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dc.contributor.authorMai, Jiangquanen_US
dc.contributor.authorLu, Haipengen_US
dc.contributor.authorLau, Tsz-Kien_US
dc.contributor.authorPeng, Shih-Haoen_US
dc.contributor.authorHsu, Chain-Shuen_US
dc.contributor.authorHua, Wenqiangen_US
dc.contributor.authorZhao, Nien_US
dc.contributor.authorXiao, Xudongen_US
dc.contributor.authorLu, Xinhuien_US
dc.date.accessioned2018-08-21T05:54:10Z-
dc.date.available2018-08-21T05:54:10Z-
dc.date.issued2017-06-21en_US
dc.identifier.issn2050-7488en_US
dc.identifier.urihttp://dx.doi.org/10.1039/c7ta00292ken_US
dc.identifier.urihttp://hdl.handle.net/11536/145625-
dc.description.abstractTernary organic solar cell is a promising strategy for improving the power conversion efficiency (PCE) of single-junction organic solar cells by broadening the light absorption spectrum with the incorporation of two electron donors and one acceptor or one donor and two acceptors. However, in many cases the optimized loading of the third component is so small that its contribution to the light absorption is limited. Following our previously proposed selection rule for the two polymers capable of comparable loadings, we report in this work a ternary system composed of two morphologically compatible polymers with distinct chemical structures that can achieve a high PCE of 9.0% with a mass ratio of 1:1. Besides the expected improvement in short circuit current due to the broadening of the absorption spectrum, the fill factor of the ternary device is improved significantly. We attribute it to the balanced electron and hole mobility and reduced recombination benefiting from the high morphology compatibility of the system.en_US
dc.language.isoen_USen_US
dc.titleHigh efficiency ternary organic solar cell with morphology-compatible polymersen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c7ta00292ken_US
dc.identifier.journalJOURNAL OF MATERIALS CHEMISTRY Aen_US
dc.citation.volume5en_US
dc.citation.spage11739en_US
dc.citation.epage11745en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000403228200031en_US
Appears in Collections:Articles