Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/114884
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dc.contributorDepartment of Electrical and Electronic Engineering-
dc.contributorResearch Institute for Smart Energy-
dc.contributorPhotonics Research Institute-
dc.contributorMainland Development Office-
dc.creatorChen, Ren_US
dc.creatorZhang, Ten_US
dc.creatorRuan, Qen_US
dc.creatorWu, Len_US
dc.creatorXu, Zen_US
dc.creatorSu, Yen_US
dc.creatorCao, Zen_US
dc.creatorLi, Qen_US
dc.creatorXiao, Ben_US
dc.creatorMa, Ren_US
dc.creatorCai, YPen_US
dc.creatorJia, Ten_US
dc.creatorLiu, Sen_US
dc.creatorLi, Gen_US
dc.date.accessioned2025-09-01T01:53:17Z-
dc.date.available2025-09-01T01:53:17Z-
dc.identifier.issn1001-604Xen_US
dc.identifier.urihttp://hdl.handle.net/10397/114884-
dc.language.isoenen_US
dc.publisherShanghai Institute of Organic Chemistry (Chinese Academy of Sciences) and Wiley-VCHen_US
dc.rightsThis is an open access article under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits use, distribution and reproduction in any medium, provided the original work is properly cited.en_US
dc.rights© 2025 The Authors. Chinese Journal of Chemistry published by SIOC, CAS, Shanghai and Wiley-VCH GmbHen_US
dc.rightsThe following publication Chen, R., Zhang, T., Ruan, Q., Wu, L., Xu, Z., Su, Y., Cao, Z., Li, Q., Xiao, B., Ma, R., Cai, Y.-P., Jia, T., Liu, S. and Li, G. (2025), Non-Halogenated Solvent Processed Ternary All-Polymer Solar Cell with PCE of 18.55% Enabled by Two Compatible Polymer Acceptors†. Chin. J. Chem., 43: 2120-2128 is available at https://doi.org/10.1002/cjoc.70075.en_US
dc.subjectAll-polymer solar cellsen_US
dc.subjectGuest selectionen_US
dc.subjectNonradiative recombinationen_US
dc.subjectPolymer acceptorsen_US
dc.subjectPower conversion efficiencyen_US
dc.subjectTernary constructionen_US
dc.titleNon-halogenated solvent processed ternary all-polymer solar cell with PCE of 18.55% enabled by two compatible polymer acceptorsen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage2120en_US
dc.identifier.epage2128en_US
dc.identifier.volume43en_US
dc.identifier.issue17en_US
dc.identifier.doi10.1002/cjoc.70075en_US
dcterms.abstractHerein, a theory-guided ternary construction case on boosting power conversion efficiency (PCE) for all-polymer solar cell (all-PSC) is reported, where guest acceptor's characteristics include high miscibility with host polymer acceptor, significantly larger optical bandgap, and improved luminescence. Consequently, with only 10 wt% PFFO-Th (third component) addition, the PCE of binary control is promoted to 18.55% from 16.69%, a 11.1% relative increase, demonstrating the great effectiveness of this ternary strategy. Besides, the realized 18.55% efficiency is at state-of-the-art level of all-PSCs processed by ortho-xylene, a widely acknowledged green non- halogenated solvent by the field. This study shares new thought on designing high-performance photovoltaic devices with reduced energy losses and favorable charge dynamics, which would nourish future development on all-PSCs, and even other organic electronics.-
dcterms.abstractGraphical abstract: [Figure not available: see fulltext.]-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationChinese journal of chemistry, 1 Sept 2025, v. 43, no. 17, p. 2120-2128en_US
dcterms.isPartOfChinese journal of chemistryen_US
dcterms.issued2025-09-01-
dc.identifier.scopus2-s2.0-105007010354-
dc.identifier.eissn1614-7065en_US
dc.description.validate202509 bcch-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_TA-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThis work was financially supported by Guangdong Natural Science Foundation (No. 2021B1515120073), the Guangdong Provincial Science and Technology Foundation (No. 2022A0505050068), the Jiangxi Provincial Natural Science Foundation (No. 20224BAB204033), Hubei Provincial Natural Science Foundation of China (2024AFB950), and Excellent Discipline Cultivation Project by JHUN (2023XKZ031). R. Ma acknowledges the support from PolyU Distinguished Postdoctoral Fellowship (1-YW4C).en_US
dc.description.pubStatusPublisheden_US
dc.description.TAWiley (2025)en_US
dc.description.oaCategoryTAen_US
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