Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/118538
DC FieldValueLanguage
dc.contributorDepartment of Applied Physics-
dc.creatorQiu, J-
dc.creatorZhu, H-
dc.creatorShao, B-
dc.creatorShi, Y-
dc.creatorXu, S-
dc.creatorAbulikemu, M-
dc.creatorLiu, J-
dc.creatorZheng, Z-
dc.creatorJamal, A-
dc.creatorAlsaiari, HA-
dc.creatorAqeel, S-
dc.creatorGereige, I-
dc.creatorZhang, F-
dc.creatorYin, J-
dc.creatorLi, C-
dc.creatorBakr, OM-
dc.date.accessioned2026-04-20T07:19:52Z-
dc.date.available2026-04-20T07:19:52Z-
dc.identifier.issn0002-7863-
dc.identifier.urihttp://hdl.handle.net/10397/118538-
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.titleTailored electron-deficient macrocycles guiding the perovskite crystallization process for solar cellsen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage42061-
dc.identifier.epage42069-
dc.identifier.volume147-
dc.identifier.issue45-
dc.identifier.doi10.1021/jacs.5c15639-
dcterms.abstractPerovskite solar cells (PSCs) exhibit impressive power conversion efficiencies (PCEs), but their stability still falls short of industrial commercialization requirements, primarily due to inherent defects and halide ion migration within the perovskite materials. To address this shortcoming, we developed a novel electron-deficient biphen[n]arene macrocycle molecule, NBP[2], synthesized through the condensation of the monomer 2,2″,4,4″-tetramethoxy-4’,6’-dinitro-1,1’:3′,1″-terphenyl (NP) with paraformaldehyde. When the macrocyclic molecule is introduced into the perovskite film via the antisolvent injection method, it functions as a regulator of the crystallization process of perovskite and an inhibitor of halide anion migration. In addition, NBP[2] can effectively bind with uncoordinated halide ions and Pb²⁺, reducing intrinsic defects through Lewis acid–base and cation−π interactions. As a result, NBP[2]-modified PSCs achieve a PCE of up to 25.38% (compared to 23.89% for the control) and retain 95.8% of their initial efficiency after 1000 h of maximum power point tracking under 1-sun illumination at room temperature in an N₂ atmosphere.-
dcterms.accessRightsembargoed accessen_US
dcterms.bibliographicCitationJournal of the American Chemical Society, 12 Nov. 2025, v. 147, no. 45, p. 42061-42069-
dcterms.isPartOfJournal of the American Chemical Society-
dcterms.issued2025-11-12-
dc.identifier.scopus2-s2.0-105021306013-
dc.identifier.pmid41152154-
dc.identifier.eissn1520-5126-
dc.description.validate202604 bcjz-
dc.description.oaNot applicableen_US
dc.identifier.SubFormIDG001457/2026-01en_US
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextJ. Q, S. X., Z. Z., and C. L acknowledge funding support from the National Natural Science Foundation of China (22301218) and the Natural Science Foundation of Tianjin City (23JCZDJC00660). B.S. thanks funding support from the China Scholarship Council (No. 202006070004). J.Y. acknowledges financial support from National Natural Science Foundation of China (62422512), Hong Kong Polytechnic University (Grant no. P0053682) and a grant from the Research Grants Council of the Hong Kong Special Administrative Region, China (Project No. 15300724). This work was supported by Saudi Aramco and King Abdullah University of Science and Technology (KAUST). We also acknowledge the Supercomputing Laboratory at KAUST for the computational resources.en_US
dc.description.pubStatusPublisheden_US
dc.date.embargo2026-10-28en_US
dc.description.oaCategoryGreen (AAM)en_US
Appears in Collections:Journal/Magazine Article
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Embargo End Date 2026-10-28
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