Journal article
Potentiostatic Modulation of the Direction of Light-Induced Electron Transfer in a Heterosupermolecule
The Journal of Physical Chemistry Part B, Vol.102(50), pp.10272-10278
1998
Abstract
Described is the covalent assembly of heterosupermolecules from TiO2 nanocrystal (TiO2), ruthenium complex (R) and viologen (V) components. Also described is their covalent organization to form a heterosupramolecular assembly. Effective function modulation has proved possible via an intrinsic substrate formed by the TiO2 nanocrystal components. Specifically, under open circuit conditions or upon application of a sufficiently positive potential to the intrinsic substrate, visible light excitation of the ruthenium complex component results in electron transfer to the TiO2 nanocrystal component (95%). Alternatively, upon application of a sufficiently negative potential to the intrinsic substrate, visible light excitation of the ruthenium complex component results in electron transfer to both the TiO2 nanocrystal (48%) and the viologen components (52%). Considered are some implications of these findings for the development of practical devices based on heterosupramolecular function that is addressable and modulatable on the nanometer scale.
Details
- Title
- Potentiostatic Modulation of the Direction of Light-Induced Electron Transfer in a Heterosupermolecule
- Authors
- Geoffrey Will (Author) - University College DublinGerrit Boschloo (Author) - University College DublinRobin Hoyle (Author) - University College DublinS. Nagaraja Rao (Author) - University College DublinDonald Fitzmaurice (Corresponding Author) - University College Dublin
- Publication details
- The Journal of Physical Chemistry Part B, Vol.102(50), pp.10272-10278
- Publisher
- American Chemical Society
- DOI
- 10.1021/jp9828843
- ISSN
- 1520-5207
- Organisation Unit
- School of Science, Technology and Engineering
- Language
- English
- Record Identifier
- 99737878802621
- Output Type
- Journal article
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- Chemistry, Physical
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