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Preparation and Characterization of Francisite Solid Solutions Cu3Bi(Se1−xTexO3)2O2Br (x = 0−1): Possibility for Francisites as Starting Materials for Oxide van der Waals Ferromagnets

  • Maria Markina
  • , Tatyana Vasilchikova
  • , Elena Kuznetsova
  • , Peter Berdonosov
  • , Andrey Olenev
  • , Seung Hwan Chung
  • , Hyun Joo Koo
  • , Myung Hwan Whangbo
  • , Alexander Vasiliev
  • Lomonosov Moscow State University
  • National University of Science and Technology "MISiS"
  • Sine Theta Ltd.
  • Kyung Hee University
  • North Carolina State University

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

We synthesized the solid solutions Cu3Bi-(Se1−xTexO3)2O2Br (x = 0, 0.25, 0.5, 0.75, 1) for the first time and characterized their structures by X-ray diffraction (XRD) measurements and their magnetic properties by electron spin resonance (ESR), magnetic susceptibility, magnetization, and specific heat measurements as well as by density functional theory (DFT) calculations. The Neél temperature TN and the critical field μ0HC needed for the metamagnetic transition increase with x, while the magnetization at a given magnetic field and the Curie− Weiss temperature Θ decrease with x. We show that the tendency for the interlayer antiferromagnetic (AFM) coupling in francisites is not explained by interlayer spin exchange but by the interlayer high-spin orbital interaction that occur across the van der Waals (vdW) gaps, hence indicating that francisites are vdW ferromagnets. This is surprising because, so far, well-established vdW ferromagnets are either layered tellurides or layered iodides. The trends in TN, μ0HC, and the magnetization of Cu3Bi(Se1−xTexO3)2O2Br as a function of x are well explained by the interlayer AFM interactions, and that in the Θ is explained by the intralayer spin exchanges. We proposed how one might modify francisites to make their interlayer interactions ferromagnetic (FM) hence leading to oxide vdW ferromagnets (Figure Presented).

Original languageEnglish
Pages (from-to)511-520
Number of pages10
JournalChemistry of Materials
Volume35
Issue number2
DOIs
StatePublished - Jan 24 2023
Externally publishedYes

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