CoS nanowires mediated by superionic conductor Ag2S for boosted oxygen evolution

被引:29
作者
Cheng, Shiqing [1 ]
Zhang, Rongxian [1 ]
Zhu, Wenjuan [2 ]
Ke, Wentao [1 ]
Li, Eryan [2 ]
机构
[1] Jiangsu Univ, Sch Chem & Chem Engn, Zhenjiang 212013, Jiangsu, Peoples R China
[2] Hefei Normal Univ, Sch Chem & Chem Engn, Hefei 230601, Peoples R China
基金
中国国家自然科学基金;
关键词
Oxygen evolution reaction; Catalysis; Silver sulfide; Cobalt sulfide; REDUCED GRAPHENE OXIDE; BIFUNCTIONAL ELECTROCATALYST; EFFICIENT ELECTROCATALYST; AIR ELECTRODE; POROUS CARBON; NICKEL FOAM; CATALYST; NANOSTRUCTURES; NANOCRYSTALS; FABRICATION;
D O I
10.1016/j.apsusc.2020.146106
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
Oxygen evolution reaction (OER) is an important semi-reaction involved in water splitting and metal-air battery devices. Considering the high activity of CoS for OER and the superionic conductor characteristics of Ag2S, Co-Ag sulfide catalyst was synthesized by a simple solvothermal method. Small amounts of Ag2S species in the reaction system mediates the formation of CoS nanowires, which is in contrast to irregular particles obtained without Ag2S. Ag2S species with superionic conductor characteristics acing as a catalyst induces the growth of CoS nanowires via a non-typical solution-liquid-solid mechanism. The thus formed Ag+ mediated CoS nanowires show improved electrical conductivity and prominent catalytic activity, and only requires an overpotential of 293 mV to provide a current density of 10 mA cm(-2) with Tafel slope of 55.3 dec(-1). In addition, the catalytic activity can maintain in the i-t WA for at least 30 h. The derivation of this OER catalyst after OER operation was examined, which indicates that Ag- and S- codoped CoOOH is formed on the catalyst surface after OER operation that acts as catalytic active phase for OER.
引用
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页数:10
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