Covalent synthesis of Ti-MOF for enhanced photocatalytic CO2 reduction

被引:12
作者
Wei, Zihao [1 ]
Xu, Wenquan [1 ,2 ]
Peng, Panpan [3 ]
Sun, Qi [1 ]
Li, Yaqiong [1 ]
Ding, Ning [1 ]
Zhao, Chaofeng [1 ]
Li, Shenghua [1 ,2 ]
Pang, Siping [1 ]
机构
[1] Beijing Inst Technol, Sch Mat Sci & Engn, Beijing 100081, Peoples R China
[2] Beijing Inst Technol, Yangtze Delta Reg Acad, Jiaxing 314019, Peoples R China
[3] Hubei Inst Aerosp Chemotechnol, Sci & Technol Aerosp Chem Power Lab, Xiangyang 441003, Hubei, Peoples R China
关键词
Metal-organic framework; Photocatalysis; CO2RR; Formate; ORGANIC FRAMEWORKS; CONSTRUCTION; CHEMISTRY; CLUSTERS;
D O I
10.1016/j.mcat.2024.114042
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Ti based Metal-organic frameworks materials, with their high surface area, visible light responsiveness, and abundant catalytic active sites, have emerged as efficient photocatalysts. However, the number of reports on titanium-based MOFs is limited, mainly due to the challenges associated with their synthesis. In this study, based on the covalent strategy of imine condensation, a novel Ti-MOF was designed and synthesized by rational selection of aldehyde ligands. The photocatalytic CO2 reduction performance of the Ti-MOF was evaluated, and it exhibited a remarkable generation rate of formate ions at 46.0 mu mol g- 1 h- 1, which is more than 6 times higher than that of MOF-902 constructed with the same titanium cluster. The rational selection of aldehyde ligands resulted in a relatively superior band structure for the Ti-MOF, characterized by a narrowed bandgap and a significantly negative shift of the conduction band, leading to enhanced photocatalytic ability.
引用
收藏
页数:6
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