纳米技术
电解质
快离子导体
材料科学
瓶颈
储能
离子电导率
固态
离子键合
计算机科学
工程物理
离子
电极
工程类
化学
物理
有机化学
功率(物理)
物理化学
量子力学
嵌入式系统
作者
Jianguo Sun,Xingyang Wang,Hao Yuan,Yu Liu,Jing Yang,Qi Zhao,Yulin Gao,Tuo Wang,Yong‐Wei Zhang,John Wang
出处
期刊:Small
[Wiley]
日期:2023-12-27
卷期号:20 (20)
被引量:9
标识
DOI:10.1002/smll.202308849
摘要
Abstract All‐solid‐state batteries (ASSBs) represent a highly promising next‐generation energy storage technology owing to their inherently high safety, device reliability, and potential for achieving high energy density in the post‐ara of lithium‐ion batteries, and therefore extensive searches are ongoing for ideal solid‐state electrolytes (SSEs). Though promising, there is still a huge barrier that limits the large‐scale applications of ASSBs, where there are a couple of bottleneck technical issues. In this perspective, a novel category of electrolytes known as frameworked electrolytes (FEs) are examined, where the solid frameworks are intentionally designed to contain 3D ionic channels at sub‐nano scales, rendering them macroscopically solid. The distinctive structural design of FEs gives rise to not only high ionic conductivity but also desirable interfaces with electrode solids. This is achieved through the presence of sub‐nano channels within the framework, which exhibit significantly different ion diffusion behavior due to the confinement effect. This perspective offers a compelling insight into the potential of FEs in the pursuit of ASSBs, where FEs offer an exciting opportunity to overcome the limitations of traditional solid‐state electrolytes and propel the development of ASSBs as the holy grail of energy storage technology.
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