快离子导体
锂(药物)
材料科学
离子电导率
离子键合
结晶
电解质
猝灭(荧光)
化学物理
化学工程
无机化学
物理化学
离子
化学
内分泌学
有机化学
工程类
物理
荧光
医学
量子力学
电极
作者
Ajay Gautam,Marcel Sadowski,Nils Prinz,Henrik Eickhoff,Nicolò Minafra,Michael Ghidiu,Sean P. Culver,Karsten Albe,Thomas F. Fässler,Mirijam Zobel,Wolfgang G. Zeier
标识
DOI:10.1021/acs.chemmater.9b03852
摘要
Lithium argyrodite superionic conductors are currently being investigated as solid electrolytes for all-solid-state batteries. Recently, in the lithium argyrodite Li6PS5X (X = Cl, Br, and I), a site-disorder between the anions S2– and X– has been observed, which strongly affects the ionic transport and appears to be a function of the halide present. In this work, we show how such a disorder in Li6PS5Br can be engineered via the synthesis method. By comparing fast cooling (i.e., quenching) to more slowly cooled samples, we find that the anion site-disorder is higher at elevated temperatures, and that fast cooling can be used to kinetically trap the desired disorder, leading to higher ionic conductivities as shown by impedance spectroscopy in combination with ab initio molecular dynamics. Furthermore, we observe that after milling, a crystalline lithium argyrodite can be obtained within 1 min of heat treatment. This rapid crystallization highlights the reactive nature of mechanical milling and shows that long reaction times with high energy consumption are not needed in this class of materials. The fact that site-disorder induced via quenching is beneficial for ionic transport provides an additional approach for the optimization and design of lithium superionic conductors.
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