Magneto-optical activity of f-f transitions in ErFe3(BO3)4 and ErAl3(BO3)4 single crystals

被引:13
作者
Malakhovskii, A. V. [1 ]
Sukhachev, A. L. [1 ]
Sokolov, V. V. [2 ]
Kutsak, T. V. [2 ]
Bondarev, V. S. [1 ,2 ]
Gudim, I. A. [1 ]
机构
[1] Russian Acad Sci, LV Kirensky Phys Inst, Siberian Branch, Krasnoyarsk 660036, Russia
[2] Siberian Fed Univ, Krasnoyarsk 660041, Russia
关键词
Magnetic circular dichroism; Natural circular dichroism; Rare earth ferroborates; Rare earth alumoborates; Electronic structure; CIRCULAR-DICHROISM SPECTRA; GREEN UP-CONVERSION; SPECTROSCOPIC PROPERTIES; ER3+; ABSORPTION; GROWTH; LASER; PR3+; HO3+; YB;
D O I
10.1016/j.jmmm.2015.02.051
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Absorption, magnetic circular dichroism and natural circular dichroism spectra of ErEe(3)(BO3)(4) and ErA(l)3(BO3)(4) single crystals were measured as a function of temperature in the range of 90-293 K. It was found out that magneto-optical activity of the same f-f transitions in the studied crystals substantially differed and their temperature dependences did not follow the Curie-Weiss law in contrast to the properties of allowed transitions. The observed phenomena were accounted for by the nature of f-f transitions allowance. Properties of the transition I-4(15/2) -> S-4(3/2) were studied in detail. In particular, the Zeeman splitting and the natural optical activity of the absorption lines composed of the transition were determined. The vibronic line with the very large natural optical activity was revealed and identified. Two nonequivalent Er3+ ion positions with the opposite chirality were found out in one of the excited states. Polarization properties of the I-4(15/2) -> S-4(3/2) transition in the ErFe3(BO3)(4) crystal have shown that the local symmetry of Er3+ ion in this crystal in the range of 90-293 K is lower than the D-3 one. From the heat capacity measurements it was revealed, that the first order structural phase transition to lower symmetry occurred in ErFe3(BO3)(4) at 433-439 K. (C)15 Elsevier By. All rights reserved.
引用
收藏
页码:255 / 265
页数:11
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