Tuning Electronic Structure of CuCo2O4 Spinel via Mn-Doping for Enhancing Oxygen Evolution Reaction

被引:26
作者
He, Xuanmeng [1 ]
Qiao, Tong [1 ]
Li, Beijun [1 ]
Zhang, Zeqin [1 ]
Wang, Shaolan [1 ]
Wang, Xinzhen [2 ]
Liu, Hui [1 ]
机构
[1] Shaanxi Univ Sci & Technol, Sch Mat Sci & Engn, Shaanxi Key Lab Green Preparat & Functionalizat In, Xian 710021, Shaanxi, Peoples R China
[2] Shandong Univ Sci & Technol, Sch Mat Sci & Engn, Qingdao 266590, Shandong, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
CuCo2O4; electronic structure; Mn-doping; oxygen evolution reaction; oxygen vacancies; WATER OXIDATION; HYDROGEN-PRODUCTION; FACILE SYNTHESIS; EFFICIENT; ELECTROCATALYSTS; NANOPARTICLES; COBALT; COMBUSTION; ENERGY;
D O I
10.1002/celc.202200933
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Cobalt-based spinel oxide is a promising electrocatalyst for oxygen evolution reaction (OER) because of its low cost, excellent activity and stability. Herein, we designed the CuMnxCo2O4 electrocatalyst with tunable electronic structure via Mn-doping to enhance OER performance. Results showed that the CuMn0.5Co2O4 catalyst prepared by calcined at 600 C exhibited high crystalline without impurity phase, and possessed the enhanced Co2+/Co3+ ratio and high concentration of oxygen vacancies, which were facilitated to enhance OER performance. Electrochemical test results showed the CuMn0.5Co2O4 catalyst had high OER performance with a low overpotential of 340 mV at the current density of 10 mA.cm and a smaller Tafel slope of 69.8 mV.dec TOF and ECSA results illustrated that the more intrinsic catalytic activity on the CuMn0.5Co2O4 catalyst. After 1000 cycles, the catalyst exhibited high stability with the 8 1.7% of current retention rate. The OER activity enhancement mechanism of was further analyzed, which were mainly ascribed to the conversion of variable Co2+/Co3+ and enhanced oxygen vacancies.
引用
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页数:10
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