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Title: Photoexcited energy transfer in a weakly coupled dimer

Abstract

Nonadiabatic excited-state molecular dynamics (NA-ESMD) simulations have been performed in order to study the time-dependent exciton localization during energy transfer between two chromophore units of the weakly coupled anthracene dimer dithia-anthracenophane (DTA). Simulations are done at both low temperature (10 K) and room temperature (300 K). The initial photoexcitation creates an exciton which is primarily localized on a single monomer unit. Subsequently, the exciton experiences an ultrafast energy transfer becoming localized on either one monomer unit or the other, whereas delocalization between both monomers never occurs. In half of the trajectories, the electronic transition density becomes completely localized on the same monomer as the initial excitation, while in the other half, it becomes completely localized on the opposite monomer. In this article, we present an analysis of the energy transfer dynamics and the effect of thermally induced geometry distortions on the exciton localization. Finally, simulated fluorescence anisotropy decay curves for both DTA and the monomer unit dimethyl anthracene (DMA) are compared. As a result, our analysis reveals that changes in the transition density localization caused by energy transfer between two monomers in DTA is not the only source of depolarization and exciton relaxation within a single DTA monomer unit canmore » also cause reorientation of the transition dipole.« less

Authors:
 [1];  [2];  [2];  [1]
  1. Univ. Nacional de Quilmes, Bernal (Argentina)
  2. Los Alamos National Lab. (LANL), Los Alamos, NM (United States)
Publication Date:
Research Org.:
Los Alamos National Lab. (LANL), Los Alamos, NM (United States)
Sponsoring Org.:
USDOE
OSTI Identifier:
1227902
Report Number(s):
LA-UR-14-28224
Journal ID: ISSN 1520-6106
Grant/Contract Number:  
PICT-2010-2375; AC52-06NA25396
Resource Type:
Accepted Manuscript
Journal Name:
Journal of Physical Chemistry. B, Condensed Matter, Materials, Surfaces, Interfaces and Biophysical Chemistry
Additional Journal Information:
Journal Volume: 119; Journal Issue: 24; Journal ID: ISSN 1520-6106
Publisher:
American Chemical Society
Country of Publication:
United States
Language:
English
Subject:
36 MATERIALS SCIENCE; energy transfer; fluorescence anisotropy; excited states; bichromophore

Citation Formats

Hernandez, Laura Alfonso, Nelson, Tammie, Tretiak, Sergei, and Fernandez-Alberti, Sebastian. Photoexcited energy transfer in a weakly coupled dimer. United States: N. p., 2015. Web. doi:10.1021/jp510557f.
Hernandez, Laura Alfonso, Nelson, Tammie, Tretiak, Sergei, & Fernandez-Alberti, Sebastian. Photoexcited energy transfer in a weakly coupled dimer. United States. doi:10.1021/jp510557f.
Hernandez, Laura Alfonso, Nelson, Tammie, Tretiak, Sergei, and Fernandez-Alberti, Sebastian. Thu . "Photoexcited energy transfer in a weakly coupled dimer". United States. doi:10.1021/jp510557f. https://www.osti.gov/servlets/purl/1227902.
@article{osti_1227902,
title = {Photoexcited energy transfer in a weakly coupled dimer},
author = {Hernandez, Laura Alfonso and Nelson, Tammie and Tretiak, Sergei and Fernandez-Alberti, Sebastian},
abstractNote = {Nonadiabatic excited-state molecular dynamics (NA-ESMD) simulations have been performed in order to study the time-dependent exciton localization during energy transfer between two chromophore units of the weakly coupled anthracene dimer dithia-anthracenophane (DTA). Simulations are done at both low temperature (10 K) and room temperature (300 K). The initial photoexcitation creates an exciton which is primarily localized on a single monomer unit. Subsequently, the exciton experiences an ultrafast energy transfer becoming localized on either one monomer unit or the other, whereas delocalization between both monomers never occurs. In half of the trajectories, the electronic transition density becomes completely localized on the same monomer as the initial excitation, while in the other half, it becomes completely localized on the opposite monomer. In this article, we present an analysis of the energy transfer dynamics and the effect of thermally induced geometry distortions on the exciton localization. Finally, simulated fluorescence anisotropy decay curves for both DTA and the monomer unit dimethyl anthracene (DMA) are compared. As a result, our analysis reveals that changes in the transition density localization caused by energy transfer between two monomers in DTA is not the only source of depolarization and exciton relaxation within a single DTA monomer unit can also cause reorientation of the transition dipole.},
doi = {10.1021/jp510557f},
journal = {Journal of Physical Chemistry. B, Condensed Matter, Materials, Surfaces, Interfaces and Biophysical Chemistry},
number = 24,
volume = 119,
place = {United States},
year = {2015},
month = {1}
}

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