Photo-recycling the sacrificial electron donor: Towards sustainable hydrogen evolution in a biphasic system
- 1. Laboratoire d'Électrochimie Physique et Analytique. École Polytechnique Fédérale de Lausanne, EPFL, Valais Wallis Rue de l'industrie, 17, 1950 Sion (Switzerland)
- 2. The Bernal Institute and Department of Chemical Sciences, University of Limerick (UL) Limerick V94 T9PX, Ireland
Description
H2 may be evolved biphasically using a polarised liquid|liquid interface, acting as a “proton pump”, in combination with organic soluble metallocenes as electron donors. Sustainable H2 production requires methodologies to recycle the oxidised donor. Herein, the photo-recycling of decamethylferrocenium cations (DcMFc+) using aqueous core-shell semiconductor CdSe@CdS nanoparticles is presented. Negative polarisation of the liquid|liquid interface is required to extract DcMFc+ to the aqueous phase. This facilitates the efficient capture of electrons by DcMFc+ on the surface of the photo-excited CdSe@CdS nanoparticles, with hydrophobic DcMFc subsequently partitioning back to the organic phase and resetting the system. TiO2 (P25) and CdSe semiconductor nanoparticles failed to recycle DcMFc+ due to their lower conduction band energy levels. During photo-recycling, CdS (on CdSe) may be self-oxidised and photo-corrode, instead of water acting as the hole scavenger.
Notes
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2020_ChemPhysChem_Manuscript_Open_Access.pdf
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Additional details
Funding
- Science Foundation Ireland
- Designing Reactive Functionalised Soft Interfaces _ Self-healing soft materials for solar energy conversion, energy storage, and sustainable low cost hydrogen production 13/SIRG/2137
- European Commission
- SOFT-PHOTOCONVERSION – Solar Energy Conversion without Solid State Architectures: Pushing the Boundaries of Photoconversion Efficiencies at Self-healing Photosensitiser Functionalised Soft Interfaces 716792