Photoelectrochemical H-2 Evolution with a Hydrogenase Immobilized on a TiO2-Protected Silicon Electrode

Authors
Lee, Chong-YongPark, Hyun S.Fontecilla-Camps, Juan C.Reisner, Erwin
Issue Date
2016-05-10
Publisher
John Wiley & Sons Ltd.
Citation
Angewandte Chemie International Edition, v.55, no.20, pp.5971 - 5974
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 H-2. 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 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.
Keywords
ACTIVE-SITE; REDUCTION; PHOTOCATHODE; OXIDATION; ENZYME; OXIDE; TIO2; ACTIVE-SITE; REDUCTION; PHOTOCATHODE; OXIDATION; ENZYME; OXIDE; TIO2; hydrogen evolution; hydrogenase; photoelectrochemistry; semiconductors; TiO2
ISSN
1433-7851
URI
https://pubs.kist.re.kr/handle/201004/124068
DOI
10.1002/anie.201511822
Appears in Collections:
KIST Article > 2016
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