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Triphenylamine/Tetracyanobutadiene‐Based π‐Conjugated Push–Pull Molecules End‐Capped with Arene Platforms: Synthesis, Photophysics, and Photovoltaic Response
Author(s) -
Simón Marqués Pablo,
Castán José María Andrés,
Raul Benedito A. L.,
Londi Giacomo,
Ramirez Ivan,
Pshenichnikov Maxim S.,
Beljonne David,
Walzer Karsten,
Blais Martin,
Allain Magali,
Cabanetos Clément,
Blanchard Philippe
Publication year - 2020
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.202002810
Subject(s) - triphenylamine , photoexcitation , photochemistry , moiety , excited state , molecule , materials science , photoluminescence , conjugated system , singlet state , optoelectronics , chemistry , stereochemistry , organic chemistry , polymer , atomic physics , physics , composite material
π‐Conjugated push–pull molecules based on triphenylamine and 1,1,4,4‐tetracyanobuta‐1,3‐diene (TCBD) have been functionalized with different terminal arene units. In solution, these highly TCBD‐twisted systems showed a strong internal charge transfer band in the visible spectrum and no detectable photoluminescence (PL). Photophysical and theoretical investigations revealed very short singlet excited state deactivation time of ≈10 ps resulting from significant conformational changes of the TCBD‐arene moiety upon photoexcitation, opening a pathway for non‐radiative decay. The PL was recovered in vacuum‐processed films or when the molecules were dispersed in a PMMA matrix leading to a significant increase of the excited state deactivation time. As shown by cyclic voltammetry, these molecules can act as electron donors compared to C 60 . Hence, vacuum‐processed planar heterojunction organic solar cells were fabricated leading to a maximum power conversion efficiency of ca. 1.9 % which decreases with the increase of the arene size.