Sol-gel synthesis and electrical properties of ceria-based solid electrolytes

1999 ◽  
Vol 42 (2) ◽  
pp. 159-163 ◽  
Author(s):  
Kai Jiang ◽  
Jian Meng ◽  
Zhiqi He ◽  
Yufang Ren ◽  
Qiang Su
2020 ◽  
Vol 685 ◽  
pp. 178511
Author(s):  
Austėja Diktanaitė ◽  
Giedrė Gaidamavičienė ◽  
Edvardas Kazakevičius ◽  
Algimantas Kežionis ◽  
Artūras Žalga

Open Ceramics ◽  
2021 ◽  
pp. 100175
Author(s):  
Naohiro Horiuchi ◽  
Kaede Ryu ◽  
Akiko Nagai ◽  
Toshinori Okura ◽  
Kimihiro Yamashita

2001 ◽  
Vol 12 (2) ◽  
pp. 219-224 ◽  
Author(s):  
Yawen Zhang ◽  
Yu Yang ◽  
Shujian Tian ◽  
Chunsheng Liao ◽  
Chunhua Yan

Membranes ◽  
2019 ◽  
Vol 9 (9) ◽  
pp. 109 ◽  
Author(s):  
Jadra Mosa ◽  
Jonh Fredy Vélez ◽  
Mario Aparicio

Organic/inorganic hybrid membranes that are based on GTT (GPTMS-TMES-TPTE) system while using 3-Glycidoxypropyl-trimethoxysilane (GPTMS), Trimethyletoxisilane (TMES), and Trimethylolpropane triglycidyl ether (TPTE) as precursors have been obtained while using a combination of organic polymerization and sol-gel synthesis to be used as electrolytes in Li-ion batteries. Self-supported materials and thin-films solid hybrid electrolytes that were doped with Lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) were prepared. The hybrid network is based on highly cross-linked structures with high ionic conductivity. The dependency of the crosslinked hybrid structure and polymerization grade on ionic conductivity is studied. Ionic conductivity depends on triepoxy precursor (TPTE) and the accessibility of Li ions in the organic network, reaching a maximum ionic conductivity of 1.3 × 10−4 and 1.4 × 10−3 S cm−1 at room temperature and 60 °C, respectively. A wide electrochemical stability window in the range of 1.5–5 V facilitates its use as solid electrolytes in next-generation of Li-ion batteries.


2012 ◽  
Vol 22 ◽  
pp. s110-s114 ◽  
Author(s):  
Dong XU ◽  
Bin JIANG ◽  
Lei JIAO ◽  
Feng-dan CUI ◽  
Hong-xing XU ◽  
...  

2010 ◽  
Vol 181 (1-2) ◽  
pp. 33-36 ◽  
Author(s):  
Y.X. Gao ◽  
X.P. Wang ◽  
W.G. Wang ◽  
Q.F. Fang

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