化学
催化作用
光敏剂
人工光合作用
钌
量子产额
光催化
光化学
电化学
配体(生物化学)
营业额
组合化学
分子
电子转移
氧化还原
产量(工程)
有机化学
荧光
生物化学
物理
受体
材料科学
电极
量子力学
物理化学
冶金
作者
Tomoya Ishizuka,Atsushi Hosokawa,T Kawanishi,Hiroaki Kotani,Yipeng Zhi,Takahiko Kojima
摘要
The promise of artificial photosynthesis to solve environmental and energy issues such as global warming and the depletion of fossil fuels has inspired intensive research into photocatalytic systems for CO2 reduction to produce value-added chemicals such as CO and CH3OH. Among the photocatalytic systems for CO2 reduction, self-photosensitizing catalysts, bearing the functions of both photosensitization and catalysis, have attracted considerable attention recently, as such catalysts do not depend on the efficiency of electron transfer from the photosensitizer to the catalyst. Here, we have synthesized and characterized a dinuclear RuII complex bearing two molecules of a tripodal hexadentate ligand as chelating and linking ligands by X-ray crystallography to establish the structure explicitly and have used various spectroscopic and electrochemical methods to elucidate the photoredox characteristics. The dinuclear complex has been revealed to act as a self-photosensitizing catalyst, which acts not only as a photosensitizer but also as a catalyst for CO2 reduction. The dinuclear RuII complex is highly durable and performs efficient and selective CO2 reduction to produce CO with a turnover number of 2400 for 26 h. The quantum yield of the CO formation is also very high─19.7%─and the catalysis is efficient, even at a low concentration (∼1.5%) of CO2.
科研通智能强力驱动
Strongly Powered by AbleSci AI