Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/115513
DC FieldValueLanguage
dc.contributorResearch Institute for Advanced Manufacturingen_US
dc.contributorDepartment of Industrial and Systems Engineeringen_US
dc.creatorSun, Yen_US
dc.creatorWang, Cen_US
dc.creatorRen, Cen_US
dc.creatorZhang, Den_US
dc.creatorLi, Ken_US
dc.creatorCheung, CFen_US
dc.creatorChen, Zen_US
dc.date.accessioned2025-10-02T06:23:47Z-
dc.date.available2025-10-02T06:23:47Z-
dc.identifier.issn0749-6419en_US
dc.identifier.urihttp://hdl.handle.net/10397/115513-
dc.language.isoenen_US
dc.publisherPergamon Pressen_US
dc.subjectAdditive manufacturingen_US
dc.subjectHigh entropy alloysen_US
dc.subjectIntermediate temperatureen_US
dc.subjectTensile propertyen_US
dc.subjectChemical orderingen_US
dc.subjectIn-situ precipitationen_US
dc.titleMultiscale chemical ordering heterogeneity facilitates exceptional strength and ductility in additively manufactured Ti-added AlCoCrFeNi₂.₁ high-entropy alloys at intermediate temperaturesen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume190en_US
dc.identifier.doi10.1016/j.ijplas.2025.104373en_US
dcterms.abstractThe remarkable mechanical properties of high-entropy alloys at room and cryogenic temperatures have garnered significant attention in recent years. However, their poor mechanical performance at intermediate temperatures has hindered their practical application in many contexts. This study examines the effect of Ti addition on the intermediate-temperature tensile properties of additively manufactured AlCoCrFeNi2.1 eutectic high-entropy alloys. The findings demonstrate that Ti addition improves the alloy's tensile properties through several vital mechanisms. Ti addition significantly increases back-stress, which dominates strain-hardening behavior. At 400 °C, Ti addition promotes the formation of chemically long-range ordered and spinodal decomposition, facilitating multi-mode dislocation behavior characterized by coexisting planar and wavy slip. This enhances work-hardening, thereby achieving improved strength-ductility synergy. At 600 °C, the long-range ordered and spinodal decomposition evolved into nanoscale D03 precipitates that allow dislocation pinning and contribute to high strength while preserving good ductility. Moreover, Ti addition induces a rounded dual-phase microstructure, where the face-centered cubic phase serves as an adhesive layer, preventing crack propagation along the phase boundary. These mechanisms synergistically enhance strength and ductility at intermediate temperatures, making Ti-modified AlCoCrFeNi2.1 high-entropy alloys highly suitable for applications in the 400-600 °C temperature range.en_US
dcterms.accessRightsembargoed accessen_US
dcterms.bibliographicCitationInternational journal of plasticity, July 2025, v. 190, 104373en_US
dcterms.isPartOfInternational journal of plasticityen_US
dcterms.issued2025-07-
dc.identifier.scopus2-s2.0-105008498148-
dc.identifier.artn104373en_US
dc.description.validate202510 bcwcen_US
dc.description.oaNot applicableen_US
dc.identifier.SubFormIDG000210/2025-07-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThe work described in this paper was mainly supported by the research studentship from the Research and Innovation Office of The Hong Kong Polytechnic University (Project codes: RJHP, BBX5, CD9E, and UARQ) and the Shenzhen-Hong Kong-Macau Technology Research Program (Project No: SGDX20220530110804030 and SGDX20230821092100002). The authors would also like to express their sincere thanks to the funding support from the State Key Laboratories in Hong Kong from the Innovation and Technology Commission (ITC) of the Government of the Hong Kong Special Administrative Region (HKSAR), China. The authors would like to thank the reviewers for their insightful comments and suggestions, which have significantly improved the clarity and quality of this manuscript.en_US
dc.description.pubStatusPublisheden_US
dc.date.embargo2027-07-31en_US
dc.description.oaCategoryGreen (AAM)en_US
Appears in Collections:Journal/Magazine Article
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Embargo End Date 2027-07-31
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