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Ultrafast electron and hole transfer dynamics of a solar cell dye containing hole acceptors on mesoporous TiO2 and Al2O3
Univ Siegen, Phys Chem, Adolf Reichwein Str 2, D-57076 Siegen, Germany..
Univ Siegen, Phys Chem, Adolf Reichwein Str 2, D-57076 Siegen, Germany..
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry - Ångström, Physical Chemistry.
Univ Siegen, Phys Chem, Adolf Reichwein Str 2, D-57076 Siegen, Germany..
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2017 (English)In: Physical Chemistry, Chemical Physics - PCCP, ISSN 1463-9076, E-ISSN 1463-9084, Vol. 19, no 10, 7158-7166 p.Article in journal (Refereed) Published
Abstract [en]

The stability of dye cations against recombination with conduction band electrons in mesoporous TiO2 electrodes is a key property for improving light harvesting in dye-sensitised solar cells. Using ultrafast transient broadband absorption spectroscopy, we monitor efficient intramolecular hole transfer in the solar cell dye E6 having two peripheral triarylamine acceptors. After photoexcitation, two hole transfer mechanisms are identified: a concerted mechanism for electron injection and hole transfer (2.4 ps) and a sequential mechanism with time constants of 3.9 ps and 30 ps. This way the dye retards unwanted recombination with a TiO2 conduction band electron by quickly moving the hole further away from the surface. Contact of the E6/TiO2 surface with the solvent acetonitrile has almost no influence on the electron injection and hole transfer kinetics. Fast hole transfer (2.8 ps) is also observed on a "non-injecting'' Al2O3 surface generating a radical cation-radical anion species with a lifetime of 530 ps. The findings confirm the good intramolecular hole transfer properties of this dye on both thin films. In contrast, intramolecular hole transfer does not occur in the mid-polar organic solvent methyl acetate. This is confirmed by TDDFT calculations suggesting a polarity-induced reduction of the driving force for hole transfer. In methyl acetate, only the relaxation of the initially photoexcited core chromophore is observed including solvent relaxation processes of the electronically excited state S-1/ICT.

Place, publisher, year, edition, pages
Royal Society of Chemistry, 2017. Vol. 19, no 10, 7158-7166 p.
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Physical Chemistry
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URN: urn:nbn:se:uu:diva-321151DOI: 10.1039/c6cp08609hISI: 000396148600029PubMedID: 28230867OAI: oai:DiVA.org:uu-321151DiVA: diva2:1092341
Available from: 2017-05-02 Created: 2017-05-02 Last updated: 2017-05-02Bibliographically approved

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