First principle study of magnetism and vacancy energetics in a near equimolar NiFeMnCr high entropy alloy

We report the results of ab initio calculations of a novel NiFeMnCr high entropy alloy (HEA) with potential applications as a high performance structural material. The bulk and defect property variations due to chemical disordering and magnetic frustration have been studied using both supercell and...

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Bibliographic Details
Published inJournal of applied physics Vol. 125; no. 15
Main Authors Li, Congyi, Yin, Junqi, Odbadrakh, Khorgolkhuu, Sales, Brian C., Zinkle, Steven J., Stocks, G. Malcolm, Wirth, Brian D.
Format Journal Article
LanguageEnglish
Published Melville American Institute of Physics 21.04.2019
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Summary:We report the results of ab initio calculations of a novel NiFeMnCr high entropy alloy (HEA) with potential applications as a high performance structural material. The bulk and defect property variations due to chemical disordering and magnetic frustration have been studied using both supercell and coherent potential approximation-based techniques. While magnetic frustration due to the presence of multiple 3d transition metals can severely affect the accuracy of vacancy formation energy in first-principles calculations, this effect should be suppressed at intermediate and high temperatures. An efficient approach to evaluate the chemical potential in HEA is constructed and implemented. Vacancy formation energies are computed based on the chemical potential. The statistical distribution of formation energies is weakly dependent upon the chemical identity of the vacancy. On the other hand, the calculated vacancy migration energies show that Fe is more likely to have a large migration barrier than Cr, Mn, or Ni. Finally, atomic-level stresses are computed. A qualitative model to explain the elemental segregation trend in HEA is built upon the atomic-level stress calculation results and provides a reasonable qualitative agreement with ion irradiation experimental data of a NiFeMnCr HEA.
Bibliography:USDOE
AC05-00OR22725; SC0006661
ISSN:0021-8979
1089-7550
DOI:10.1063/1.5086172