Universal Anion-Interface-Confinement Strategy to Regulate Robust Solid-Electrolyte Interphase for Lithium Metal Batteries
Source abstract
Abstract
The inherent high reactivity of lithium metal and the nonuniform deposition/stripping behavior of Li + during the cycle lead to the deterioration of performance and safety risks of lithium metal batteries. Herein, we designed and fabricated a multifunctional ferroelectric (β-PVDF) composite separator with dipole directional arrangement. Detailed characterization indicates that the directional arrangement of negative dipoles caused by spontaneous polarization of ferroelectric coatings induces anion interface confinement and promotes the complete reduction of lithium salts, thereby constructing a robust solid-electrolyte interphase (SEI) rich in inorganic species on the Li metal anode surface. The SEI can ensure the uniform distribution and rapid migration of Li + as well as high interface stability. As a result, the Li||Li symmetrical cell with ferroelectric composite separator achieves an ultralong cycle life of more than 4000 h at 2.5 mA/cm 2 to 2.5 mAh/cm 2 . The full cell with a high mass loading (12 mg/cm 2 ) of the LiFePO 4 cathode shows a high capacity retention of 96.84% after 960 cycles. This universal strategy may provide a perspective for regulating SEI chemistry by introducing functional coatings with multiphysical fields to regulate and limit anion migration.
Source: openalex_inverted_index · 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
State Key Laboratory of Powder Metallurgy
Central South University
Hunan Key Laboratory of Applied Environmental Photocatalysis
Changsha University
Funding
State Key Laboratory of Powder Metallurgy · Natural Science Foundation of Hunan Province · Education Department of Hunan Province · National Natural Science Foundation of China · Natural Science Foundation of Changsha
References (25)
Show source-provided references
1. 10.1002/advs.20210111110.1002/advs.202101111 ↗
2. 10.1002/aenm.20240010810.1002/aenm.202400108 ↗
3. 10.1021/acsenergylett.3c0091010.1021/acsenergylett.3c00910 ↗
4. 10.1002/advs.20150021310.1002/advs.201500213 ↗
5. 10.1002/adma.20221120310.1002/adma.202211203 ↗
6. 10.1039/D3TA04676A10.1039/D3TA04676A ↗
7. 10.1016/j.matt.2021.09.02510.1016/j.matt.2021.09.025 ↗
8. 10.1002/adma.20230737010.1002/adma.202307370 ↗
9. 10.1021/acs.chemrev.0c0110010.1021/acs.chemrev.0c01100 ↗
10. 10.1126/science.aam601410.1126/science.aam6014 ↗
11. 10.1038/s41570-022-00387-510.1038/s41570-022-00387-5 ↗
12. 10.1016/j.cej.2023.14439110.1016/j.cej.2023.144391 ↗
13. 10.1002/polb.2214510.1002/polb.22145 ↗
14. 10.1016/j.matchemphys.2011.03.07410.1016/j.matchemphys.2011.03.074 ↗
15. 10.1016/j.jece.2022.10839910.1016/j.jece.2022.108399 ↗
16. 10.1038/s41467-023-36853-x10.1038/s41467-023-36853-x ↗
17. 10.1021/cr030203g10.1021/cr030203g ↗
18. 10.1021/acs.nanolett.0c0320610.1021/acs.nanolett.0c03206 ↗
19. 10.1016/j.ensm.2018.09.02410.1016/j.ensm.2018.09.024 ↗
20. 10.1016/j.xcrp.2022.10105710.1016/j.xcrp.2022.101057 ↗
21. 10.1126/sciadv.aau924510.1126/sciadv.aau9245 ↗
22. 10.1002/adfm.20210222810.1002/adfm.202102228 ↗
23. 10.1002/anie.20201200510.1002/anie.202012005 ↗
24. 10.1038/s41560-024-01494-x10.1038/s41560-024-01494-x ↗
25. 10.1016/j.nanoen.2020.10548110.1016/j.nanoen.2020.105481 ↗