首页 | 本学科首页   官方微博 | 高级检索  
     


Electron paramagnetic resonance study of Fe3+ ions at octahedral and tetrahedral mirror symmetry sites in the LiScGeO4 crystal
Authors:A.?A.?Galeev  author-information"  >  author-information__contact u-icon-before"  >  mailto:akhmet.galeev@ksu.ru"   title="  akhmet.galeev@ksu.ru"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author,N.?M.?Khasanova,C.?Rudowicz,G.?S.?Shakurov,G.?R.?Bulka,N.?M.?Nizamutdinov,V.?M.?Vinokurov
Affiliation:(1) School of Physics and Engineering, Zhengzhou University, Zhengzhou, 450052, People’s Republic of China;
Abstract:An electron paramagnetic resonance (EPR) study of a synthetic single crystal of LiScGeO4 doped with Cr ions carried out earlier at the X- and Q-bands at 300, K has indicated additional weak lines. A detailed analysis of these EPR lines, which were tentatively attributed to the Fe3+ ions at two different mirror symmetry sites, is presented in this paper. The angular dependences in the three crystallographic planes were resolved by fitting the two distinct spectra denoted Fe3+(I) and Fe3+(II) with a spin Hamiltonian (S=5/2) of monoclinic symmetry. The rank-4 crystal field tensors at tetrahedral and octahedral sites were calculated with the point-charge model to determine the principal axis orientations of their cubic, tetragonal and trigonal components. A comparative analysis of the zero-field splitting tensors and the crystal field ones indicates that Fe3+(I) ions substitute for Sc3+ at octahedral sites and Fe3+(II) ions substitute for Ge4+ at tetrahedral sites with no significant distorition of the coordination polyhedra in the structure of LiScGeO4.
Keywords:
本文献已被 SpringerLink 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号