丁二腈
电解质
离子电导率
聚合
硒化物
电化学
材料科学
锂(药物)
二聚体
无机化学
化学工程
电导率
离子键合
金属
化学
电极
有机化学
离子
溶剂
物理化学
冶金
聚合物
工程类
医学
硒
复合材料
内分泌学
作者
Jian‐Fang Wu,Zixing Wang,Jun Jin,Zi-Xiang Kong,Shi Chen,Jilei Liu
出处
期刊:Nano Letters
[American Chemical Society]
日期:2025-01-03
被引量:3
标识
DOI:10.1021/acs.nanolett.4c04164
摘要
Solid-state metallic potassium batteries (SSMPBs) afresh have attracted incremental attention because of their potential to supplement solid-state metallic lithium batteries. However, SSMPBs suffer poor electrochemical performances due to the low ionic conductivity of solid electrolytes and huge electrode/electrolyte interfacial resistance. Herein, high-rate SSMPBs are achieved by in situ ring-opening polymerization of 1,3-dioxolane with succinonitrile as a plasticizer and Al(OTf)3 as the catalyst, where the succinonitrile enables short-chain polyether electrolytes. The in situ polymerized electrolytes deliver a high ionic conductivity of 4.5 × 10–5 S cm–1 at room temperature and excellent stabilities at high oxidation potentials (4.2 V vs K+/K) and against metallic K anodes. All these result in SSMPBs with a discharge capacity of 69 mAh g–1 under a high rate of 100 mA g–1 and a retention of 88.8% after 100 cycles, and the rate and capacity retention are higher than those in previous work on SSMPBs.
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