Local chemical order enables an ultrastrong and ductile high-entropy alloy in a cryogenic environment

材料科学 晶体孪晶 打滑(空气动力学) 合金 延展性(地球科学) 极限抗拉强度 纳米技术 复合材料 蠕动 热力学 微观结构 物理
作者
Lifang Sun,Zhufeng He,Nan Jia,Yanxin Guo,Shuang Jiang,Yuliang Yang,Yuxin Liu,Xianjun Guan,Y.F. Shen,Haile Yan,Peter K. Liaw
出处
期刊:Science Advances [American Association for the Advancement of Science]
卷期号:10 (48) 被引量:8
标识
DOI:10.1126/sciadv.adq6398
摘要

Owing to superior strength-ductility combination and great potential for applications in extreme conditions, high-entropy alloys (HEAs) with the face-centered cubic (FCC) structure have drawn enormous attention. However, the FCC structure limits yield strength and makes the alloys unable to meet ever-increasing demands for exploring the universe. Here, we report a strategy to obtain FCC materials with outstanding mechanical properties in both ambient and cryogenic environments, via exploiting dynamic development of the interstitial-driven local chemical order (LCO). Dense laths composed of the multiscaled LCO domains evolve from planar-slip bands that form in the prior thermomechanical processing, contributing to ultrahigh yield strengths over a wide temperature range. During cryogenic tensile deformation, LCO further develops and promotes remarkable dislocation cross-slip. Together with the deformation-driven transformation and twinning, these factors lead to satisfactory work hardening. The cryogenic loading–promoted LCO, also revealed by ab initio calculations, opens an avenue for designing advanced cryogenic materials.
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