Photoelectrocatalytic hydrogen generation coupled with reforming of glucose into valuable chemicals using a nanostructured WO3 photoanode

Coupling the photo-oxidation of biomass derived substrates with water splitting in a photoelectrochemical (PEC) cell is a broadly discussed approach intended to enhance efficiency of hydrogen generation at the cathode. Here, we report a PEC device employing a nanostructured semitransparent WO 3 phot...

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Veröffentlicht in:Communications chemistry 2022-10, Vol.5 (1), p.1-10, Article 125
Hauptverfasser: Jakubow-Piotrowska, Katarzyna, Witkowski, Bartłomiej, Augustynski, Jan
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Sprache:eng
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Zusammenfassung:Coupling the photo-oxidation of biomass derived substrates with water splitting in a photoelectrochemical (PEC) cell is a broadly discussed approach intended to enhance efficiency of hydrogen generation at the cathode. Here, we report a PEC device employing a nanostructured semitransparent WO 3 photoanode that, irradiated with simulated solar light achieves large photocurrents of 6.5 mA cm −2 through oxidation of glucose, a common carbohydrate available in nature that can be obtained by processing waste biomass. The attained photocurrents are in a large part due to the occurrence of the photocurrent doubling, where oxidation of glucose by the photogenerated positive hole is followed by injection by the formed intermediate of an electron into the conduction band of WO 3. Selection of an appropriate supporting electrolyte enabled effective reforming of glucose into valuable products: gluconic and glucaric acids, erythrose and arabinose with up to 64% total Faradaic yield attained at ca 15% glucose conversion. Coupling the photo-oxidation of biomass-derived substrates with water splitting in a photoelectrochemical cell enables efficient hydrogen generation at the cathode. Here, a photoelectrochemical device employing a nanostructured WO 3 photoanode displays photocurrents of 6.5 mA cm −2 through oxidation of glucose, in turn producing valuable products in the form of gluconic and glucaric acids, erythrose and arabinose.
ISSN:2399-3669
2399-3669
DOI:10.1038/s42004-022-00745-w