Toward All-Solid-State Lithium Batteries: Three-Dimensional Visualization of Lithium Migration in β-Li3PS4 Ceramic Electrolyte

被引:53
作者
Seitzman, Natalie [1 ]
Guthrey, Harvey [2 ]
Sulas, Dana B. [2 ]
Platt, Heather A. S. [3 ]
Al-Jassim, Mowafak [2 ]
Pylypenko, Svitlana [1 ]
机构
[1] Colorado Sch Mines, Dept Chem, Mat Sci Program, Golden, CO 80401 USA
[2] Natl Renewable Energy Lab, Golden, CO 80401 USA
[3] Solid Power Inc, Louisville, CO 80027 USA
关键词
X-RAY; METAL ANODE; DEPOSITION;
D O I
10.1149/2.0301816jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
All-solid lithium batteries are an attractive next-generation technology that use ion-conducting solids such as beta-Li3PS4 (LPS) to enable use of a lithium metal anode, which increases theoretical capacity and widens the stable voltage window over traditional lithium-ion systems. These ion-conductive solids also provide increased safety by replacing flammable liquid electrolytes. Although solid-state electrolytes are significantly more stable and dendrite-resistant than traditional liquid electrolytes, lithium anodes in all-solid systems may nevertheless grow dendrites under high stress or repeated cycling, leading to short circuits and premature battery breakdown. For this reason, we study the formation and propagation of Li metal features within solid electrolytes using synchrotron-based X-ray tomography with in-situ current-voltage cycling supported by our custom sample platform. Our results demonstrate the ability of this technique to delineate different layers of the Li/LPS/Li structure with spatial resolution approaching 1 mu m. At this resolution, we are able to detect expansion of voids, especially in early stages of cycling. This expansion of voids is observed throughout the volume of the symmetric cells and visually resembles propagation of cracks resulting from interactions between the Li metal and pre-existing voids in the LPS electrolyte. (C) 2018 The Electrochemical Society.
引用
收藏
页码:A3732 / A3737
页数:6
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