Highly Robust Rhenium(I) Bipyridyl Complexes Containing Dipyrromethene-BF2 Chromophores for Visible Light-Driven CO2 Reduction

被引:11
作者
Qiu, Li-Qi [1 ]
Yang, Zhi-Wen [1 ]
Yao, Xiangyang [1 ]
Li, Xiao-Yang [1 ]
He, Liang-Nian [1 ]
机构
[1] Nankai Univ, Coll Chem, Dept State Key Lab & Inst Elementoorgan, Tianjin 300071, Peoples R China
基金
中国国家自然科学基金;
关键词
CO2; photoreduction; electron transfer efficiency; photocatalysis; solar-to-fuel; sustainable chemistry; CARBON-DIOXIDE; PHOTOCATALYTIC REDUCTION; PHOTOPHYSICAL PROPERTIES; CATALYTIC-REDUCTION; METAL-COMPLEXES; MOLECULAR DYAD; EFFICIENT; HYDROGENATION; CONVERSION; PHOSPHORESCENCE;
D O I
10.1002/cssc.202200337
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
New rhenium bipyridyl complexes with dipyrromethene-BF2 chromophores (A-ReBDP-CZ, A-ReBDP2, ReBDP-CZ, and ReBDP2) were developed for highly efficient photocatalytic carbon dioxide (CO2) reduction to carbon monoxide (CO). These catalysts consisted of two moderate electron-deficient groups (dipyrromethene-BF2, BDP) as the visible-light-harvesting antenna as well as both electron donor (N-phenylcarbazole, CZ) and acceptor (BDP) on Re bipyridyl framework. Among ReBDP-CZ and ReBDP2 complexes, the ReBDP2 incorporating two electron-deficient BDP chromophores had a longer-lived photoexcited state (182.4 mu s) and a twofold enhanced molar absorption coefficient (epsilon=157000 m(-1) cm(-1)) compared with ReBDP-CZ. Thus, ReBDP2 achieved the superior photocatalytic reactivity and stability with a CO turnover number (TONCO) value as high as 1323 and quantum yield (phi(CO)) up to 55 %, which was the most excellent photocatalysis efficiency among the single-active-site Re catalysts without additional photosensitizer. Furthermore, the acetylene-bridged linker was detrimental to the photoactivity and durability of the catalyst. In brief, two BDP-based Re bipyridyl systems with outstanding catalytic performance and significant visible-light-harvesting capabilities in the solar spectrum offer a promising strategy for solar-to-fuel conversion schemes.
引用
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页数:11
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