Dual-scale chemical ordering for cryogenic properties in CoNiV-based alloys

  • Tiwen Lu
  • , Binhan Sun
  • , Yue Li
  • , Sheng Dai
  • , Ning Yao
  • , Wenbo Li
  • , Xizhen Dong
  • , Xiyu Chen
  • , Jiacheng Niu
  • , Fan Ye
  • , Alisson Kwiatkowski da Silva
  • , Shuya Zhu
  • , Yu Xie
  • , Xiaofeng Yang
  • , Sihao Deng
  • , Jianping Tan
  • , Zhiming Li
  • , Dirk Ponge
  • , Lunhua He
  • , Xian Cheng Zhang
  • Dierk Raabe, Shan Tung Tu

Research output: Contribution to journalArticlepeer-review

7 Scopus citations

Abstract

The mechanical properties of metallic materials often degrade under harsh cryogenic conditions, posing challenges for low-temperature infrastructures1. Here we introduce a dual-scale atomic-ordering nanostructure, characterized by an exceptionally high number density of co-existing subnanoscale short-range ordering (approximately 2.4 × 1026 m−3) and nanoscale long-range ordering (approximately 4.5 × 1025 m−3) domains, within a metallic solid-solution matrix in a CoNiV-based alloy to improve the synergy of strength and ductility at low temperatures. We observe an ordering-induced increase in dislocation shear stress as well as a more rapid dislocation multiplication owing to the dislocation blocking effect of nanoscale long-range ordering and the associated generation of new dislocations. The latter effect also releases stress concentrations at nanoscale long-range-ordered obstacles that otherwise would promote damage initiation and failure. Consequently, the alloy shows a strength–elongation product of 76 GPa % with a yield strength of approximately 1.2 GPa at 87 K, outperforming materials devoid of such ordering hierarchy, containing only short-range ordered or coherent precipitates of a few tens of nanometres. Our results highlight the impact of dual co-existing chemical ordering on the mechanical properties of complex alloys and offer guidelines to control these ordering states to enhance their mechanical performance for cryogenic applications.

Original languageEnglish
Pages (from-to)385-391
Number of pages7
JournalNature
Volume645
Issue number8080
DOIs
StatePublished - Sep 11 2025
Externally publishedYes

Funding

Open access funding provided by Max Planck Society. X.-C.Z. acknowledges the financial support from the National Key Research and Development Programme (2022YFB4602100) and the National Natural Science Foundation of China (52205152, 52321002, U21B2077), New Cornerstone Science Foundation. T.L. acknowledges the financial support from Shanghai Super Postdoctoral Incentive Plan (2021103) and Shanghai Pujiang Programme (23FJD023). B.S. acknowledges the financial support from the National Key Research and Development Project (2023YFB3712103), the National Natural Science Foundation of China (52275147) and the Shanghai Gaofeng Project for University Academic Program Development. S. Dai acknowledges the the National Natural Science Foundation of China (22376062), the Science and Technology Commission of Shanghai Municipality (24DX1400200 and 22ZR1415700) and the Fundamental Research Funds for the Central Universities. We thank J. Shi and T. He for discussions on the neutron diffraction analysis.

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