Tuning interface density and electronic structure of NiS/Ni3S4 by Mo, Co co-doping for efficient urea electrooxidation reaction

被引:9
|
作者
Huang, Wen [1 ]
Yuan, Yahui [1 ]
Wang, Kaili [1 ]
Cao, Qiuhan [1 ]
Zhao, Yongjie [1 ]
Sun, Xiujuan [1 ]
Ding, Rui [1 ]
Gao, Ping [1 ]
Cai, Weiwei [2 ]
Liu, Enhui [1 ]
机构
[1] Xiangtan Univ, Coll Chem, Key Lab Environmentally Friendly Chem & Applicat, Minist Educ, Hunan 411105, Peoples R China
[2] China Univ Geoscinces, Fac Mat Sci & Chem, Sustainable Energy Lab, Wuhan 430074, Peoples R China
基金
中国国家自然科学基金;
关键词
Interface density; Electron modulation; Flower-like structure; Urea oxidation reaction; Mo; Co co-doping; Urea fuel cell; HIGHLY EFFICIENT; OXIDATION; ELECTROCATALYSTS; PERFORMANCE; CATALYST;
D O I
10.1016/j.jelechem.2022.116242
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Electrocatalysts exhibiting impressive catalytic capability and strong stability for urea oxidation reaction (UOR) are highly desired for direct urea fuel cells (DUFCs). Herein, a series of flower-like Mo, Co co-doped NiS/Ni3S4 heterostructure (Mo, Co-NSH) are controllable synthesized by a one-step hydrothermal method and utilized as catalysts for UOR. Taking advantages of massive heterojunctions, tunable electronic configuration and hierarchical flower-like topological structure together, the optimized component demonstrates advanced UOR performance compared to pure NiS/Ni3S4 and mono Co/Mo element doped NiS/Ni3S4, it delivers 147.1 mA cm(-2) at 1.6 V vs. RHE and works for more than 18 h without decay. The assembly direct urea hydrogen peroxide fuel cell (DUHPFC) with Mo-0.05, Co-NSH catalyst has an open-circuit voltage of 0.86 V and a maximum power density of 5.96 mW cm(-2) at 27 degrees C. The work provides a promising avenue for exploiting efficient electrocatalysts on both multi-metal doping and heterojunction engineering for electrochemical energy conversion and sewage treatment applications.
引用
收藏
页数:9
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