电解质
离子电导率
阳极
材料科学
电化学
掺杂剂
钇
电导率
电化学窗口
锂(药物)
化学工程
快离子导体
无机化学
兴奋剂
化学
冶金
电极
物理化学
氧化物
内分泌学
工程类
医学
光电子学
作者
Yang Xia,Jiaojiao Li,Jun Zhang,Xiaozheng Zhou,Hui Huang,Xinping He,Yongping Gan,Zhen Xiao,Jun Zhang
标识
DOI:10.1016/j.jpowsour.2022.231846
摘要
The inferior electrochemical stability towards Li anode and relatively low ionic conductivity at room temperature of argyrodite Li6PS5Cl (LPSCl) electrolytes are the intractable challenges for all-solid-state lithium batteries (ASSLBs). Herein, in order to fully address the aforementioned issues, yttrium ion (Y3+) employed as dopant is designed to substitute for P5+ in LPSCl to boost the Li + mobility in electrolyte, as well as to ameliorate the interface stability to Li anode. By introducing appropriate Y3+ dopant, the optimized LPSCl-0.02Y electrolyte exhibits high ionic conductivity of 3.3 × 10−3 S cm−1 at 25 °C, which is 2 times higher than that of the pristine LPSCl (1.5 × 10−3 S cm−1). Benefitting from the high ionic conductivity, LPSCl-0.02Y is endowed with superior inhibition ability of Li dendrite nucleation and growth from Li anode, thereby significantly enhancing the (electro)chemical interfacial stability. Impressively, LiNi0.8Co0.1Mn0.1O2/Li cell with LPSCl-0.02Y electrolyte delivers high initial discharge capacity (165 mA h g−1 at 0.05C), robust cycling stability (93 mA h g−1 after 100 cycles) and remarkable rate capability (130 mA h g−1 at 0.2C). This rationally designed Y-doped LPSCl electrolyte is highly expected to pave the road for the practical application of ASSLBs, and to deepen the understanding of aliovalent substitution mechanism.
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