Transition of lithium growth mechanisms in liquid electrolytes

被引:1298
作者
Bai, Peng [1 ]
Li, Ju [2 ,3 ]
Brushett, Fikile R. [1 ]
Bazant, Martin Z. [1 ,4 ,5 ,6 ]
机构
[1] MIT, Dept Chem Engn, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[2] MIT, Dept Nucl Sci & Engn, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[3] MIT, Dept Mat Sci & Engn, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[4] MIT, Dept Math, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[5] Stanford Univ, Dept Mat Sci & Engn, Stanford, CA 94305 USA
[6] Stanford Univ, SUNCAT Interfacial Sci & Catalysis, Stanford, CA 94305 USA
关键词
DENDRITIC GROWTH; ION BATTERIES; METAL; ELECTRODEPOSITION; LI; MORPHOLOGY; DEPOSITION; ANODES; LAYER; SALTS;
D O I
10.1039/c6ee01674j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Next-generation high-energy batteries will require a rechargeable lithium metal anode, but lithium dendrites tend to form during recharging, causing short-circuit risk and capacity loss, by mechanisms that still remain elusive. Here, we visualize lithium growth in a glass capillary cell and demonstrate a change of mechanism from root-growing mossy lithium to tip-growing dendritic lithium at the onset of electrolyte diffusion limitation. In sandwich cells, we further demonstrate that mossy lithium can be blocked by nanoporous ceramic separators, while dendritic lithium can easily penetrate nanopores and short the cell. Our results imply a fundamental design constraint for metal batteries ("Sand's capacity''), which can be increased by using concentrated electrolytes with stiff, permeable, nanoporous separators for improved safety.
引用
收藏
页码:3221 / 3229
页数:9
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