Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/117197
DC FieldValueLanguage
dc.contributorDepartment of Industrial and Systems Engineeringen_US
dc.contributorResearch Institute for Advanced Manufacturingen_US
dc.contributorDepartment of Mechanical Engineeringen_US
dc.creatorYang, Wen_US
dc.creatorQian, Len_US
dc.creatorLuo, Jen_US
dc.creatorLu, Wen_US
dc.creatorGao, Zen_US
dc.creatorCheung, CFen_US
dc.creatorRuan, Hen_US
dc.creatorWang, YJen_US
dc.creatorYang, XSen_US
dc.date.accessioned2026-02-06T08:21:49Z-
dc.date.available2026-02-06T08:21:49Z-
dc.identifier.issn1359-6454en_US
dc.identifier.urihttp://hdl.handle.net/10397/117197-
dc.language.isoenen_US
dc.publisherElsevier Ltden_US
dc.subjectCompositionally complex alloysen_US
dc.subjectCrystalline-amorphous nanostructureen_US
dc.subjectDeformation-induced crystallizationen_US
dc.subjectGrain coalescenceen_US
dc.subjectLaser surface remeltingen_US
dc.titleAmorphous phase crystallization-involved cooperative deformation mechanism in a crystalline-amorphous nanostructured compositionally complex alloyen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume302en_US
dc.identifier.doi10.1016/j.actamat.2025.121673en_US
dcterms.abstractCrystalline-amorphous nanostructured metals, comprising extremely refined nanograins encapsulated by nanoscale amorphous phase acting as grain boundaries (GBs), exhibit exceptional mechanical properties with sustained strengthening, primarily due to unique dislocation-mediated cooperative deformation mechanisms. However, the atomic-scale understanding of dislocation activities, their interaction with nanograins and amorphous GBs, and the resulting microstructural change during plastic deformation remain elusive. In this work, a crystalline-amorphous nanostructured layer is fabricated on a Fe<inf>45</inf>Mn<inf>35</inf>Cr<inf>10</inf>Co<inf>10</inf> compositionally complex alloy via laser surface remelting. High-resolution transmission electron microscopy (HRTEM), complemented by atomistic molecular dynamics (MD) simulations, reveals the atomic-scale dynamic cooperative deformation behavior. The results show that partial dislocations initially nucleate at the nanograin/amorphous GB interfaces, forming faulted bands across nanograins. As deformation progresses, these dislocations accumulate and induce local atomic rearrangements within the amorphous zones. This activity promotes fragmentation of disordered regions, enabling further dislocation nucleation and initiating a disorder-to-order transition that drives progressive crystallization of the amorphous GBs. Such crystallization progressively thins the amorphous GBs, transforming them into conventional sharp boundaries. Continued dislocation movement in the GBs trigger slight rotations of adjacent nanograins, particularly those with small misorientations, facilitating grain coalescence for coarsening. These findings offer profound insights into the cooperative co-deformation mechanisms in crystalline-amorphous nanostructures which are beneficial for enhanced mechanical properties through microstructural optimization.en_US
dcterms.accessRightsembargoed accessen_US
dcterms.bibliographicCitationActa materialia, 1 Jan. 2026, v. 302, 121673en_US
dcterms.isPartOfActa materialiaen_US
dcterms.issued2026-01-01-
dc.identifier.scopus2-s2.0-105020925487-
dc.identifier.eissn1873-2453en_US
dc.identifier.artn121673en_US
dc.description.validate202602 bchyen_US
dc.description.oaNot applicableen_US
dc.identifier.SubFormIDG000841/2026-01-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThis work was supported by the grants from the Research Grants Council of the Hong Kong Special Administrative Region, China (Nos. PolyU15210123), Guangdong Basic and Applied Basic Research Foundation (No. 2024A1515010781), PolyU grants (Nos. 1-BBRA, 1-YXB4, and 1-YWBC), and the funding support to the State Key Laboratories in Hong Kong from the Innovation and Technology Commission (ITC) of the Government of the HKASR, China. WY and ZG were supported by the grants from the Research Committee of PolyU under student account codes RK3J and RHVR, respectively.en_US
dc.description.pubStatusPublisheden_US
dc.date.embargo2028-01-01en_US
dc.description.oaCategoryGreen (AAM)en_US
Appears in Collections:Journal/Magazine Article
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Embargo End Date 2028-01-01
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