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Probing electronic coupling in excitonically coupled heterodimer complexes by two-color three-pulse photon echoes
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Zeitschriftentitel: | The Journal of Chemical Physics |
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Personen und Körperschaften: | , |
In: | The Journal of Chemical Physics, 121, 2004, 21, S. 10556-10565 |
Format: | E-Article |
Sprache: | Englisch |
veröffentlicht: |
AIP Publishing
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Schlagwörter: |
author_facet |
Mančal, Tomáš Fleming, Graham R. Mančal, Tomáš Fleming, Graham R. |
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author |
Mančal, Tomáš Fleming, Graham R. |
spellingShingle |
Mančal, Tomáš Fleming, Graham R. The Journal of Chemical Physics Probing electronic coupling in excitonically coupled heterodimer complexes by two-color three-pulse photon echoes Physical and Theoretical Chemistry General Physics and Astronomy |
author_sort |
mančal, tomáš |
spelling |
Mančal, Tomáš Fleming, Graham R. 0021-9606 1089-7690 AIP Publishing Physical and Theoretical Chemistry General Physics and Astronomy http://dx.doi.org/10.1063/1.1807816 <jats:p>Following the earlier work of Yang et al. [J. Chem. Phys. 110 (1999) 2983] analytical expressions for the downhill and uphill resonant two-color three-pulse photon echo peak shift (2C-3PEPS) of a heterodimer system are derived in the impulsive limit. It is shown how to obtain information about coupling between the components of the dimer from the combined one- and two-color peak shift measurements. Further analytical relations are derived which enable site specific information about the environment of the components, including the relative difference of the inhomogeneity and the difference between the energy-gap correlation functions on the heterodimer sites to be obtained. The simulations show only a very small influence of the laser pulse length on the measured values of coupling coefficient and other relevant quantities suggesting that current 2C-3PEPS measurements can find practical application in directly measuring couplings in excitonically coupled heterodimer complexes.</jats:p> Probing electronic coupling in excitonically coupled heterodimer complexes by two-color three-pulse photon echoes The Journal of Chemical Physics |
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10.1063/1.1807816 |
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The Journal of Chemical Physics |
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title |
Probing electronic coupling in excitonically coupled heterodimer complexes by two-color three-pulse photon echoes |
title_unstemmed |
Probing electronic coupling in excitonically coupled heterodimer complexes by two-color three-pulse photon echoes |
title_full |
Probing electronic coupling in excitonically coupled heterodimer complexes by two-color three-pulse photon echoes |
title_fullStr |
Probing electronic coupling in excitonically coupled heterodimer complexes by two-color three-pulse photon echoes |
title_full_unstemmed |
Probing electronic coupling in excitonically coupled heterodimer complexes by two-color three-pulse photon echoes |
title_short |
Probing electronic coupling in excitonically coupled heterodimer complexes by two-color three-pulse photon echoes |
title_sort |
probing electronic coupling in excitonically coupled heterodimer complexes by two-color three-pulse photon echoes |
topic |
Physical and Theoretical Chemistry General Physics and Astronomy |
url |
http://dx.doi.org/10.1063/1.1807816 |
publishDate |
2004 |
physical |
10556-10565 |
description |
<jats:p>Following the earlier work of Yang et al. [J. Chem. Phys. 110 (1999) 2983] analytical expressions for the downhill and uphill resonant two-color three-pulse photon echo peak shift (2C-3PEPS) of a heterodimer system are derived in the impulsive limit. It is shown how to obtain information about coupling between the components of the dimer from the combined one- and two-color peak shift measurements. Further analytical relations are derived which enable site specific information about the environment of the components, including the relative difference of the inhomogeneity and the difference between the energy-gap correlation functions on the heterodimer sites to be obtained. The simulations show only a very small influence of the laser pulse length on the measured values of coupling coefficient and other relevant quantities suggesting that current 2C-3PEPS measurements can find practical application in directly measuring couplings in excitonically coupled heterodimer complexes.</jats:p> |
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author | Mančal, Tomáš, Fleming, Graham R. |
author_facet | Mančal, Tomáš, Fleming, Graham R., Mančal, Tomáš, Fleming, Graham R. |
author_sort | mančal, tomáš |
container_issue | 21 |
container_start_page | 10556 |
container_title | The Journal of Chemical Physics |
container_volume | 121 |
description | <jats:p>Following the earlier work of Yang et al. [J. Chem. Phys. 110 (1999) 2983] analytical expressions for the downhill and uphill resonant two-color three-pulse photon echo peak shift (2C-3PEPS) of a heterodimer system are derived in the impulsive limit. It is shown how to obtain information about coupling between the components of the dimer from the combined one- and two-color peak shift measurements. Further analytical relations are derived which enable site specific information about the environment of the components, including the relative difference of the inhomogeneity and the difference between the energy-gap correlation functions on the heterodimer sites to be obtained. The simulations show only a very small influence of the laser pulse length on the measured values of coupling coefficient and other relevant quantities suggesting that current 2C-3PEPS measurements can find practical application in directly measuring couplings in excitonically coupled heterodimer complexes.</jats:p> |
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series | The Journal of Chemical Physics |
source_id | 49 |
spelling | Mančal, Tomáš Fleming, Graham R. 0021-9606 1089-7690 AIP Publishing Physical and Theoretical Chemistry General Physics and Astronomy http://dx.doi.org/10.1063/1.1807816 <jats:p>Following the earlier work of Yang et al. [J. Chem. Phys. 110 (1999) 2983] analytical expressions for the downhill and uphill resonant two-color three-pulse photon echo peak shift (2C-3PEPS) of a heterodimer system are derived in the impulsive limit. It is shown how to obtain information about coupling between the components of the dimer from the combined one- and two-color peak shift measurements. Further analytical relations are derived which enable site specific information about the environment of the components, including the relative difference of the inhomogeneity and the difference between the energy-gap correlation functions on the heterodimer sites to be obtained. The simulations show only a very small influence of the laser pulse length on the measured values of coupling coefficient and other relevant quantities suggesting that current 2C-3PEPS measurements can find practical application in directly measuring couplings in excitonically coupled heterodimer complexes.</jats:p> Probing electronic coupling in excitonically coupled heterodimer complexes by two-color three-pulse photon echoes The Journal of Chemical Physics |
spellingShingle | Mančal, Tomáš, Fleming, Graham R., The Journal of Chemical Physics, Probing electronic coupling in excitonically coupled heterodimer complexes by two-color three-pulse photon echoes, Physical and Theoretical Chemistry, General Physics and Astronomy |
title | Probing electronic coupling in excitonically coupled heterodimer complexes by two-color three-pulse photon echoes |
title_full | Probing electronic coupling in excitonically coupled heterodimer complexes by two-color three-pulse photon echoes |
title_fullStr | Probing electronic coupling in excitonically coupled heterodimer complexes by two-color three-pulse photon echoes |
title_full_unstemmed | Probing electronic coupling in excitonically coupled heterodimer complexes by two-color three-pulse photon echoes |
title_short | Probing electronic coupling in excitonically coupled heterodimer complexes by two-color three-pulse photon echoes |
title_sort | probing electronic coupling in excitonically coupled heterodimer complexes by two-color three-pulse photon echoes |
title_unstemmed | Probing electronic coupling in excitonically coupled heterodimer complexes by two-color three-pulse photon echoes |
topic | Physical and Theoretical Chemistry, General Physics and Astronomy |
url | http://dx.doi.org/10.1063/1.1807816 |