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Efficient intramolecular energy transfer in single endcapped conjugated polymer molecules in the absence of appreciable spectral overlap
被引:49
作者:

Becker, K
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机构: Univ Munich, Photon & Optoelect Grp, Dept Phys, D-8000 Munich, Germany

Lupton, JM
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机构: Univ Munich, Photon & Optoelect Grp, Dept Phys, D-8000 Munich, Germany

Feldmann, J
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机构: Univ Munich, Photon & Optoelect Grp, Dept Phys, D-8000 Munich, Germany

Setayesh, S
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机构: Univ Munich, Photon & Optoelect Grp, Dept Phys, D-8000 Munich, Germany

Grimsdale, AC
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机构: Univ Munich, Photon & Optoelect Grp, Dept Phys, D-8000 Munich, Germany

Müllen, K
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机构: Univ Munich, Photon & Optoelect Grp, Dept Phys, D-8000 Munich, Germany
机构:
[1] Univ Munich, Photon & Optoelect Grp, Dept Phys, D-8000 Munich, Germany
[2] Univ Munich, CENS, D-8000 Munich, Germany
[3] Max Planck Inst Polymer Res, D-55128 Mainz, Germany
关键词:
D O I:
10.1021/ja056469h
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Intramolecular energy transfer is investigated in an endcapped conjugated polymer on the single molecule level at low temperature. While light harvesting in one dimension is on average inefficient in the ensemble, the efficiency scatters widely on the single molecule level, with some molecules exhibiting near-unity transfer probability from the polymer backbone donor to the acceptor endcap. This transfer occurs in the absence of spectral overlap between donor and acceptor, as the electronic and vibronic transitions narrow substantially at low temperatures once inhomogeneous disorder broadening is overcome. The results illustrate how far-field absorption and emission characteristics of molecular transitions are insufficient to describe resonant energy transfer processes following Förster theory in multichromophoric aggregates. Rather, exciton trapping due to efficient multiphonon emission has to be invoked with a possible contribution of strong polaronic coupling. Copyright © 2006 American Chemical Society.
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页码:680 / 681
页数:2
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