Volume 5, Issue 6
Full Paper

Complexing‐Coprecipitation Method to Synthesize Catalysts of Cobalt, Nitrogen‐Doped Carbon, and CeO2 Nanosheets for Highly Efficient Oxygen Reduction

Xiaoqing Wang

State Key Laboratory of Silicon Materials, School of Materials Science and Engineering, Zhejiang University, Hangzhou, 310027 China

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Jijian Xu

State Key Laboratory of Silicon Materials, School of Materials Science and Engineering, Zhejiang University, Hangzhou, 310027 China

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Zongxiao Wu

State Key Laboratory of Silicon Materials, School of Materials Science and Engineering, Zhejiang University, Hangzhou, 310027 China

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Dr. Mingjia Zhi

Corresponding Author

E-mail address: mingjia_zhi@zju.edu.cn

State Key Laboratory of Silicon Materials, School of Materials Science and Engineering, Zhejiang University, Hangzhou, 310027 China

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Prof. Zhanglian Hong

Corresponding Author

E-mail address: hong_zhanglian@zju.edu.cn

State Key Laboratory of Silicon Materials, School of Materials Science and Engineering, Zhejiang University, Hangzhou, 310027 China

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Prof. Fuqiang Huang

Corresponding Author

E-mail address: huangfq@mail.sic.ac.cn

State Key Laboratory of Silicon Materials, School of Materials Science and Engineering, Zhejiang University, Hangzhou, 310027 China

State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai, 200050 China

State Key Laboratory of Rare Earth Materials Chemistry and Applications College of Chemistry and Molecular Engineering, Peking University, Beijing, 100871 China

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First published: 14 April 2019
Citations: 1

Abstract

The oxygen reduction reaction (ORR) is the key cathode reaction in renewable‐energy technologies. Developing highly efficient, low‐cost, methanol‐tolerant and durable ORR catalysts is highly needed. In this research, we reported a simple complexing‐coprecipitation method to synthesize CeO2 nanosheets encapsulated by a nitrogen‐doped carbon (NC) layer with uniformly dispersed Co nanoparticles catalysts on the surface. In particular, the 0.5Co‐NC‐CeO2 sample exhibits high ORR catalytic activity with an onset potential of 875 mV (vs. RHE), a diffusion‐limited current density of 4.72 mA/cm2 and a positive half‐wave potential of 817 mV (vs RHE), while 20% Pt/C presents an onset potential of 934 mV (vs. RHE), a diffusion limited current density of 5.8 mA/cm2 and half‐wave potential of 850 mV (vs. RHE). In addition, the catalyst 0.5Co‐NC‐CeO2 also possesses a robust durability, that is the half‐wave potential exhibits a negative shift of only 17 mV after 1000 cycles. The enhanced ORR performance can be attributed to the synergistic effect among Co, the nitrogen‐doped carbon layer and CeO2. The results demonstrated here have implications in designing non‐Pt ORR catalysts.

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