Application of Rod-Like Li6PS5Cl Directly Synthesized by a Liquid Phase Process to Sheet-Type Electrodes for All-Solid-State Lithium Batteries
Source abstract
Abstract
All-solid-state lithium batteries employing sulfide-based solid electrolytes have emerged as promising next-generation batteries for large-scale energy storage applications because of their safety and high energy density. Among them, Li 6 PS 5 X (X = Cl, Br, I) with an argyrodite structure synthesized by planetary milling exhibits a rather high lithium ion conductivity of 10 −2 – 10 −3 S cm −1 at room temperature. Unfortunately, the planetary milling process has the disadvantage of producing the solid electrolytes with large, round-shaped particles. Recently, the solid electrolytes have been synthesized by not the mechanical milling but the liquid-phase process, which facilitates synthesis of sub-micrometer- to nanometer-sized solid electrolyte particles. It is important to reduce the particle size of the solid electrolyte to promote intimate contact with the active material in the composite cathode. Here, rod-like Li 6 PS 5 Cl solid electrolyte with a high ionic conductivity of 1.1 × 10 −3 S cm −1 at room temperature was, for the first time, directly prepared by a liquid phase process using only a stirring method. SEM images showed the electrolyte had a rod-like morphology with a length of 20–30 μm and a width of 2–3 μm. The composite cathode was prepared from a slurry and the cell performances were investigated.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Battery Materials and Technologies · Advancements in Battery Materials · Inorganic Chemistry and Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (36)
Show source-provided references
1. 10.5796/electrochemistry.80.74910.5796/electrochemistry.80.749 ↗
2. 10.1016/j.ssi.2007.05.02010.1016/j.ssi.2007.05.020 ↗
3. 10.1016/j.apsusc.2018.02.27010.1016/j.apsusc.2018.02.270 ↗
4. 10.1016/j.ssi.2015.09.01010.1016/j.ssi.2015.09.010 ↗
5. 10.1016/j.jpowsour.2015.05.09310.1016/j.jpowsour.2015.05.093 ↗
6. 10.1039/C8TA07652A10.1039/C8TA07652A ↗
7. 10.1021/acs.chemmater.7b0484210.1021/acs.chemmater.7b04842 ↗
8. 10.1021/acs.nanolett.6b0175410.1021/acs.nanolett.6b01754 ↗
9. 10.1021/acs.nanolett.6b0344810.1021/acs.nanolett.6b03448 ↗
10. 10.1016/j.jpowsour.2014.08.02410.1016/j.jpowsour.2014.08.024 ↗
11. 10.1007/s11581-017-2035-810.1007/s11581-017-2035-8 ↗
12. 10.1016/j.ssi.2012.06.00810.1016/j.ssi.2012.06.008 ↗
13. 10.1016/j.jpowsour.2017.11.03110.1016/j.jpowsour.2017.11.031 ↗
14. 10.1149/1.177521810.1149/1.1775218 ↗
15. 10.1007/s10008-011-1572-810.1007/s10008-011-1572-8 ↗
16. 10.1016/j.jpowsour.2018.06.01110.1016/j.jpowsour.2018.06.011 ↗
17. 10.1016/j.ssi.2015.11.01910.1016/j.ssi.2015.11.019 ↗
18. 10.2109/jcersj2.1801110.2109/jcersj2.18011 ↗
19. 10.1021/acsami.5b0936710.1021/acsami.5b09367 ↗
20. 10.1016/j.jnoncrysol.2011.08.03010.1016/j.jnoncrysol.2011.08.030 ↗
21. Krishnan R. S. , in Essays in Structural Chemistry, Downs A. J. Long D. A. Staveley L. A. K. Editors, p. 189, Springer US, Boston, MA (1971).
22. 10.1016/j.apcatb.2016.10.07310.1016/j.apcatb.2016.10.073 ↗
23. 10.1016/j.electacta.2016.09.15510.1016/j.electacta.2016.09.155 ↗
24. 10.1016/j.jpowsour.2015.05.09310.1016/j.jpowsour.2015.05.093 ↗
25. 10.1021/ja311089510.1021/ja3110895 ↗
26. 10.1038/3505004710.1038/35050047 ↗
27. 10.1002/aenm.20180003510.1002/aenm.201800035 ↗
28. 10.1021/cm901819c10.1021/cm901819c ↗
29. 10.1149/1.193361610.1149/1.1933616 ↗
30. 10.1021/acs.nanolett.7b0033010.1021/acs.nanolett.7b00330 ↗
31. 10.1039/C7TA01147D10.1039/C7TA01147D ↗
32. 10.2109/jcersj2.1811410.2109/jcersj2.18114 ↗
33. 10.1016/j.ceramint.2017.08.17610.1016/j.ceramint.2017.08.176 ↗
34. 10.1002/adma.20150500810.1002/adma.201505008 ↗
35. 10.1149/1.300597210.1149/1.3005972 ↗
36. 10.1021/acsami.7b0113710.1021/acsami.7b01137 ↗