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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Drokina T. V., Petrakovskii G. A., Molokeev M. S., Misyul S. V., Bondarev V. S., Velikanov D. A., Frontzek M., Schefer J.
Заглавие : Crystal and magnetic structures, phase transitions in quasi-one-dimensional pyroxenes Na0.5Li0.5FeGe2O6
Коллективы : Ministry of Education and Science of the Russian Federation of Siberian Federal University
Место публикации : J. Magn. Magn. Mater.: Elsevier Science, 2015. - Vol. 385. - P.243-249. - ISSN 0304, DOI 10.1016/j.jmmm.2015.03.016. - ISSN 18734766(eISSN)
Примечания : Cited References:25. - Neutron beam time at the cold neutron powder diffractometer DMC at the Swiss spallation neutron source SINQ Paul Scherrer Institut, Switzerland is gratefully acknowledged. MF acknowledges funding from the European Community's Seventh Framework Programme (FP7/2007-2013) under Grant Agreement no. 290605 (PSIFELLOW/COFUND). This work was also supported by Ministry of Education and Science of the Russian Federation of Siberian Federal University 2014 year (Assignment no. 3.2534.2014/K).
Предметные рубрики: CLINOPYROXENE-TYPE LIFEGE2O6
NAFESI2O6
LIFESI2O6
Ключевые слова (''Своб.индексиров.''): phase transition--magnetic structure--pyroxene--magnetic properties--calorimetric measurements
Аннотация: The possibility of cation substitution in pyroxenes allows the investigation the gradual change of structural and magnetic properties under doping in these compounds. Here, Na0.5Li0.5FeGe2O6 was prepared by the standard solid-phase reaction method and has been investigated using X-ray and neutron powder diffraction, and further characterized by magnetic and calorimetric measurements. The crystal structure of Na0.5Li0.5FeGe2O6 at 300 K is monoclinic C2/c (a=10.0333(1), b=8.8136(1), c=5.5295(9) Å, β=108.921(1)°). Calorimetric investigations indicate a displacive first order phase transition at T=271±1 K which is accompanied by the appearance of superstructure reflections in the X-ray patterns. At this transition Na0.5Li0.5FeGe2O6 undergoes a space group change from C2/c to P21/c (a=9.9692(3), b=8.8545(3), c=5.4752(2) Å, β=108.494(1)°). Magnetic order has been found below the Néel temperature TN≈18 K and has been refined from neutron diffraction. The quasi-low-dimensional magnetic spin system Na0.5Li0.5FeGe2O6 exhibits a collinear antiferromagnetic structure with the space group Pa21/c and the doubling of the unit cell along the crystallographic a-axis of the pyroxene crystal (propagation vector k=(1/2, 0, 0)). The critical modes which are responsible for the phase transition from C2/c to P21/c symmetry and for the magnetic transition from paramagnetic to antiferromagnetic state have been determined and their role in the transition is described. They are also the relevant mechanism driving the magnetic order in LiFeGe2O6.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Drokina T. V., Petrakovskii G. A., Molokeev M. S., Bondarev V. S., Velikanov D. A.
Заглавие : Synthesis and study of structural, thermodynamic, and magnetic properties of NaxLi1–xFeGe2O6 (x = 0.1–0.9) compounds
Место публикации : Phys. Solid State: MAIK Nauka-Interperiodica / Springer, 2016. - Vol. 58, Is. 7. - P.1361-1370. - ISSN 10637834 (ISSN), DOI 10.1134/S1063783416070143
Примечания : Cited References: 20
Предметные рубрики: CLINOPYROXENE-TYPE LiFeGe2O6
PHASE-TRANSITION
PYROXENES
TEMPERATURE
LiFeSi2O6
CRYSTAL
Аннотация: The properties of NaxLi1–xFeGe2O6 (x = 0.1–0.9) solid solutions obtained via a solid-phase synthesis have been measured by X-ray diffraction, calorimetry, and magnetic method. The order–disorder transformations in low-dimensional NaxLi1–xFeGe2O6 (x = 0.1–0.9) spin systems with predominately antiferromagnetic exchange interaction have been revealed in the low-temperature susceptibility dependences. The study of thermal and physical properties has confirmed that substituting the sodium ions with the lithium ones induces the first-order structural phase transitions of the displacement type which are characterized by a symmetry change in monoclinic crystals from high-temperature C2/c space group to low-temperature P21/c space group. © 2016, Pleiades Publishing, Ltd.
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