Luminescence quenching by inter-chain aggregates in substituted polythiophenes

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Luminescence quenching by inter-chain aggregates in substituted polythiophenes. / Ruseckas, Arvydas; Namdas, Ebinazar B.; Theander, Mathias; Svensson, Mattias; Yartsev, Arkady; Zigmantas, Donatas; Andersson, Mats R.; Inganas, Olle; Sundström, Villy.

I: Journal of Photochemistry and Photobiology, A: Chemistry, Vol. 144, Nr. 1, 2001, s. 3-12.

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Ruseckas, Arvydas ; Namdas, Ebinazar B. ; Theander, Mathias ; Svensson, Mattias ; Yartsev, Arkady ; Zigmantas, Donatas ; Andersson, Mats R. ; Inganas, Olle ; Sundström, Villy. / Luminescence quenching by inter-chain aggregates in substituted polythiophenes. I: Journal of Photochemistry and Photobiology, A: Chemistry. 2001 ; Vol. 144, Nr. 1. s. 3-12.

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TY - JOUR

T1 - Luminescence quenching by inter-chain aggregates in substituted polythiophenes

AU - Ruseckas, Arvydas

AU - Namdas, Ebinazar B.

AU - Theander, Mathias

AU - Svensson, Mattias

AU - Yartsev, Arkady

AU - Zigmantas, Donatas

AU - Andersson, Mats R.

AU - Inganas, Olle

AU - Sundström, Villy

N1 - The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Chemical Physics (S) (011001060)

PY - 2001

Y1 - 2001

N2 - Time-resolved photo luminescence spectra measured in solid films of two polythiophene derivatives with different chain packing allow to distinguish emission of intra-chain excitations from the luminescence of inter-chain aggregates. Aggregate luminescence is red shifted by about 0.1 eV relative to intra-chain emission and shows vibronic coupling to the C=C bond stretch with the Huang-Phys factor of S approximate to 1.5, which is twice bigger than that of the intra-chain emission. Combining time resolved luminescence data with femtosecond transient absorption, we show that the dynamic quenching of the luminescence in films with dense chain packing is mainly due to excitation energy transfer to aggregates. The radiative lifetime of the lowest excited state of the aggregate with the optical gap of 1.84-1.9 eV is estimated to be about 20 ns. The aggregate contribution to the total luminescence in the polythiophene films with dense chain packing is about 50% and does not change significantly with temperature. (C) 2001 Elsevier Science B.V. All rights reserved.

AB - Time-resolved photo luminescence spectra measured in solid films of two polythiophene derivatives with different chain packing allow to distinguish emission of intra-chain excitations from the luminescence of inter-chain aggregates. Aggregate luminescence is red shifted by about 0.1 eV relative to intra-chain emission and shows vibronic coupling to the C=C bond stretch with the Huang-Phys factor of S approximate to 1.5, which is twice bigger than that of the intra-chain emission. Combining time resolved luminescence data with femtosecond transient absorption, we show that the dynamic quenching of the luminescence in films with dense chain packing is mainly due to excitation energy transfer to aggregates. The radiative lifetime of the lowest excited state of the aggregate with the optical gap of 1.84-1.9 eV is estimated to be about 20 ns. The aggregate contribution to the total luminescence in the polythiophene films with dense chain packing is about 50% and does not change significantly with temperature. (C) 2001 Elsevier Science B.V. All rights reserved.

KW - pairs

KW - electron

KW - films

KW - ultrafast

KW - luminescence

KW - conjugated polymers

KW - excitation energy transfer

KW - physical dimers

U2 - 10.1016/S1010-6030(01)00517-2

DO - 10.1016/S1010-6030(01)00517-2

M3 - Article

VL - 144

SP - 3

EP - 12

JO - Journal of Photochemistry and Photobiology A: Chemistry

JF - Journal of Photochemistry and Photobiology A: Chemistry

SN - 1873-2666

IS - 1

ER -