Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/117756
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dc.contributorDepartment of Applied Physics-
dc.creatorWang, Len_US
dc.creatorLiu, Yen_US
dc.creatorYang, Jen_US
dc.creatorXu, Xen_US
dc.creatorShao, Ben_US
dc.creatorZhu, Hen_US
dc.creatorCai, Hen_US
dc.creatorSun, Ten_US
dc.creatorYin, Jen_US
dc.creatorAlshareef, HNen_US
dc.creatorBakr, OMen_US
dc.creatorZhu, Yen_US
dc.creatorMohammed, OFen_US
dc.date.accessioned2026-03-05T07:56:09Z-
dc.date.available2026-03-05T07:56:09Z-
dc.identifier.urihttp://hdl.handle.net/10397/117756-
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.rights© 2025 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., Liu, Y., Yang, J., Xu, X., Shao, B., Zhu, H., ... & Mohammed, O. F. (2025). Lattice Expansion Enables Large Surface Carrier Diffusion in WS2 Monolayer. ACS Energy Letters, 10(4), 1741-1750 is available at https://doi.org/10.1021/acsenergylett.5c00307.en_US
dc.titleLattice expansion enables large surface carrier diffusion in WS₂ monolayeren_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage1741en_US
dc.identifier.epage1750en_US
dc.identifier.volume10en_US
dc.identifier.issue4en_US
dc.identifier.doi10.1021/acsenergylett.5c00307en_US
dcterms.abstractTwo-dimensional (2D) materials hold great promise for next-generation optoelectronic devices, with photogenerated charge carrier transport being critical to their performance. However, the influence of photoexcitation-induced commensurate lattice thermal effects on surface charge carrier dynamics is poorly understood. Traditional photon-pump/photon-probe methods have constraints in capturing the subtle yet critical surface dynamics, especially for these ultrathin materials due to challenges in spatial resolution and penetration depth. In this study, we utilized scanning ultrafast electron microscopy (SUEM), a technique that offers unparalleled sensitivity to surface phenomena that are entirely inaccessible through other methods. Our findings reveal a ∼1.4% negative thermal expansion at elevated temperatures, inducing internal strain that modifies the electronic structure and significantly enhances surface carrier transport, resulting in an order-of-magnitude improvement in photodetection performance. Moreover, we demonstrate that photoinduced charge carrier diffusion occurs predominantly within the first tens of picoseconds after photoexcitation, a regime characterized by thermal excitation resulting from carrier–phonon interactions. These results establish a direct link among lattice thermal expansion, carrier dynamics, and optoelectronic performance.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationACS energy letters, 11 Apr. 2025, v. 10, no. 4, p. 1741-1750en_US
dcterms.isPartOfACS energy lettersen_US
dcterms.issued2025-04-11-
dc.identifier.scopus2-s2.0-105000392115-
dc.identifier.eissn2380-8195en_US
dc.description.validate202603 bcch-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOS-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThis work was supported by King Abdullah University of Science and Technology (KAUST). Y. Liu, H. Cai, T. Sun and Y. Zhu acknowledge National Key Research and Development Program of China (2022YFE0113800) and the National Natural Science Foundation of China (22122505, 22075250, 21771161). J. Yang acknowledges financial support from the National Natural Science Foundation of China (No. 12347160), the Key Scientific Research Project of Colleges and Universities in He’nan Province (No. 24A140022), and the Natural Science Foundation of He’nan (No. 242300421671). J. Yin acknowledges financial support from Hong Kong Polytechnic University (grant no. P0042930, P0050410 and P0053682) and grants from the Research Grants Council of the Hong Kong Special Administrative Region, China (project no. PolyU 25300823 and PolyU 15300724), and National Natural Science Foundation of China (62422512).en_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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