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Enhanced luminescence properties of highly threaded conjugated polyelectrolytes with potassium counter-ions upon blending with poly(ethylene oxide)

Abstract:
The photophysics and electroluminescence (EL) of thin films of unthreaded and cyclodextrin-encapsulated poly(4, 4′ -diphenylenevinylene) (PDV) with potassium countercations, blended with poly(ethylene oxide) (PEO) are investigated as a function of the PEO concentration. We show that three main factors contribute to increasing the photoluminescence (PL) quantum efficiency as a result of suppressed intermolecular interactions, namely: the high degree of encapsulation of the polyrotaxanes, the relatively large countercation (e.g., compared to lithium), and the complexation of the rotaxanes with PEO. By facilitating cationic transport to the negative electrodes, PEO also leads to devices with enhanced electron injection and improved charge balance, whose operation therefore resembles that of "virtually unipolar" light-emitting electrochemical cells. This effect, together with the enhanced PL efficiency, leads to higher EL efficiency for both polyrotaxanes and unthreaded polymers, upon addition of the PEO. We show that the concurrent exploitation of the various strategies above lead to an overall EL efficiency that is approximately twice the value previously reported for Li-based PDV. A blueshift of the EL spectrum during the devices turn-on is also reported and analyzed in terms of interference and doping effects. © 2010 American Institute of Physics.
Publication status:
Published

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Publisher copy:
10.1063/1.3372616

Authors


More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Organic Chemistry
Role:
Author


Journal:
JOURNAL OF APPLIED PHYSICS More from this journal
Volume:
107
Issue:
12
Pages:
124509-124509
Publication date:
2010-06-15
DOI:
ISSN:
0021-8979


Language:
English
Pubs id:
pubs:66174
UUID:
uuid:9e52ebc9-2572-421b-85dc-61058866e712
Local pid:
pubs:66174
Source identifiers:
66174
Deposit date:
2012-12-19

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