Spectroscopic evidence of spinel phase clustering in solid solutions Hg1-x CrxSe (0.03 ≤ x ≤ 0.1)

被引:12
作者
Lamonova, K. [1 ]
Ivanchenko, I. [2 ]
Orel, S. [1 ]
Paranchich, S. [3 ]
Tkach, V. [4 ]
Zhitlukhina, E. [1 ]
Popenko, N. [2 ]
Pashkevich, Yu [1 ]
机构
[1] NASU, AA Galkin Donetsk Inst Phys & Engn, UA-83114 Donetsk, Ukraine
[2] NASU, Usikov Inst Radiophys & Elect, UA-61085 Kharkov, Ukraine
[3] Chernivtsi Natl Univ, UA-58012 Chernovtsy, Ukraine
[4] NASU, VN Bakul Inst Superhard Mat, UA-04074 Kiev, Ukraine
关键词
ORBIT-COUPLING CONSTANTS; MAGNETIC SEMICONDUCTORS; EXCHANGE INTERACTIONS; IONS; EPR;
D O I
10.1088/0953-8984/21/4/045603
中图分类号
O469 [凝聚态物理学];
学科分类号
070205 ;
摘要
The diluted magnetic semiconductors Hg1-xCrxSe (0.03 <= x <= 0.1) were prepared by the solid state recrystallization method. The structure microanalysis of the Hg1-xCrxSe compounds, performed by using a scanning electron spectrometer, has shown that the HgCr2Se4 spinel-like inclusions are present in the host matrix Hg1-xCrxSe and their amount increases when the chromium content grows. ESR studies of Hg1-xCrxSe samples were carried out in the temperature range 4.2-300 K. ESR spectra of the samples with different chromium contents demonstrate the same g-factors at room temperature and similar fine structure development with the temperature decrease. Numerical studies of g-factors, performed by the modified crystal field approach (MCFA), allowed us to reveal that Cr2+/Cr3+ ions in the tetrahedral environment of the solid solution Hg1-xCrxSe cannot lead to the ESR signal. The experimental g-factor is well reproduced by a numerical g-factor for Cr3+ ions located in the octahedral environment, being specific for the HgCr2Se4 spinel phase. The onset of the ESR fine structure is determined by the trigonal distortions of the (CrSe6)(9-) octahedral cell. From our study it has been found that the spinel clusters are present in the Hg1-xCrxSe solid solution even at low chromium content.
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页数:9
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