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Amorphous martensite in β-Ti alloys

Author

Listed:
  • Long Zhang

    (Chinese Academy of Sciences
    IFW Dresden, Institute for Complex Materials)

  • Haifeng Zhang

    (Chinese Academy of Sciences)

  • Xiaobing Ren

    (Xi’an Jiaotong University
    National Institute for Materials Science)

  • Jürgen Eckert

    (Austrian Academy of Sciences
    Montanuniversität Leoben)

  • Yandong Wang

    (University of Science and Technology Beijing)

  • Zhengwang Zhu

    (Chinese Academy of Sciences)

  • Thomas Gemming

    (IFW Dresden, Institute for Complex Materials)

  • Simon Pauly

    (IFW Dresden, Institute for Complex Materials)

Abstract

Martensitic transformations originate from a rigidity instability, which causes a crystal to change its lattice in a displacive manner. Here, we report that the martensitic transformation on cooling in Ti–Zr–Cu–Fe alloys yields an amorphous phase instead. Metastable β-Ti partially transforms into an intragranular amorphous phase due to local lattice shear and distortion. The lenticular amorphous plates, which very much resemble α′/α″ martensite in conventional Ti alloys, have a well-defined orientation relationship with the surrounding β-Ti crystal. The present solid-state amorphization process is reversible, largely cooling rate independent and constitutes a rare case of congruent inverse melting. The observed combination of elastic softening and local lattice shear, thus, is the unifying mechanism underlying both martensitic transformations and catastrophic (inverse) melting. Not only do we reveal an alternative mechanism for solid-state amorphization but also establish an explicit experimental link between martensitic transformations and catastrophic melting.

Suggested Citation

  • Long Zhang & Haifeng Zhang & Xiaobing Ren & Jürgen Eckert & Yandong Wang & Zhengwang Zhu & Thomas Gemming & Simon Pauly, 2018. "Amorphous martensite in β-Ti alloys," Nature Communications, Nature, vol. 9(1), pages 1-8, December.
  • Handle: RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-02961-2
    DOI: 10.1038/s41467-018-02961-2
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