Fe-Ni co-doping strategy in perovskite for developing an efficient oxygen evolution electrocatalyst

被引:0
|
作者
Liu, Huimin [1 ,2 ]
Wei, Lianwei [1 ,2 ]
Zheng, Hui [1 ,2 ]
Tang, Kaibin [1 ,2 ]
机构
[1] Univ Sci & Technol China, Hefei Natl Res Ctr Phys Sci Microscale, Hefei 230026, Peoples R China
[2] Univ Sci & Technol China, Dept Chem, Hefei 230026, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
Electrocatalysis; Oygen evolution reaction; Fe-Ni co-doping; Perovskite oxide; WATER OXIDATION; PERFORMANCE; HYDROGEN; REDUCTION; CATALYSTS; SURFACE;
D O I
10.1063/1674-0068/cjcp2204072
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
The high reaction barrier of the oxygen evolution reaction (OER) has always been the bottleneck of the water decomposition reaction, so low-cost, high-performance and stable catalysts are urgently needed currently. Herein, we designed an effective OER electrocatalyst BaCo0.6Fe0.2Ni0.2O3-delta (BCFN) by a codoping strategy. The overpotential of BCFN at a current density of 10 mA/cm(2) reaches 310 mV, and possesses a Tafel slope of 50.2 mV/dec. The catalytic capability of BCFN is much stronger than that of Fe-doped BaCo0.8Fe0.2O3-delta (360 mV), Ni-doped BaCo0.8Ni0.2O3-delta (375 mV), and benchmark IrO2 with excellent performance (329 mV). At the same time, BCFN is also a fairly stable alkaline OER catalyst. After 500-cycle scans, BCFN still shows high catalytic activity without significant decrease in catalytic performance. Electrochemical experiments show that BCFN has the fastest reaction kinetics and the lowest charge transfer resistance among the materials in this work. In addition, a large amount of highly oxidative oxygen O-2(2-)/O- and hydroxyl groups OH- on the surface of BCFN are conducive to the occurrence of OER, thereby increasing the reaction rate. This work provides a universal strategy to develop high-performance electrocatalysts for electrochemical energy conversion technology.
引用
收藏
页码:764 / 772
页数:9
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