Cortizo-Lacalle, Diego and Howells, Calvyn T and Pandey, Upendra K and Cameron, Joseph and Findlay, Neil J and Inigo, Anto Regis and Tuttle, Tell and Skabara, Peter J and Samuel, Ifor DW (2014) Solution processable diketopyrrolopyrrole (DPP) cored small molecules with BODIPY end groups as novel donors for organic solar cells. In: BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY, 10 . pp. 2683-2695.
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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 PC71BM 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.
Item Type: | Journal Article |
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Publication: | BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY |
Publisher: | BEILSTEIN-INSTITUT |
Additional Information: | Copyright for this article belongs to the BEILSTEIN-INSTITUT, TRAKEHNER STRASSE 7-9, FRANKFURT AM MAIN, 60487, GERMANY |
Keywords: | BODIPY; diketopyrrolopyrrole; organic semiconductors; organic solar cells; thiophene |
Department/Centre: | Division of Interdisciplinary Sciences > Interdisciplinary Centre for Energy Research |
Date Deposited: | 21 Jan 2015 06:40 |
Last Modified: | 12 Oct 2018 15:33 |
URI: | http://eprints.iisc.ac.in/id/eprint/50731 |
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