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Efficient Conversion of CO2 to Methane Photocatalyzed by Conductive Black Titania

Guoheng Yin

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

University of Chinese Academy of Sciences, Beijing, 100049 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 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 China

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Jijian Xu

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

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Dr. Tianquan Lin

State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai, 200050 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 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: 25 July 2017
Citations: 20
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Abstract

One of the major challenges encountered in CO2 utilization is the development of available and cost‐efficient catalysts with sufficient activity, selectivity, and stability for the generation of useful methane. Here, conductive black titania, TiO2−x , is found to be efficient in photocatalyzing the reduction of CO2 to CH4. This unique material comprises a crystalline core–amorphous shell structure (TiO2@TiO2−x ) with numerous surface oxygen vacancies, which facilitates the adsorption and chemical activation of CO2 molecules. Under full solar irradiation, the optimized 500‐TiO2−x material with narrowed band gap and intermediate states below the conduction band tail exhibits a high space‐time yield of CH4 of 14.3 μmol g−1 h−1, with 74 % selectivity and excellent photostability. The present findings can make a significant contribution, not only to develop the surface electron‐modified black TiO2 catalyst to boost photocatalytic efficiency, but also to establish a really viable and convenient CH4 production process for CO2 conversion and renewable solar energy storage.