Volume 24, Issue 9
Full Paper

Efficient Reduction of CO2 to CO Using Cobalt–Cobalt Oxide Core–Shell Catalysts

Guoheng Yin

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

University of Chinese Academy of Sciences, Beijing, 100049 P. R. China

These authors contributed equally to this work.

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Xiaotao Yuan

Beijing National Laboratory for Molecular Sciences and State Key Laboratory of Rare Earth Materials Chemistry and Applications, College of Chemistry and Molecular Engineering, Peking University, Beijing, 100871 P. R. China

These authors contributed equally to this work.

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Dr. Xianlong Du

Key Laboratory of Interfacial Physics and Technology, Shanghai Institute of Applied Physics, Chinese Academy of Sciences, Shanghai, 201800 P. R. China

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Dr. Wei Zhao

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

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Dr. Qingyuan Bi

Corresponding Author

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

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

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Prof. Dr. Fuqiang Huang

Corresponding Author

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

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

Beijing National Laboratory for Molecular Sciences and State Key Laboratory of Rare Earth Materials Chemistry and Applications, College of Chemistry and Molecular Engineering, Peking University, Beijing, 100871 P. R. China

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First published: 04 December 2017
Citations: 16

Abstract

The route of converting CO2 to CO by reverse water‐gas shift (RWGS) reaction is of particular interest due to the direct use of CO as feedstock in many significant industrial processes. Here, an engineered cobalt–cobalt oxide core–shell catalyst (Co@CoO) with nanochains structure has been made for the efficient reduction of CO2 to useful CO. Owing to the excellent performance for H2 activation of metal nanoparticles and the enhanced absorption and activation for CO2 molecule of defective metal oxides, the unique synergistic effect of metallic Co and encapsulating coordinatively unsaturated CoO species shows high performance for clean generation of CO under moderate and practical conditions. Furthermore, with N‐dopant into the defective CoO shell, the Co@CoO‐N achieves the highest conversion of 19.2 % and an exceptional CO evolution rate of 96 mL min−1 gcat−1 at 523 K with a gas hourly space velocity (GHSV) of 42,000 mL gcat−1 h−1, which is comparable with the previously reported materials under identical conditions.