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Proceedings Paper

Beyond vibrationally mediated electron transfer: interfacial charge injection on a sub-10-fs time scale
Author(s): Robert Huber; Jacques E. Moser; Michael Gratzel; Josef L. Wachtveitl
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Paper Abstract

The electron transfer (ET) from organic dye molecules to semiconductor-colloidal systems is characterized by a special energetic situation with a charge transfer reaction from a system of discrete donor levels to a continuum of acceptor states. If these systems show a strong electronic coupling they are amongst the fastest known ET systems with transfer times of less than 10 fs. In the first part a detailed discussion of the direct observation of an ET reaction with a time constant of about 6 fs will be given, with an accompanying argumentation concerning possible artifacts or other interfering signal contributions. In a second part we will try to give a simple picture for the scenario of such superfast ET reactions and one main focus will be the discussion of electronic dephasing and its consequences for the ET reaction. The actual ET process can be understood as a kind of dispersion process of the initially located electron into the colloid representing a real motion of charge density from the alizarin to the colloid.

Paper Details

Date Published: 4 December 2003
PDF: 11 pages
Proc. SPIE 5223, Physical Chemistry of Interfaces and Nanomaterials II, (4 December 2003); doi: 10.1117/12.506722
Show Author Affiliations
Robert Huber, J. W. Goethe-Univ. Frankfurt am Main (Germany)
Jacques E. Moser, Ecole Polytechnique Federale de Lausanne (Switzerland)
Michael Gratzel, Ecole Polytechnique Federale de Lausanne (Switzerland)
Josef L. Wachtveitl, J. W. Goethe-Univ. Frankfurt am Main (Germany)

Published in SPIE Proceedings Vol. 5223:
Physical Chemistry of Interfaces and Nanomaterials II
Tianquan Lian; Hai-Lung Dai, Editor(s)

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