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Photoreduction of CO(2) with a Formate Dehydrogenase Driven by Photosystem II Using a Semi-artificial Z-Scheme Architecture

[Image: see text] Solar-driven coupling of water oxidation with CO(2) 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 CO(2) to formate. We employ a semi-artif...

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Detalles Bibliográficos
Autores principales: Sokol, Katarzyna P., Robinson, William E., Oliveira, Ana R., Warnan, Julien, Nowaczyk, Marc M., Ruff, Adrian, Pereira, Inês A. C., Reisner, Erwin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307851/
https://www.ncbi.nlm.nih.gov/pubmed/30452863
http://dx.doi.org/10.1021/jacs.8b10247
Descripción
Sumario:[Image: see text] Solar-driven coupling of water oxidation with CO(2) 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 CO(2) 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 CO(2) fixation to formate. From a synthetic point of view, it represents a proof-of-principle system utilizing precious-metal-free catalysts for selective CO(2)-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.