Relaxation dynamics of excitons in thin quaterthiophene films on different substrates

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  • Philipps-Universität Marburg
  • Julius-Maximilians-Universität Würzburg
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Details

OriginalspracheEnglisch
Seiten (von - bis)9-15
Seitenumfang7
FachzeitschriftChemical Physics Letters
Jahrgang314
Ausgabenummer1-2
PublikationsstatusVeröffentlicht - 26 Nov. 1999
Extern publiziertJa

Abstract

We compare picosecond time-resolved photoluminescence spectra of thin polycrystalline films of quaterthiophene (4T) vapour deposited on two different substrates: highly oriented pyrolytic graphite (HOPG) and glass. At zero time delay, both films show the same highly resolved vibrational fine structure as isolated 4T molecules. The fine structure remains over time on HOPG, but vanishes within the first 100 ps on glass and is replaced by emission from two luminescent traps. The results explain the line broadening in time-integrated (cw) spectra and yield information on the luminescence quenching in polycrystalline organic films.

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Relaxation dynamics of excitons in thin quaterthiophene films on different substrates. / Hopmeier, M.; Gebauer, W.; Oestreich, Michael et al.
in: Chemical Physics Letters, Jahrgang 314, Nr. 1-2, 26.11.1999, S. 9-15.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Hopmeier M, Gebauer W, Oestreich M, Sokolowski M, Umbach E, Mahrt RF. Relaxation dynamics of excitons in thin quaterthiophene films on different substrates. Chemical Physics Letters. 1999 Nov 26;314(1-2):9-15. doi: 10.1016/S0009-2614(99)01116-1
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title = "Relaxation dynamics of excitons in thin quaterthiophene films on different substrates",
abstract = "We compare picosecond time-resolved photoluminescence spectra of thin polycrystalline films of quaterthiophene (4T) vapour deposited on two different substrates: highly oriented pyrolytic graphite (HOPG) and glass. At zero time delay, both films show the same highly resolved vibrational fine structure as isolated 4T molecules. The fine structure remains over time on HOPG, but vanishes within the first 100 ps on glass and is replaced by emission from two luminescent traps. The results explain the line broadening in time-integrated (cw) spectra and yield information on the luminescence quenching in polycrystalline organic films.",
author = "M. Hopmeier and W. Gebauer and Michael Oestreich and M. Sokolowski and E. Umbach and Mahrt, {R. F.}",
note = "Funding information: We thank Dr. Naarmann, BASF AG, for providing the 4T material. We are grateful to Prof. H. B{\"a}ssler, Prof. W.W. R{\"u}hle, and Dr. H. Egelhaaf for stimulating discussions. This work was supported by the Deutsche Forschungsgemeinschaft through SFB383 and through project Um 6/4-1. Financial support by the Fond der Chemischen Industrie is gratefully acknowledged.",
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TY - JOUR

T1 - Relaxation dynamics of excitons in thin quaterthiophene films on different substrates

AU - Hopmeier, M.

AU - Gebauer, W.

AU - Oestreich, Michael

AU - Sokolowski, M.

AU - Umbach, E.

AU - Mahrt, R. F.

N1 - Funding information: We thank Dr. Naarmann, BASF AG, for providing the 4T material. We are grateful to Prof. H. Bässler, Prof. W.W. Rühle, and Dr. H. Egelhaaf for stimulating discussions. This work was supported by the Deutsche Forschungsgemeinschaft through SFB383 and through project Um 6/4-1. Financial support by the Fond der Chemischen Industrie is gratefully acknowledged.

PY - 1999/11/26

Y1 - 1999/11/26

N2 - We compare picosecond time-resolved photoluminescence spectra of thin polycrystalline films of quaterthiophene (4T) vapour deposited on two different substrates: highly oriented pyrolytic graphite (HOPG) and glass. At zero time delay, both films show the same highly resolved vibrational fine structure as isolated 4T molecules. The fine structure remains over time on HOPG, but vanishes within the first 100 ps on glass and is replaced by emission from two luminescent traps. The results explain the line broadening in time-integrated (cw) spectra and yield information on the luminescence quenching in polycrystalline organic films.

AB - We compare picosecond time-resolved photoluminescence spectra of thin polycrystalline films of quaterthiophene (4T) vapour deposited on two different substrates: highly oriented pyrolytic graphite (HOPG) and glass. At zero time delay, both films show the same highly resolved vibrational fine structure as isolated 4T molecules. The fine structure remains over time on HOPG, but vanishes within the first 100 ps on glass and is replaced by emission from two luminescent traps. The results explain the line broadening in time-integrated (cw) spectra and yield information on the luminescence quenching in polycrystalline organic films.

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U2 - 10.1016/S0009-2614(99)01116-1

DO - 10.1016/S0009-2614(99)01116-1

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VL - 314

SP - 9

EP - 15

JO - Chemical Physics Letters

JF - Chemical Physics Letters

SN - 0009-2614

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