金属锂
溶剂
固态
电池(电)
锂(药物)
金属
材料科学
无机化学
化学
化学工程
纳米技术
物理化学
有机化学
电极
热力学
阳极
物理
工程类
功率(物理)
医学
内分泌学
作者
Bin Qiu,Feng Xu,Jie Huang,Ying Wu,Kaiming Huang,Jinyu Gao,Chuanxin He,Peixin Zhang,Hongwei Mi
出处
期刊:Nano Letters
[American Chemical Society]
日期:2024-07-11
卷期号:24 (29): 8872-8879
被引量:6
标识
DOI:10.1021/acs.nanolett.4c01453
摘要
Parlous structure integrity of the cathode and erratic interfacial microdynamics under high potential take responsibility for the degradation of solid-state lithium metal batteries (LMBs). Here, high-voltage LMBs have been operated by modulating the polymer electrolyte intrinsic structure through an intermediate dielectric constant solvent and further inducing the gradient solid-state electrolyte interphase. Benefiting from the chemical adsorption between trimethyl phosphate (TMP) and the cathode, the gradient interphase rich in LiPFxOy and LiF is induced, thereby ensuring the structural integrity and interface compatibility of the commercial LiNi0.8Co0.1Mn0.1O2 (NCM811) cathode even at the 4.9 V cutoff voltage. Eventually, the specific capacity of NCM811|Li full cell based on TMP-modulated polymer electrolyte increased by 27.7% from 4.5 to 4.9 V. Such a universal screening method of electrolyte solvents and its derived electrode interfacial manipulation strategy opens fresh avenues for quasi-solid-state LMBs with high specific energy.
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