Structural Transition and Atomic Ordering in the Non-Stoichiometric Double Perovskite Sr2FexMo2-xO6.

ChemInform ◽  
2003 ◽  
Vol 34 (24) ◽  
Author(s):  
G. Y. Liu ◽  
G. H. Rao ◽  
X. M. Feng ◽  
H. F. Yang ◽  
Z. W. Ouyang ◽  
...  
2003 ◽  
Vol 353 (1-2) ◽  
pp. 42-47 ◽  
Author(s):  
G.Y. Liu ◽  
G.H. Rao ◽  
X.M. Feng ◽  
H.F. Yang ◽  
Z.W. Ouyang ◽  
...  

2012 ◽  
Vol 1454 ◽  
pp. 3-13
Author(s):  
Akira Ohtomo ◽  
Suvankar Chakraverty ◽  
Hisanori Mashiko ◽  
Takayoshi Oshima ◽  
Masashi Kawasaki

ABSTRACTWe report on the atomic ordering of B-site transition-metals and magnetic properties in double-perovskite oxides, La2CrFeO6 (LCFO) and La2VMnO6 (LVMO), which have never been reported to exist in ordered forms. These double-perovskite oxides are particularly interesting because of possible ferromagnetism (expected from the Kanamori-Goodenough rule for LCFO) and half-metallic antiferromagnetism (predicted for LVMO). Using pulsed-laser deposition technique with single solid-solution targets, we have prepared epitaxial films in ordered forms. Despite similar ionic characters of constituent transition-metals in each compound, the maximum B-site order attained was surprisingly high, ∼90% for LCFO and ∼80% for LVMO, suggesting a significant role of epitaxial stabilization in the spontaneous ordering process. Magnetization and valence state characterizations revealed that the magnetic ground state of both compounds was coincidently ferrimagnetic with saturation magnetization of ∼2μBper formula unit, unlike those predicted theoretically. In addition, they were found to be insulating with optical band-gaps of 1.6 eV and 0.9 eV for LCFO and LVMO, respectively. Our results present a wide opportunity to explore novel magnetic properties of binary transition-metal perovskites upon epitaxial stabilization of the ordered phase.


Author(s):  
Caroline Andreazza-Vignolle ◽  
Pascal Andreazza ◽  
Jérome Pirart ◽  
Asseline Lemoine

2022 ◽  
Vol 892 ◽  
pp. 162034
Author(s):  
Evgenii V. Sterkhov ◽  
Nikolay M. Chtchelkatchev ◽  
Elena V. Mostovshchikova ◽  
Roman E. Ryltsev ◽  
Sergey A. Uporov ◽  
...  

Nanoscale ◽  
2019 ◽  
Vol 11 (36) ◽  
pp. 17004-17009 ◽  
Author(s):  
Ruijing Fu ◽  
Yaping Chen ◽  
Xue Yong ◽  
Zhiwei Ma ◽  
Lingrui Wang ◽  
...  

The pressure-induced bandgap evolution of double perovskite Cs2AgBiBr6 nanocrystals is highly related to the orbital interactions, associated with the tilting and distortion of [AgBr6]5− and [BiBr6]3− octahedra under pressure.


2003 ◽  
Vol 15 (12) ◽  
pp. 2053-2060 ◽  
Author(s):  
G Y Liu ◽  
G H Rao ◽  
X M Feng ◽  
H F Yang ◽  
Z W Ouyang ◽  
...  

2010 ◽  
Vol 663-665 ◽  
pp. 1036-1040
Author(s):  
Zhen Feng Xu ◽  
Jun Liang ◽  
Juan Pei ◽  
Yan Yan Yin ◽  
Chang Li

Ordered double perovskite oxides (Sr2-3xLa2xBax)FeMoO6 (0≤x≤0.3) have been investigated in this work. X-ray powder diffraction reveals that the crystal structure of the compounds changes from a tetragonal I4/m lattice to a cubic Fm 3m lattice around x=0.2. Though the nominal average size of the A site cation of (Sr2-3xLa2xBax)FeMoO6 is designed to be almost independent of x, the refinements of the crystal structure show that the lattice constants increase with x in both the tetragonal and the cubic phase regions due to electron doping. As the x increases, the degree of cationic ordering on the B site is decreased pronouncedly, while the Curie temperature of the compounds is nearly unchanged.


Author(s):  
Jianfa Zhao ◽  
Xiao Wang ◽  
Xi Shen ◽  
Christoph J. Sahle ◽  
Cheng Dong ◽  
...  

2018 ◽  
Author(s):  
Julian Steele ◽  
Masoumeh Keshavarz ◽  
Elke Debroye ◽  
Haifeng Yuan ◽  
Johan Hofkens ◽  
...  

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