Solution processable diketopyrrolopyrrole (DPP) cored small molecules with BODIPY end groups as novel donors for organic solar cells

Diego Cortizo-Lacalle, Calvyn T. Howells, Upendra K. Pandey, Joseph Cameron, Neil J. Findlay, Anto Regis Inigo, Tell Tuttle, Peter J. Skabara, Ifor D.W. Samuel

    Research output: Contribution to journalArticlepeer-review

    23 Scopus citations

    Abstract

    Two novel triads based on a diketopyrrolopyrrole (DPP) central core and two 4,4-difluoro-4-bora-3a,4a-diaza- s - indacene (BODIPY) units attached by thiophene rings have been synthesised having high molar extinction coefficients. These triads were characterised and used as donor materials in small molecule, solution processable organic solar cells. Both triads were blended with PC 71 BM as an acceptor in different ratios by wt % and their photovoltaic properties were studied. For both the triads a modest photovoltaic performance was observed, having an efficiency of 0.65%. Moreover, in order to understand the ground and excited state properties and vertical absorption profile of DPP and BODIPY units within the triads, theoretical DFT and TDDFT calculations were performed.

    Original languageBritish English
    Pages (from-to)2683-2695
    Number of pages13
    JournalBeilstein Journal of Organic Chemistry
    Volume10
    DOIs
    StatePublished - 18 Nov 2014

    Keywords

    • BODIPY
    • Diketopyrrolopyrrole
    • Organic semiconductors
    • Organic solar cells
    • Thiophene

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