Photoreduction of CO2 with a Formate Dehydrogenase Driven by Photosystem II Using a Semi-artificial Z-Scheme Architecture

被引:118
作者
Sokol, Katarzyna P. [1 ]
Robinson, William E. [1 ]
Oliveira, Ana R. [2 ]
Warnan, Julien [1 ]
Nowaczyk, Marc M. [3 ]
Ruff, Adrian [4 ]
Pereira, Ines A. C. [2 ]
Reisner, Erwin [1 ]
机构
[1] Univ Cambridge, Dept Chem, Lensfield Rd, Cambridge CB2 1EW, England
[2] Univ NOVA Lisboa, Inst Tecnol Quim & Biol Antonio Xavier ITQB NOVA, Av Republ, P-2780157 Oeiras, Portugal
[3] Ruhr Univ Bochum, Fac Biol & Biotechnol, Plant Biochem, Univ Str 150, D-44780 Bochum, Germany
[4] Ruhr Univ Bochum, Fac Chem & Biochem, Analyt Chem Ctr Electrochem Sci, Univ Str 150, D-44780 Bochum, Germany
基金
英国工程与自然科学研究理事会; 欧盟地平线“2020”;
关键词
CARBON-DIOXIDE; FORMIC-ACID; ELECTROCHEMICAL CONVERSION; PHOTORESPIRATORY BYPASS; ZINC PORPHYRIN; REDUCTION; FIXATION; WATER; PHOTOSYNTHESIS; HYDROGEN;
D O I
10.1021/jacs.8b10247
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Solar-driven coupling of water oxidation with CO2 reduction sustains life on our planet and is of high priority in contemporary energy research. Here, we report a photoelectrochemical tandem device that performs photocatalytic reduction of CO2 to formate. We employ a semi-artificial design, which wires a W-dependent formate dehydrogenase (FDH) cathode to a photoanode containing the photosynthetic water oxidation enzyme, Photosystem II, via a synthetic dye with complementary light absorption. From a biological perspective, the system achieves a metabolically inaccessible pathway of light-driven CO2 fixation to formate. From a synthetic point of view, it represents a proof-of-principle system utilizing precious-metal-free catalysts for selective CO2-to-formate conversion using water as an electron donor. This hybrid platform demonstrates the translatability and versatility of coupling abiotic and biotic components to create challenging models for solar fuel and chemical synthesis.
引用
收藏
页码:16418 / 16422
页数:5
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