Dye‐Sensitized Photocatalysis: Hydrogen Evolution and Alcohol‐to‐Aldehyde Oxidation without Sacrifical Electron Donor

Author:

Romito Deborah1ORCID,Govind Chinju2ORCID,Nikolaou Vasilis1ORCID,Fernández‐Terán Ricardo J.2ORCID,Stoumpidi Aspasia3,Agapaki Eleni3ORCID,Charalambidis Georgios4ORCID,Diring Stéphane1ORCID,Vauthey Eric2ORCID,Coutsolelos Athanassios G.35ORCID,Odobel Fabrice1ORCID

Affiliation:

1. Nantes Université, CNRS, CEISAM, UMR 6230 F-44000 Nantes France

2. Department of Physical Chemistry University of Geneva 30 Quai Ernest-Ansermet CH-1211 Geneva Switzerland

3. Laboratory of Bioinorganic Chemistry, Department of Chemistry University of Crete Voutes Campus 70013 Heraklion Crete Greece

4. Theoretical and Physical Chemistry Institute National Hellenic Research Foundation 48 Vassileos Constantinou Avenue 11635 Athens Greece

5. Institute of Electronic Structure and Laser (IESL) Foundation for Research and Technology – Hellas (FORTH), Vassilika Vouton GR 70013 Heraklion Crete Greece

Abstract

AbstractThere is a growing interest in developing dye‐sensitized photocatalytic systems (DSPs) to produce molecular hydrogen (H2) as alternative energy source. To improve the sustainability of this technology, we replaced the sacrificial electron donor (SED), typically an expensive and polluting chemical, with an alcohol oxidation catalyst. This study demonstrates the firstdye‐sensitized system using a diketopyrrolopyrrole dye covalently linked to 2,2,6,6‐tetramethyl‐1‐piperidine‐N‐oxyl (TEMPO) based catalyst for simultaneous H2 evolution and alcohol‐to‐aldehyde transformation operating in water with visible irradiation.

Funder

Agence Nationale de la Recherche

HORIZON EUROPE Marie Sklodowska-Curie Actions

Hellenic Foundation for Research and Innovation

Foundation for Research and Technology-Hellas

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Publisher

Wiley

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