离子电导率
离子键合
钨
电解质
扩散
兴奋剂
正交晶系
钠
空位缺陷
活化能
离子
电导率
化学
快离子导体
离子半径
无机化学
分析化学(期刊)
材料科学
物理化学
结晶学
晶体结构
热力学
电极
物理
有机化学
光电子学
色谱法
作者
Xuyong Feng,Hong Fang,Pengcheng Liu,Nan Wu,Ethan C. Self,Liang Yin,Pengbo Wang,Xiang Li,Puru Jena,Jagjit Nanda,David Mitlin
标识
DOI:10.1002/ange.202110699
摘要
Abstract A strategy for modifying the structure of solid‐state electrolytes (SSEs) to reduce the cation diffusion activation energy is presented. Two heavily W‐doped sodium thioantimonate SSEs, Na 2.895 W 0.3 Sb 0.7 S 4 and Na 2.7 W 0.3 Sb 0.7 S 4 are designed, both exhibiting exceptionally low activation energy and enhanced room temperature (RT) ionic conductivity; 0.09 eV, 24.2 mS/cm and 0.12 eV, 14.5 mS/cm. At −15 °C the Na 2.895 W 0.3 Sb 0.7 S 4 displays a total ionic conductivity of 5.5 mS/cm. The 30 % W content goes far beyond the 10–12 % reported in the prior studies, and results in novel pseudo‐cubic or orthorhombic structures. Calculations reveal that these properties result from a combination of multiple diffusion mechanisms, including vacancy defects, strongly correlated modes and excessive Na‐ions. An all‐solid‐state battery (ASSB) using Na 2.895 W 0.3 Sb 0.7 S 4 as the primary SSE and a sodium sulfide (Na 2 S) cathode achieves a reversible capacity of 400 mAh g −1 .
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