2D Vertically Conductive Metal─Organic Framework Electrolytes: Will They Outperform 3D MOFs for Solid State Batteries?

材料科学 纳米技术 储能 快离子导体 导电体 电解质 金属有机骨架 锂(药物) 工程物理 电极 工程类 化学 复合材料 内分泌学 物理化学 吸附 功率(物理) 有机化学 物理 医学 量子力学
作者
Zixin Hong,Hao Yuan,Hengcai Wu,Jianguo Sun,Jing Yang,Yong‐Wei Zhang,Jiaping Wang,John Wang
出处
期刊:Small [Wiley]
被引量:3
标识
DOI:10.1002/smll.202408394
摘要

Lithium-ion batteries are currently the mainstream for almost all portables, and quickly expand in electrical vehicles and grid storage applications. However, they are challenged by the poor safety regarding organic liquid electrolytes and relatively low energy density. Solid-state batteries, characterized by using solid-state electrolytes (SSEs), are recognized as the next-generation energy technology, owing to their intrinsically high safety and potentially superior energy density. However, developing SSEs is impeded by several key factors, including low ionic conductivity, interfacial issues, and high-cost in industrial scales. Recently, a novel category of SSEs, known as frameworked electrolytes (FEs), has emerged as a formidable contender for the transition to all-solid-state batteries. FEs exhibit a unique macroscopically solid-state nature and microscopically sub-nanochannels offering high ionic conductivity. In this perspective, the unique lithium-ion transport mechanisms within FEs are explored and 2D vertically conductive metal-organic framework (MOF) is proposed as an even more promising FE candidate. The abundant active sites in the 1D sub-nanochannels of 2D vertically conductive MOFs facilitate efficient ion transport, favorable interfacial compatibility, and scalable industrial applications. This perspective aims to boost the emergence of novel SSEs, promoting the realization of long-expected all-solid-state batteries and inspiring future energy storage solutions.
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