Journal article
Photo-recycling the Sacrificial Electron Donor: Towards Sustainable Hydrogen Evolution in a Biphasic System.
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Ge P
Laboratoire d'Électrochimie Physique et Analytique, École Polytechnique Fédérale de Lausanne, EPFL, Valais Wallis, Rue de l'industrie, 17, 1950, SION, Switzerland.
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Hojeij M
Laboratoire d'Électrochimie Physique et Analytique, École Polytechnique Fédérale de Lausanne, EPFL, Valais Wallis, Rue de l'industrie, 17, 1950, SION, Switzerland.
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Scanlon MD
The Bernal Institute and Department of Chemical Sciences, University of Limerick (UL), Limerick, V94 T9PX, Ireland.
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Girault HH
Laboratoire d'Électrochimie Physique et Analytique, École Polytechnique Fédérale de Lausanne, EPFL, Valais Wallis, Rue de l'industrie, 17, 1950, SION, Switzerland.
Published in:
- Chemphyschem : a European journal of chemical physics and physical chemistry. - 2020
English
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.
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Language
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Open access status
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closed
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Identifiers
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Persistent URL
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https://sonar.ch/global/documents/120530
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