Recent advances and future prospects on Ni3S2-Based electrocatalysts for efficient alkaline water electrolysis

被引:50
作者
Wang, Shiwen [1 ]
Geng, Zhen [1 ]
Bi, Songhu [1 ]
Wang, Yuwei [1 ]
Gao, Zijian [1 ]
Jin, Liming [1 ]
Zhang, Cunman [1 ]
机构
[1] Tongji Univ, Clean Energy Automot Engn Ctr, Sch Automot Studies, Shanghai 201804, Peoples R China
关键词
Alkaline water electrolysis; Hydrogen; Electrocatalysts; STABLE BIFUNCTIONAL ELECTROCATALYSTS; HYDROGEN EVOLUTION ACTIVITY; LAYERED DOUBLE HYDROXIDES; NI3S2 NANOSHEET ARRAY; ONE-STEP SYNTHESIS; OXYGEN-EVOLUTION; HIGHLY EFFICIENT; NICKEL FOAM; NI FOAM; NANOWIRE ARRAYS;
D O I
10.1016/j.gee.2023.02.011
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
Green hydrogen (H2) produced by renewable energy powered alkaline water electrolysis is a promising alternative to fossil fuels due to its high energy density with zero -carbon emissions. However, efficient and economic H2 production by alkaline water electrolysis is hindered by the sluggish hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). Therefore, it is imperative to design and fabricate high -active and low-cost non -precious metal catalysts to improve the HER and OER performance, which affects the energy efficiency of alkaline water electrolysis. Ni3S2 with the heazlewoodite structure is a potential electrocatalyst with near -metal conductivity due to the Ni-Ni metal network. Here, the review comprehensively presents the recent progress of Ni3S2-based electrocatalysts for alkaline water electrocatalysis. Herein, the HER and OER mechanisms, performance evaluation criteria, preparation methods, and strategies for performance improvement of Ni3S2-based electrocatalysts are discussed. The challenges and perspectives are also analyzed. (c) 2023 Institute of Process Engineering, Chinese Academy of Sciences. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co., Ltd. This is an open access article under the CC BY -NC -ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:659 / 683
页数:25
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