离子电导率
中子衍射
材料科学
电解质
电导率
快离子导体
分析化学(期刊)
退火(玻璃)
陶瓷
离子
相(物质)
锂(药物)
无机化学
化学工程
化学
晶体结构
结晶学
物理化学
电极
复合材料
工程类
内分泌学
医学
色谱法
有机化学
作者
R. Prasada Rao,Neeraj Sharma,Vanessa K. Peterson,Stefan Adams
标识
DOI:10.1016/j.ssi.2012.09.014
摘要
Lithium-ion conducting argyrodites Li6PS5X (X = Cl, Br, I) are a promising class of fast-ion conductors for all-solid state Li-ion batteries. To gain a deeper insight into the phase formation of Li6PS5Cl, in situ neutron diffraction studies are carried out on a stoichiometric ball-milled precursor mixture during thermal treatment. The evolution of the S2 −/Cl− anion disorder and its correlation with ionic conductivity are reported here. In contrast to earlier reports, an argyrodite phase is found to form between 80 and 150 °C, but the phase shows only moderate conductivity when crystallized at such low temperatures and further thermal treatment is required to access the highly conducting phase. The maximum room-temperature ionic conductivity of 1.1 × 10− 3 S/cm is observed for samples annealed at intermediate temperatures (250 °C). When ball-milled glass-ceramic precursors for Li6PS5Cl are crystallized with a constant slow heating rate, the initially formed argyrodite phase is found to be Li7PS6, which is then gradually converted into Li6PS5Cl at higher temperatures. The industrial requirements for minimizing cost by using lower annealing temperatures thus need to be balanced with the requirements of obtaining the highest conducting composition of the phase for performance in all-solid state batteries.
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