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Push–Pull Triphenylamine Chromophore Syntheses and Optoelectronic Characterizations
Author(s) -
Jeux Victorien,
Segut Olivier,
Demeter Dora,
Alévêque Olivier,
Leriche Philippe,
Roncali Jean
Publication year - 2015
Publication title -
chempluschem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.801
H-Index - 61
ISSN - 2192-6506
DOI - 10.1002/cplu.201402386
Subject(s) - triphenylamine , chromophore , acceptor , organic solar cell , molecule , materials science , electron acceptor , fullerene , electrochemistry , planar , heterojunction , photochemistry , optoelectronics , chemistry , electrode , physics , organic chemistry , polymer , composite material , computer graphics (images) , computer science , condensed matter physics
A series of push–pull molecules combining a diarylamine donor block with various electron‐acceptor units through phenylthienyl (PT) and bithienyl (TT) π‐conjugating spacers have been synthesized. Optical and electrochemical results, supported by theoretical calculations, show that the electronic properties of the molecules can be modulated by varying the strength of the acceptor group and/or the structure of the conjugating spacer. As a first evaluation of the potential of these compounds as donors in organic solar cells (OSC), simple planar heterojunction (PHJ) prototypes using fullerene C 60 as electron acceptor have been fabricated. Most OSCs exhibit analogous photoconversion efficiencies in the 1.5–2 % range. Their characteristics are discussed in terms of structure–properties relationships.