电解质
材料科学
阳极
电流密度
聚合物
化学工程
金属锂
相间
图层(电子)
快离子导体
锂(药物)
电极
纳米技术
复合材料
物理化学
化学
生物
物理
工程类
内分泌学
医学
量子力学
遗传学
作者
Nan Wu,Yutao Li,Andrei Dolocan,Wei Li,Henghui Xu,Biyi Xu,Nicholas S. Grundish,Zhiming Cui,Haibo Jin,John B. Goodenough
标识
DOI:10.1002/adfm.202000831
摘要
Abstract Solid‐state polymer electrolytes provide better flexibility and electrode contact than their ceramic counterparts, making them a worthwhile pursuit for all‐solid‐state lithium‐metal batteries. However, their large Li/solid state electrolyte interfacial resistance, small critical current density, and rapid lithium dendrite growth during cycling still limit their viability. Owing to these restrictions, all‐solid‐state cells with solid polymer electrolytes must be cycled above room‐temperature and with a small current density. These problems can be mitigated with an in situ formed artificial solid electrolyte interphase that rapidly conducts Li + ions. Herein, a Li 3 P layer formed in situ at the Li‐metal/solid polymer electrolyte interphase is reported that significantly reduces the electrode/electrolyte interfacial resistance. Additionally, this layer increases the wettability of the solid polymer by the metallic lithium anode, allowing for the critical current density of lithium symmetric cells to be doubled by homogenizing the current density at the interface. All‐solid‐state Li/Li symmetric cells and Li/LiFePO 4 cells with the Li 3 P layer show improved cycling performance with a high current density.
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