Stabilizing Li-Metal Electrode via Anion-Induced Desolvation in a Covalent Organic Framework Separator
Source abstract
Abstract
Although Li-metal batteries have been widely used as high-capacity batteries, they are highly susceptible to electrolytes that lead to dendritic or dead Li growth, which significantly reduces the stability of Li-metal electrodes. Herein, we report an anionic covalent organic framework (sulfonate COF: Bd-COF) as a Li + -solvate dissociator that strips solvent molecules from encapsulated Li + to stabilize Li-metal electrodes. The homogeneous and dense ionic COF separator was prepared using a template-assisted interface in-suit polymerization engineering. Notably, the well-developed anionic groups within the COF channels could as counter-charge ligands to Li +, that adsorb Li + -solvates and induce their partial desolvation. Meanwhile, the ordered anionic groups on the surface of COF pores provide continuous ion channels for Li + migration, facilitating the removal of solvent molecules from Li + -solvated species. Combined with the dense nanoporous feature, the COF membrane was found to be effective in suppressing Li-dendrites and parasitic reactions. The Bd-COF/Celgard membrane realizes uniform Li deposition on Li-metal electrodes, exhibiting excellent cycling performance in Li-symmetric batteries and high-voltage Li-metal batteries with LiNi 0.6 Mn 0.2 Co 0.2 O 2 cathodes, showcasing the application prospects of ion-conductive covalent organic frameworks in lithium battery separators.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Battery Materials and Technologies · Advancements in Battery Materials · Covalent Organic Framework Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Institute of Nuclear and New Energy Technology
Tsinghua University
Funding
Ministry of Science and Technology of the People's Republic of China · Tsinghua University · National Natural Science Foundation of China
References (56)
Show source-provided references
1. 10.1038/3510464410.1038/35104644 ↗
2. 10.1038/natrevmats.2016.1310.1038/natrevmats.2016.13 ↗
3. 10.1002/adma.20180056110.1002/adma.201800561 ↗
4. 10.1039/c3cs60177c10.1039/c3cs60177c ↗
5. 10.1038/s41565-018-0183-210.1038/s41565-018-0183-2 ↗
6. 10.1021/acs.chemrev.8b0042210.1021/acs.chemrev.8b00422 ↗
7. 10.1039/C9CS00838A10.1039/C9CS00838A ↗
8. 10.1038/nnano.2017.1610.1038/nnano.2017.16 ↗
9. 10.1126/science.aap878710.1126/science.aap8787 ↗
10. 10.1007/s12274-023-5441-410.1007/s12274-023-5441-4 ↗
11. 10.1016/j.ensm.2022.03.03310.1016/j.ensm.2022.03.033 ↗
12. 10.1126/science.abm630410.1126/science.abm6304 ↗
13. 10.1016/j.ccr.2022.21443110.1016/j.ccr.2022.214431 ↗
14. 10.1002/adma.20200128410.1002/adma.202001284 ↗
15. 10.1021/jacs.0c0597010.1021/jacs.0c05970 ↗
16. 10.1002/anie.20210519010.1002/anie.202105190 ↗
17. 10.1038/s41467-022-28643-810.1038/s41467-022-28643-8 ↗
18. 10.1021/acsnano.2c0476710.1021/acsnano.2c04767 ↗
19. 10.1002/anie.20141126210.1002/anie.201411262 ↗
20. 10.1002/adma.20150500410.1002/adma.201505004 ↗
21. 10.1021/jacs.0c1131310.1021/jacs.0c11313 ↗
22. 10.1002/advs.20180236510.1002/advs.201802365 ↗
23. 10.1002/smll.20200107010.1002/smll.202001070 ↗
24. 10.1021/jacs.2c0570110.1021/jacs.2c05701 ↗
25. 10.1002/ange.20221890810.1002/ange.202218908 ↗
26. 10.1002/anie.20150170610.1002/anie.201501706 ↗
27. 10.1002/aenm.20210032110.1002/aenm.202100321 ↗
28. 10.1007/s40820-024-01485-310.1007/s40820-024-01485-3 ↗
29. 10.1002/adma.20241302210.1002/adma.202413022 ↗
30. 10.1002/adfm.20210008310.1002/adfm.202100083 ↗
31. 10.1038/nmat461110.1038/nmat4611 ↗
32. 10.1002/adfm.20170555310.1002/adfm.201705553 ↗
33. 10.1039/D0CS00786B10.1039/D0CS00786B ↗
34. 10.1002/anie.20201579010.1002/anie.202015790 ↗
35. 10.1002/ange.20240651110.1002/ange.202406511 ↗
36. 10.1002/anie.20171063310.1002/anie.201710633 ↗
37. 10.1002/ange.20230745910.1002/ange.202307459 ↗
38. 10.1038/s41563-021-01052-w10.1038/s41563-021-01052-w ↗
39. 10.1038/s41467-022-33868-810.1038/s41467-022-33868-8 ↗
40. 10.1002/adma.20170443610.1002/adma.201704436 ↗
41. 10.1016/j.ensm.2022.02.01410.1016/j.ensm.2022.02.014 ↗
42. 10.1021/jacs.9b0244810.1021/jacs.9b02448 ↗
43. 10.1016/j.ensm.2019.10.01810.1016/j.ensm.2019.10.018 ↗
44. 10.1002/advs.20230808710.1002/advs.202308087 ↗
45. 10.1021/acsenergylett.4c0194110.1021/acsenergylett.4c01941 ↗
46. 10.1016/j.joule.2020.06.01610.1016/j.joule.2020.06.016 ↗
47. 10.1038/s41565-019-0604-x10.1038/s41565-019-0604-x ↗
48. 10.1002/adma.20220600910.1002/adma.202206009 ↗
49. 10.1002/adma.20231307610.1002/adma.202313076 ↗
50. 10.1038/s41557-024-01585-y10.1038/s41557-024-01585-y ↗
51. 10.1038/s41467-021-27841-010.1038/s41467-021-27841-0 ↗
52. 10.1039/D0CS01017K10.1039/D0CS01017K ↗
53. 10.1039/D3CS00151B10.1039/D3CS00151B ↗
54. 10.1016/j.joule.2020.06.01110.1016/j.joule.2020.06.011 ↗
55. 10.1002/anie.20210412410.1002/anie.202104124 ↗
56. 10.1002/adma.20220133910.1002/adma.202201339 ↗