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Ti substitution for Mn in MnCoGe - the magnetism of Mn0.9Ti 0.1CoGe

  • J. L. Wang
  • , P. Shamba
  • , W. D. Hutchison
  • , M. F. Md. Din
  • , J. C. Debnath
  • , M. Avdeev
  • , R. Zeng
  • , S. J. Kennedy
  • , S. J. Campbell
  • , S. X. Dou

    Research output: Contribution to journalArticlepeer-review

    23 Citations (Scopus)

    Abstract

    Bulk magnetization measurements (5-320 K; 0-8 T) reveal that below room temperature Mn0.9Ti0.1CoGe exhibits two magnetic phase transitions at ∼178 K and ∼280 K. Neutron diffraction measurements (3-350 K) confirm that the transition at ∼178 K is due to the structural change from the low-temperature orthorhombic TiNiSi-type structure (space group Pnma) to the higher temperature hexagonal Ni2In-type structure (space group P63/mmc), while the transition at ∼280 K originates from the transition from ferromagnetism to paramagnetism. The magnetocaloric behaviour of Mn0.9Ti0.1CoGe around Tstr ∼ 178 K and TC ∼ 280 K as determined via the magnetic field and temperature dependences of DC magnetisation are given by the maximum values of the magnetic entropy changes ΔSM max = 6.6J kg1 K 1 around Tstr ∼ 178 K, and ΔSM max = 4.2 J kg1 K1 around TC ∼ 280 K for a magnetic field change of ΔB = 0-8 T. Both structural entropy - due to the unit cell expansion of ∼4.04% - and magnetic entropy - due to an increase in the magnetic moment of ∼31% - are found to contribute significantly to the total entropy change around Tstr. Critical analysis of the transition around TC ∼ 280 K leads to exponents similar to values derived from a mean field theory, consistent with long-range ferromagnetic interactions. It was found that the field dependence of ΔSM max can be expressed as ΔSMmax ∠Bn with n = 1 for the structural transition around T str and n = 2/3 for the ferromagnetic transition around TC thereby confirming the second order nature of this latter transition.
    Original languageEnglish
    Pages (from-to)475-479
    Number of pages5
    JournalJournal of Alloys and Compounds
    Volume577
    DOIs
    Publication statusPublished - 2013

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