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Issue 7, 2016
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Understanding the effect of solvent vapor annealing on solution-processed A–D–A oligothiophene bulk-heterojunction solar cells: the role of alkyl side chains

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Abstract

Solution-processed bulk heterojunction solar cells consisting of the previously developed dithienopyrrole containing A–D–A oligothiophenes (A = acceptor, D = donor unit) and [6,6]-phenyl-C71-butyric acid methyl ester (PC71BM) with power conversion efficiency up to 7.1% after solvent vapor annealing (SVA) are demonstrated. The influence of the position of the alkyl side chains attached to the thiophene units on the SVA, and the usage of either PC61BM or PC71BM as acceptor, is investigated in more detail by negative secondary ion mass spectrometry (SIMS), Kelvin probe force microscopy (KPFM), photoluminescence (PL), and grazing-incidence X-ray diffraction spectroscopy (GIWAXS). It was found that besides increased crystallinity and domain sizes, the active layers consisting of two different isomers which we will refer to in the following as isomer 1 or isomer 2 had different compositions after SVA treatment. In the former, a more or less homogeneously-mixed D:A blend was observed, whereas the latter showed a vertical gradient of PCBM in the active layer and much stronger phase segregation on the surface. These findings correlate well with the differences in solar cell performance of both isomers, before and after SVA.

Graphical abstract: Understanding the effect of solvent vapor annealing on solution-processed A–D–A oligothiophene bulk-heterojunction solar cells: the role of alkyl side chains

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Supplementary files

Article information


Submitted
25 Sep 2015
Accepted
06 Dec 2015
First published
07 Dec 2015

J. Mater. Chem. A, 2016,4, 2571-2580
Article type
Paper
Author version available

Understanding the effect of solvent vapor annealing on solution-processed A–D–A oligothiophene bulk-heterojunction solar cells: the role of alkyl side chains

C. D. Wessendorf, A. Perez-Rodriguez, J. Hanisch, A. P. Arndt, I. Ata, G. L. Schulz, A. Quintilla, P. Bäuerle, U. Lemmer, P. Wochner, E. Ahlswede and E. Barrena, J. Mater. Chem. A, 2016, 4, 2571
DOI: 10.1039/C5TA07713C

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