EPR of lithium-sodium tetragermanate single crystal doped with copper ion

Автор(и)

  • M. P. Trubitsyn Research Institute for Energy Efficient Technologies and Materials Sciences, Oles Honchar Dnipro National University, Dnipro, Ukraine; Institute of Physics of the Czech Academy of Sciences, Prague, Czech Republic https://orcid.org/0000-0001-7993-7733
  • A. O. Diachenko Research Institute for Energy Efficient Technologies and Materials Sciences, Oles Honchar Dnipro National University, Dnipro, Ukraine https://orcid.org/0000-0003-4786-8897
  • O. A. Bibikova Research Institute for Energy Efficient Technologies and Materials Sciences, Oles Honchar Dnipro National University, Dnipro, Ukraine
  • Ye. V. Skrypnik Research Institute for Energy Efficient Technologies and Materials Sciences, Oles Honchar Dnipro National University, Dnipro, Ukraine
  • V. R. Kolbunov Research Institute for Energy Efficient Technologies and Materials Sciences, Oles Honchar Dnipro National University, Dnipro, Ukraine https://orcid.org/0000-0003-0430-1591
  • M. D. Volnianskii Research Institute for Energy Efficient Technologies and Materials Sciences, Oles Honchar Dnipro National University, Dnipro, Ukraine

DOI:

https://doi.org/10.15421/332512

Ключові слова:

lithium-sodium tetragermanate crystal, Cu2+ doping ion, electron paramagnetic resonance

Анотація

For the first time electron paramagnetic resonance (EPR) spectra are studied in lithium-sodium tetragermanate (LiNaGe4O9) single crystal doped with copper impurity. The hyperfine quadruplets of two-valent Cu2+ ions (3d9, S =1/2, I = 3/2) are detected. The angular variations of the EPR spectra are studied in crystal planes at 295 K. The components of g-factor and hyperfine interaction tensor A are calculated. The EPR spectra anisotropy testifies the triclinic symmetry of the Cu2+ ions position in the lattice. The symmetry of the impurity site as well as the ratio of the ionic charges and radii give evidence that Cu2+ centers are substituted for Li+ ions in the LiNaGe4O9 crystal lattice. The charge imbalance of the dopant is presumably compensated by non-stoichiometric lithium ions vacancies.

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Опубліковано

2025-12-26

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