法拉第效率
电解质
纳米技术
材料科学
储能
电导率
溶解
电极
电池(电)
工艺工程
光学(聚焦)
聚合物电解质
电流(流体)
高效能源利用
计算机科学
自行车
燃料电池
工程物理
阳离子聚合
离子
能量转换
能量密度
低能
作者
Valentino G. Martello,Alessandro Piovano,Matteo Bonomo,Mircea Dincă,Silvia Bordiga,Claudio Gerbaldi
标识
DOI:10.1021/acsenergylett.5c02431
摘要
The development of solid-state electrolytes is a major focus in energy storage, offering improvements in both safety and performance. In chloride-ion batteries (CIBs), where electrode dissolution in liquid electrolytes remains a critical challenge, solid-state alternatives are especially attractive. Herein, we demonstrate for the first time the suitability of a metal-organic framework (MOF) as a quasi-solid-state single-ion electrolyte for CIBs. The cationic Al-based MOF MIP-213 ([Al18(μ2-OH)24(OH2)12(mdip)6]-6Cl·6H2O) exhibits a chloride ion conductivity of 1.1 × 10-6 S cm-1 at 25 °C, is nonflammable, electrochemically stable up to 4.2 V vs Li+/Li, and enables single-ion transport in a Li|MIP-213|FeOCl full cell over 100 cycles with Coulombic efficiency > 90%, while maintaining structural integrity. Although further optimization of the CIB components will be needed to enable cycling at higher current regimes and approach practical application, these findings establish MOFs as promising platforms for designing stable and efficient quasi-solid-state batteries.
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