光电阴极
人工光合作用
格式化
氧化剂
分解水
材料科学
电子转移
化学工程
电化学
电极
化学
光催化
光化学
催化作用
电子
物理
有机化学
量子力学
物理化学
工程类
作者
Su Keun Kuk,Jinha Jang,Jin‐Hyun Kim,Young‐Jun Lee,Young Sin Kim,Bonhyeong Koo,Yang Woo Lee,Jong Wan Ko,Byungha Shin,Jung‐Kul Lee,Chan Beum Park
出处
期刊:Chemsuschem
[Wiley]
日期:2020-03-17
卷期号:13 (11): 2940-2944
被引量:34
标识
DOI:10.1002/cssc.202000459
摘要
Green plants convert sunlight into high-energy chemicals by coupling solar-driven water oxidation in the Z-scheme and CO2 fixation in the Calvin cycle. In this study, formate dehydrogenase from Clostridium ljungdahlii (ClFDH) is interfaced with a TiO2 -coated CuFeO2 and CuO mixed (ClFDH-TiO2 |CFO) electrode. In this biohybrid photocathode, the TiO2 layer enhances the photoelectrochemical (PEC) stability of the labile CFO photocathode and facilitates the transfer of photoexcited electrons from the CFO to ClFDH. Furthermore, inspired by the natural photosynthetic scheme, the photobiocathode is combined with a water-oxidizing, FeOOH-coated BiVO4 (FeOOH|BiVO4 ) photoanode to assemble a wireless Z-scheme biocatalytic PEC device as a semi-artificial leaf. The leaf-like structure effects a bias-free biocatalytic CO2 -to-formate conversion under visible light. Its rate of formate production is 2.45 times faster than that without ClFDH. This work is the first example of a wireless solar-driven semi-biological PEC system for CO2 reduction that uses water as an electron feedstock.
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