Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/108998
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dc.contributorDepartment of Applied Physicsen_US
dc.creatorWang, Len_US
dc.creatorNughays, Ren_US
dc.creatorYin, Jen_US
dc.creatorShih, CHen_US
dc.creatorGuo, TFen_US
dc.creatorMohammed, OFen_US
dc.creatorChergui, Men_US
dc.date.accessioned2024-09-12T06:45:03Z-
dc.date.available2024-09-12T06:45:03Z-
dc.identifier.urihttp://hdl.handle.net/10397/108998-
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.rights© 2024 The Authors. Published by American Chemical Societyen_US
dc.rightsThis article is licensed under CC-BY 4.0 (https://creativecommons.org/licenses/by/4.0/)en_US
dc.rightsThe following publication Wang, L., Nughays, R., Yin, J., Shih, C.-H., Guo, T.-F., Mohammed, O. F., & Chergui, M. (2024). Band Gap Renormalization at Different Symmetry Points in Perovskites. ACS Photonics, 11(6), 2273-2281 is available at https://doi.org/10.1021/acsphotonics.4c00082.en_US
dc.subjectBroad-band UV transient absorptionen_US
dc.subjectGlobal lifetime analysisen_US
dc.subjectMany-body interactionsen_US
dc.subjectPhotoexcitationen_US
dc.subjectUltrafast spectral responseen_US
dc.titleBand gap renormalization at different symmetry points in perovskitesen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage2273en_US
dc.identifier.epage2281en_US
dc.identifier.volume11en_US
dc.identifier.issue6en_US
dc.identifier.doi10.1021/acsphotonics.4c00082en_US
dcterms.abstractUsing ultrafast broad-band transient absorption (TA) spectroscopy of photoexcited MAPbBr3 thin films with probe continua in the visible and the mid- to deep-ultraviolet (UV) ranges, we capture the ultrafast renormalization at the fundamental gap at the R symmetry point of the Brillouin zone (BZ) and a higher energy gap at the M symmetry point. Advanced global lifetime analysis and lifetime density distribution analysis are applied to extract quantitative information. Our work confirms the similarity of the response at both high-symmetry points, which indicates a band edge renormalization that rises within the instrument response function (IRF, ∼250 fs) and decays in ca. 400–600 fs, undergoing an energy red shift of 90–150 meV. The reported time scale corresponds to the decay of free carriers into neutral excitons. The ability to monitor different high-symmetry points in photoexcited perovskites opens exciting prospects for the characterization of a large class of materials and for photonic applications.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationACS photonics, 19 June 2024, v. 11, no. 6, p. 2273-2281en_US
dcterms.isPartOfACS photonicsen_US
dcterms.issued2024-06-19-
dc.identifier.scopus2-s2.0-85193582439-
dc.identifier.eissn2330-4022en_US
dc.description.validate202409 bcchen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberCDCF_2023-2024-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextKing Abdullah University of Science and Technology, KAUST; Malawi University of Science and Technology, MUST; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung, SNF; European Research Council, ERC; European Research Council, ERC; Hong Kong Polytechnic University, PolyU; Hong Kong Polytechnic University, PolyUen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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