Structural and magnetic properties of the ordered perovskite Pb2CoTeO6

被引:33
|
作者
Ivanov, S. A. [2 ]
Nordblad, P. [3 ]
Mathieu, R. [3 ]
Tellgren, R. [1 ]
Ritter, C. [4 ]
机构
[1] Uppsala Univ, Angstrom Lab, Dept Chem Mat, Uppsala, Sweden
[2] Karpov Inst Phys Chem, Moscow, Russia
[3] Uppsala Univ, Angstrom Lab, Dept Engn Sci, Uppsala, Sweden
[4] Inst Laue Langevin, Grenoble, France
基金
瑞典研究理事会; 俄罗斯基础研究基金会;
关键词
NEUTRON POWDER DIFFRACTION; DIELECTRIC-PROPERTIES; TELLURIUM; FERROELECTRICS; CRYSTAL;
D O I
10.1039/c0dt00558d
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The complex perovskite Pb2CoTeO6 (PCTO) has been prepared as polycrystalline powders by a solid state reaction route, and the crystal structure and magnetic properties have been investigated using a combination of X-ray and neutron powder diffraction, electron microscopy, dielectric, calorimetric and magnetic measurements. It was shown that at room temperature this compound adopts a trigonal perovskite structure, space group R (3) over bar (a = 5.6782(1) angstrom, c = 13.8552(3) angstrom). The compound undergoes a number of temperature-induced phase transitions and adopts four different structures in the temperature range 5 500 K: monoclinic in P2(1)/n (5 < T < 125 K, tilt system (a(+)b(-)b(-))), monoclinic in I2/m (125 < T < 210 K, tilt system (a(0)b(-)b(-))), rhombohedral in R (3) over bar (210 < T < 370 K, tilt system (a(-)a(-)a(-))), and finally cubic in Fm (3) over barm (above 370 K without any tilting). These structural phase transitions are coupled to changes in the dielectric constant and the heat capacity around 210 and 370 K. A long-range antiferromagnetically ordered state has been identified from neutron powder diffraction and magnetic studies at different temperatures. Magnetic diffraction peaks were registered below the transition at about 16 K and a possible model for the magnetic structure is proposed. Possible coexistence of long-range ordering of the electrical dipoles and the magnetic moments at low temperatures making PCTO a potential multiferroic candidate is discussed.
引用
收藏
页码:11136 / 11148
页数:13
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