Gel Polymer Electrolyte with High Li+ Transference Number Enhancing the Cycling Stability of Lithium Anodes
Source abstract
Abstract
Lithium anodes suffer from severe safety problems in liquid electrolyte systems that result from an unstable Li plating/stripping process and Li dendrite growth, leading to rapid degradation of Li metal batteries. A polyethylene (PE)-supported gel polymer electrolyte (GPE) with excellent electrolyte uptake/retention capability was simply prepared in this paper by the construction of cross-linked polymer networks (PNs) on the surface of a poly(ethylenimine)-primed PE separator to stabilize the lithium anode. The highly delocalized negative charge of p-styrene sulfonate groups on PNs plays a role in regulating the Li+ and anion transport, giving rise to a high Li+ transference number. This GPE extended the electrochemical stability to 4.8 V and improved the stability of interface between the electrolyte and lithium metal anode (reduced overpotential and suppressed lithium dendrites) during storage and repeated lithium plating/stripping cycling. The Li metal anode-based battery employing this GPE exhibits excellent cycling stability and C-rate capability.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Battery Materials and Technologies · Advancements in Battery Materials · Advanced Battery Technologies Research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Research Center of Nanoscience and Nanotechnology, Shanghai University, Shanghai 200444, China
Department of Chemistry-Ångström Laboratory, Uppsala University, Uppsala 75121, Sweden
Emerging Industries Institute, Shanghai University, Jiaxing, Zhejiang 314006, China
Funding
Vetenskapsr?det · National Natural Science Foundation of China
References (40)
Show source-provided references
1. 10.1016/j.ensm.2017.12.00210.1016/j.ensm.2017.12.002 ↗
2. 10.1038/natrevmats.2016.1310.1038/natrevmats.2016.13 ↗
3. 10.1002/admi.20170109710.1002/admi.201701097 ↗
4. 10.1021/acs.chemrev.7b0011510.1021/acs.chemrev.7b00115 ↗
5. 10.1038/nnano.2017.1610.1038/nnano.2017.16 ↗
6. 10.1021/acsenergylett.6b0025910.1021/acsenergylett.6b00259 ↗
7. 10.1021/acs.chemmater.6b0524710.1021/acs.chemmater.6b05247 ↗
8. 10.1016/j.jpowsour.2015.06.04410.1016/j.jpowsour.2015.06.044 ↗
9. 10.1021/acs.chemmater.7b0009110.1021/acs.chemmater.7b00091 ↗
10. 10.1021/acs.chemmater.7b0149610.1021/acs.chemmater.7b01496 ↗
11. 10.1007/s12274-017-1647-710.1007/s12274-017-1647-7 ↗
12. 10.1246/cl.17028410.1246/cl.170284 ↗
13. 10.5796/electrochemistry.85.55910.5796/electrochemistry.85.559 ↗
14. 10.1002/adfm.20170034810.1002/adfm.201700348 ↗
15. 10.1073/pnas.161948911410.1073/pnas.1619489114 ↗
16. 10.1002/adma.20170000710.1002/adma.201700007 ↗
17. 10.1016/j.nanoen.2017.01.02810.1016/j.nanoen.2017.01.028 ↗
18. 10.1002/aenm.20170265710.1002/aenm.201702657 ↗
19. 10.1002/smll.20170300110.1002/smll.201703001 ↗
20. 10.1002/aenm.20170218410.1002/aenm.201702184 ↗
21. 10.1021/acsenergylett.7b0079210.1021/acsenergylett.7b00792 ↗
22. 10.1021/acsami.5b0609610.1021/acsami.5b06096 ↗
23. 10.1021/acs.macromol.5b0119310.1021/acs.macromol.5b01193 ↗
24. 10.1016/j.polymer.2016.07.09010.1016/j.polymer.2016.07.090 ↗
25. 10.1021/acsami.6b0960110.1021/acsami.6b09601 ↗
26. 10.3144/expresspolymlett.2017.510.3144/expresspolymlett.2017.5 ↗
27. 10.1021/acs.jpclett.6b0266210.1021/acs.jpclett.6b02662 ↗
28. 10.1021/am508149n10.1021/am508149n ↗
29. 10.1016/j.electacta.2017.10.12010.1016/j.electacta.2017.10.120 ↗
30. 10.1016/j.jpowsour.2016.06.05010.1016/j.jpowsour.2016.06.050 ↗
31. 10.1021/acs.chemmater.6b0219010.1021/acs.chemmater.6b02190 ↗
32. 10.4236/msa.2012.3606010.4236/msa.2012.36060 ↗
33. 10.1039/c4ta03570d10.1039/c4ta03570d ↗
34. 10.1016/j.electacta.2016.03.18910.1016/j.electacta.2016.03.189 ↗
35. 10.1002/aenm.20110068710.1002/aenm.201100687 ↗
36. 10.1039/c1jm12246k10.1039/c1jm12246k ↗
37. 10.1016/j.jpowsour.2009.10.08510.1016/j.jpowsour.2009.10.085 ↗
38. 10.1039/c3ee40795k10.1039/c3ee40795k ↗
39. 10.1002/adfm.20140093510.1002/adfm.201400935 ↗
40. 10.1149/1.160668610.1149/1.1606686 ↗