电解质
材料科学
碳酸乙烯酯
化学工程
锂(药物)
聚合
阳极
离子电导率
三氟甲磺酸
无机化学
催化作用
有机化学
化学
聚合物
电极
复合材料
物理化学
内分泌学
工程类
医学
作者
Shufeng Song,Weiling Gao,Guanming Yang,Yanfang Zhai,Jianyao Yao,Liyang Lin,Weiping Tang,Ning Hu,Li Lu
标识
DOI:10.1016/j.mtener.2021.100893
摘要
Building safe and high-energy-density lithium metal batteries (LMBs) is currently being pursued to sustain our modern lifestyles. However, new electrolyte engineering is rigorously required that is capable of simultaneously providing good protection on lithium metal anode and sustaining high oxidative stability at the cathode, besides sufficient bulk conductivity and low interfacial resistance. Here, we report a novel hybrid poly-ether/carbonate ester quasi-solid-state electrolyte with high oxidative stability formed by a simple and efficient in situ polymerization of strategy, in which ring-opening polymerization of ether-based 1,3-dioxolane (DOL) and ester-based ethylene carbonate (EC)-ethylmethyl carbonate (EMC) is initiated by rare-earth triflate catalyst Sc(OTf)3 at room temperature. Such electrolyte engineering not only achieves a sufficiently high ionic conductivity of 5 × 10−4 S cm−1 but enables a high anodic voltage limit of 5 V while maintaining feasible battery manufacture technology. The hybrid poly-DOL/EC/EMC quasi-solid-state electrolyte is capable of producing a stable solid electrolyte interphase (SEI) featuring Li plating/stripping over 500 h at 0.5 mA cm−2 and decreased charge transfer resistance. The derived Li||LiFePO4 quasi-solid-state LMB, benefited from the enhanced oxidative stability of electrolyte, exhibits a notable capacity of 169 mAh g−1 at 1C with no capacity decay after 300 cycles.
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