An enhanced non-noble perovskite-based oxygen electrocatalyst for efficient oxygen reduction and evolution reactions

被引:14
|
作者
Chen, Feiming [1 ]
Xue, Lichun [1 ]
Shang, Zhenxi [1 ]
Zhang, Zhenbao [1 ]
Chen, Dengjie [1 ]
机构
[1] Jinan Univ, Coll Chem & Mat Sci, Guangdong Engn & Technol Res Ctr Graphene Mat & P, Dept Chem, Guangzhou 510632, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Ba0.5Sr0.5Co0.8Fe0.2O3-delta; g-C3N4; Perovskite oxide; Oxygen reduction reaction; Oxygen evolution reaction; GRAPHITIC CARBON NITRIDE; HIGHLY-EFFICIENT; BA0.5SR0.5CO0.8FE0.2O3-DELTA PEROVSKITE; GRAPHENE OXIDE; FUEL-CELLS; PERFORMANCE; CATALYSTS; DESIGN; CATHODE; G-C3N4;
D O I
10.1016/j.jssc.2019.121119
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Developing cost-effective and efficient bifunctional electrocatalysts for oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) is of considerable importance for fuel cells and metal-air batteries. In this work, a non-precious composite (i.e., Ba0.5Sr0.5Co0.8Fe0.2O3-delta (BSCF), g-C3N4 and Vulcan carbon (VC)) labeled as BSCF/g-C3N4-VC was developed via ultrasonically mixing. The formed BSCF/g-C3N4-VC exhibited improved ORR and OER activity compared with the individual g-C3N4 and BSCF, as well as the composites of g-C3N4-VC and BSCF/VC. The critical roles of BSCF, g-C3N4, and VC for boosting ORR and OER have been clearly demonstrated. Apparently, the prepared composite overcame major limitations of perovskite-type BSCF and g-C3N4, i.e., the relatively low specific surface area (similar to 0.27 m(2) g(-1)) of the former and the extremely low electronic conductivity of the latter. Moreover, the significantly enhanced electrocatalytic activity could be attributed to the synergistic effect between g-C3N4, BSCF, and VC. Our results suggest that facilely compositing carbon materials (e.g. VC and g-C3N4) with perovskite-type oxides (e.g. BSCF) will open a new path for the development of highly efficient oxygen electrocatalysts.
引用
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页数:9
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