A - and B - Site Order in (Na1/2La1/2)(Mg1/3Ta2/3)O3 Perovskites

1998 ◽  
Vol 547 ◽  
Author(s):  
L. Dupont ◽  
L. Chai ◽  
P.K. Davies

AbstractThe “1:2” family of A2+(B2+1/3B+5+2/3)O3 (e.g. B2+ = Mg, Ni, Zn; B5+ = Nb, Ta) mixed metal perovskites typically adopt a 1:2 layered ordered structure when A = Ba and Sr, and a 1:1 ordered doubled perovskite structure for A = Pb. To understand the stability of the cation order in these systems and explore how the different cation correlations affect their dielectric and ferroelectric properties, the response of several members of this family of perovskites to a series of chemical substitutions and thermal treatments have been explored. In this paper we present results for a system where the divalent A cation is replaced by a 1:1 mixture of Na+ and La3+. At all temperatures this substitution stabilizes 1:1 B-site ordering. Below ~ 950°C an additional ordering reaction occurs on the A sub-lattice with Na and La occupying alternate layers along the c axis. The formation of different orientational variants of the A-site ordered phase produces a twinned nano-domain structure which in turn perturbs the length-scale, but not the symmetry, of the order on the B-site lattice. The presence of (Na1/2La1/2) on the A-site is apparently effective in destabilizing the 1:2 layering of the B-site cations observed in alkaline earth systems, possibly through unfavorable local charge imbalances.

2019 ◽  
Author(s):  
Nga Phung ◽  
Hans Köbler ◽  
Diego Di Girolamo ◽  
Thi Tuyen Ngo ◽  
Gabrielle Sousa e Silva ◽  
...  

2007 ◽  
Vol 1034 ◽  
Author(s):  
V. A. Khomchenko ◽  
D. A. Kiselev ◽  
J. M. Vieira ◽  
Li Jian ◽  
A. M. L. Lopes ◽  
...  

AbstractInvestigation of crystal structure, magnetic and local ferroelectric properties of the diamagnetically-doped Bi1−xAxFeO3 (A= Ca, Sr, Pb, Ba; x= 0.2, 0.3) ceramic samples has been carried out. It has been shown that the solid solutions have a rhombohedrally distorted perovskite structure described by the space group R3c. Piezoresponse force microscopy data have revealed the existence of the spontaneous ferroelectric polarization in the samples at room temperature. Magnetization measurements have shown that the magnetic state of these compounds is determined by the ionic radius of the substituting elements. A-site substitution with the biggest ionic radius ions has been found to suppress the spiral spin structure of BiFeO3 and to result in the appearance of weak ferromagnetism. The magnetic properties have been discussed in terms of doping- induced changes in the magnetic anisotropy.


2008 ◽  
Vol 64 (a1) ◽  
pp. C512-C512
Author(s):  
G.J. Thorogood ◽  
B.J. Kennedy ◽  
V.K. Peterson ◽  
M.M. Elcombe ◽  
G.J. Kearley ◽  
...  

2021 ◽  
Vol 74 ◽  
Author(s):  
Susanne G.E.T. Escher ◽  
Helen D. Duncan ◽  
Alexey A. Sokol ◽  
Scott M. Woodley

ABSTRACT A systematic DFT study is performed on (MgO)B, (CaO)n, (SrO)n, and (BaO)n clusters with 6 < n < 50, and which display a cuboid 2X2X2 atomic motif seen in the bulk, rock-salt, configuration. The stability and energy progression of these clusters are used to predict the energies of infinitely long nanorods, or nanowires, slabs, and the bulk global minimum energy. Keywords: Alkaline earth metal oxides, nanoclusters, nanorods, DFT.


1991 ◽  
Vol 10 (1) ◽  
pp. 215-219 ◽  
Author(s):  
E. A. Weiss ◽  
G. M. Gilmartin ◽  
J. R. Nevins

RSC Advances ◽  
2019 ◽  
Vol 9 (68) ◽  
pp. 39932-39944 ◽  
Author(s):  
Ho-Chen Hsieh ◽  
Ping-Wen Tsai ◽  
Yuan-Chia Chang ◽  
Sheng-Feng Weng ◽  
Hwo-Shuenn Sheu ◽  
...  

Alkaline earth metal substitutions on the A-site of pyrochlore oxide MxLa2−xCe1.8Ru0.2O7−δ (M = Mg, Ca) were studied as catalyst materials for oxidative/autothermal steam reforming of ethanol (OSRE/ATR).


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