scholarly journals A New Lithium‐Ion Conductor LiTaSiO 5 : Theoretical Prediction, Materials Synthesis, and Ionic Conductivity

2019 ◽  
Vol 29 (37) ◽  
pp. 1904232 ◽  
Author(s):  
Qi Wang ◽  
Jian‐Fang Wu ◽  
Ziheng Lu ◽  
Francesco Ciucci ◽  
Wei Kong Pang ◽  
...  
2020 ◽  
Vol 13 (06) ◽  
pp. 2050031
Author(s):  
Yue Jiang ◽  
Zhiwei Hu ◽  
Ming’en Ling ◽  
Xiaohong Zhu

Since the lithium-ion conductor Li[Formula: see text]GeP2S[Formula: see text] (LGPS) with a super high room-temperature conductivity of 12[Formula: see text]mS/cm was first reported in 2011, sulfide-type solid electrolytes have been paid much attention. It was suggested by Kwon et al. [J. Mater. Chem. A 3, 438 (2015)] that some excess lithium ions in LGPS, namely, Li[Formula: see text]Ge[Formula: see text] P[Formula: see text]S[Formula: see text], could further improve their ionic conductivities, and the highest conductivity of 14.2[Formula: see text]mS/cm was obtained at [Formula: see text] though a larger lattice parameter that occurred at [Formula: see text]. In this study, we focus on these two different chemical compositions of LGPS with [Formula: see text] and [Formula: see text], respectively. Both samples were prepared using the same experimental process. Their lattice parameter, microstructure and room-temperature ionic conductivity were compared in detail. The results show that the main phase is the tetragonal LGPS phase but with a nearly identical amount of orthorhombic LGPS phase coexisting in both samples. Bigger lattice parameters, larger grain sizes and higher ionic conductivities are simultaneously achieved in Li[Formula: see text]Ge[Formula: see text]P[Formula: see text]S[Formula: see text] ([Formula: see text]), exhibiting an ultrahigh room-temperature ionic conductivity of 18.8[Formula: see text]mS/cm.


2004 ◽  
Vol 822 ◽  
Author(s):  
Flávio L. Souza ◽  
Paulo R. Bueno ◽  
Ronaldo C. Faria ◽  
Elson Longo ◽  
Edson R. Leite

AbstractA new nanocomposite electrolyte was synthesized using a simple non-hydrolytic sol-gel route without specific treatment of the reagents. The nanocomposite ion conductor was prepared with citric acid, tetraethyl orthosilicate and ethylene glycol, forming polyester chains. The time-consuming drying step that is a necessary part of most chemical syntheses was not required in the preparation of the present nanocomposite electrolyte of the polyelectrolyte class, because only Li+ is mobile in the polymeric chain. The effects of the concentration of Li, SiO 2 and SnO2nanoparticles were investigated in terms of Li+ ionic conductivity. Conductivity measurements as a function of the metal oxide nanocrystal content in the nanocomposite revealed a significant increase in conductivity at approximately 5 and 10 wt % of nanoparticles. The new nanocomposite conductor proved to be fully amorphous at room temperature, with a vitreous transition temperature of approximately 228K (−45°C). The material is solid and transparent, displaying an ionic conductivity of 10−4to 10−5 (O.cm)−1at room temperature presenting excellent reproducibility of all these characteristics. Cyclic voltammetry measurements indicate that the hybrid electrolyte possesses outstanding electrochemical stability.


2018 ◽  
Vol 166 (3) ◽  
pp. A5168-A5173 ◽  
Author(s):  
Daisuke Mori ◽  
Kaoru Sugimoto ◽  
Yasuaki Matsuda ◽  
Kenta Ohmori ◽  
Tetsuhiro Katsumata ◽  
...  

2008 ◽  
Vol 179 (21-26) ◽  
pp. 867-870 ◽  
Author(s):  
Y. Tomita ◽  
H. Matsushita ◽  
K. Kobayashi ◽  
Y. Maeda ◽  
K. Yamada

2018 ◽  
Vol 6 (39) ◽  
pp. 19231-19240 ◽  
Author(s):  
Minjie Xuan ◽  
Weidong Xiao ◽  
Hongjie Xu ◽  
Yonglong Shen ◽  
Zhenzhen Li ◽  
...  

A solid electrolyte with superb Li+ conductivity through tuning of the lattice chemistry in Li6PS5Cl. The ionic conductivity is enhanced through the combined effect of excess Li and substitution of S with Te.


2017 ◽  
Vol 140 ◽  
pp. 417-423 ◽  
Author(s):  
Wojciech Zając ◽  
Mateusz Tarach ◽  
Anita Trenczek-Zając

2019 ◽  
Vol 10 (1) ◽  
Author(s):  
David G. Mackanic ◽  
Xuzhou Yan ◽  
Qiuhong Zhang ◽  
Naoji Matsuhisa ◽  
Zhiao Yu ◽  
...  

AbstractThe emergence of wearable electronics puts batteries closer to the human skin, exacerbating the need for battery materials that are robust, highly ionically conductive, and stretchable. Herein, we introduce a supramolecular design as an effective strategy to overcome the canonical tradeoff between mechanical robustness and ionic conductivity in polymer electrolytes. The supramolecular lithium ion conductor utilizes orthogonally functional H-bonding domains and ion-conducting domains to create a polymer electrolyte with unprecedented toughness (29.3 MJ m−3) and high ionic conductivity (1.2 × 10−4 S cm−1 at 25 °C). Implementation of the supramolecular ion conductor as a binder material allows for the creation of stretchable lithium-ion battery electrodes with strain capability of over 900% via a conventional slurry process. The supramolecular nature of these battery components enables intimate bonding at the electrode-electrolyte interface. Combination of these stretchable components leads to a stretchable battery with a capacity of 1.1 mAh cm−2 that functions even when stretched to 70% strain. The method reported here of decoupling ionic conductivity from mechanical properties opens a promising route to create high-toughness ion transport materials for energy storage applications.


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