Interface engineering of NiMoSx heterostructure nanorods for efficient oxygen evolution reaction

被引:15
作者
Mao, Xiaoqing [1 ]
Shen, Pei Kang [1 ]
机构
[1] Guangxi Univ, Collaborat Innovat Ctr Sustainable Energy Mat, Sch Chem & Chem Engn, Nanning 530004, Peoples R China
关键词
Oxygen evolution reaction; Sulfide; Heterostructure; Interface engineering; Water splitting; HYDROGEN EVOLUTION; FACILE SYNTHESIS; ELECTROCATALYSTS; OXIDATION; CATALYSTS; HETEROINTERFACES; NANOPARTICLES; FABRICATION; REDUCTION; SULFIDE;
D O I
10.1016/j.jcis.2022.07.157
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
The development of electrocatalyst with efficient and stability for water oxidation is the key to enhance the efficiency of water electrolysis. Interface engineering can modify the local electronic structure of active sites, which is one of the important strategy to enhance catalytic activity. Herein, we synthesized NiMoSx heterostructure nanorods by simple hydrothermal method. The self supporting electrode of NiMoSx heterostructure nanorods grown in situ on nickel foam can reduce the indirect contact resistance between the substrate and the catalyst, and promote the timely release of bubbles produced by the oxygen evolution reaction. The heterogeneous interface in NiMoSx can provide abundant electroactive centers and optimize the adsorption energy of active intermediates. NiMoSx heterostructure nanorods showed excellent oxygen evolution catalytic activity (g100 = 279 mV, g1000 = 436 mV, Tafel slope b = 72.3 mV dec-1) and more than 200 hours of sustainable durability in 1 M KOH. When NiMoSx heterostructure nanorods are used as anode materials for water electrolysis, the electrolytic cell could obtain 10 mA cm-2 at 1.48 V. The current research results not only show that NiMoSx nanostructure is an excellent oxygen evolution electrocatalyst, At the same time, it also provides a valuable interface regulation method for the design of high-performance heterostructure electrocatalyst.@2022 Elsevier Inc. All rights reserved.
引用
收藏
页码:513 / 523
页数:11
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