Controllable Crosslinking Enables High‐Ionic‐Conductivity Polymer Electrolyte for Solid‐State Sodium Metal Batteries
Source abstract
Abstract
ABSTRACT Ultraviolet (UV) photo‐crosslinking technology is a research focus in the fabrication of solid‐state polymer electrolytes (SPEs) due to its efficiency, low energy consumption, and eco‐friendliness. However, its inherent uncontrollability elevates polymer network crystallinity, severely compromising ionic conductivity. This study fabricates SPEs with high ionic conductivity through controllable photo‐crosslinking. By strategically incorporating mono‐functional vinyl ethylene carbonate (VEC) into poly (ethylene glycol) diacrylate (PEGDA) to consume crosslinking sites and form “dead‐end” structures, thereby achieving synergistic regulation of crystallinity and crosslinking density. The optimized electrolyte (P 1.5 V 1.5 NB) exhibited a high ionic conductivity of 1.39 × 10 – 3 S cm −1 at 30°C and a wide electrochemical stability window of 4.8 V (vs. Na + /Na). Na‖P 1.5 V 1.5 NB‖Na 3 V 2 (PO 4 ) 3 (NVP) cell delivering 92.62 mAh g −1 at 2C with 89.26% capacity retention after 1000 cycles. This strategy delivers a novel strategy for developing SPEs with high ionic conductivity via controllable photo‐crosslinking, substantially enhancing the electrochemical performance of solid‐state sodium metal batteries (SSMBs).
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Advanced Battery Materials and Technologies · Thermal Expansion and Ionic Conductivity · Advancements in Battery Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
National Engineering Research Center of Vacuum Metallurgy Faculty of Metallurgical and Energy Engineering Kunming University of Science and Technology Kunming China
Key Laboratory for Nonferrous Vacuum Metallurgy of Yunnan Province Kunming China
Frontiers Science Center for New Organic Matter Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education) College of Chemistry Nankai University Tianjin China
Funding
National Natural Science Foundation of China
References (63)
Show source-provided references
1. 10.1002/adma.20231125610.1002/adma.202311256 ↗
2. 10.1016/j.ensm.2025.10455510.1016/j.ensm.2025.104555 ↗
3. 10.1039/D3EE02082G10.1039/D3EE02082G ↗
4. 10.1007/s11431‐024‐2797‐910.1007/s11431‐024‐2797‐9 ↗
5. 10.1021/acs.chemrev.4c0101210.1021/acs.chemrev.4c01012 ↗
6. 10.1039/D2CS01029A10.1039/D2CS01029A ↗
7. 10.1007/s41918‐023‐00196‐410.1007/s41918‐023‐00196‐4 ↗
8. 10.1016/j.chempr.2018.12.00210.1016/j.chempr.2018.12.002 ↗
9. 10.1002/adma.20200072110.1002/adma.202000721 ↗
10. 10.1002/adfm.20221358410.1002/adfm.202213584 ↗
11. 10.1021/acs.chemrev.2c0068610.1021/acs.chemrev.2c00686 ↗
12. 10.1038/s41578‐021‐00320‐010.1038/s41578‐021‐00320‐0 ↗
13. 10.1021/acsenergylett.4c0304310.1021/acsenergylett.4c03043 ↗
14. 10.1016/j.cej.2022.13484310.1016/j.cej.2022.134843 ↗
15. 10.1016/j.jpowsour.2023.23351810.1016/j.jpowsour.2023.233518 ↗
16. 10.1002/adfm.20241117110.1002/adfm.202411171 ↗
17. 10.1002/adfm.20250100510.1002/adfm.202501005 ↗
18. 10.1016/j.jmps.2009.03.00310.1016/j.jmps.2009.03.003 ↗
19. 10.1021/cr300519710.1021/cr3005197 ↗
20. 10.1021/acs.chemrev.9b0081010.1021/acs.chemrev.9b00810 ↗
21. 10.1016/S0079‐6700(01)00004‐110.1016/S0079‐6700(01)00004‐1 ↗
22. 10.1016/j.progpolymsci.2016.04.00210.1016/j.progpolymsci.2016.04.002 ↗
23. 10.1021/ar800075n10.1021/ar800075n ↗
24. 10.1002/adfm.20220808310.1002/adfm.202208083 ↗
25. 10.1016/j.progpolymsci.2024.10184710.1016/j.progpolymsci.2024.101847 ↗
26. 10.1021/acs.macromol.9b0017710.1021/acs.macromol.9b00177 ↗
27. 10.1016/S0009‐2509(01)00287‐110.1016/S0009‐2509(01)00287‐1 ↗
28. 10.1038/s41467‐025‐62742‐610.1038/s41467‐025‐62742‐6 ↗
29. 10.1016/0032‐3861(87)90258‐810.1016/0032‐3861(87)90258‐8 ↗
30. 10.1016/j.progpolymsci.2016.12.01110.1016/j.progpolymsci.2016.12.011 ↗
31. 10.1016/0079‐6700(95)00027‐510.1016/0079‐6700(95)00027‐5 ↗
32. 10.1007/s40820‐024‐01498‐y10.1007/s40820‐024‐01498‐y ↗
33. 10.1007/s41918‐018‐0011‐210.1007/s41918‐018‐0011‐2 ↗
34. 10.1016/j.etran.2023.10026410.1016/j.etran.2023.100264 ↗
35. 10.1016/j.ensm.2024.10318110.1016/j.ensm.2024.103181 ↗
36. 10.1016/j.apmate.2024.10018110.1016/j.apmate.2024.100181 ↗
37. 10.1007/s41918‐025‐00242‐310.1007/s41918‐025‐00242‐3 ↗
38. 10.1016/j.jpowsour.2019.22717510.1016/j.jpowsour.2019.227175 ↗
39. 10.1016/j.ensm.2022.08.01910.1016/j.ensm.2022.08.019 ↗
40. 10.1002/appl.20230003010.1002/appl.202300030 ↗
41. 10.26599/NRE.2023.912005010.26599/NRE.2023.9120050 ↗
42. 10.1016/j.mtener.2024.10157410.1016/j.mtener.2024.101574 ↗
43. 10.1016/j.jechem.2024.06.05210.1016/j.jechem.2024.06.052 ↗
44. 10.1016/j.jpowsour.2019.01.01710.1016/j.jpowsour.2019.01.017 ↗
45. 10.1002/smtd.20240222010.1002/smtd.202402220 ↗
46. 10.1002/eem2.1267010.1002/eem2.12670 ↗
47. 10.1002/aenm.20240080810.1002/aenm.202400808 ↗
48. 10.1021/acsami.1c0754710.1021/acsami.1c07547 ↗
49. 10.1002/aenm.20230394010.1002/aenm.202303940 ↗
50. 10.1002/adfm.20231095710.1002/adfm.202310957 ↗
51. 10.1016/j.jechem.2025.04.07610.1016/j.jechem.2025.04.076 ↗
52. 10.1016/j.jechem.2025.04.07410.1016/j.jechem.2025.04.074 ↗
53. 10.1016/0032‐3861(79)90268‐410.1016/0032‐3861(79)90268‐4 ↗
54. 10.1063/1.172379110.1063/1.1723791 ↗
55. 10.1002/anie.20210919010.1002/anie.202109190 ↗
56. 10.1002/anie.20230873810.1002/anie.202308738 ↗
57. 10.1002/mame.20240038310.1002/mame.202400383 ↗
58. 10.1016/0378‐3812(81)80010‐610.1016/0378‐3812(81)80010‐6 ↗
59. 10.1016/j.ensm.2025.10453310.1016/j.ensm.2025.104533 ↗
60. 10.1021/acsaem.1c0157310.1021/acsaem.1c01573 ↗
61. 10.1002/sus2.7000410.1002/sus2.70004 ↗
62. 10.1021/acsenergylett.5c0102510.1021/acsenergylett.5c01025 ↗
63. 10.1016/j.jcis.2024.04.04610.1016/j.jcis.2024.04.046 ↗