journal article·2024-01-12

Dynamic Al–O Interactions Enable Uniform Al Deposition toward High Energy-Density and Practical Al Metal Batteries

Long Yao, Shunlong Ju, Guanglin Xia, Dalin Sun, Xuebin Yu

ACS Energy Letters· Volume 9· Issue 1
Publisher page

Abstract

Al batteries exhibit high crustal abundance and theoretical energy density, making them promising candidates as next-generation batteries. However, the poor Al plating/stripping at the Al anode severely limits their potential application. Herein, MXene-induced atomically dispersed MN 4 sites (M = Co, Ni, Cu) containing axial O coordination (MN 4 O 2 ) are demonstrated to show a synergistic effect of dynamic Al–O interactions to induce Al homogeneous deposition. As an example, the single-atomic Co modified Al anode exhibits negligible nucleation overpotential and a long plating lifespan even under unprecedented conditions (areal capacity of 10 mAh cm –2, current density of 40 mA cm –2 ). A practical 323 Wh kg –1 metal Al–S battery is well demonstrated under a 7 mg cm –2 high sulfur loading. These findings provide atomic-scale insights for the regulation of Al deposition and provide an avenue to stabilize the metal Al battery under practical high energy density conditions.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advancements in Battery Materials · MXene and MAX Phase Materials · Advanced Battery Materials and Technologies

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Materials Science, Fudan University, Shanghai 200433, China

Institute of Energy Materials Science, University of Shanghai for Science and Technology, Shanghai 200093, China

Funding

Shanghai Municipal Education Commission · National Natural Science Foundation of China

References (35)

Show source-provided references
1. 10.1126/science.abg395410.1126/science.abg3954 ↗
2. 10.1038/nature1434010.1038/nature14340 ↗
3. 10.1038/s41586-022-04983-910.1038/s41586-022-04983-9 ↗
4. 10.1021/acs.chemrev.0c0125710.1021/acs.chemrev.0c01257 ↗
5. 10.1038/s41560-020-00728-y10.1038/s41560-020-00728-y ↗
6. 10.1038/s41467-021-26056-710.1038/s41467-021-26056-7 ↗
7. 10.1038/s41560-021-00797-710.1038/s41560-021-00797-7 ↗
8. 10.1016/j.ensm.2020.09.01310.1016/j.ensm.2020.09.013 ↗
9. 10.1021/jacs.0c0505410.1021/jacs.0c05054 ↗
10. 10.1038/s41467-022-28238-310.1038/s41467-022-28238-3 ↗
11. 10.1021/jacs.2c0482010.1021/jacs.2c04820 ↗
12. 10.1021/acs.chemrev.0c0059410.1021/acs.chemrev.0c00594 ↗
13. 10.1021/acs.nanolett.1c0053410.1021/acs.nanolett.1c00534 ↗
14. 10.1021/jacs.8b1297310.1021/jacs.8b12973 ↗
15. 10.1002/adma.20200330010.1002/adma.202003300 ↗
16. 10.1016/j.ensm.2020.11.01110.1016/j.ensm.2020.11.011 ↗
17. 10.1002/eem2.1244910.1002/eem2.12449 ↗
18. 10.1002/aenm.20200065110.1002/aenm.202000651 ↗
19. 10.1002/adma.20170689510.1002/adma.201706895 ↗
20. 10.1039/C9EE00536F10.1039/C9EE00536F ↗
21. 10.1002/adma.20190739910.1002/adma.201907399 ↗
22. 10.1002/adma.20210120410.1002/adma.202101204 ↗
23. 10.1039/C8EE02694G10.1039/C8EE02694G ↗
24. 10.1038/s41467-020-18062-y10.1038/s41467-020-18062-y ↗
25. 10.1021/acs.nanolett.1c0053410.1021/acs.nanolett.1c00534 ↗
26. 10.1002/anie.20210255210.1002/anie.202102552 ↗
27. 10.1038/nnano.2016.3210.1038/nnano.2016.32 ↗
28. 10.1002/aenm.20210197610.1002/aenm.202101976 ↗
29. 10.1002/adma.20210502910.1002/adma.202105029 ↗
30. 10.1021/jacs.7b0643710.1021/jacs.7b06437 ↗
31. 10.1016/j.gee.2017.10.00210.1016/j.gee.2017.10.002 ↗
32. 10.1039/D0TA08505G10.1039/D0TA08505G ↗
33. 10.1021/acsami.7b0702410.1021/acsami.7b07024 ↗
34. 10.1002/anie.20220269610.1002/anie.202202696 ↗
35. 10.1016/j.jpowsour.2015.02.13110.1016/j.jpowsour.2015.02.131 ↗