scholarly journals Novel Li3ClO based glasses with superionic properties for lithium batteries

2014 ◽  
Vol 2 (15) ◽  
pp. 5470-5480 ◽  
Author(s):  
M. H. Braga ◽  
J. A. Ferreira ◽  
V. Stockhausen ◽  
J. E. Oliveira ◽  
A. El-Azab

Glassy electrolytes with superior ionic conductivity at room temperature, wide electrochemical stability window and impressive lifecycle in Li-metal cells were developed.

Materials ◽  
2021 ◽  
Vol 14 (14) ◽  
pp. 3840
Author(s):  
Adrien Méry ◽  
Steeve Rousselot ◽  
David Lepage ◽  
Mickaël Dollé

All-solid-state lithium batteries (ASSLB) are very promising for the future development of next generation lithium battery systems due to their increased energy density and improved safety. ASSLB employing Solid Polymer Electrolytes (SPE) and Solid Composite Electrolytes (SCE) in particular have attracted significant attention. Among the several expected requirements for a battery system (high ionic conductivity, safety, mechanical stability), increasing the energy density and the cycle life relies on the electrochemical stability window of the SPE or SCE. Most published works target the importance of ionic conductivity (undoubtedly a crucial parameter) and often identify the Electrochemical Stability Window (ESW) of the electrolyte as a secondary parameter. In this review, we first present a summary of recent publications on SPE and SCE with a particular focus on the analysis of their electrochemical stability. The goal of the second part is to propose a review of optimized and improved electrochemical methods, leading to a better understanding and a better evaluation of the ESW of the SPE and the SCE which is, once again, a critical parameter for high stability and high performance ASSLB applications.


2017 ◽  
Vol 5 (34) ◽  
pp. 18012-18019 ◽  
Author(s):  
Guang Yang ◽  
Chalathorn Chanthad ◽  
Hyukkeun Oh ◽  
Ismail Alperen Ayhan ◽  
Qing Wang

Ionic liquid-based solid electrolytes with outstanding room-temperature ionic conductivity and excellent electrochemical stability are developed for all-solid-state Li metal batteries.


2021 ◽  
Author(s):  
Jianwen Liang ◽  
Eveline van der Maas ◽  
Jing Luo ◽  
Xiaona Li ◽  
Ning Chen ◽  
...  

Abstract Understanding the relationship between structure, ionic conductivity, and synthesis is the key to the development of solid electrolytes for all-solid-state Lithium batteries. Here, we investigate chloride solid electrolytes with compositions Li3 − 3xM1+xCl6 (-0.14 < x ≤ 0.5, M = Tb, Dy, Ho, Y, Er, Tm). When x > 0.04, a trigonal to orthorhombic phase transition occurs in the isostructural Li-Dy-Cl, Li-Ho-Cl, Li-Y-Cl, Li-Er-Cl and Li-Tm-Cl solid electrolytes. The new orthorhombic phase shows a four-fold increase in ionic conductivity up to 1.3×10− 3 S cm− 1 at room temperature for Li2.73Ho1.09Cl6 (x = 0.09) when compared to the trigonal Li3HoCl6. For isostructural Li-Dy-Cl, Li-Y-Cl, Li-Er-Cl and Li-Tm-Cl solid electrolytes, about one order of magnitude increase in ionic conductivities are observed for the orthorhombic structure compared to the trigonal structure. Using the Li-Ho-Cl components as an example, detailed studies of its structure, phase transition, ionic conductivity, air stability and electrochemical stability have been made. Molecular dynamics simulations based on density functional theory reveal that the different cations arrangement in the orthorhombic structure leads to a higher lithium diffusivity as compared to the trigonal structure, rationalizing the improved ionic conductivities of the new Li-M-Cl electrolytes. All-solid-state batteries of In/Li2.73Ho1.09Cl6/NMC811 demonstrate excellent electrochemical performance at both room temperature and − 10°C. As relevant to the vast number of isostructural halide electrolytes, the present structure control strategy provides guidance for the design of novel halide superionic conductors.


2013 ◽  
Vol 743-744 ◽  
pp. 53-58 ◽  
Author(s):  
Rui Yang ◽  
Shi Chao Zhang ◽  
Lan Zhang ◽  
Xiao Fang Bi

Solid polymer electrolytes (SPEs) which were composed of poly (ethylene oxide) (PEO), poly (lithium acrylate) (PLiAA), and LiClO4were prepared in order to investigate the influence of LiClO4content on the ionic conductivity of the electrolyte. All of the membranes were investigated by XRD, DSC, and EIS, et.al. The dependence of SPEs conductivity on temperature was measured, and the maximum ionic conductivity is 5.88×10-6S/cm at 293 K for membrane which is composed of PEO+PLiAA+15wt% LiClO4. The electrochemical stability window of the PEO+PLiAA+15wt% LiClO4is 4.75 V verse Li.


Electrochem ◽  
2021 ◽  
Vol 2 (3) ◽  
pp. 390-414
Author(s):  
Md Mozammal Raju ◽  
Fadhilah Altayran ◽  
Michael Johnson ◽  
Danling Wang ◽  
Qifeng Zhang

As an essential part of solid-state lithium-ion batteries, solid electrolytes are receiving increasing interest. Among all solid electrolytes, garnet-type Li7La3Zr2O12 (LLZO) has proven to be one of the most promising electrolytes because of its high ionic conductivity at room temperature, low activation energy, good chemical and electrochemical stability, and wide potential window. Since the first report of LLZO, extensive research has been done in both experimental investigations and theoretical simulations aiming to improve its performance and make LLZO a feasible solid electrolyte. These include developing different methods for the synthesis of LLZO, using different crucibles and different sintering temperatures to stabilize the crystal structure, and adopting different methods of cation doping to achieve more stable LLZO with a higher ionic conductivity and lower activation energy. It also includes intensive efforts made to reveal the mechanism of Li ion movement and understand its determination of the ionic conductivity of the material through molecular dynamic simulations. Nonetheless, more insightful study is expected in order to obtain LLZO with a higher ionic conductivity at room temperature and further improve chemical and electrochemical stability, while optimal multiple doping is thought to be a feasible and promising route. This review summarizes recent progress in the investigations of crystal structure and preparation of LLZO, and the impacts of doping on the lithium ionic conductivity of LLZO.


2016 ◽  
Vol 120 (25) ◽  
pp. 5691-5702 ◽  
Author(s):  
Saeed Kazemiabnavi ◽  
Zhengcheng Zhang ◽  
Katsuyo Thornton ◽  
Soumik Banerjee

2016 ◽  
Vol 4 (14) ◽  
pp. 5191-5197 ◽  
Author(s):  
Jingchao Chai ◽  
Jianjun Zhang ◽  
Pu Hu ◽  
Jun Ma ◽  
Huiping Du ◽  
...  

A polytetrafluoroethylene supported poly(methylethyl α-cyanoacrylate) with high ionic conductivity and excellent electrochemical stability is developed for high-voltage LiNi0.5Mn1.5O4/Li battery.


2020 ◽  
Vol 13 (5) ◽  
pp. 1429-1461 ◽  
Author(s):  
Xiaona Li ◽  
Jianwen Liang ◽  
Xiaofei Yang ◽  
Keegan R. Adair ◽  
Changhong Wang ◽  
...  

This review focuses on fundamental understanding, various synthesis routes, chemical/electrochemical stability of halide-based lithium superionic conductors, and their potential applications in energy storage as well as related challenges.


2021 ◽  
Author(s):  
Ruixue Zhang ◽  
Wanying Zhao ◽  
Zhenzhen Liu ◽  
Shanghai Wei ◽  
Yigang Yan ◽  
...  

In situ formed amorphous LiBH4·1/2NH3 on the surface of Al2O3 nanoparticles results in an enhanced ion conductivity of 1.1 × 10−3 S cm−1 at room temperature.


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