Long-range energy migration in photoexcited polymers

Authors
Yu, JWKim, JKCho, HNKim, DYKim, CYSong, NWKim, D
Issue Date
2000-07
Publisher
AMER CHEMICAL SOC
Citation
MACROMOLECULES, v.33, no.15, pp.5443 - 5447
Abstract
Excitation migration dynamics and the energy-transfer process in a donor-acceptor pair system on photoexcitation have been investigated by using static and time-resolved photoluminescence (PL) measurements. The PL spectrum of poly(N-vinylcarbazole) (PVK) was fully superposed on the electronic absorption spectrum of poly(9,9'-di-n-hexyl-2,7-fluorenylvinylene (PDHFV) to fulfill a requirement for an efficient Forster-type energy transfer. In the PL spectrum of a blended PVK film with 0.5 wt % PDHFV on photoexcitation at 340 nm, the PL emission of PDHFV, which exhibits little absorbance at the excitation wavelength, prevailed over the PL emission of PVK. The PL spectrum of a bilayered structure with a PVK layer thickness of 4 mu m and a PDHFV layer thickness of 80 nm, which was prepared by spin-casting PDHFV solution in trichloroethylene on a PVK film, also showed the PL emission of PDHFV on photoexcitation of the PVK layer at 340 nm without a trace of the PL emission of PVK. Excitation energy migration through a PVK bulk was observed up to a PVK thickness of 23 mu m. A time-correlated single-photon counting (TCSPC) study deduced an energy migration velocity of 3.5 x 10(6) cm/s and a dwell time between each hopping of 85 fs, respectively, in the PVK bulk of the bilayered structures with a PDHFV layer thickness of 10 or 80 nm.
Keywords
LIGHT-EMITTING-DIODES; CONJUGATED POLYMERS; ELECTROLUMINESCENCE; BLENDS; POLY(N-VINYLCARBAZOLE); CONFINEMENT; RELAXATION; exciton migration
ISSN
0024-9297
URI
https://pubs.kist.re.kr/handle/201004/141271
DOI
10.1021/ma0001483
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KIST Article > 2000
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