Correlation between conjugation length and non-radiative relaxation rate in poly(p-phenylene vinylene): A picosecond photoluminescence study

K. S. Wong; D. D.C. Bradley; W. Hayes; J. F. Ryan; R. H. Friend; H. Lindenberger; S. Roth

doi:10.1088/0022-3719/20/11/002

Correlation between conjugation length and non-radiative relaxation rate in poly(p-phenylene vinylene): A picosecond photoluminescence study

K. S. Wong, D. D.C. Bradley, W. Hayes, J. F. Ryan, R. H. Friend, H. Lindenberger, S. Roth

Research output: Contribution to journal › Article › peer-review

80 Scopus citations

Abstract

Time-resolved photoluminescence of poly(p-phenylene vinylene) in the picosecond regime shows that the non-radiative decay rate increases with increasing polymer chain conjugation length and that the luminescence decay is much faster for excitation parallel to the polymer chain than for perpendicular excitation. The results provide evidence for bimolecular recombination processes. © 1987 IOP Publishing Ltd.

Original language	English (US)
Journal	Journal of Physics C: Solid State Physics
Volume	20
Issue number	11
DOIs	https://doi.org/10.1088/0022-3719/20/11/002
State	Published - Apr 20 1987
Externally published	Yes

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10.1088/0022-3719/20/11/002

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@article{9295a0e1db9a4068ac487b06539b10d7,

title = "Correlation between conjugation length and non-radiative relaxation rate in poly(p-phenylene vinylene): A picosecond photoluminescence study",

abstract = "Time-resolved photoluminescence of poly(p-phenylene vinylene) in the picosecond regime shows that the non-radiative decay rate increases with increasing polymer chain conjugation length and that the luminescence decay is much faster for excitation parallel to the polymer chain than for perpendicular excitation. The results provide evidence for bimolecular recombination processes. {\textcopyright} 1987 IOP Publishing Ltd.",

author = "Wong, {K. S.} and Bradley, {D. D.C.} and W. Hayes and Ryan, {J. F.} and Friend, {R. H.} and H. Lindenberger and S. Roth",

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T1 - Correlation between conjugation length and non-radiative relaxation rate in poly(p-phenylene vinylene): A picosecond photoluminescence study

AU - Wong, K. S.

AU - Bradley, D. D.C.

AU - Hayes, W.

AU - Ryan, J. F.

AU - Friend, R. H.

AU - Lindenberger, H.

AU - Roth, S.

N1 - Generated from Scopus record by KAUST IRTS on 2019-11-27

PY - 1987/4/20

Y1 - 1987/4/20

N2 - Time-resolved photoluminescence of poly(p-phenylene vinylene) in the picosecond regime shows that the non-radiative decay rate increases with increasing polymer chain conjugation length and that the luminescence decay is much faster for excitation parallel to the polymer chain than for perpendicular excitation. The results provide evidence for bimolecular recombination processes. © 1987 IOP Publishing Ltd.

AB - Time-resolved photoluminescence of poly(p-phenylene vinylene) in the picosecond regime shows that the non-radiative decay rate increases with increasing polymer chain conjugation length and that the luminescence decay is much faster for excitation parallel to the polymer chain than for perpendicular excitation. The results provide evidence for bimolecular recombination processes. © 1987 IOP Publishing Ltd.

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U2 - 10.1088/0022-3719/20/11/002

DO - 10.1088/0022-3719/20/11/002

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SN - 0022-3719

VL - 20

JO - Journal of Physics C: Solid State Physics

JF - Journal of Physics C: Solid State Physics

IS - 11

ER -

Correlation between conjugation length and non-radiative relaxation rate in poly(p-phenylene vinylene): A picosecond photoluminescence study

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