Porphyrin-Based Two-Dimensional Metal-Organic framework nanosheets for efficient photocatalytic CO2 transformation

被引:26
作者
Shi, Quan [1 ]
Chen, Ming-Hui [1 ]
Xiong, Ji [1 ]
Li, Ting [1 ]
Feng, Ya-Qing [1 ,2 ,3 ]
Zhang, Bao [1 ,2 ,3 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Tianjin 300350, Peoples R China
[2] Tianjin Collaborat Innovat Ctr Chem Sci & Engn, Tianjin 300072, Peoples R China
[3] Haihe Lab Sustainable Chem Transformat, Tianjin 300192, Peoples R China
基金
中国国家自然科学基金;
关键词
Porphyrin; Metal -organic framework; Photocatalysis; CO; 2; transformation; PHOTOREDUCTION; CONVERSION; EPOXIDES; CATALYST;
D O I
10.1016/j.cej.2023.148301
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
2D metal - organic framework (MOF) nanosheets have been demonstrated to exhibit excellent properties and prospects in various aspects, especially in photocatalysis. However, the design and direct preparation of 2D MOF photocatalyst is highly desirable but still challenging. Herein, a novel 2D porphyrin-based MOF Fe-DBP(Co), which is assembled by dicarboxylic porphyrin ligands and the unprecedented undecametallic ferric-oxo clusters, is designed and developed. The unique nanosheet morphology and assembled layered structure endows the photocatalyst with higher electron-hole separation efficiency and longer photogenerated carrier lifetime compared to the analogous MOFs. Consequently, Fe-DBP(Co) exhibits strikingly excellent and stable photocatalytic performance in CO2 cycloaddition, and the reaction rate of 103.2 mmol center dot g- 1 center dot h-1 is among the state-ofthe-art cases for MOF-photocatalyzed CO2 cycloaddition. The underlying mechanism investigation suggested that photogenerated electrons transferred from CoDBP ligands to the Fe clusters, and the abundant electrons and holes promoted the generation of Fe(II) and Co(III) respectively, leading to excellent catalytic performance. This work proposes a new strategy to design and develop efficient MOF photocatalysts for photocatalytic transformation of CO2.
引用
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页数:10
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