Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/103582
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dc.contributorDepartment of Electrical and Electronic Engineeringen_US
dc.contributorResearch Institute for Smart Energyen_US
dc.contributorDepartment of Applied Physicsen_US
dc.contributorSchool of Fashion and Textilesen_US
dc.creatorZhang, Hen_US
dc.creatorChen, Zen_US
dc.creatorQin, Men_US
dc.creatorRen, Zen_US
dc.creatorLiu, Ken_US
dc.creatorHuang, Jen_US
dc.creatorShen, Den_US
dc.creatorWu, Zen_US
dc.creatorZhang, Yen_US
dc.creatorHao, Jen_US
dc.creatorLee, CSen_US
dc.creatorLu, Xen_US
dc.creatorZheng, Zen_US
dc.creatorYu, Wen_US
dc.creatorLi, Gen_US
dc.date.accessioned2023-12-28T09:08:13Z-
dc.date.available2023-12-28T09:08:13Z-
dc.identifier.issn0935-9648en_US
dc.identifier.urihttp://hdl.handle.net/10397/103582-
dc.language.isoenen_US
dc.publisherWiley-VCH Verlag GmbH & Co. KGaAen_US
dc.rights© 2021 Wiley-VCH GmbHen_US
dc.rightsThis is the peer reviewed version of the following article: H. Zhang, Z. Chen, M. Qin, Z. Ren, K. Liu, J. Huang, D. Shen, Z. Wu, Y. Zhang, J. Hao, C.-s. Lee, X. Lu, Z. Zheng, W. Yu, G. Li, Multifunctional Crosslinking-Enabled Strain-Regulating Crystallization for Stable, Efficient α-FAPbI3-Based Perovskite Solar Cells. Adv. Mater. 2021, 33, 2008487, which has been published in final form at https://doi.org/10.1002/adma.202008487. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. This article may not be enhanced, enriched or otherwise transformed into a derivative work, without express permission from Wiley or by statutory rights under applicable legislation. Copyright notices must not be removed, obscured or modified. The article must be linked to Wiley’s version of record on Wiley Online Library and any embedding, framing or otherwise making available the article or pages thereof by third parties from platforms, services and websites other than Wiley Online Library must be prohibited.en_US
dc.subjectα-FAPbI3en_US
dc.subjectCrosslinkingen_US
dc.subjectDefect passivationen_US
dc.subjectPerovskite solar cellsen_US
dc.subjectStrain regulationen_US
dc.titleMultifunctional crosslinking-enabled strain-regulating crystallization for stable, efficient α-FAPbI₃-based perovskite solar cellsen_US
dc.typeJournal/Magazine Articleen_US
dc.description.otherinformationTitle on author's file: Multi-functional Cross-linking Enabled Strain Regulating Crystallization for Stable, Efficient α-FAPbI3-based Perovskite Solar Cellsen_US
dc.identifier.volume33en_US
dc.identifier.issue29en_US
dc.identifier.doi10.1002/adma.202008487en_US
dcterms.abstractα-Formamidinium lead triiodide (α-FAPbI3) represents the state-of-the-art for perovskite solar cells (PSCs) but experiences intrinsic thermally induced tensile strain due to a higher phase-converting temperature, which is a critical instability factor. An in situ crosslinking-enabled strain-regulating crystallization (CSRC) method with trimethylolpropane triacrylate (TMTA) is introduced to precisely regulate the top section of perovskite film where the largest lattice distortion occurs. In CSRC, crosslinking provides in situ perovskite thermal-expansion confinement and strain regulation during the annealing crystallization process, which is proven to be much more effective than the conventional strain-compensation (post-treatment) method. Moreover, CSRC with TMTA successfully achieves multifunctionality simultaneously: the regulation of tensile strain, perovskite defects passivation with an enhanced open-circuit voltage (VOC = 50 mV), and enlarged perovskite grain size. The CSRC approach gives significantly enhanced power conversion efficiency (PCE) of 22.39% in α-FAPbI3-based PSC versus 20.29% in the control case. More importantly, the control PSCs’ instability factor—residual tensile strain—is regulated into compression strain in the CSRC perovskite film through TMTA crosslinking, resulting in not only the best PCE but also outstanding device stability in both long-term storage (over 4000 h with 95% of initial PCE) and light soaking (1248 h with 80% of initial PCE) conditions.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationAdvanced materials, 22 July 2021, v. 33, no. 29, 2008487en_US
dcterms.isPartOfAdvanced materialsen_US
dcterms.issued2021-07-22-
dc.identifier.eissn1521-4095en_US
dc.identifier.artn2008487en_US
dc.description.validate202312 bcchen_US
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumbera2553-n12-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextShenzhen Science and Technology Innovation Commission; Research Institute for Smart Energy (RISE); University Supporting Fund; Sir Sze‐yuen Chung Endowed Professorship Fund, Hong Kong Polytechnic University; Shenzhen Science and Technology Innovation Commission; Research Institute for Smart Energy (RISE)en_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryGreen (AAM)en_US
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