电解质
锂(药物)
材料科学
化学工程
准固态
聚合物
剥脱关节
扩散
纳米技术
化学
复合材料
电极
热力学
物理
工程类
内分泌学
物理化学
医学
色素敏化染料
石墨烯
作者
Jun Cheng,Guangmei Hou,Qiong Chen,Deping Li,Kaikai Li,Qunhui Yuan,Jiajun Wang,Lijie Ci
标识
DOI:10.1016/j.cej.2021.132343
摘要
Polyoxyethylene (PEO)-based electrolyte is one of the most promising solid-state electrolyte (SSE) candidates for all-solid-state batteries due to its high flexible and salt solubility. Recently, morphological control on active fillers is confirmed as a critical issue affecting the performance of SSE. However, the lack of comprehensive research is hindering the understanding over the growth mechanism of the structured active fillers. Especially, compared with other dimensions, the studies on the growth mechanism of two-dimensional (2D) active fillers are quite limited due to the difficulties in physical methods such as exfoliation. Herein, sheet-like LLZAO (Li6.25La3Zr2Al0.25O12) (SL) is synthesized by bottom-up method to upgrade PEO matrix (SL@PEO). In addition, the growth mechanism of SL is proposed, which provides a new sight for morphology control over inorganic solid electrolytes. The SL structure provides continuous interfaces between the fillers and the polymer matrix, which ensures rapid diffusion of lithium ions. In addition, the SL can provide more nature barriers for electrolyte to suppress the lithium dendrites growth. The lithium symmetric cells adopting SL@PEO present prolonged cycling stability and higher critical current density compared with the control samples. The assembled all-solid-state LiFePO4/SL@PEO/Li batteries exhibit superior cycling stability and rate capability.
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