Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/117552
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dc.contributorDepartment of Applied Physics-
dc.contributorDepartment of Applied Biology and Chemical Technology-
dc.contributorResearch Institute for Smart Energy-
dc.creatorZou, Ben_US
dc.creatorNg, HMen_US
dc.creatorLi, Zen_US
dc.creatorWang, Yen_US
dc.creatorWang, Qen_US
dc.creatorChen, Den_US
dc.creatorYao, Zen_US
dc.creatorLi, Hen_US
dc.creatorLi, Cen_US
dc.creatorZeng, Xen_US
dc.creatorLiu, Wen_US
dc.creatorHalpert, JEen_US
dc.creatorHu, Hen_US
dc.creatorDuan, Cen_US
dc.creatorZhu, Zen_US
dc.creatorWu, Ten_US
dc.creatorWong, WYen_US
dc.creatorZhang, ZGen_US
dc.creatorYan, Hen_US
dc.creatorYu, Hen_US
dc.date.accessioned2026-02-26T03:46:50Z-
dc.date.available2026-02-26T03:46:50Z-
dc.identifier.urihttp://hdl.handle.net/10397/117552-
dc.language.isoenen_US
dc.publisherWiley-VCH Verlag GmbH & Co. KGaAen_US
dc.rights© 2025 The Author(s). Advanced Science published by Wiley-VCH GmbH. This 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.rightsThe following publication B. Zou, H. M. Ng, Z. Li, et al. “ Indoor Organic Photovoltaics with Over 29% Efficiency and Great Stability Enabled by Giant Dimeric Acceptors with Hypsochromic Absorption and High Glass Transition Temperature.” Adv. Sci. 12, no. 44 (2025): e12690 is available at https://doi.org/10.1002/advs.202512690.en_US
dc.subjectGiant dimeric acceptorsen_US
dc.subjectHigh glass transition temperatureen_US
dc.subjectHypsochromic absorptionen_US
dc.subjectIndoor photovoltaicsen_US
dc.subjectOperation and mechanical stabilityen_US
dc.titleIndoor organic photovoltaics with over 29% efficiency and great stability enabled by giant dimeric acceptors with hypsochromic absorption and high glass transition temperatureen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume12en_US
dc.identifier.issue44en_US
dc.identifier.doi10.1002/advs.202512690en_US
dcterms.abstractIndoor organic photovoltaics (IOPVs) are an emerging LED light recycling technology with promising applications such as indoor off-grid ecosystem for the Internet of Things. However, efficient and stable IOPVs based on giant dimeric acceptors (GDAs) are rarely reported due to the dearth of GDAs with hypsochromic absorption (absorption onset < 850 nm) and good crystallinity. Herein, two hypsochromic GDAs are proposed with different fluorination degrees, namely DY4FO-V and DY6FO-V, and process a systematic study of hypsochromic acceptor materials from the small molecule to dimers and polymer. Interestingly, both hypsochromic GDAs possess better crystallinity, thus faster carrier transport and suppress recombination than small-molecule and polymer acceptor-based devices. With extra fluorination, PM6:DY6FO-V exhibits higher external quantum efficiency response and tighter packing compared with PM6:DY4FO-V. As a result, PM6:DY6FO-V delivers a champion efficiency over 29% under a LED illumination of 2000 lux (2600 k), positioning it the highest values for GDA-based IOPVs. Meanwhile, the high glass transition temperature of DY6FO-V endowed corresponding devices with great photostability and enhanced mechanical stability in flexible devices, demonstrating the feasibility of practical applications of the DY6FO-V-based IOPVs. This research underscores the huge potential of developing hypsochromic GDAs for highly efficient IOPVs with superior stability.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationAdvanced science, 27 Nov. 2025, v. 12, no. 44, e12690en_US
dcterms.isPartOfAdvanced scienceen_US
dcterms.issued2025-11-27-
dc.identifier.scopus2-s2.0-105019064946-
dc.identifier.pmid41092357-
dc.identifier.eissn2198-3844en_US
dc.identifier.artne12690en_US
dc.description.validate202602 bcch-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOS-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextB.Z., H.M.N., and Z.L. contributed equally to this work. H.Y. acknowledges the support from the Strategic Hiring Scheme start-up fund of the Hong Kong Polytechnic University (Project ID: P0056175; Work Programme: 1-BDDV) and the Hong Kong Research Grant Council (General Research Fund project 16303024, 16310824), National Natural Science Foundation of China (NSFC, No. 22505209). H. Yan appreciates the support from the Hong Kong Research Grants Council (Research fellow scheme RFS2021-6S05, RIF project R6021-18, CRF project C6023-19G), Zhongshan Municipal Bureau of Science and Technology (No. ZSST20SC02). Z.-G. Zhang appreciates the support from the Beijing Natural Science Foundation (2192043), the National Natural Science Foundation of China (Nos. 52373168, 22175014, 52373176), the Strategic Priority Research Program of the Chinese Academy of Sciences (Grant No. XDB0520102), the Fundamental Research Funds for the Central Universities (QNTD20). A portion of this work is based on the data obtained at Beijing Synchrotron Radiation Facility (BSRF) and Shanghai Synchrotron Radiation Facility (SSRF).en_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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