)2 electrode with a durable stability of 35 mA cm-2 for 100 h. This work offers an effective approach to construct crystalline-amorphous materials for efficient alkaline HER. (c) 2023 Elsevier B.V. All rights reserved.
引用
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页数:9
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