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Eur. Phys. J. Appl. Phys. 36, 245-249 (2006)
DOI: 10.1051/epjap:2006141
Synthesis, characterization and application of donor-acceptor block copolymers in nanostructured bulk heterojunction solar cells
M. Sommer and M. ThelakkatApplied Functional Polymers, University of Bayreuth, 95440 Bayreuth, Germany
Mukundan.Thelakkat@uni-bayreuth.de
(Received: 21 July 2006 / Received in final form: 25 September 2006 / Accepted: 11 October 2006 / Published online: 10 January 2007 )
Abstract
The synthesis and properties of two semiconducting donor-acceptor (D-A)
block copolymers and their application in nanostructured bulk heterojunction
solar cells are reported. The donor segments were obtained via nitroxide
mediated polymerization of either bis(4-methoxyphenyl)-4'-vinylphenylamine
or
N,N'-bis(4-methoxyphenyl)-N-phenyl-N'-4-vinylphenyl-[1,1'biphenyl]-4,4'-diamine.
Narrow-distributed macroinitiators,
poly{bis(4-methoxyphenyl)-4'-vinylphenylamine} (PvDMTPA) and
poly{N,N'-bis(4-methoxyphenyl)-N-phenyl-N'-4-vinylphenyl-[1,1'biphenyl]-4,4'-diamine}
(PvDMTPD) were used to polymerize the acceptor monomer perylene diimide
acrylate (PerAcr) to yield block copolymers with well-defined molecular
weights. Different diblock copolymers, PvDMTPA-block-PPerAcr and
PvDMTPD-block-PPerAcr, with high perylene diimide weight fractions were prepared.
The block copolymers exhibited efficient fluorescence quenching.
Transmission electron microscopy revealed wire-like and worm-like
nanostructures throughout bulk samples. Thin film photovoltaic devices
showed short circuit currents
of up to 1.21 mA/cm2 and power conversion efficiencies
of 0.32% under AM 1.5 illumination conditions.
78.66.Qn - Polymers; organic compounds.
81.16.Dn - Self-assembly.
81.20.Ka - Chemical synthesis; combustion synthesis.
© EDP Sciences 2006
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