journal article·2024-07-12Open access

Compliant Solid Polymer Electrolytes (SPEs) for Enhanced Anode-Electrolyte Interfacial Stability in All-Solid-State Lithium–Metal Batteries (LMBs)

William R. Fullerton, Christopher Y. Li

ACS Applied Polymer Materials· Volume 6· Issue 13

Abstract

High Resolution Image Download MS PowerPoint Slide Practical application of high energy density lithium–metal batteries (LMBs) has remained elusive over the last several decades due to their unstable and dendritic electrodeposition behavior. Solid polymer electrolytes (SPEs) with sufficient elastic modulus have been shown to attenuate dendrite growth and extend cycle life. Among different polymer architectures, network SPEs have demonstrated promising overall performance in cells using lithium metal anodes. However, fine-tuning network structures to attain adequate lithium electrode interfacial contact and stable electrodeposition behavior at extended cycling remains a challenge. In this work, we designed a series of comb-chain cross-linker-based network SPEs with tunable compliance by introducing free dangling chains into the SPE network. These dangling chains were used to tune the SPE ionic conductivity, ductility, and compliance. Our results demonstrate that increasing network compliance and ductility improves anode-electrolyte interfacial adhesion and reduces voltage hysteresis. SPEs with 56.3 wt % free dangling chain content showed a high Coulombic efficiency of 93.4% and a symmetric cell cycle life 1.9× that of SPEs without free chains. Additionally, the improved anode compliance of these SPEs led to reduced anode-electrolyte interfacial resistance growth and greater capacity retention at 92.8% when cycled at 1C in Li|SPE|LiFePO 4 half cells for 275 cycles.
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

Department of Materials Science and Engineering, Drexel University, Philadelphia, Pennsylvania 19104, United States

Funding

National Science Foundation

References (63)

Show source-provided references
1. 10.1021/cm901452z10.1021/cm901452z ↗
2. 10.1039/C3EE40795K10.1039/C3EE40795K ↗
3. 10.1039/C6TA02621D10.1039/C6TA02621D ↗
4. 10.1038/nenergy.2016.11410.1038/nenergy.2016.114 ↗
5. 10.1038/nnano.2017.1610.1038/nnano.2017.16 ↗
6. 10.1038/s41578-019-0103-610.1038/s41578-019-0103-6 ↗
7. 10.1016/S0167-2738(02)00080-210.1016/S0167-2738(02)00080-2 ↗
8. 10.1021/acs.chemrev.0c0027510.1021/acs.chemrev.0c00275 ↗
9. 10.1016/j.xcrp.2020.10011910.1016/j.xcrp.2020.100119 ↗
10. 10.1038/s41578-019-0165-510.1038/s41578-019-0165-5 ↗
11. 10.1149/1.160668610.1149/1.1606686 ↗
12. 10.1149/1.185085410.1149/1.1850854 ↗
13. 10.1149/2.030203jes10.1149/2.030203jes ↗
14. 10.1149/2.030303jes10.1149/2.030303jes ↗
15. 10.1149/2.117309jes10.1149/2.117309jes ↗
16. 10.1149/2.0721507jes10.1149/2.0721507jes ↗
17. 10.1149/2.0321514jes10.1149/2.0321514jes ↗
18. 10.1149/1.347423210.1149/1.3474232 ↗
19. 10.1016/j.jpowsour.2014.04.06510.1016/j.jpowsour.2014.04.065 ↗
20. 10.1016/j.elecom.2015.05.00110.1016/j.elecom.2015.05.001 ↗
21. 10.1039/C9EE01548E10.1039/C9EE01548E ↗
22. 10.1149/1.137902810.1149/1.1379028 ↗
23. 10.1038/nmat306610.1038/nmat3066 ↗
24. 10.1038/nenergy.2016.3010.1038/nenergy.2016.30 ↗
25. 10.1016/j.joule.2019.06.01710.1016/j.joule.2019.06.017 ↗
26. 10.1038/s41563-019-0438-910.1038/s41563-019-0438-9 ↗
27. 10.1021/acsami.9b0253710.1021/acsami.9b02537 ↗
28. 10.1021/ja502133j10.1021/ja502133j ↗
29. 10.1002/adma.20150205910.1002/adma.201502059 ↗
30. 10.1039/C6SC01813K10.1039/C6SC01813K ↗
31. 10.1073/pnas.180338511510.1073/pnas.1803385115 ↗
32. 10.1021/acs.nanolett.0c0303310.1021/acs.nanolett.0c03033 ↗
33. 10.1021/acs.macromol.0c0047510.1021/acs.macromol.0c00475 ↗
34. 10.1021/acsami.1c1318610.1021/acsami.1c13186 ↗
35. 10.1016/j.cej.2021.13344210.1016/j.cej.2021.133442 ↗
36. 10.1016/j.jpowsour.2018.07.00810.1016/j.jpowsour.2018.07.008 ↗
37. 10.1002/adma.20180414210.1002/adma.201804142 ↗
38. 10.1002/anie.20191047810.1002/anie.201910478 ↗
39. 10.1021/acs.macromol.9b0230510.1021/acs.macromol.9b02305 ↗
40. 10.1021/acsaem.1c0285710.1021/acsaem.1c02857 ↗
41. 10.1002/admi.20180144510.1002/admi.201801445 ↗
42. 10.1016/j.ensm.2020.04.00210.1016/j.ensm.2020.04.002 ↗
43. 10.1038/s41560-019-0349-710.1038/s41560-019-0349-7 ↗
44. 10.1002/anie.20190158210.1002/anie.201901582 ↗
45. 10.1038/s41598-020-61373-910.1038/s41598-020-61373-9 ↗
46. 10.1149/1945-7111/ac2d8b10.1149/1945-7111/ac2d8b ↗
47. 10.1021/acs.macromol.5b0172410.1021/acs.macromol.5b01724 ↗
48. 10.1039/C7TA00371D10.1039/C7TA00371D ↗
49. 10.1021/acscentsci.6b0026010.1021/acscentsci.6b00260 ↗
50. 10.1126/sciadv.add051010.1126/sciadv.add0510 ↗
51. 10.1016/j.joule.2023.07.02210.1016/j.joule.2023.07.022 ↗
52. 10.1016/j.cej.2020.12651710.1016/j.cej.2020.126517 ↗
53. 10.1016/j.jpowsour.2017.11.08210.1016/j.jpowsour.2017.11.082 ↗
54. 10.1016/j.jpowsour.2017.11.07810.1016/j.jpowsour.2017.11.078 ↗
55. 10.1016/j.joule.2019.03.02210.1016/j.joule.2019.03.022 ↗
56. 10.1016/j.jpowsour.2018.08.07710.1016/j.jpowsour.2018.08.077 ↗
57. 10.1016/j.ensm.2019.03.00410.1016/j.ensm.2019.03.004 ↗
58. 10.1002/aenm.20190276710.1002/aenm.201902767 ↗
59. 10.1002/aenm.20210372010.1002/aenm.202103720 ↗
60. 10.1038/s41467-022-35636-010.1038/s41467-022-35636-0 ↗
61. 10.1021/acsami.9b0998510.1021/acsami.9b09985 ↗
62. 10.1021/cm047846c10.1021/cm047846c ↗
63. 10.1002/adfm.20080078910.1002/adfm.200800789 ↗