Impact of temperature-dependent local and global spin order in RMnO3 compounds for spin-phonon coupling and electromagnon activity

被引:4
作者
Elsaesser, S. [1 ]
Schiebl, M. [2 ]
Mukhin, A. A. [3 ]
Balbashov, A. M. [4 ]
Pimenov, A. [2 ]
Geurts, J. [1 ]
机构
[1] Univ Wurzburg, Phys Inst EP3, D-97074 Wurzburg, Germany
[2] Vienna Univ Technol, Inst Solid State Phys, A-1040 Vienna, Austria
[3] Russian Acad Sci, Prokhorov Gen Phys Inst, Moscow 119991, Russia
[4] Tech Univ, Moscow Power Engn Inst, Ul Krasnokazarmennaya 14, Moscow 111250, Russia
基金
奥地利科学基金会;
关键词
RMnO3; multiferroics; electromagnon; Raman spectroscopy; spin-phonon coupling; MULTIFERROICS; MANGANITES;
D O I
10.1088/1367-2630/aa55ed
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
The orthorhombic rare-earth manganite compounds RMnO3 show a global magnetic order for T < T-N, and several representatives are multiferroic with a cycloidal spin ground state order for T < T-cycl < T-N approximate to 40 K. We deduce from the temperature dependence of spin-phonon coupling in Raman spectroscopy for a series of RMnO3 compounds that their spin order locally persists up to about twice TN. Along the same line, our observation of the persistence of the electromagnon in GdMnO3 up to T approximate to 100 K is attributed to a local cycloidal spin order for T > T-cycl, in contrast to the hitherto assumed incommensurate sinusoidal phase in the intermediate temperature range. The development of the magnetization pattern can be described in terms of an order-disorder transition at T-cycl within a pseudospin model of localized spin cycloids with opposite chirality.
引用
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页数:7
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