电解质
电化学
锂(药物)
材料科学
金属
化学工程
X射线光电子能谱
准固态
电化学窗口
离子电导率
化学
纳米技术
电极
冶金
物理化学
色素敏化染料
医学
工程类
内分泌学
作者
Long Pan,Shuo Sun,Genxi Yu,Xiong Xiong Liu,Shengfa Feng,Wei Zhang,Muhammadali Turgunov,Sheng Wang,ZhengMing Sun
标识
DOI:10.1016/j.cej.2022.137682
摘要
Solid electrolytes are fundamental for next-generation solid-state Li-metal batteries that promise high energy density and safety. However, various solid electrolytes suffer from chemical/electrochemical instability against Li metal and poor interfacial contact with electrodes. Herein, a polymer-in-salt (PiS) artificial protection layer composed of fluoropolymer in highly-concentrated lithium salt (labeled as PiSPL) is introduced to address these problems using NASICON-type Li1.3Al0.3Ti1.7(PO4)3 (LATP) as a typical solid electrolyte. The resulted PiSPL layer exhibits small thickness (10 μm), good chemical/electrochemical stability, and excellent ionic conductivity (0.5 and 1.8 mS cm−1 at 25 and 60 °C, respectively). These properties endow the LATP/Li interface with improved contact, favorable Li+ diffusion, and, most importantly, inhibited interfacial reactions, which is examined using ex-situ X-ray photoelectron spectroscopy and electrochemical analyses and morphological observations. Consequently, Li||[email protected]||Li symmetric cells can deliver small overpotentials at various current densities and long lifetime at 0.16 mA cm−2 over 400 h. On the contrary, the same configuration cells with LATP die after only 50 h. Moreover, the LiFePO4||[email protected]||Li solid-state full cells exhibit excellent rate capability (124.0 mA h g−1 at 2.0C) and cyclability (148.9 and 140.6 mA h g−1 after 200 cycles at 0.2C and 300 cycles at 1.0C, respectively). The PiS strategy represents a general and effective approach to stabilize various solid electrolyte/Li interfaces to push solid-state Li-metal batteries forward.
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