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Azobenzene-equipped Covalent triazine polymers for Visible-Light-Driven photocatalytic reduction of CO2 to CH4

Qi Huang, Zhen Zhan Orcid Logo, Yuanting Qiao Orcid Logo, Xueting Pan, Shaojun Xu Orcid Logo, Bien Tan Orcid Logo, Chunfei Wu Orcid Logo

Fuel, Volume: 361, Start page: 130646

Swansea University Author: Yuanting Qiao Orcid Logo

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Abstract

Covalent triazine polymers, as large π conjugated, highly porous, nitrogen riched organic semiconductors, can play a key role in tackling the fuel energy crisis and global warming issues. However, their development in photocatalytic CO2 reduction is still rare. More effective strategies to enhance C...

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Published in: Fuel
ISSN: 0016-2361
Published: Elsevier BV 2024
Online Access: Check full text

URI: https://cronfa.swan.ac.uk/Record/cronfa67098
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Abstract: Covalent triazine polymers, as large π conjugated, highly porous, nitrogen riched organic semiconductors, can play a key role in tackling the fuel energy crisis and global warming issues. However, their development in photocatalytic CO2 reduction is still rare. More effective strategies to enhance CO2 reduction activity need to be explored. Herein, different amounts of azobenzene pendants functionalized CTPs: Azo-CTP0, Azo-CTP1, Azo-mCTP1 and Azo-CTP2, were fabricated for photocatalytic CO2 reduction with Pd loaded. Among them, Azo-mCTP1 displayed the highest CO2 uptake capacity up to 48.2 cm3 g−1 (2.15 mmol g−1) at 273 K, and the highest CH4 evolution rate in the water system, with selectivity highly up to 97 %. Apart from that, the azobenzene functionalization of Azo-CTP0 could significantly boost the CO2 reduction efficiency by 4 times. Therefore, this study provides a potentially general approach for accurately modifying organic semiconductors to enhance photocatalytic performance.
Keywords: Azobenzene contained; Covalent triazine polymers (CTPs); photocatalytic CO2 conversion
College: Faculty of Science and Engineering
Funders: The authors sincerely appreciate the financial support from the China Scholarship Council. We also appreciate the isotopic GC-MS support from Center for Experimental Chemistry, School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology. This project has received funding from the European Union’s Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie grant agreement No 823745.
Start Page: 130646