Flexible Composite Solid Electrolyte Facilitating Highly Stable “Soft Contacting” Li–Electrolyte Interface for Solid State Lithium‐Ion Batteries
Source abstract
Abstract
Abstract A flexible composite solid electrolyte membrane consisting of inorganic solid particles (Li1.3Al0.3Ti1.7(PO4)3), polyethylene oxide (PEO), and boronized polyethylene glycol (BPEG) is prepared and investigated. This membrane exhibits good stability against lithium dendrite, which can be attributed to its well‐designed combination components: the compact inorganic lithium ion conducting layer provides the membrane with good mechanical strength and physically barricades the free growth of lithium dendrite; while the addition of planar BPEG oligomers not only disorganizes the crystallinity of the PEO domain, leading to good ionic conductivity, but also facilitates a “soft contact” between interfaces, which not only chemically enables homogeneous lithium plating/stripping on the lithium metal anode, but also reduces the polarization effects. In addition, by employing this membrane to a LiFePO4/Li cell and testing its galvanostatic cycling performances at 60 °C, capacities of 158.2 and 94.2 mA h g−1 are delivered at 0.1 C and 2 C, respectively.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Advanced Battery Technologies Research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Advanced Materials Shenzhen Graduate School Peking University Shenzhen 518055 P. R. China
South China Academy of Advanced Optoeletronics South China Normal University Guangzhou 510006 P. R. China
Funding
National Materials Genome Project · Guangdong Innovation Team Project · Shenzhen Science and Technology Research
References (38)
Show source-provided references
1. 10.1038/451652a10.1038/451652a ↗
2. 10.1021/cm901452z10.1021/cm901452z ↗
3. 10.1038/3510464410.1038/35104644 ↗
4. 10.1038/nnano.2016.20710.1038/nnano.2016.207 ↗
5. 10.1039/C6MH00218H10.1039/C6MH00218H ↗
6. 10.1038/1973010.1038/19730 ↗
7. 10.1016/S0378-7753(99)00529-710.1016/S0378-7753(99)00529-7 ↗
8. 10.1016/j.jpowsour.2007.06.23410.1016/j.jpowsour.2007.06.234 ↗
9. 10.1016/j.electacta.2012.06.03810.1016/j.electacta.2012.06.038 ↗
10. 10.1038/natrevmats.2016.10310.1038/natrevmats.2016.103 ↗
11. 10.1021/jp510077z10.1021/jp510077z ↗
12. 10.1039/C5EE01941A10.1039/C5EE01941A ↗
13. 10.1016/j.ssi.2011.06.00110.1016/j.ssi.2011.06.001 ↗
14. 10.1039/C3CC49588D10.1039/C3CC49588D ↗
15. 10.1021/jp305945410.1021/jp3059454 ↗
16. 10.1038/2881810.1038/28818 ↗
17. 10.1002/aenm.20150026510.1002/aenm.201500265 ↗
18. 10.1021/acs.jpcc.6b1113610.1021/acs.jpcc.6b11136 ↗
19. 10.1021/acs.nanolett.5b0060010.1021/acs.nanolett.5b00600 ↗
20. 10.1016/j.jpowsour.2014.10.07810.1016/j.jpowsour.2014.10.078 ↗
21. 10.1149/1.208659710.1149/1.2086597 ↗
22. 10.1016/j.ssi.2014.07.01810.1016/j.ssi.2014.07.018 ↗
23. 10.1021/acs.inorgchem.5b0282110.1021/acs.inorgchem.5b02821 ↗
24. 10.1039/C5TA08545D10.1039/C5TA08545D ↗
25. 10.1016/0032-3861(73)90146-810.1016/0032-3861(73)90146-8 ↗
26. 10.1016/S0013-4686(99)00383-710.1016/S0013-4686(99)00383-7 ↗
27. 10.1016/j.jpowsour.2010.08.02010.1016/j.jpowsour.2010.08.020 ↗
28. 10.1039/C4PY00123K10.1039/C4PY00123K ↗
29. 10.1021/acsami.6b0900810.1021/acsami.6b09008 ↗
30. 10.1021/j100058a00910.1021/j100058a009 ↗
31. 10.1002/anie.20160753910.1002/anie.201607539 ↗
32. 10.1088/0022-3727/41/22/22300110.1088/0022-3727/41/22/223001 ↗
33. 10.1016/j.ssi.2015.06.00110.1016/j.ssi.2015.06.001 ↗
34. 10.1021/nl503125u10.1021/nl503125u ↗
35. 10.1002/adma.20150612410.1002/adma.201506124 ↗
36. 10.1016/j.nanoen.2016.09.00210.1016/j.nanoen.2016.09.002 ↗
37. 10.1016/j.elecom.2015.05.00110.1016/j.elecom.2015.05.001 ↗
38. 10.1016/j.jpowsour.2016.09.04910.1016/j.jpowsour.2016.09.049 ↗