The influence of siloxane side-chains on the photovoltaic performance of a conjugated polymer. Issue 16 (15th March 2019)

• Record Type: Journal Article
• Authors: Heintges, Gaël H. L.; Hendriks, Koen H.; Colberts, Fallon J. M.; Li, Mengmeng; Li, Junyu; Janssen, René A. J.
• Is Part Of: RSC advances. Volume 9:Issue 16(2019)
• Page Start: 8740
• Page End: 8747
• Publication Date: 2019-03-15
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c9ra00816k
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : Molecular weight and intrinsic solubility affect the photovoltaic performance for a diketopyrrolopyrrole polymer with mixed alkyl and siloxane side chains. Abstract : The effect of gradually replacing the branched alkyl side chains of a diketopyrrolopyrrole (DPP) conjugated polymer by linear side chains containing branched siloxane end groups on the photovoltaic performance of blends of these polymers with a common fullerene acceptor is investigated. With an increasing proportion of siloxane side chains, the molecular weight and solubility of the polymers decreases. While the siloxane containing polymers exhibit a higher hole mobility in field-effect transistors, their performance in solar cells is less than the polymer with only alkyl sides chains. Using grazing-incidence wide-angle X-ray scattering, transmission electron microscopy, and fluorescence spectroscopy we identify two main reasons for the reduced performance of siloxane containing polymers in solar cells. The first one is a somewhat coarser phase-separated morphology with slightly wider polymer fibers. This is unexpected as often the fiber width is inversely correlated with polymer solubility. The second one is stronger non-radiative decay of the pristine polymers containing siloxane side chains.