Strong electronic coupling of CoNi and N-doped-carbon for efficient urea-assisted H2 production at a large current density

被引:108
作者
Qian, Guangfu [1 ]
Chen, Jinli [1 ]
Jiang, Wenjie [1 ]
Yu, Tianqi [1 ]
Tan, Kexin [1 ]
Yin, Shibin [1 ,2 ]
机构
[1] Guangxi Univ, Coll Chem & Chem Engn, Coll Light Ind & Food Engn, Guangxi Key Lab Electrochem Energy Mat, Nanning, Peoples R China
[2] Guangxi Univ, Coll Chem & Chem Engn, Coll Light Ind & Food Engn, Guangxi Key Lab Electrochem Energy Mat, 100 Daxue Rd, Nanning 530004, Peoples R China
基金
中国国家自然科学基金;
关键词
carbon-encapsulated structure; catalyst; hydrogen production; large current density; urea-assisted water electrolysis; HYDROGEN; ELECTROCATALYSTS; WATER; CATALYST; NANOMATERIALS; OXIDATION; LDH;
D O I
10.1002/cey2.368
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
Exploiting efficient urea oxidation reaction (UOR) and hydrogen evolution reaction (HER) catalysts are significant for energy-saving H-2 production through urea-assisted water electrolysis, but it is still challenging. Herein, carbon-encapsulated CoNi coupled with CoNiMoO (CoNi@CN-CoNiMoO) is prepared by solvothermal method and calcination to enhance the activity/stability of urea-assisted water electrolysis at large current density. It exhibits good activity for UOR (E-10/1,E-000 = 1.29/1.40 V) and HER (E-10/-1000 = -45/-245 mV) in 1.0 M KOH + 0.5 M urea solution. For the UOR||HER system, CoNi@CN-CoNiMoO only needs 1.58 V at 500 mA cm(-2) and shows good stability. Density functional theory calculation suggests that the strong electronic interaction at the interface between NiCo alloy and N-doping-carbon layers can optimize the adsorption/desorption energy of UOR/HER intermediates and accelerate the water dissociation, which can expedite urea decomposition and Volmer step, thus increasing the UOR and HER activity, respectively. This work provides a new solution to design UOR/HER catalysts for H-2 production through urea-assisted water electrolysis.
引用
收藏
页数:13
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