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Article: Photocarrier-induced persistent structural polarization in soft-lattice lead halide perovskites

TitlePhotocarrier-induced persistent structural polarization in soft-lattice lead halide perovskites
Authors
Issue Date2023
Citation
Nature Nanotechnology, 2023, v. 18, n. 4, p. 357-364 How to Cite?
AbstractThe success of the lead halide perovskites in diverse optoelectronics has motivated considerable interest in their fundamental photocarrier dynamics. Here we report the discovery of photocarrier-induced persistent structural polarization and local ferroelectricity in lead halide perovskites. Photoconductance studies of thin-film single-crystal CsPbBr3 at 10 K reveal long-lasting persistent photoconductance with an ultralong photocarrier lifetime beyond 106 s. X-ray diffraction studies reveal that photocarrier-induced structural polarization is present up to a critical freezing temperature. Photocapacitance studies at cryogenic temperatures further demonstrate a systematic local phase transition from linear dielectric to paraelectric and relaxor ferroelectric under increasing illumination. Our theoretical investigations highlight the critical role of photocarrier–phonon coupling and large polaron formation in driving the local relaxor ferroelectric phase transition. Our findings show that this photocarrier-induced persistent structural polarization enables the formation of ferroelectric nanodomains at low temperature, which suppress carrier recombination and offer the possibility of exploring intriguing carrier–phonon interplay and the rich polaron photophysics.
Persistent Identifierhttp://hdl.handle.net/10722/356283
ISSN
2023 Impact Factor: 38.1
2023 SCImago Journal Rankings: 14.577
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorQian, Qi-
dc.contributor.authorWan, Zhong-
dc.contributor.authorTakenaka, Hiroyuki-
dc.contributor.authorKeum, Jong K.-
dc.contributor.authorSmart, Tyler J.-
dc.contributor.authorWang, Laiyuan-
dc.contributor.authorWang, Peiqi-
dc.contributor.authorZhou, Jingyuan-
dc.contributor.authorRen, Huaying-
dc.contributor.authorXu, Dong-
dc.contributor.authorHuang, Yu-
dc.contributor.authorPing, Yuan-
dc.contributor.authorDuan, Xiangfeng-
dc.date.accessioned2025-05-27T07:21:59Z-
dc.date.available2025-05-27T07:21:59Z-
dc.date.issued2023-
dc.identifier.citationNature Nanotechnology, 2023, v. 18, n. 4, p. 357-364-
dc.identifier.issn1748-3387-
dc.identifier.urihttp://hdl.handle.net/10722/356283-
dc.description.abstractThe success of the lead halide perovskites in diverse optoelectronics has motivated considerable interest in their fundamental photocarrier dynamics. Here we report the discovery of photocarrier-induced persistent structural polarization and local ferroelectricity in lead halide perovskites. Photoconductance studies of thin-film single-crystal CsPbBr3 at 10 K reveal long-lasting persistent photoconductance with an ultralong photocarrier lifetime beyond 106 s. X-ray diffraction studies reveal that photocarrier-induced structural polarization is present up to a critical freezing temperature. Photocapacitance studies at cryogenic temperatures further demonstrate a systematic local phase transition from linear dielectric to paraelectric and relaxor ferroelectric under increasing illumination. Our theoretical investigations highlight the critical role of photocarrier–phonon coupling and large polaron formation in driving the local relaxor ferroelectric phase transition. Our findings show that this photocarrier-induced persistent structural polarization enables the formation of ferroelectric nanodomains at low temperature, which suppress carrier recombination and offer the possibility of exploring intriguing carrier–phonon interplay and the rich polaron photophysics.-
dc.languageeng-
dc.relation.ispartofNature Nanotechnology-
dc.titlePhotocarrier-induced persistent structural polarization in soft-lattice lead halide perovskites-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1038/s41565-022-01306-x-
dc.identifier.pmid36702955-
dc.identifier.scopuseid_2-s2.0-85146853498-
dc.identifier.volume18-
dc.identifier.issue4-
dc.identifier.spage357-
dc.identifier.epage364-
dc.identifier.eissn1748-3395-
dc.identifier.isiWOS:000922940000002-

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