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Disorder in M n+1 AX n phases at the atomic scale

  • Chenxu Wang
  • , Tengfei Yang
  • , Cameron L. Tracy
  • , Chenyang Lu
  • , Hui Zhang
  • , Yong Jie Hu
  • , Lumin Wang
  • , Liang Qi
  • , Lin Gu
  • , Qing Huang
  • , Jie Zhang
  • , Jingyang Wang
  • , Jianming Xue
  • , Rodney C. Ewing
  • , Yugang Wang
  • Stanford University
  • Peking University
  • University of Michigan, Ann Arbor
  • Monash University
  • CAS - Institute of Physics
  • CAS - Ningbo Institute of Material Technology and Engineering
  • CAS - Institute of Metal Research

Research output: Contribution to journalArticlepeer-review

79 Scopus citations

Abstract

Atomic disordering in materials alters their physical and chemical properties and can subsequently affect their performance. In complex ceramic materials, it is a challenge to understand the nature of structural disordering, due to the difficulty of direct, atomic-scale experimental observations. Here we report the direct imaging of ion irradiation-induced antisite defects in M n+1 AX n phases using double C S -corrected scanning transmission electron microscopy and provide compelling evidence of order-to-disorder phase transformations, overturning the conventional view that irradiation causes phase decomposition to binary fcc-structured M n+1 X n . With the formation of uniformly distributed cation antisite defects and the rearrangement of X anions, disordered solid solution γ-(M n+1 A)X n phases are formed at low ion fluences, followed by gradual transitions to solid solution fcc-structured (M n+1 A)X n phases. This study provides a comprehensive understanding of the order-to-disorder transformations in M n+1 AX n phases and proposes a method for the synthesis of new solid solution (M n+1 A)X n phases by tailoring the disorder.

Original languageEnglish
Article number622
JournalNature Communications
Volume10
Issue number1
DOIs
StatePublished - 1 Dec 2019
Externally publishedYes

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