Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/115290
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dc.contributorDepartment of Applied Physicsen_US
dc.creatorKwok, CKen_US
dc.creatorNg, Hen_US
dc.creatorGao, Cen_US
dc.creatorHu, Hen_US
dc.creatorDela, Peña, TAen_US
dc.creatorLai, JYLen_US
dc.creatorChen, Len_US
dc.creatorXie, Len_US
dc.creatorLi, MJen_US
dc.creatorWu, Jen_US
dc.creatorZhang, Gen_US
dc.creatorWong, WYen_US
dc.creatorYan, Hen_US
dc.creatorYu, Hen_US
dc.date.accessioned2025-09-19T03:23:51Z-
dc.date.available2025-09-19T03:23:51Z-
dc.identifier.issn2050-7488en_US
dc.identifier.urihttp://hdl.handle.net/10397/115290-
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.rights© The Royal Society of Chemistry 2025en_US
dc.rightsThis article is Open Access Attribution-NonCommercial 3.0 Unported (CC BY-NC 3.0) (https://creativecommons.org/licenses/by-nc/3.0/)en_US
dc.rightsThe following publication Kwok, C. H., Ng, H. M., Gao, C., Hu, H., Peña, T. A. D., Lai, J. Y. L., ... & Yu, H. (2025). Central π-conjugated extension in quinoxaline-based small-molecule acceptors as guest components enabling high-performance ternary organic solar cells. Journal of Materials Chemistry A, 13(20), 14765-14772 is available at https://doi.org/10.1039/d5ta00204d.en_US
dc.titleCentral π-conjugated extension in quinoxaline-based small-molecule acceptors as guest components enabling high-performance ternary organic solar cellsen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage14765en_US
dc.identifier.epage14772en_US
dc.identifier.volume13en_US
dc.identifier.issue20en_US
dc.identifier.doi10.1039/d5ta00204den_US
dcterms.abstractTernary strategies have critical roles in pursuing high efficiencies for organic solar cells (OSCs). However, the optimization of ternary systems relies heavily on understanding the compatibility and performance of different guest/host combinations. To establish design principles of quinoxaline (Qx)-based small-molecule acceptors (SMAs) as guest components for ternary OSCs, a new Qx-SMA named Qx-Ac and two reported Qx-SMAs named Qx-B and Qx-Pn were synthesized by extending the central Qx core with benzene (B), acenaphthene (Ac) and phenanthrene (Pn), respectively. After blending with PM6:BTP-eC9 (17.55%), Qx-Ac (18.51%) and Qx-Pn (18.11%) devices exhibited superior phase segregation and lower energy disorder. The improvement in Qx-Pn devices was dampened by inferior absorption, while the use of Qx-B (17.56%) did not improve the device at all. This work delineates the significant influence of Qx core extension on ternary guest compatibility, providing valuable insights and guidance for the design of ternary systems towards higher efficiencies for OSCs.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationJournal of materials chemistry A, 2025, v. 13, no. 20, p. 14765-14772en_US
dcterms.isPartOfJournal of materials chemistry Aen_US
dcterms.issued2025-
dc.identifier.scopus2-s2.0-105003230494-
dc.identifier.eissn2050-7496en_US
dc.description.validate202509 bchyen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberCDCF_2024-2025, OA_TA-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextH. Yu appreciates the support from the Strategic Hiring Scheme start-up fund of the Hong Kong Polytechnic University (Project ID: P0056175; Work Programme: BDDV) and the Hong Kong Research Grants Council (GRF project 16303024 and 16310824). H. Yan appreciates the support from the National Key Research and Development Program of China (No. 2019YFA0705900) funded by MOST, the Basic and Applied Research Major Program of Guangdong Province (No. 2019B030302007), the National Natural Science Foundation of China (NSFC, No. 22075057), the Shen Zhen Technology and Innovation Commission through (Shenzhen Fundamental Research Program, JCYJ20200109140801751), the Hong Kong Research Grants Council (research fellow scheme RFS2021-6S05, RIF project R6021-18, CRF project C6023-19G, GRF project 16310019, 16310020, 16309221, 16309822), Hong Kong Innovation and Technology Commission (ITCCNERC14SC01) and Foshan-HKUST (Project No. FSUST19-CAT0202), Zhongshan Municipal Bureau of Science and Technology (No. ZSST20SC02), Guangdong-Hong Kong-Macao Joint Laboratory (No. 2023B1212120003) and Tencent Xplorer Prize. We also would like to express our gratitude to beamline BL16B1 at Shanghai Synchrotron Radiation Facility (SSRF) for their support during the GIWAXS experiment. RSoXS measurement was conducted at ALS BL 11.0.1.2, supported by the Office of Science, Office of Basic Energy Sciences, of the U.S. Department of Energy under Contract No. DE-AC02-05CH11231. W. Y. W. is grateful to the financial support from the RGC Senior Research Fellowship Scheme (SRFS2021-5S01), Research Institute for Smart Energy (CDAQ), Research Centre for Organic Electronics (CE0P), Research Centre for Carbon-Strategic Catalysis (CE2L) and Miss Clarea Au for the Endowed Professorship in Energy (847S).en_US
dc.description.pubStatusPublisheden_US
dc.description.TARSC (2025)en_US
dc.description.oaCategoryTAen_US
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