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Photoelectrochemical H2 Evolution with a Hydrogenase Immobilized on a TiO2-Protected Silicon Electrode.


ABSTRACT: 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 TiO2-coated p-Si photocathode for the photo-reduction of protons to H2. The immobilized hydrogenase exhibits activity on Si attributable to a bifunctional TiO2 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|TiO2|hydrogenase photocathode displays visible-light driven production of H2 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.

SUBMITTER: Lee CY 

PROVIDER: S-EPMC4982046 | biostudies-literature | 2016 May

REPOSITORIES: biostudies-literature

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Photoelectrochemical H<sub>2</sub> Evolution with a Hydrogenase Immobilized on a TiO<sub>2</sub>-Protected Silicon Electrode.

Lee Chong-Yong CY   Park Hyun S HS   Fontecilla-Camps Juan C JC   Reisner Erwin E  

Angewandte Chemie (Weinheim an der Bergstrasse, Germany) 20160408 20


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<sub>2</sub>-coated p-Si photocathode for the photo-reduction of protons to H<sub>2</sub>. The immobilized hydrogenase exhibits activity on Si attributable to a bifunctional TiO<sub>2</sub> layer, which protects the Si ele  ...[more]

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