丁二腈
材料科学
电解质
化学工程
离子电导率
沉积(地质)
电极
锂(药物)
枝晶(数学)
无机化学
纳米技术
物理化学
化学
工程类
古生物学
内分泌学
几何学
生物
医学
数学
沉积物
作者
Diandian Han,Pengfei Wang,Ping Li,Juan Shi,Jing Liu,Pengjing Chen,Lipeng Zhai,Liwei Mi,Yongzhu Fu
标识
DOI:10.1021/acsami.1c16498
摘要
Lithium (Li) metal has emerged as a promising electrode material for high-energy-density batteries. However, serious Li dendrite issues during cycling have plagued the safety and cyclability of the batteries, thus limiting the practical application of Li metal batteries. Herein, we prepare a novel metal-organic-framework-based (MOF-based) succinonitrile electrolyte, which enables homogeneous and fast Li-ion (Li+) transport for dendrite-free Li deposition. Given the appropriate aperture size of the MOF skeleton, the targeted electrolyte can allow only small-size Li+ to pass through its pores, which effectively guides uniform Li+ transport. Specially, Li ions are coordinated by the C═N of the MOF framework and the C≡N of succinonitrile, which could accelerate Li+ migration jointly. These characteristics afford an excellent quasi-solid-state electrolyte with a high ionic conductivity of 7.04 × 10-4 S cm-1 at room temperature and a superior Li+ transference number of 0.68. The Li/LiFePO4 battery with the MOF-based succinonitrile electrolyte exhibits dendrite-free Li deposition during the charge process, accompanied by a high capacity retention of 98.9% after 100 cycles at 0.1C.
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