材料科学
金属间化合物
脆性
合金
复式(建筑)
纳米结构
软化
纳米晶
位错
可塑性
同种类的
高熵合金
产量(工程)
成核
化学物理
纳米技术
钛合金
声子
材料设计
工作(物理)
复合材料
结构材料
化学工程
作者
Shaohua Gao,Yi Yang,Xiaoxuan Fan,Jinyu Zhang,Shuaiyang Liu,J H Li,Hui Wang,W Song,G W Liu,Jun Sun
摘要
ABSTRACT Chemically homogeneous intermetallic nanoprecipitates (INPs), despite their high strength, are intrinsically hard and brittle and often suffer from glide‐plane softening, which can strengthen alloys but severely degrade uniform elongation. This strength–ductility trade‐off is further exacerbated at cryogenic temperatures by the inherent brittleness of bcc‐based phases in precipitate‐strengthened fcc/bcc duplex alloys. Here we propose a strategy that overcomes these limitations through the design of structurally complex INPs, i.e., the ductile B2 multicomponent INPs (MINPs) assembled with dispersive nanocores and a chemical‐heterogeneity shell, in duplex fcc/bcc Fe 58 Ni 16 Cr 16 Al 10 (at%) medium‐entropy alloys (Fe‐MEAs). Within the bcc constituent, these coherent core–shell B2 MINPs serve the dual role of dislocation sources and obstacles, analogous to the ordinary incoherent B2 MINPs that trigger twinning‐induced plasticity in the fcc constituent, yet they are substantially more effective in load transfer for high yield strength and in self‐hardening for large uniform elongation. Critically, the core–shell nanostructure suppresses the glide‐plane softening typical of conventional INPs and promotes the activation of unusual ⟨111⟩ dislocation multiplication and interactions under cryogenic conditions. This work demonstrates a structural complexification strategy for designing self‐hardening MINPs, opening a pathway to ductile, high‐strength materials for advanced cryogenic structural applications.
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