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Effects of orientation at the phthalocyanine-CdSe interface on the electron transfer characteristics

A phthalocyanine molecule adsorbed on the (101[combining macron]0) surface of wurtzite CdSe is theoretically modeled by the DFT method. We have found that a linker does not affect substantially the redox properties of phthalocyanine, while saturation of the macrocycle with peripheral substituent gro...

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Published in:Physical chemistry chemical physics : PCCP 2017-04, Vol.19 (16), p.10511-10517
Main Authors: Golovanov, V V, Nazarchuk, B V, Golovanova, V V, Tkachenko, N V, Rantala, T T
Format: Article
Language:English
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Summary:A phthalocyanine molecule adsorbed on the (101[combining macron]0) surface of wurtzite CdSe is theoretically modeled by the DFT method. We have found that a linker does not affect substantially the redox properties of phthalocyanine, while saturation of the macrocycle with peripheral substituent groups causes a downward shift in the energy position of its frontier orbitals that can hinder electron injection to the CdSe surface. Tilting of the phthalocyanine molecule relative to the surface also leads to the lowering of its molecular electronic levels relative to the bands of CdSe. At a tilting angle of 30°, the LUMO level of the dye appears to be lower than the conduction band minimum of cadmium selenide, which makes the electron transfer to its hybridized surface unfavorable. By contrast, the HOMO level of the phenylbutyric acid linker provides a suitable intermediate channel for the hole transfer from the valence band of CdSe to the phthalocyanine that points to the possible acceptor behavior of the phthalocyanine molecule in its hybrids with CdSe nanostructures.
ISSN:1463-9076
1463-9084
DOI:10.1039/c7cp00833c