离子电导率
电化学
兴奋剂
电解质
锂(药物)
卤化物
材料科学
快离子导体
电导率
储能
固态
纳米技术
化学工程
离子键合
离子液体
无机化学
离子
工程物理
化学
电极
光电子学
物理化学
有机化学
物理
工程类
医学
功率(物理)
量子力学
内分泌学
催化作用
作者
Pengfei Du,Peng Zhang,Zhenyang Shen,Yongmei Zhou,Ying Liu,Qingtao Wang
出处
期刊:Nanoscale
[Royal Society of Chemistry]
日期:2025-01-01
卷期号:17 (26): 15856-15865
被引量:1
摘要
All-solid-state lithium batteries (ASSLBs) are garnering increasing attention as a state-of-the-art energy storage technology. Halide solid electrolytes have emerged as a focal point of research in recent years, owing to their straightforward preparation methods and high ionic conductivity at room temperature. In this study, Bi-doped Li2ZrCl6 was synthesized using a high-energy ball milling method. The Bi3+ ion effectively replaces some of the Zr4+ ions. Due to its lower valence state and larger ionic radius, the concentration of Li+ in the electrolyte increases, and the lattice volume increases, which facilitates Li+ migration. Consequently, the ionic conductivity of modified Li2.15Zr0.85Bi0.15Cl6 at room temperature is 4.9 × 10-4 S cm-1, more than double that of Li2ZrCl6. This enhancement was further validated through cyclic voltammetry and wet air stability tests, which confirmed that Bi3+ doping not only significantly improves the electrochemical high-pressure oxidation stability of Li2ZrCl6 but also enhances its stability in humid air. Additionally, charge/discharge tests on ASSLB using Li2.15Zr0.85Bi0.15Cl6 as the electrolyte demonstrated that Bi doping enhances the electrochemical performance of Li2ZrCl6, leading to improvements in discharge specific capacity and cycle life.
科研通智能强力驱动
Strongly Powered by AbleSci AI