光电流
光电阴极
甲酸脱氢酶
光电化学
材料科学
化学
串联
电解质
格式化
电催化剂
能量转换效率
化学工程
分解水
电极
纳米技术
人工光合作用
电化学
光电子学
催化作用
光催化
有机化学
物理化学
复合材料
电子
工程类
物理
量子力学
作者
Elaine A. Moore,Virgil Andrei,Ana Rita Oliveira,Ana Margarida Coito,Inês Pereira,Erwin Reisner
标识
DOI:10.1002/anie.202110867
摘要
Semi-artificial photoelectrochemistry can combine state-of-the-art photovoltaic light-absorbers with enzymes evolved for selective fuel-forming reactions such as CO2 reduction, but the overall performance of such hybrid systems has been limited to date. Here, the electrolyte constituents were first tuned to establish an optimal local environment for a W-formate dehydrogenase to perform electrocatalysis. The CO2 reductase was then interfaced with a triple cation lead mixed-halide perovskite through a hierarchically structured porous TiO2 scaffold to produce an integrated photocathode achieving a photocurrent density of -5 mA cm-2 at 0.4 V vs. the reversible hydrogen electrode during simulated solar light irradiation. Finally, the combination with a water-oxidizing BiVO4 photoanode produced a bias-free integrated biophotoelectrochemical tandem device (semi-artificial leaf) with a solar CO2 -to-formate energy conversion efficiency of 0.8 %.
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