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Alkylated-C60 based soft materials: regulation of self-assembly and optoelectronic properties by chain branching
Author(s) -
Hongguang Li,
Sukumaran Santhosh Babu,
Sarah T. Turner,
Dieter Neher,
Martin J. Hollamby,
Tomohiro Seki,
Shiki Yagai,
Yonekazu Deguchi,
Helmuth Möhwald,
Takashi Nakanishi
Publication year - 2013
Publication title -
journal of materials chemistry c
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.899
H-Index - 128
eISSN - 2050-7534
pISSN - 2050-7526
DOI - 10.1039/c3tc00066d
Subject(s) - materials science , polymer solar cell , fullerene , thermotropic crystal , chemical engineering , acceptor , liquid crystal , lamellar structure , energy conversion efficiency , solar cell , organic solar cell , active layer , side chain , substituent , photoactive layer , branching (polymer chemistry) , nanotechnology , layer (electronics) , organic chemistry , optoelectronics , polymer , liquid crystalline , composite material , physics , chemistry , thin film transistor , engineering , condensed matter physics
Derivatization of fullerene (C60) with branched aliphatic chains softens C60-based materials and enables the formation of thermotropic liquid crystals and room temperature nonvolatile liquids. This work demonstrates that by carefully tuning parameters such as type, number and substituent position of the branched chains, liquid crystalline C60 materials with mesophase temperatures suited for photovoltaic cell fabrication and room temperature nonvolatile liquid fullerenes with tunable viscosity can be obtained. In particular, compound 1, with branched chains, exhibits a smectic liquid crystalline phase extending from 84 °C to room temperature. Analysis of bulk heterojunction (BHJ) organic solar cells with a ca. 100 nm active layer of compound 1 and poly(3-hexylthiophene) (P3HT) as an electron acceptor and an electron donor, respectively, reveals an improved performance (power conversion efficiency, PCE: 1.6 ± 0.1%) in comparison with another compound, 10 (PCE: 0.5 ± 0.1%). The latter, in contrast to 1, carries linear aliphatic chains and thus forms a highly ordered solid lamellar phase at room temperature. The solar cell performance of 1 blended with P3HT approaches that of PCBM/P3HT for the same active layer thickness. This indicates that C 60 derivatives bearing branched tails are a promising class of electron acceptors in soft (flexible) photovoltaic devices. © 2013 The Royal Society of Chemistry.

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