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Microwave-assisted hydrothermal synthesis of MOFs-derived bimetallic CuCo-N/C electrocatalyst for efficient oxygen reduction reaction.

Authors :
Kang, Xiaomin
Fu, Guodong
Song, Zhongxin
Huo, Ge
Si, Fengzhan
Deng, Xiaohui
Fu, Xian-Zhu
Luo, Jing-Li
Source :
Journal of Alloys & Compounds. Jul2019, Vol. 795, p462-470. 9p.
Publication Year :
2019

Abstract

The oxygen reduction reaction (ORR) plays a significant role in energy conversion technologies such as metal-air batteries and fuel cells. The development of efficient ORR electrocatalyst is highly desirable to achieve the fast oxygen reduction. In this work, the bimetallic Cu and Co embedded nitrogen-doped carbon (CuCo-N/C) is fabricated as efficient electrocatalyst for ORR. The incorporation of Cu-precursor into Co-based zeolitic imidazolate frameworks (ZIF) is innovated here to synergistically enhance the activity of Co. Surprisingly, the addition of Cu can also increase the nitrogen content in the CuCo-N/C catalysts, which could generate more active sites and result in the improvement of ORR activity. The optimized CuCo-N/C catalysts exhibit superior ORR performance with a half-wave potential of 0.85 V (vs. RHE), a limiting current density of 5.61 mA cm−2 and enhanced long-term durability comparing with the state-of-the-art Pt/C catalysts. Benefiting from the unique structure, the as-made CuCo-N/C catalysts as electrode for Zn-air battery delivers excellent performance with a peak power density of 66.9 mW cm−2, a high open circuit voltage of 1.468 V, and a voltage degradation of about 1.4% after 12 h discharging, which is much better than that of Pt/C catalysts. • A CuCo-N/C catalyst is obtained by a fast and efficient microwave-assisted method. • High N content and bimetallic Cu/Co contribute to the enhanced ORR performance. • The CuCo-N/C electrode delivers excellent performance in Zn-air battery. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09258388
Volume :
795
Database :
Academic Search Index
Journal :
Journal of Alloys & Compounds
Publication Type :
Academic Journal
Accession number :
136645647
Full Text :
https://doi.org/10.1016/j.jallcom.2019.04.325