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Triphenylamine-Based Push–Pull σ–C60 Dyad As Photoactive Molecular Material for Single-Component Organic Solar Cells: Synthesis, Characterizations, and Photophysical Properties
Author(s) -
Antoine Labrunie,
Julien Gorenflot,
Maxime Babics,
Olivier Alévêque,
Sylvie DabosSeig,
Ahmed H. Balawi,
Zhipeng Kan,
Markus Wohlfahrt,
Eric Levillain,
Piétrick Hudhomme,
Pierre M. Beaujuge,
Frédéric Laquai,
Clément Cabanetos,
Philippe Blanchard
Publication year - 2018
Publication title -
chemistry of materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.741
H-Index - 375
eISSN - 1520-5002
pISSN - 0897-4756
DOI - 10.1021/acs.chemmater.8b01117
Subject(s) - triphenylamine , ultrafast laser spectroscopy , organic solar cell , photocurrent , photoluminescence , electron mobility , materials science , photochemistry , quenching (fluorescence) , chemistry , optoelectronics , spectroscopy , organic chemistry , polymer , optics , fluorescence , physics , quantum mechanics
A push–pull σ–C60 molecular dyad was synthesized via Huisgen-type click chemistry and used as photoactive material for single-component organic solar cells. Steady-state photoluminescence (PL) experiments of the dyad in solution show a significant quenching of the emission of the push–pull moiety. Spin-casting of a solution of the dyad results in homogeneous and smooth thin films, which exhibit complete PL quenching in line with ultrafast photoinduced electron-transfer in the solid state. Spectroelectrochemistry reveals the optical signatures of radical cations and radical anions. Evaluation of the charge carrier mobility by space-charge limited current measurements gives an electron-mobility of μe = 4.3 × 10–4 cm2 V–1 s–1, ca. 50 times higher than the hole-mobility. Single-component organic solar cells yield an open-circuit voltage Voc of 0.73 V and a short-circuit current density of 2.1 mA cm–2; however, a poor fill factor FF (29%) is obtained, resulting in low power conversion efficiency of only 0.4%. ...

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