ChemInform Abstract: Ion Conducting Behavior in (Lu1-xMx)2(WO4)3 Solid Solutions (M: Sm, Ho, Er) with the Sc2(WO4)3 Type Structure.

ChemInform ◽  
2010 ◽  
Vol 33 (15) ◽  
pp. no-no
Author(s):  
Nobuhito Imanaka ◽  
Joachim Koehler ◽  
Shinji Tamura ◽  
Gin-ya Adachi
Keyword(s):  
Solid Solutions ◽  
Type Structure ◽  
Ion Conducting

New trivalent ion conducting solid electrolyte with the NASICON type structure

2004 ◽  
Vol 379 (1-2) ◽  
pp. 262-265 ◽  
Author(s):  
Y. Hasegawa ◽  
S. Tamura ◽  
N. Imanaka ◽  
G. Adachi
Keyword(s):  
Solid Electrolyte ◽  
Type Structure ◽  
Nasicon Type ◽  
Ion Conducting

Solid solutions in the system Ag2S–Ag2Se

1992 ◽  
Vol 7 (8) ◽  
pp. 2219-2224 ◽  
Author(s):  
N.E. Pingitore ◽  
B.F. Ponce ◽  
M.P. Eastman ◽  
F. Moreno ◽  
C. Podpora
Keyword(s):  
Solid Solution ◽  
Solid Solutions ◽  
Type Structure ◽  
Solid Solution Series ◽  
X Ray Diffraction ◽  
Compositional Gradient ◽  
X Ray ◽  
Optical Electron ◽  
Discrete Phase ◽  
Diffraction Peaks

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.

Fast Solid-State Li Ion Conducting Garnet-Type Structure Metal Oxides for Energy Storage

2015 ◽  
Vol 6 (2) ◽  
pp. 292-299 ◽  
Author(s):  
Venkataraman Thangadurai ◽  
Dana Pinzaru ◽  
Sumaletha Narayanan ◽  
Ashok Kumar Baral
Keyword(s):  
Energy Storage ◽  
Solid State ◽  
Metal Oxides ◽  
Type Structure ◽  
Li Ion ◽  
Ion Conducting

Water-stable lithium ion conducting solid electrolyte of the Li1.4Al0.4Ti1.6−xGex(PO4)3 system (x=0–1.0) with NASICON-type structure

2013 ◽  
Vol 253 ◽  
pp. 175-180 ◽  
Author(s):  
Peng Zhang ◽  
Masaki Matsui ◽  
Atsushi Hirano ◽  
Yasuo Takeda ◽  
Osamu Yamamoto ◽  
...  
Keyword(s):  
Solid Electrolyte ◽  
Lithium Ion ◽  
Type Structure ◽  
Nasicon Type ◽  
Ion Conducting

Flexible Fast Lithium Ion Conducting Ceramic Electrolyte

2013 ◽  
Vol 1496 ◽  
Author(s):  
Koichi Hamamoto ◽  
Danila Matveev ◽  
Toshiaki Yamaguchi ◽  
Hirofumi Sumi ◽  
Toshio Suzuki ◽  
...  
Keyword(s):  
Crystalline Phase ◽  
Room Temperature ◽  
Lithium Ion ◽  
Sheet Forming ◽  
Type Structure ◽  
Bending Stress ◽  
Large Area ◽  
Casting Method ◽  
Ceramic Electrolyte ◽  
Ion Conducting

ABSTRACTLarge-area fast lithium ion conducting ceramic thin freestanding sheets was successfully prepared using a sheet forming technique. This ceramic sheet contains the crystalline phase of Li1+x+yAlxTi2-xSiyP3-yO12 with the NASICON type structure. The ceramic sheet showed maximum overall conductivity over 10−3 S cm−1 at room temperature. And, the developed thin ceramic sheet has sufficient flexibility against bending stress. Because a thin large-area ceramic electrolyte sheet was prepared using less energy compared with a conventional glass casting method, it is suitable for practical use.

The ion conducting properties of perovskite solid solutions (La1/2Li1/3+X)TiO3

2005 ◽  
Vol 2 (1) ◽  
pp. 192-195 ◽  
Author(s):  
E. A. Fortalnova ◽  
A. V. Mosunov ◽  
M. G. Safronenko ◽  
N. U. Venskovskii ◽  
and E. D. Politova
Keyword(s):  
Solid Solutions ◽  
Ion Conducting
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