1992
DOI: 10.1103/physrevb.46.11636
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Theory of Faraday rotation and susceptibility of rare-earth trifluorides

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Cited by 31 publications
(21 citation statements)
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“…Cerium Fluoride is superionic [16], the fluorine ions having high mobility, which could account for part of its observed radiation hardness. It is also paramagnetic, a characteristics which influences the Faraday rotation in a magnetic field [17]. Fluorine ions labelled F 1 in literature [18] account for most of the Cerium Fluoride conductivity and hence their mobility might help repair defects.…”
Section: Cerium Fluoridementioning
confidence: 99%
“…Cerium Fluoride is superionic [16], the fluorine ions having high mobility, which could account for part of its observed radiation hardness. It is also paramagnetic, a characteristics which influences the Faraday rotation in a magnetic field [17]. Fluorine ions labelled F 1 in literature [18] account for most of the Cerium Fluoride conductivity and hence their mobility might help repair defects.…”
Section: Cerium Fluoridementioning
confidence: 99%
“…[6] have reported theoretical investigations on the magnetic properties and magneto-optical properties of CeF 3 using experimental data on temperature behavior of the magnetic dc-susceptibility and Faraday rotation measured in CeF 3 single crystal [7]. Mixed-valent behavior of Ce-ion in CeF 3 has been suggested [6] to agree with results of the theoretical calculations and the experimental data. An Important role of the super-exchange magnetic field (caused by super-exchange interaction between Ce 3+ ions) in the splitting of the Ce 3+ crystal field levels has been considered in the Ref.…”
Section: Introductionmentioning
confidence: 54%
“…Xu and M. Duan in Ref. [6] described the inverse susceptibility in CeF 3 (experimental data from Ref. [7]) rather well in the temperature range T > 50 K taking the mixed-valent behavior of the Ce 3+ ions into account using a very simple model of the crystal field.…”
Section: Discussionmentioning
confidence: 99%
“…We have shown theoretically that the intra-ionic 4f n → 4f n−1 5d electric dipole transition is the main origin of the giant MO enhancement of rare earth ions in some compounds [14][15][16]. Since the energy difference between the 3d n and 3d n−1 4p configurations in the 3d ions is much larger than that between the 4f n and 4f n−1 5d configurations in the rare earth ions, for 3d ions, the factor ω 2 /(ω 2 ng − ω 2 ) (see Eq.…”
Section: Introductionmentioning
confidence: 99%