电解质
X射线光电子能谱
锂(药物)
阳极
阴极
材料科学
化学工程
分解
金属
无机化学
化学
电极
物理化学
有机化学
医学
工程类
冶金
内分泌学
作者
Chenxi Xiao,Xiaotong Liu,Weiping Li,Xianghe Ma,Ju Qian,Xinrong Lin
标识
DOI:10.1002/batt.202400078
摘要
Abstract The electrolyte stability under high‐voltage conditions considerably limits the upper cut‐off potential of solid‐state electrolytes (SSEs) and therefore the energy density of all‐solid‐state batteries (ASSBs). In this work, metal‐organic frameworks (MOFs) were fluorinated to lower the energy level of HOMO orbital and allow access to a 4F‐MOF that exhibit enhanced anodic stability. The composited 4F‐MOF/PEO electrolyte could not only transport Li + ions in the ordered framework channels, but also provide a remarkable high‐voltage stability up to 5.0 V, shielding oxidative decomposition that would otherwise occur at around 3.9 V for conventional PEO electrolytes. In addition, stable lithium deposition was demonstrated for more than 1,300 hours at 0.1 mA ⋅ cm −2 , while reversible charge‐discharge cycling performance was delivered in assembled Li||LiNi 0.5 Mn 1.5 O 4 (LNMO) ASSBs up to 5.0 V. Post‐mortem X‐ray photoelectron spectroscopy (XPS) investigation on cathodes revealed presence of a LiF‐rich cathode electrolyte interface (CEI), supporting promoted stability towards high‐voltage ASSBs.
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