错误:搜索内容不能为空,请输入英文关键词
错误:关键词超出字数限制,请精简
高级检索

EPR and superposition-model analysis of zero-field splitting parameters for Mn2+ doped in ZnNbOF5.6(H2O) and CoNbOF5.6(H2O) single crystals

  • Shish Pal Rathee,
  • S. S. Hooda

摘要

The electron paramagnetic resonance (EPR) and crystallographic data have been previously documented in literature for Mn2 + doped zinc pentafluorooxodiobate (V) hexahydrate ZnNbOF5.6H20 (CPH) and cobalt pentafluorooxonibotae (V) hexahydrate CoNbO5.6H2O single crystal. In this study, a theoretical investigation of these crystals has been conducted using the superposition model (SPM). The superposition model (SPM) distinguish the geometrical and physical properties that are essential in crystal field parameters. By employing a simple linear least square fit of parameters to intrinsic parameters, the zero field splitting parameters (ZFS) of Mn2+ in ZPH and CPH can be determined from crystal structure din the lattice. This observation suggests that Mn2 + effectively replace Zn2+ and Co2+. The SPM analysis, relying on the assumption of n no. of identical structure around host and guest ions, consider only the immediately coordinated ions. Close agreement between theoretical values of \({b}_{0}^{2}\) b 0 2 is achieved by adopting a reference distance of R0 = 0.22 nm. The exponent power law t2 = 7 ± 1 and t4 = 10 ± 1 are determined for Mn2+ surrounded by oxygen. The fine structure constants are indicative of the specific arrangement of ligands nearby all the impurity ions, with zero-field splitting parameters \({b}_{2}^{0}\) b 2 0 , \({b}_{2}^{2}\) b 2 2 , \({b}_{4}^{ 0}\) b 4 0 , \({b}_{4}^{2}\) b 4 2 and \({b}_{4}^{4}\) b 4 4 showing sensitivity in the case where Mn2+ ions are coordinated by oxygen in single crystals. The results obtained from the superposition model align well with the experimental findings, especially when accounting for local distortion around the Mn2+ ion at substitutional site in the host crystal. This paper aims to investigate the local distortion caused by substituting Mn2+ in the host crystal, exploring its potential impact on its magnetic properties.