Conductivity and dielectric constant of the polymeric solid electrolyte, (PEO)8NH4SO3CF3, in the 100 Hz to 1010 Hz range

1985 ◽  
Vol 17 (2) ◽  
pp. 101-106 ◽  
Author(s):  
S ANSARI ◽  
M BRODWIN ◽  
M STAINER ◽  
S DRUGER ◽  
M RATNER ◽  
...  
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Qilei Liu ◽  
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Xinyang Wang ◽  
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pp. 1771-1775 ◽  
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Eishun Tsuchida ◽  
Hiroyuki Ohno ◽  
Norihisa Kobayashi ◽  
Hajime Ishizaka

1995 ◽  
Vol 196 (6) ◽  
pp. 1813-1820 ◽  
Author(s):  
Miharu Seki ◽  
Kojiro Sato ◽  
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Takayuki Kobayashi ◽  
Ryutoku Yosomiya

2001 ◽  
Vol 4 (11) ◽  
pp. A177 ◽  
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Masayuki Morita ◽  
Nobuko Yoshimoto ◽  
Shin Yakushiji ◽  
Masashi Ishikawa

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2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Hirotada Gamo ◽  
Atsushi Nagai ◽  
Atsunori Matsuda

AbstractSynthesis technology for sulfide-based solid electrolytes based on liquid-phase processing has attracted significant interest in relation to achieving the optimal design for all-solid-state batteries. Herein, guidelines to solvent selection for the liquid-phase synthesis of superionic conductor Li7P3S11 are described through systematic examination. 70Li2S–30P2S5 system, a source of Li7P3S11, is treated via a wet chemical reaction using eight organic solvents with different physical and chemical properties (i.e., dielectric constant, molecule structure, and boiling point). We reveal that the solvent’s polarity, characterized by the dielectric constant, plays an important role in the formation of crystalline Li7P3S11 via wet chemical reaction. In addition, acetonitrile (ACN) solvent with a high dielectric constant was found to lead to high-purity crystalline Li7P3S11 and intrinsically high ionic conductivity. Further, solvents with a high boiling point and ring structures that cause steric hindrance were found to be unfavorable for the wet chemical synthesis of Li7P3S11 solid electrolyte. Overall, we demonstrate that ACN solvent is the most suitable for the liquid-phase synthesis of a crystalline Li7P3S11 solid electrolyte with high purity based on its dielectric constant, molecular structure, and boiling point.


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