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Interfacial exciplex formation in bilayers of conjugated polymers
被引:5
|作者:
Nobuyasu, R. S.
[1
]
Araujo, K. A. S.
[1
]
Cury, L. A.
[1
]
Jarrosson, T.
[2
]
Serein-Spirau, F.
[2
]
Lere-Porte, J. -P.
[2
]
Dias, F. B.
[3
]
Monkman, A. P.
[3
]
机构:
[1] Univ Fed Minas Gerais, Dept Fis, Inst Ciencias Exatas, BR-31270901 Belo Horizonte, MG, Brazil
[2] Ecole Natl Super Chim Montpellier, Inst Charles Gerhardt, UMR CNRS 5253, Equipe AM2N, F-34296 Montpellier 05, France
[3] Univ Durham, Dept Phys, Durham DH1 3LE, England
基金:
英国工程与自然科学研究理事会;
关键词:
AMPLIFIED SPONTANEOUS EMISSION;
POLYFLUORENE COPOLYMER;
ENERGY-TRANSFER;
EFFICIENCY;
FILMS;
DEVICES;
D O I:
10.1063/1.4827097
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
The donor-acceptor interactions in sequential bilayer and blend films are investigated. Steady-state and time-resolved photoluminescence (PL) were measured to characterize the samples at different geometries of photoluminescence collection. At standard excitation, with the laser incidence at 45 degrees of the normal direction of the sample surface, a band related to the aggregate states of donor molecules appears for both blend and bilayer at around 540 nm. For the PL spectra acquired from the edge of the bilayer, with the laser incidence made at normal direction of the sample surface (90 degrees geometry), a new featureless band emission, red-shifted from donor and acceptor emission regions was observed and assigned as the emission from interfacial exciplex states. The conformational complexity coming from donor/acceptor interactions at the heterojunction interface of the bilayer is at the origin of this interfacial exciplex emission. (C) 2013 AIP Publishing LLC.
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页数:8
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