A strong regioregularity effect in self-organizing conjugated polymer films and high-efficiency polythiophene: Fullerene solar cells

Youngkyoo Kim, Steffan Cook, Sachetan M. Tuladhar, Stelios A. Choulis, Jenny Nelson, James R. Durrant, Donal D.C. Bradley, Mark Giles, Iain Mc Culloch, Chang Sik Ha, Moonhor Ree

    Research output: Chapter in Book/Report/Conference proceedingChapter

    20 Scopus citations

    Abstract

    Low-cost photovoltaic energy conversion using conjugated molecular materials has become increasingly feasible through the development of organic ‘bulk heterojunction (BHJ)’ structures1−7, where efficient light-induced charge separation is enabled by a large-area donor–acceptor interface2,3. The highest efficiencies have been achieved using blends of poly(3-hexylthiophene) (P3HT) and a fullerene derivative8–12, but performance depends critically on the material properties and processing conditions. This variability is believed to be influenced by the self-organizing properties of P3HT, which means that both optical13,14and electronic15,16properties are sensitive to the molecular packing. However, the relationship between molecular nanostructure, optoelectronic properties of the blend material and device performance has not yet been demonstrated. Here we focus on the influence of polymer regioregularity (RR) on the molecular nanostructure, and hence on the resulting material properties and device performance.We find a strong influence of RR on solar-cell performance, which can be attributed to enhanced optical absorption and transport resulting from the organization of P3HT chains and domains. Further optimization of devices using the highest RR material resulted in a power conversion efficiency of 4.4%, even without optimization of electrodes7.
    Original languageEnglish (US)
    Title of host publicationMaterials for Sustainable Energy: A Collection of Peer-Reviewed Research and Review Articles from Nature Publishing Group
    PublisherWorld Scientific Publishing Co.
    ISBN (Print)9789814317665
    DOIs
    StatePublished - Jan 1 2010

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