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Photovoltaic Investigation of New Co-polymers Based on Thiophene, Fluorine and Phenylene
Conferences & Talks
30 November 2010
We have investigated a series of new electron donor co-polymers (LaPPS-35) in organic thin-film solar cells. Copolymerization allows us to create new materials by tailoring unit ratios with a combination of properties and behaviors of different materials. The co-polymers used in this study were composed of thiophene, phenylene and fluorine units, where the thiophene content was kept constant while the fluorine/phenylene ratio was varied. For every copolymer ratio, we report results in three different structures: monolayer, bilayer and bulk heterojunction. Using vapor-deposited C60 as the electron acceptor in bilayer structures, we show the effect of altering the thickness of both the copolymer and fullerene films. Bilayer devices were further analyzed using a model for charge transport, which indicated a dependence of effective mobility on film thickness. For the bulk heterojunction system [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) was used as the electron acceptor. For both the bilayer and heterojection cells it was found that a 1:1 ratio of phenylene:fluorine units led to the highest device performance, and initial bulk hetereojunction devices using this polymer showed a peak external quantum efficiency of 33% and a AM1.5 power conversion efficiency of 0.7%.
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