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Azobenzene-equipped Covalent triazine polymers for Visible-Light-Driven photocatalytic reduction of CO2 to CH4
被引:6
|作者:
Huang, Qi
[1
]
Zhan, Zhen
[2
]
Qiao, Yuanting
[1
]
Pan, Xueting
[1
]
Xu, Shaojun
[3
,4
,5
]
Tan, Bien
[2
]
Wu, Chunfei
[1
]
机构:
[1] Queens Univ Belfast, Sch Chem & Chem Engn, Belfast BT7 1NN, North Ireland
[2] Huazhong Univ Sci & Technol, Sch Chem & Chem Engn, Key Lab Mat Chem Energy Convers & Storage, Minist Educ, Luoyu Rd 1037, Wuhan 430074, Peoples R China
[3] Univ Manchester, Dept Chem Engn, Manchester M13 9PL, England
[4] Rutherford Appleton Lab, UK Catalysis Hub, Res Complex Harwell, Harwell OX11 0FA, England
[5] Cardiff Univ, Sch Chem, Cardiff CF10 3AT, Wales
来源:
关键词:
Azobenzene contained;
Covalent triazine polymers (CTPs);
photocatalytic CO2 conversion;
FACILE SYNTHESIS;
CARBON-DIOXIDE;
FRAMEWORKS;
CAPTURE;
D O I:
10.1016/j.fuel.2023.130646
中图分类号:
TE [石油、天然气工业];
TK [能源与动力工程];
学科分类号:
0807 ;
0820 ;
摘要:
Covalent triazine polymers, as large pi 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, AzomCTP1 and Azo-CTP2, were fabricated for photocatalytic CO2 reduction with Pd loaded. Among them, AzomCTP1 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.
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页数:9
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