Electronic and magnetic properties of boron substituted CuFeO2 delafossite oxide


Ezircan A., Aslan M. S., Miyazaki H., Akyol M., Ozkendir O. M., EKİCİBİL A., ...More

Philosophical Magazine, 2024 (SCI-Expanded) identifier

  • Publication Type: Article / Article
  • Publication Date: 2024
  • Doi Number: 10.1080/14786435.2024.2337197
  • Journal Name: Philosophical Magazine
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, PASCAL, Aerospace Database, Chemical Abstracts Core, Communication Abstracts, Compendex, INSPEC, Metadex, Civil Engineering Abstracts
  • Keywords: absorption spectroscopy, electronic structure, Magnetic materials, oxides
  • Çukurova University Affiliated: Yes

Abstract

Synchrotron x-ray diffraction (SR-XRD) and X-ray absorption fine structure spectroscopy (XAFS) were used to investigate the crystal and electronic properties of boron-substituted CuFeO2 material at room temperature. Without boron substitution, the polycrystalline structures of the trigonal (rhombohedral) ‘ (Formula presented.) ’ CuFeO2 (87.7%) and hexagonal ‘P63/mmc’ (12.3%), which were also present in each sample but in different proportions, were utilised to identify the base material. XRD patterns revealed that, beyond 10% boron substitution, the metal–oxygen bonds (Fe-O and Cu-O) weakened, resulting in the formation of new tetragonal ‘I41/amd’ CuFe2O4 crystals. Although the CuFeO2 structure was preserved, it is conceivable that the presence of other crystal structures could lead to the formation of new features. This state arose as a result of CuFe2O4 crystallization and the impact of boron activity on the surrounding oxygen structures. By measuring magnetisation at both swept temperatures (10–300 K) and applied magnetic fields (±30 kOe), the magnetic properties of the samples were investigated. In the 10–300 K temperature range, the polycrystalline samples exhibit a ferromagnetic property without a magnetic phase transition. This suggests that replacing B with Fe in CuFe1−xBxO2 does not influence the primary magnetic property of CuFeO2. The samples’ saturation magnetisation (Ms) values gradually fall as the B substitution content increases with Fe. This is because there's a chance that the non-transition metal B in CuFe1−xBxO2 will boost antiferromagnetic superexchange Cu-O interactions while lowering the p-d exchange interaction.