Disorder influenced optical properties of α-sexithiophene single crystals and thin evaporated films

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • R. N. Marks
  • M. Muccini
  • E. Lunedi
  • R. H. Michel
  • M. Murgia
  • R. Zamboni
  • C. Taliani
  • G. Horowitz
  • F. Garnier
  • M. Hopmeier
  • Michael Oestreich
  • Rainer E. Mahrt

Externe Organisationen

  • Consiglio Nazionale delle Ricerche (CNR)
  • Centre national de la recherche scientifique (CNRS)
  • Philipps-Universität Marburg
Forschungs-netzwerk anzeigen

Details

OriginalspracheEnglisch
Seiten (von - bis)49-56
Seitenumfang8
FachzeitschriftChemical Physics
Jahrgang227
Ausgabenummer1-2
PublikationsstatusVeröffentlicht - 1 Feb. 1998
Extern publiziertJa

Abstract

We report measurements on steady state and time resolved photoluminescence (PL) and PL-excitation (PLE) of sexithiophene single crystals and evaporated thin films. In contrast to the broad spectral features usually observed even in crystals, we have observed for the first time sharp emission peaks from the single crystal superimposed on a broader background. The broad background is due to emission from defect states, which are observable in PLE measurements and site-selective PL. These defect states are visible both in films and crystals, but their density and nature are strongly dependent on the growth conditions. Additionally in the film a fast energy transfer from the primary excited molecular states to defect states is observed on a sub 100 ps timescale whereas the fluorescence lifetime of these defects is around 700 ps.

Zitieren

Disorder influenced optical properties of α-sexithiophene single crystals and thin evaporated films. / Marks, R. N.; Muccini, M.; Lunedi, E. et al.
in: Chemical Physics, Jahrgang 227, Nr. 1-2, 01.02.1998, S. 49-56.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Marks, RN, Muccini, M, Lunedi, E, Michel, RH, Murgia, M, Zamboni, R, Taliani, C, Horowitz, G, Garnier, F, Hopmeier, M, Oestreich, M & Mahrt, RE 1998, 'Disorder influenced optical properties of α-sexithiophene single crystals and thin evaporated films', Chemical Physics, Jg. 227, Nr. 1-2, S. 49-56. https://doi.org/10.1016/S0301-0104(97)00274-7
Marks, R. N., Muccini, M., Lunedi, E., Michel, R. H., Murgia, M., Zamboni, R., Taliani, C., Horowitz, G., Garnier, F., Hopmeier, M., Oestreich, M., & Mahrt, R. E. (1998). Disorder influenced optical properties of α-sexithiophene single crystals and thin evaporated films. Chemical Physics, 227(1-2), 49-56. https://doi.org/10.1016/S0301-0104(97)00274-7
Marks RN, Muccini M, Lunedi E, Michel RH, Murgia M, Zamboni R et al. Disorder influenced optical properties of α-sexithiophene single crystals and thin evaporated films. Chemical Physics. 1998 Feb 1;227(1-2):49-56. doi: 10.1016/S0301-0104(97)00274-7
Marks, R. N. ; Muccini, M. ; Lunedi, E. et al. / Disorder influenced optical properties of α-sexithiophene single crystals and thin evaporated films. in: Chemical Physics. 1998 ; Jahrgang 227, Nr. 1-2. S. 49-56.
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title = "Disorder influenced optical properties of α-sexithiophene single crystals and thin evaporated films",
abstract = "We report measurements on steady state and time resolved photoluminescence (PL) and PL-excitation (PLE) of sexithiophene single crystals and evaporated thin films. In contrast to the broad spectral features usually observed even in crystals, we have observed for the first time sharp emission peaks from the single crystal superimposed on a broader background. The broad background is due to emission from defect states, which are observable in PLE measurements and site-selective PL. These defect states are visible both in films and crystals, but their density and nature are strongly dependent on the growth conditions. Additionally in the film a fast energy transfer from the primary excited molecular states to defect states is observed on a sub 100 ps timescale whereas the fluorescence lifetime of these defects is around 700 ps.",
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note = "Funding information: We are grateful to Prof. H. B~issler and Prof. W.W. Riihle for stimulating discussions. This work was partly supported by the European Community (SELOA and LEDFOS), Sonderforschungsbereich 383 and the Volkswagen-Stiftung. RFM gratefully acknowledges financial support by the Deutsche Forschungsgemeinschaft. We are grateful to Hama- matsu Photonics Italia for financial support with the PMA-11 Optical Multichannel Analyser.",
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TY - JOUR

T1 - Disorder influenced optical properties of α-sexithiophene single crystals and thin evaporated films

AU - Marks, R. N.

AU - Muccini, M.

AU - Lunedi, E.

AU - Michel, R. H.

AU - Murgia, M.

AU - Zamboni, R.

AU - Taliani, C.

AU - Horowitz, G.

AU - Garnier, F.

AU - Hopmeier, M.

AU - Oestreich, Michael

AU - Mahrt, Rainer E.

N1 - Funding information: We are grateful to Prof. H. B~issler and Prof. W.W. Riihle for stimulating discussions. This work was partly supported by the European Community (SELOA and LEDFOS), Sonderforschungsbereich 383 and the Volkswagen-Stiftung. RFM gratefully acknowledges financial support by the Deutsche Forschungsgemeinschaft. We are grateful to Hama- matsu Photonics Italia for financial support with the PMA-11 Optical Multichannel Analyser.

PY - 1998/2/1

Y1 - 1998/2/1

N2 - We report measurements on steady state and time resolved photoluminescence (PL) and PL-excitation (PLE) of sexithiophene single crystals and evaporated thin films. In contrast to the broad spectral features usually observed even in crystals, we have observed for the first time sharp emission peaks from the single crystal superimposed on a broader background. The broad background is due to emission from defect states, which are observable in PLE measurements and site-selective PL. These defect states are visible both in films and crystals, but their density and nature are strongly dependent on the growth conditions. Additionally in the film a fast energy transfer from the primary excited molecular states to defect states is observed on a sub 100 ps timescale whereas the fluorescence lifetime of these defects is around 700 ps.

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EP - 56

JO - Chemical Physics

JF - Chemical Physics

SN - 0301-0104

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ER -

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