Illumination of exciton migration in rodlike luminescent conjugated polymers by single-molecule spectroscopy
Author(s) -
C. F. Wang,
J. D. White,
Thong Leng Lim,
J.H. Hsu,
Shenghao Yang,
Wunshain Fann,
KangYung Peng,
S. A. Chen
Publication year - 2003
Publication title -
physical review. b, condensed matter
Language(s) - English
Resource type - Journals
eISSN - 1095-3795
pISSN - 0163-1829
DOI - 10.1103/physrevb.67.035202
Subject(s) - polymer , materials science , exciton , luminescence , spectroscopy , polystyrene , chemical physics , molecule , fluorescence , photoluminescence , emission spectrum , conjugated system , molecular physics , spectral line , photochemistry , optics , optoelectronics , condensed matter physics , chemistry , physics , organic chemistry , quantum mechanics , composite material , astronomy
[[abstract]]©2003 APS - Single-molecule spectroscopy is used to study the time-dependent spectral behavior of a short rodlike Poly(phenylene vinylene) (PPV) derivative polymer spin cast in a polystyrene matrix. The fluorescent time trace is characterized by stepwise intensity emission with constant spectral composition, punctuated by abrupt intensity changes, which are usually accompanied by abrupt spectral changes. In contrast to coiled long chain polymers, defect-free rodlike polymers exhibit multiple-emission sites, each with its characteristic invariant spectrum. The distribution of spectral jumps in the emission spectrum reflects the distribution of the effective conjugation length. This implies the energy transfer (i.e., thermalized exciton migration) along the polymer backbone is inefficient. A static disorder induced conjugation length distribution model with limited energy transfer can be used in understanding the photophysics of an isolated polymer.[[fileno]]2020116010087[[department]]化學工程學
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