材料科学
过电位
阳极
电解质
化学工程
电导率
阴极
硫化物
X射线光电子能谱
离子电导率
快离子导体
电化学
无机化学
电极
冶金
物理化学
化学
工程类
作者
Bereket Woldegbreal Taklu,Wei‐Nien Su,Yosef Nikodimos,Keseven Lakshmanan,Nigusu Tiruneh Temesgen,Pei-Xuan Lin,Shi‐Kai Jiang,Chen‐Jui Huang,Di‐Yan Wang,Hwo‐Shuenn Sheu,She‐Huang Wu,Bing‐Joe Hwang
出处
期刊:Nano Energy
[Elsevier]
日期:2021-09-22
卷期号:90: 106542-106542
被引量:84
标识
DOI:10.1016/j.nanoen.2021.106542
摘要
The decent ductileness, high ionic conductivity, low cost, and versatility over synthesis methods make Li-argyrodite a promising for all-solid-state lithium batteries. However, its serious interfacial incompatibility with Li anode, dendrite growth, and intrinsic air instability impedes its practicability. Herein, we report a CuCl dual doped Li-argyrodite sulfide superb-conductor (Li6+3xP1−xCuxS5−xCl1+x) prepared to overcome these issues via ball-mill free synthesis approach. The maximum Li+ conductivity of 4.34 mS cm−1 at room temperature with ultrawide voltage stability up to 8 V vs. Li/Li+ was achieved in Li6.3P0.9Cu0.1S4.9Cl1.1 (LPSC-1) via a both composite and planar electrode system and can suppress dendrite formation at a current density of 3 mA cm−2 at 50 оC. The symmetrical cell cycled at 0.1 and 1 mA cm−2 also demonstrates remarkable reversibility with negligible overpotential alteration for more than 2400 h and 400 h. An ex-situ XPS and AC impedance analysis proved enhanced interfacial compatibility at Li | SE and achieved a critical current density of 3 mA cm−2. More interestingly, incorporating soft acid Cu in LPSC-1 boosts the air stability and suppresses H2S generation by two-folds. The XRD for the LPSC-1 before and after air exposure proves the decrease in the oxophilicity of the sulfide solid electrolyte.
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