Spin State of Cobalt Ions and the Magnetic Properties of Heavily Ba-Substituted Cobaltites with Perovskite Structure

2018 ◽  
Vol 255 (10) ◽  
pp. 1800315
Author(s):  
Igor Troyanchuk ◽  
Maxim Bushinsky ◽  
Nina Tereshko ◽  
Clemens Ritter ◽  
Vadim Sikolenko ◽  
...  
1997 ◽  
Vol 230-232 ◽  
pp. 756-758 ◽  
Author(s):  
Masayuki Itoh ◽  
Masami Mori ◽  
Masaru Sugahara ◽  
Touru Yamauchi ◽  
Yutaka Ueda

2013 ◽  
Vol 39 (5) ◽  
pp. 589-596 ◽  
Author(s):  
A. A. Zatsiupa ◽  
L. A. Bashkirov ◽  
G. S. Petrov ◽  
L. S. Lobanovskii ◽  
S. V. Trukhanov

2020 ◽  
Vol 10 (24) ◽  
pp. 8786
Author(s):  
Paweł Głuchowski ◽  
Ruslan Nikonkov ◽  
Robert Tomala ◽  
Wiesław Stręk ◽  
Tatsiana Shulha ◽  
...  

The aim of the work was to check how the introduction of alkali and cobalt ions into a manganese structure can affect the structural disorder and, in consequence, lead to the changes (improvements) of magnetic properties. The high-pressure sintering technique was applied to check if the external factor can modify the magnetization of manganites. Nanocrystalline La0.9A0.1Mn0.9Co0.1O3 (where A is Li, K, Na) powders were synthesized by the combustion technique. The respective powders were used for nanoceramics preparation by the high-pressure sintering technique. The structure and morphology of the compounds were studied by X-ray powder diffraction, scanning electron microscopy and energy-dispersive X-ray spectroscopy. Magnetization studies for all compounds were performed in order to check the changes induced by either codoping or the sintering pressure. It was found that the type of the dopant ion and sintering pressure produced significant changes to the magnetic properties of the studied compounds. Alkali ions lead to the stabilization of Co ions in the +2 oxidation state and the formation of positive exchange interactions Mn3+–Mn4+ and Co2+–Mn4+ and the subsequent increase in remanent magnetization. High sintering pressure leads to a decrease in grain size and reduction of long-range ferromagnetic order and lower magnetization.


2015 ◽  
Vol 17 (39) ◽  
pp. 26302-26306 ◽  
Author(s):  
Kun Tao ◽  
Qing Guo ◽  
Puru Jena ◽  
Desheng Xue ◽  
Valeri S. Stepanyuk

The possibility of using exchange interactions to manipulate the spin state of an antiferromagnetic nanostructure is explored using ab initio calculations.


1989 ◽  
Vol 12 (1) ◽  
pp. 53-56
Author(s):  
Om Parkash ◽  
N Chaturvedi ◽  
M Tiwari ◽  
Devendra Kumar
Keyword(s):  

2021 ◽  
Vol 8 (1) ◽  
pp. 20218108
Author(s):  
A. V. Bryuzgina ◽  
A. S. Urusova ◽  
I. L. Ivanov ◽  
V. A. Cherepanov

YFe1-xСоxO3 solid solutions were prepared by glycerol-nitrate technique. The homogeneity range of solid solutions was studied within the temperature range 1173 – 1573 K. A continues series of solid solution below the decomposition temperature of YСоO3, which was shown to be equal to 1266 ± 6 K, begins to narrow at higher temperatures and becomes equal to 0 ≤ x ≤ 0.1 at 1573 K. The phase diagram of the YFeO3 – YСoO3 system in the “T – composition” coordinates was divided into three fields. Similar to the parent ternary oxides, all single-phase YFe1-xСоxO3 solid solutions possess orthorhombically distorted perovskite structure (Pnma space group). Unusual behavior of orthorhombic distortions in YFe1-xСоxO3 with temperature was explained by probable changes in spin state of Co3+ ions.


Materials ◽  
2020 ◽  
Vol 13 (10) ◽  
pp. 2301
Author(s):  
Akihiro Tsuruta ◽  
Shuji Kawasaki ◽  
Masashi Mikami ◽  
Yoshiaki Kinemuchi ◽  
Yoshitake Masuda ◽  
...  

We investigated the Co substitution effect for the magnetic properties in room-temperature ferromagnetic oxide Sr3.1Y0.9Co4O10.5. The substituted element (Al and Ga) and low-spin state Co3+, which was changed from a high-spin or intermediate-spin state by Al or Ga substitution, reduced the Curie temperature to even 1.5 times lower than the temperature estimated from a simple dilution effect. Al3+ preferentially substituted for intermediate-spin-state Co3+ in the ferrimagnetic CoO6 layer and deteriorated the saturation magnetization of Sr3.1Y0.9Co4O10.5. By contrast, Ga3+ substituted for high-spin-state Co3+ in the CoO6 layer and/or the antiferromagnetic CoO4.25 layer and enhanced the saturation magnetization per Co ion. These results indicate that the magnetic properties of Sr3.1Y0.9Co4O10.5 can be controlled by selectively substituting for Co3+ with different spin states.


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