材料科学
快离子导体
电解质
无定形固体
电导率
锂(药物)
离子电导率
法拉第效率
阳极
晶界
离子
化学工程
冶金
物理化学
结晶学
微观结构
电极
化学
内分泌学
工程类
物理
医学
量子力学
作者
Kavish Kaup,David Bazak,Shahrzad Hosseini Vajargah,Xiaohan Wu,Joern Kulisch,Gillian R. Goward,Linda F. Nazar
标识
DOI:10.1002/aenm.201902783
摘要
Abstract As potential next‐generation energy storage devices, solid‐state lithium batteries require highly functional solid state electrolytes. Recent research is primarily focused on crystalline materials, while amorphous materials offer advantages by eliminating problematic grain boundaries that can limit ion transport and trigger dendritic growth at the Li anode. However, simultaneously achieving high conductivity and stability in glasses is a challenge. New quaternary superionic lithium oxythioborate glasses are reported that exhibit high ion conductivity up to 2 mS cm −1 despite relatively high oxygen: sulfur ratios of more than 1:2, that exhibit greatly reduced H 2 S evolution upon exposure to air compared to Li 7 P 3 S 11 . These monolithic glasses are prepared from vitreous melts without ball‐milling and exhibit no discernable XRD pattern. Solid‐state NMR studies elucidate the structural entities that comprise the local glass structure which dictates fast ion conduction. Stripping/plating onto lithium metal results in very low polarization at a current density of 0.1 mA cm −2 over repeated cycling. Evaluation of the optimal glass composition as an electrolyte in an all‐solid‐state battery shows it exhibits excellent cycling stability and maintains near theoretical capacity for over 130 cycles at room temperature with Coulombic efficiency close to 99.9%, opening up new avenues of exploration for these quaternary compositions.
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