Synergy of Cobalt Iron Tetrathiomolybdate Coated on Cobalt Iron Carbonate Hydroxide Hydrate Nanowire Arrays for Overall Water Splitting

被引:11
|
作者
Zhao, Jinxiu [1 ,2 ]
Ren, Xiang [1 ,2 ]
Su, Xu [1 ,2 ]
Zhang, Yong [1 ,2 ]
Yan, Tao [3 ]
Wei, Qin [1 ,2 ]
Wu, Dan [1 ,2 ]
机构
[1] Univ Jinan, Sch Chem & Chem Engn, Collaborat Innovat Ctr Green Chem Mfg & Accurate, Jinan 250022, Shandong, Peoples R China
[2] Univ Jinan, Sch Chem & Chem Engn, Key Lab Interfacial React & Sensing Anal Univ Sha, Jinan 250022, Shandong, Peoples R China
[3] Univ Jinan, Sch Water Conservancy & Environm, Jinan 250022, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
overall water splitting; electrochemical catalysts; cobalt iron tetrathiomolybdate; cobalt iron carbonate hydroxide hydrate; nanowire array; surface anion interchange; HYDROGEN EVOLUTION ELECTROCATALYSIS; EFFICIENT; ENERGY; FILM; NANOSHEETS; ALKALINE; IMPACTS; COMOO4; NI5P4; FUELS;
D O I
10.1002/celc.202000596
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Electrochemical water splitting is regarded as an ideal strategy for producing hydrogen energy. However, the ability to design efficient and durable noble-metal-free catalysts for decreasing the overpotential in the electrolysis process is in high demand. Here, it is demonstrated that cobalt iron carbonate hydroxide hydrate nanowire arrays on Ti mesh (CFOC/TM) obtained through a surface anion interchange method can lead to amorphous cobalt iron tetrathiomolybdate coated on crystalline cobalt iron carbonate hydroxide hydrate nanowire arrays on Ti mesh (CFMS@CFOC/TM), which can act as an efficient and durable water splitting electrocatalyst in alkaline media. CFMS@CFOC/TM shows good performance for the oxygen evolution and hydrogen evolution reactions, with the need for low overpotentials of 237 mV and 93 mV at 10 mA cm(-2) in 1.0 M KOH, respectively. As a 3D bifunctional electrode catalyst, it enables alkaline water splitting with excellent performance, achieving 10 mA cm(-2) at a voltage of 1.63 V with a satisfying stability performance.
引用
收藏
页码:2309 / 2313
页数:5
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