Abstract

The poor compatibility of inorganic materials (electron transport layer) with the active layer and an ultrathin film of conjugated polymers becomes the great obstacle to producing high-quality polymer solar cells with high-throughput roll-to-roll (R2R) method. Novel electron transport layer-free polymer solar cells have been constructed by integrating the conjugated aminoalkyl-functionalized polymer, poly[3-(5-(9,9-bis(3-(dimethylamino)propyl)-7-methyl-9H-fluoren-2-yl)thiophen-2-yl)-2,5-bis(2-butyloctyl)-6-(5-methylthiophen-2-yl)pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione] (PDTFN) into the active layer. PDTFN was synthesized by different Suzuki reaction conditions to gain different molecular weights- small molecular weight (PDTFN-L) and high molecular weight (PDTFN-H). It is noteworthy that PDTFN-H can significantly enhance the power conversion efficiency of the solar cells that incorporate a photoactive layer composed of poly[(3-hexylthiophene)-2,5-diyl] (P3HT) and the fullerene acceptor [6,6-phenyl-C71-butyric acid methyl ester] (PC71BM). The power conversion efficiency varies from 2.5% for ZnO transparent cathode based solar cells to 3.6% for PDTFN-H based electron transport layer-free solar cells. This improved performance can be attributed to the following reasons: the PDTFN-H can enhance cathode electron transporting by introducing the PDTFN-H into active layer without extra coating the cathode interfacial material; besides, a favorable vertical phase separation of active layer was formed due to the PDTFN-H excellent compatibility with the bulk-heterojunction. These experimental results revealed that the electron transport layer-free polymer solar cells based on PDTFN-H can be a promising novel effective fabrication with simplified manufacturing process and lower cost.

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