Construction of N-doped copper metal-organic frameworks for promoting photocatalytic carbon dioxide reduction to ethylene

被引:3
|
作者
Guo, Fan [1 ,2 ]
He, Zong-Zheng [1 ]
Wang, Peng [2 ]
Zhang, Xiao-Yu [2 ]
Yu, Hongjian [1 ]
Wang, Qin-Chao [1 ]
Sun, Wei-Yin [2 ]
机构
[1] Yangzhou Univ, Sch Chem & Chem Engn, Yangzhou 225002, Peoples R China
[2] Nanjing Univ, Coordinat Chem Inst, Nanjing Natl Lab Microstruct, Sch Chem & Chem Engn,Collaborat Innovat Ctr Adv Mi, Nanjing 210023, Peoples R China
基金
中国国家自然科学基金;
关键词
metal-organic frameworks; C-C coupling; doping; photocatalytic CO2 reduction; Cu-based catalysts; CO2; ELECTROREDUCTION; EFFICIENT; VACANCIES; SITES; WATER; C2H4;
D O I
10.1007/s11426-024-2229-2
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Engineering nonmetallic atom-doped metal-organic framework (MOF) catalyst to promote C-C coupling and realize conversion of CO2 into C2 multi-carbon hydrocarbon products is still challenging. Herein, with 2-methylimidazole as a dopant of N element, an N-doped NH2-CuBDC catalyst was obtained via a facile and simple stirring procedure. Upon illumination, compared with catalytic CO2 reduction to C1 product of CO by original MOF, N-doped NH2-CuBDC can motivate generation of C2H4, which is difficult to achieve in photocatalytic system by MOF-based catalysts. The transfer rates of photo-generated charges have been expedited due to the high electron density around Cu catalytic sites after N-doping. More importantly, C-C coupling intermediate CO-CHO* was identified by in situ Fourier transform infrared spectroscopy during the catalytic CO2 reduction reaction process, which further indicates the presence of Cu-N sites in the NH2-CuBDC can facilitate the formation of C2H4 effectively. This work uncovers a new paradigm to design photocatalysts for enhancing the reduction of CO2 to C2 products.
引用
收藏
页码:601 / 609
页数:9
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