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Lookup NU author(s): Dr Elisabetta Benazzi, Dr Joshua Karlsson, Dr Guillaume Izzet, Professor Elizabeth GibsonORCiD
This is the authors' accepted manuscript of an article that has been published in its final definitive form by Royal Society of Chemistry, 2021.
For re-use rights please refer to the publisher's terms and conditions.
© the Partner Organisations. H+ modulated charge-transfer in photoexcited covalent polyoxometalate-bodipy conjugates is described. The hybrid organic/inorganic molecular photoactive dyads are based on Keggin-type polyoxometalates (POMs, where KM = [PM11O39] and M = Mo or W) covalently grafted via an organotin linker to a bodipy (BOD) photosensitizer. The relative potentials of the photosensitizer and POM are aligned such that light-induced electron transfer from BOD to POM is permitted for the polyoxomolybdate KMoSn[BOD] but not effective for the polyoxotungstate analogue KWSn[BOD]. In both cases, the addition of acid shifts the redox potential of the POM only, to increase the driving force for electron transfer. This leads to charge-separation being switched on for KWSn[BOD] in the presence of acid. The addition of acid to KMoSn[BOD] accelerates charge-separation by an order of magnitude (from 2 ns to 200 ps) and is accompanied by a deceleration of charge recombination, leading to a charge-separated state lifetime of up to 1.3 μs. This behaviour is consistent with proton coupled electron transfer, which has previously been observed electrochemically for POMs, but this study shows, for the first time, the impact of protonation on photoinduced electron transfer.
Author(s): Benazzi E, Karlsson J, Ben M'Barek Y, Chabera P, Blanchard S, Alves S, Proust A, Pullerits T, Izzet G, Gibson EA
Publication type: Article
Publication status: Published
Journal: Inorganic Chemistry Frontiers
Year: 2021
Volume: 8
Issue: 6
Pages: 1610-1618
Print publication date: 21/03/2021
Online publication date: 21/01/2021
Acceptance date: 20/01/2021
Date deposited: 23/04/2021
ISSN (print): 2052-1545
ISSN (electronic): 2052-1553
Publisher: Royal Society of Chemistry
URL: https://doi.org/10.1039/d0qi01368d
DOI: 10.1039/d0qi01368d
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