scholarly journals A class of rare antiferromagnetic metallic oxides: double perovskite AMn3V4O12 (A = Na+, Ca2+, and La3+) and the site-selective doping effect

2015 ◽  
Vol 17 (19) ◽  
pp. 12717-12721 ◽  
Author(s):  
Guangbiao Zhang ◽  
Yuanxu Wang ◽  
Zhenxiang Cheng ◽  
Yuli Yan ◽  
Chengxiao Peng ◽  
...  

A-site-ordered double perovskite oxides will work as an ideal platform for designing novel antiferromagnetic metallic oxides.

2020 ◽  
Vol 132 (11) ◽  
pp. 4478-4485 ◽  
Author(s):  
Wenli Zhang ◽  
Zhen Cao ◽  
Wenxi Wang ◽  
Eman Alhajji ◽  
Abdul‐Hamid Emwas ◽  
...  

2020 ◽  
Vol 270 ◽  
pp. 118868 ◽  
Author(s):  
Shengli Pang ◽  
Jie Xu ◽  
Yanjing Su ◽  
Gongmei Yang ◽  
Meng Zhu ◽  
...  

2020 ◽  
Vol 4 (5) ◽  
pp. 1519-1529 ◽  
Author(s):  
Hayato Togano ◽  
Kaisei Asai ◽  
Seiji Oda ◽  
Hidekazu Ikeno ◽  
Shogo Kawaguchi ◽  
...  

Oxygen-deficient double perovskite oxides PrBaCo2O6−δ exhibit highly active hydrogen evolution reaction catalysis, which is associated with multiple factors: oxygen deficiency, high Co valence, and A-site cation ordering.


2020 ◽  
Vol 59 (11) ◽  
pp. 4448-4455 ◽  
Author(s):  
Wenli Zhang ◽  
Zhen Cao ◽  
Wenxi Wang ◽  
Eman Alhajji ◽  
Abdul‐Hamid Emwas ◽  
...  

2012 ◽  
Vol 135 (16) ◽  
pp. 6056-6060 ◽  
Author(s):  
Shoubao Zhang ◽  
Takashi Saito ◽  
Masaichiro Mizumaki ◽  
Wei-tin Chen ◽  
Takenori Tohyama ◽  
...  

RSC Advances ◽  
2020 ◽  
Vol 10 (4) ◽  
pp. 1883-1889
Author(s):  
He Huang ◽  
Pengfei Jiang ◽  
Wenliang Gao ◽  
Rihong Cong ◽  
Tao Yang

Sr2+-to-Ca2+ substitution resulted in new 1:1:1 triple-cation B-site ordered perovskites, where the structure difference lies in the orientations of GaO4-tetrahedra.


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.


1996 ◽  
Vol 451 ◽  
Author(s):  
D. Lincot ◽  
M. J. Furlong ◽  
M. Froment ◽  
R. Cortes ◽  
M. C. Bernard

ABSTRACTChalcogenide semiconductors have been deposited epitaxially from aqueous solutions either chemically or electrochemically at growth rates of up to 0.7 μmhr−1. After recalling the basic principles of these deposition processes, results are presented concerning chemically deposited CdS on InP, GaP and CuInSe2 substrates, electrodeposited CdTe on InP, and CdSAnP heterostructures. Characterisation of these structures by RHEED, TEM, HRTEM, and glazing angle X ray diffraction allows to analyse the effects of substrate orientation, polarity, lattice match plus the influence of temperature on epitaxial growth. These results are discussed in terms of self organisation and a site selective growth mechanisms due to the free enegy of formation of each compound.


2021 ◽  
Vol 33 (5) ◽  
pp. 1594-1606
Author(s):  
Monirul Shaikh ◽  
Aafreen Fathima ◽  
M. J. Swamynadhan ◽  
Hena Das ◽  
Saurabh Ghosh

Sign in / Sign up

Export Citation Format

Share Document