Transformation of Solid Solution with Spinel-Type Structure Within the Range LiMn2−x(Ni0.33Co0.33Fe0.33)xO4 (0 ≤ x ≤ 2)

2020 ◽  
Vol 41 (6) ◽  
pp. 819-826
Author(s):  
G. D. Nipan ◽  
M. N. Smirnova ◽  
D. Yu Kornilov ◽  
M. A. Kop’eva ◽  
G. E. Nikiforova ◽  
...  
2020 ◽  
Vol 62 (7) ◽  
pp. 608-617
Author(s):  
I. V. Pekov ◽  
I. P. Anikin ◽  
N. V. Chukanov ◽  
D. I. Belakovskiy ◽  
V. O. Yapaskurt ◽  
...  

1998 ◽  
Vol 281 (2) ◽  
pp. 312-317 ◽  
Author(s):  
A. López-Delgado ◽  
J.L. Martı́n de Vidales ◽  
E. Vila ◽  
F.A. López

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Myroslava Horiacha ◽  
Galyna Nychyporuk ◽  
Rainer Pöttgen ◽  
Vasyl Zaremba

Abstract Phase formation in the solid solution TbNiIn1−x Ga x at 873 K was investigated in the full concentration range by means of powder X-ray diffraction and EDX analysis. The samples were synthesized by arc-melting of the pure metals with subsequent annealing at 873 K for one month. The influence of the substitution of indium by gallium on the type of structure and solubility was studied. The solubility ranges have been determined and changes of the unit cell parameters were calculated on the basis of powder X-ray diffraction data: TbNiIn1–0.4Ga0–0.6 (ZrNiAl-type structure, space group P 6 ‾ 2 m $P‾{6}2m$ , a = 0.74461(8)–0.72711(17) and c = 0.37976(5)–0.37469(8) nm); TbNiIn0.2–0Ga0.8–1.0 (TiNiSi-type structure, space group Pnma, а = 0.68950(11)–0.68830(12), b = 0.43053(9)–0.42974(6), с = 0.74186(10)–0.73486(13) nm). The crystal structures of TbNiGa (TiNiSi type, Pnma, a = 0.69140(5), b = 0.43047(7), c = 0.73553(8) nm, wR2=0.0414, 525 F 2 values, 21 variables), TbNiIn0.83(1)Ga0.17(1) (ZrNiAl type, P 6 ‾ 2 m $P‾{6}2m$ , a = 0.74043(6), c = 0.37789(3) nm, wR2 = 0.0293, 322 F 2 values, 16 variables) and TbNiIn0.12(2)Ga0.88(2) (TiNiSi type, Pnma, a = 0.69124(6), b = 0.43134(9), c = 0.74232(11) nm, wR2 = 0.0495, 516 F 2 values, 21 variables) have been determined. The characteristics of the solid solutions and the variations of the unit cell parameters are briefly discussed.


2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Shrikant Bhat ◽  
Abhijeet Lale ◽  
Samuel Bernard ◽  
Wei Zhang ◽  
Ryo Ishikawa ◽  
...  

1992 ◽  
Vol 7 (8) ◽  
pp. 2219-2224 ◽  
Author(s):  
N.E. Pingitore ◽  
B.F. Ponce ◽  
M.P. Eastman ◽  
F. Moreno ◽  
C. Podpora

Optical, electron microprobe, and x-ray diffraction analysis of 88 samples of various compositions between Ag2S and Ag2Se synthesized at high temperature in sealed quartz tubing indicates the presence of two solid-solution series in this system at ambient (room) conditions. One series extends from Ag2S to approximately Ag2S0.4Se0.7 and has the Ag2S-III-type structure (monoclinic). The second series ranges from Ag2S0.3Se0.7 to Ag2Se and is characterized by the Ag2Se-II-type structure (orthorhombic). Members of both series, in appropriate proportions, characterize the apparent compositional gap between the two solid solutions. Gradual shifts in the locations of the x-ray diffraction peaks along the compositional gradient of each solid solution revealed an expansion of the d-spacing as the larger Se ion was substituted for S in the Ag2S-III-type structure and a contraction as S was substituted for Se in the Ag2Se-II-type structure. The reported discrete phase, Ag4SSe (aguilarite, orthorhombic), appears to be simply a member of the monoclinic Ag2S-III-type solid solution.


1984 ◽  
Vol 167 (3-4) ◽  
pp. 235-246 ◽  
Author(s):  
Torsten Lundström ◽  
Lars-Erik Tergenius ◽  
Iwami Higashi

2006 ◽  
Vol 292 (1) ◽  
pp. 129-135 ◽  
Author(s):  
Mikio Masaoka ◽  
Atsushi Kyono ◽  
Tamao Hatta ◽  
Mitsuyoshi Kimata

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