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  5. Real-time observations of TRIP-induced ultrahigh strain hardening in a dual-phase CrMnFeCoNi high-entropy alloy

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Article
English
2020

Real-time observations of TRIP-induced ultrahigh strain hardening in a dual-phase CrMnFeCoNi high-entropy alloy

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English
2020
Nature Communications
Vol 11 (1)
DOI: 10.1038/s41467-020-14641-1

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Robert O. Ritchie
Robert O. Ritchie

University of California, Berkeley

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Sijing Chen
Hyun Seok Oh
Bernd Gludovatz
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Abstract

Strategies involving metastable phases have been the basis of the design of numerous alloys, yet research on metastable high-entropy alloys is still in its infancy. In dual-phase high-entropy alloys, the combination of local chemical environments and loading-induced crystal structure changes suggests a relationship between deformation mechanisms and chemical atomic distribution, which we examine in here in a Cantor-like Cr 20 Mn 6 Fe 34 Co 34 Ni 6 alloy, comprising both face-centered cubic ( fcc ) and hexagonal closed packed ( hcp ) phases. We observe that partial dislocation activities result in stable three-dimensional stacking-fault networks. Additionally, the fraction of the stronger hcp phase progressively increases during plastic deformation by forming at the stacking-fault network boundaries in the fcc phase, serving as the major source of strain hardening. In this context, variations in local chemical composition promote a high density of Lomer-Cottrell locks, which facilitate the construction of the stacking-fault networks to provide nucleation sites for the hcp phase transformation.

How to cite this publication

Sijing Chen, Hyun Seok Oh, Bernd Gludovatz, Sang Jun Kim, Eun Soo Park, Ze Zhang, Robert O. Ritchie, Qian Yu (2020). Real-time observations of TRIP-induced ultrahigh strain hardening in a dual-phase CrMnFeCoNi high-entropy alloy. Nature Communications, 11(1), DOI: 10.1038/s41467-020-14641-1.

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Publication Details

Type

Article

Year

2020

Authors

8

Datasets

0

Total Files

0

Language

English

Journal

Nature Communications

DOI

10.1038/s41467-020-14641-1

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