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Photoelectrochemical H(2) Evolution with a Hydrogenase Immobilized on a TiO(2)‐Protected Silicon Electrode

The combination of enzymes with semiconductors enables the photoelectrochemical characterization of electron‐transfer processes at highly active and well‐defined catalytic sites on a light‐harvesting electrode surface. Herein, we report the integration of a hydrogenase on a TiO(2)‐coated p‐Si photoc...

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Detalles Bibliográficos
Autores principales: Lee, Chong‐Yong, Park, Hyun S., Fontecilla‐Camps, Juan C., Reisner, Erwin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4982046/
https://www.ncbi.nlm.nih.gov/pubmed/27570301
http://dx.doi.org/10.1002/ange.201511822
Descripción
Sumario:The combination of enzymes with semiconductors enables the photoelectrochemical characterization of electron‐transfer processes at highly active and well‐defined catalytic sites on a light‐harvesting electrode surface. Herein, we report the integration of a hydrogenase on a TiO(2)‐coated p‐Si photocathode for the photo‐reduction of protons to H(2). The immobilized hydrogenase exhibits activity on Si attributable to a bifunctional TiO(2) layer, which protects the Si electrode from oxidation and acts as a biocompatible support layer for the productive adsorption of the enzyme. The p‐Si|TiO(2)|hydrogenase photocathode displays visible‐light driven production of H(2) at an energy‐storing, positive electrochemical potential and an essentially quantitative faradaic efficiency. We have thus established a widely applicable platform to wire redox enzymes in an active configuration on a p‐type semiconductor photocathode through the engineering of the enzyme–materials interface.