Rose-like Cu-doped Ni3S2 nanoflowers decorated with thin NiFe LDH nanosheets for high-efficiency overall water and urea electrolysis

被引:58
作者
Ding, Yangyang [1 ]
Du, Xiaoqiang [1 ]
Zhang, Xiaoshuang [2 ]
机构
[1] North Univ China, Sch Chem Engn & Technol, Taiyuan 030051, Peoples R China
[2] North Univ China, Sch Sci, Taiyuan 030051, Peoples R China
关键词
Water electrolysis; Urea electrolysis; Structure-function relationship; Transition metal sulfides; Layered double hydroxides; HYDROGEN-PRODUCTION; EARTH-ABUNDANT; ELECTROCATALYSTS; EVOLUTION; OXIDATION; ARRAYS; PHOTOLYSIS; SULFIDE;
D O I
10.1016/j.apsusc.2022.152622
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
Water electrolysis is a promising way to produce green hydrogen energy but still limited by the sluggish anodic oxidation kinetics. Herein, we firstly introduced a multifunctional electrocatalyst of rose-like Cu-doped Ni3S2 nanoflowers decorated with thin NiFe LDH nanosheets (Cu-Ni3S2@NiFe LDH) with excellent hydrogen evolution reaction (HER), oxygen evolution reaction (OER) and water electrolysis performance. More impressively, CuNi3S2@NiFe LDH-200 target catalyst shows the huge potential to replace the slow OER with urea electrolysis when it is used to catalyze urea oxidation reaction (UOR). In addition, the structure-function relationship of material was highlighted and the performance of target catalyst was well revealed by analyzing the growth law of NiFe LDH on Cu-doped Ni3S(2). It's worth noting that Cu-Ni3S(2)@NiFe LDH-100 performs well for HER, while Cu-Ni3S2@NiFe LDH-200 stands out for OER and UOR. The resulting Cu-Ni3S2@NiFe LDH-200(+)//Cu-Ni3S2@NiFe LDH-100(-) electrode couple only requires 1.502 V and 1.413 V to deliver the same current density of 10 mA cm-2 for water electrolysis and urea electrolysis and catalyzed stably for over 20 h, which is one of the best catalytic activities reported so far. Our work will open a new idea to enhance the catalytic activity and stability of transition metal sulfides with layered double hydroxides.
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页数:13
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