Structural and magnetic properties of RMn2-xFexD6 compounds (R=Y, Er; x ≤ 0.2) synthesized under high deuterium pressure

被引:6
|
作者
Paul-Boncour, V. [1 ,2 ]
Filipek, S. M. [3 ]
Sato, R. [3 ]
Wierzbicki, R. [3 ]
Andre, G. [4 ]
Porcher, F. [4 ]
Reissner, M. [5 ]
Wiesinger, G. [5 ]
机构
[1] CNRS, Inst Chim & Mat Paris Est, CMTR, F-94320 Thiais, France
[2] U PEC, F-94320 Thiais, France
[3] Polish Acad Sci, Inst Phys Chem, PL-01224 Warsaw, Poland
[4] CEA Saclay, Lab Leon Brillouin, CEA CNRS, F-91191 Gif Sur Yvette, France
[5] TU Vienna, Inst Solid State Phys, A-1040 Vienna, Austria
关键词
Laves phase; Deuteride; High pressure; Magnetism; Neutron diffraction; NEUTRON-DIFFRACTION; MOSSBAUER-SPECTROSCOPY; HYDROGEN ABSORPTION; RAY-ABSORPTION; LAVES HYDRIDES; YMN2; RMN2; GD; DY;
D O I
10.1016/j.jssc.2010.12.017
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
RMn2-xFexD6 compounds were obtained by applying a deuterium pressure of several kbar to RMn2-xFex compounds for x <= 0.2 and R=Y, Er. These compounds are isostructural to RMn2D6 compounds and crystallize in a K2PtCl6 type structure with a random substitution of R and half the Mn atoms in the same 8c site whereas the other Mn atoms are located on the 4a site and surrounded by six D atoms (24e site). According to neutron powder diffraction analysis the Fe atoms are preferentially substituted on the 4a site. YMn2-xFexD6 compounds are paramagnetic and their molar susceptibility follows a modified Curie-Weiss law. ErMn2-xFexD6 compounds display a ferromagnetic behavior at 2 K, but their saturation magnetization (M-S similar to 4.0 mu(B)/f.u.) is half that of their parent compounds (M-S similar to 8.0 mu B/f.u.). The neutron diffraction patterns of ErMn1.8Fe0.2D6 display below 13 K both ferromagnetic and antiferromagnetic short range order, which can be related to a disordered distribution of Er moments. The paramagnetic temperatures of ErMn2-xFexD6 compounds are negative and decrease versus the Fe content whereas they are positive and increase for their parent compounds. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:463 / 469
页数:7
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