Combining Superionic Conduction and Favorable Decomposition Products in the Crystalline Lithium-Boron-Sulfur System: A New Mechanism for Stabilizing Solid Li-Ion Electrolytes

被引:27
作者
Sendek, Austin D. [1 ,2 ,3 ]
Antoniuk, Evan R. [4 ]
Cubuk, Ekin D. [5 ]
Ransom, Brandi [2 ]
Francisco, Brian E. [6 ]
Buettner-Garrett, Josh [6 ]
Cui, Yi [2 ]
Reed, Evan J. [2 ]
机构
[1] Stanford Univ, Dept Appl Phys, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Mat Sci & Engn, Stanford, CA 94305 USA
[3] Aionics Inc, Evanston, WY 82930 USA
[4] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
[5] Google Brain, Google Brain, CA 94043 USA
[6] Solid Power Inc, Louisville, CO 80027 USA
关键词
solid ion conductor; solid electrolyte; Li-ion battery; density functional theory; ion transport; electrochemical stability; kinetics; STATE BATTERIES; PHASE-STABILITY; DENSITY; DYNAMICS; CATHODES; GLASSES; NMR; MN; FE;
D O I
10.1021/acsami.9b19091
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
We report a solid-state Li-ion electrolyte predicted to exhibit simultaneously fast ionic conductivity, wide electrochemical stability, low cost, and low mass density. We report exceptional density functional theory (DFT)-based room-temperature single-crystal ionic conductivity values for two phases within the crystalline lithium-boron-sulfur (Li-B-S) system: 62 (+9, -2) mS cm(-1) in Li5B7S13 and 80 (-56, -41) mS cm(-1) in Li9B19S33. We report significant ionic conductivity values for two additional phases: between 0.0056 and 0.16 mS/cm(-1) in Li2B2S5 and between 0.0031 and 9.7 mS cm(-1) in Li3BS3 depending on the room-temperature extrapolation scheme used. To our knowledge, our prediction gives Li9B19S33 and Li5B7S13 the second and third highest reported DFT-computed single-crystal ionic conductivities of any crystalline material. We compute the thermodynamic electrochemical stability window widths of these materials to be 0.50 V for Li5B7S13, 0.16 V for Li2B2S5, 0.45 V for Li3BS3, and 0.60 V for Li9B19S33. Individually, these materials exhibit similar or better ionic conductivity and electrochemical stability than the best-known sulfide-based solid-state Li-ion electrolyte materials, including Li10GeP2S12 (LGPS). However, we predict that electrolyte materials synthesized from a range of compositions in the Li-B-S system may exhibit even wider thermodynamic electrochemical stability windows of 0.63 V and possibly as high as 3 V or greater. The Li-B-S system also has a low elemental cost of approximately 0.05 USD/m(2) per 10 mu m thickness, which is significantly lower than that of germanium-containing LGPS, and a comparable mass density below 2 g/cm(3). These fast-conducting phases were initially brought to our attention by a machine learning-based approach to screen over 12,000 solid electrolyte candidates, and the evidence provided here represents an inspiring success for this model.
引用
收藏
页码:37957 / 37966
页数:10
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