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dc.contributor.authorChen, Tsung-Weien_US
dc.contributor.authorYu, Jun-Yanen_US
dc.contributor.authorLin, You-Weien_US
dc.contributor.authorPeng, Shih-Haoen_US
dc.contributor.authorWu, Shang-Hsuanen_US
dc.contributor.authorSu, Yi-Jiaen_US
dc.contributor.authorKarapala, Vamsi Krishnaen_US
dc.contributor.authorHong, Lingen_US
dc.contributor.authorYao, Huifengen_US
dc.contributor.authorHou, Jianhuien_US
dc.contributor.authorHsu, Chain-Shuen_US
dc.date.accessioned2020-10-05T02:01:59Z-
dc.date.available2020-10-05T02:01:59Z-
dc.date.issued1970-01-01en_US
dc.identifier.issn2367-198Xen_US
dc.identifier.urihttp://dx.doi.org/10.1002/solr.202000357en_US
dc.identifier.urihttp://hdl.handle.net/11536/155408-
dc.description.abstractHerein, two novel nonfullerene acceptors (NFAs), DTCC-4Cl and DTSiC-4Cl, are synthesized by end-capping dithienocyclopentacarbazole (DTCC) and dithieno-silolocarbazole (DTSiC) cores with chlorinated IC (2Cl-IC) units, respectively. With the better-known advantage of having the extraordinary sigma*-pi* conjugation of silole unit embedded in the DTSiC core, DTSiC-4Cl manifests upshifted lowest unoccupied molecular orbital (LUMO), blue-shifted absorption, and increased pi-pi interaction in comparison with DTCC-4Cl. Furthermore, to elucidate the effect of bridging atoms on the photovoltaic performance, T1 is selected as the polymer donor to be blended with DTCC-4Cl and DTSiC-4Cl. T1:DTCC-4Cl-based devices exhibit a fine power conversion efficiency (PCE) of 14.43% and T1:DTSiC-4Cl-based devices exhibit a comparable PCE of 14.46%. Interestingly, the T1:DTSiC-4Cl-based devices demonstrate an additive-free feature, which is worthy of further applications. From the perspective of constructing high-performance ternary devices, DTCC-4Cl is expected to possess excellent compatibility with DTSiC-4Cl owing to its structural similarity. As anticipated, the ternary T1:DTSiC-4Cl:DTCC-4Cl-based device outperforms the binary T1:DTCC-4Cl and T1:DTSiC-4Cl-based devices, affording a decent PCE of 15.04% with aV(OC)of 0.97 V, aJ(SC) of 20.80 mA cm(-2), and an FF of 74.55% without any additive.en_US
dc.language.isoen_USen_US
dc.subjectbridging atomen_US
dc.subjectcarbazoleen_US
dc.subjectnonfullerene acceptorsen_US
dc.subjectsiloleen_US
dc.subjectternary organic solar cellsen_US
dc.titleChlorinated Carbon-Bridged and Silicon-Bridged Carbazole-Based Nonfullerene Acceptors Manifest Synergistic Enhancement in Ternary Organic Solar Cell with Efficiency over 15%en_US
dc.typeArticleen_US
dc.identifier.doi10.1002/solr.202000357en_US
dc.identifier.journalSOLAR RRLen_US
dc.citation.spage0en_US
dc.citation.epage0en_US
dc.contributor.department交大名義發表zh_TW
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentNational Chiao Tung Universityen_US
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000560826800001en_US
dc.citation.woscount0en_US
Appears in Collections:Articles