Minimized Metal Dissolution from High-Energy Nickel Cobalt Manganese Oxide Cathodes with Al2O3 Coating and Its Effects on Electrolyte Decomposition on Graphite Anodes
Source abstract
Abstract
High-energy nickel cobalt manganese oxides have been studied intensively as cathode materials for lithium-ion batteries. However, several hurdles need to be overcome to adopt these cathodes in commercial lithium-ion batteries. Herein, aluminum oxide (Al 2 O 3 ) coating was applied to high-energy nickel cobalt manganese oxides (HE-NCM, Li 1.33 Ni 0.27 Co 0.13 Mn 0.60 O 2+d ) by atomic layer deposition (ALD) and its effects on HE-NCM/graphite full cells were investigated. HE-NCM/graphite full cells have better cycling performance and efficiency when HE-NCM is coated with Al 2 O 3 . ICP-MS measurements show that the Al 2 O 3 coating can effectively prevent transition metal dissolution from HE-NCM. XPS and FT-IR analysis suggests that the surface film on HE-NCM cathodes does not change significantly with the Al 2 O 3 coating even after 50 cycles, however the surface film on graphite anodes shows a significant change. The resistance of graphite electrodes cycled with the uncoated HE-NCM is higher than that of graphite electrodes cycled with the Al 2 O 3 -coated HE-NCM due to the increased SEI thickness. The improved cycling performance of HE-NCM/graphite cells with Al 2 O 3 coating can be attributed to the minimized resistance increase on graphite as well as the suppression of cathode active material loss.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · Advanced Battery Technologies Research · Advanced Battery Materials and Technologies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (40)
Show source-provided references
1. 10.1021/jp506731v10.1021/jp506731v ↗
2. 10.1002/aenm.20150101010.1002/aenm.201501010 ↗
3. 10.1016/j.jpowsour.2016.03.10710.1016/j.jpowsour.2016.03.107 ↗
4. 10.1021/acsnano.7b0894510.1021/acsnano.7b08945 ↗
5. 10.1039/C7EE03122J10.1039/C7EE03122J ↗
6. 10.1149/2.0861412jes10.1149/2.0861412jes ↗
7. 10.1016/j.jpowsour.2013.10.04410.1016/j.jpowsour.2013.10.044 ↗
8. 10.1016/j.jpowsour.2012.01.12210.1016/j.jpowsour.2012.01.122 ↗
9. 10.1016/j.electacta.2014.04.09110.1016/j.electacta.2014.04.091 ↗
10. 10.1021/jp405158m10.1021/jp405158m ↗
11. 10.1016/j.jpowsour.2016.08.09910.1016/j.jpowsour.2016.08.099 ↗
12. 10.1149/1.351661910.1149/1.3516619 ↗
13. 10.1016/j.jpowsour.2003.09.03410.1016/j.jpowsour.2003.09.034 ↗
14. 10.1038/ncomms343710.1038/ncomms3437 ↗
15. 10.1149/2.035308jes10.1149/2.035308jes ↗
16. 10.1016/S0013-4686(01)00847-710.1016/S0013-4686(01)00847-7 ↗
17. 10.1021/cm000511k10.1021/cm000511k ↗
18. 10.1021/jp067436710.1021/jp0674367 ↗
19. 10.1038/srep2653210.1038/srep26532 ↗
20. 10.1149/2.0141903jes10.1149/2.0141903jes ↗
21. 10.1149/1.162734710.1149/1.1627347 ↗
22. 10.1149/2.1101609jes10.1149/2.1101609jes ↗
23. 10.1021/acs.chemmater.5b0430110.1021/acs.chemmater.5b04301 ↗
24. 10.1149/2.1111702jes10.1149/2.1111702jes ↗
25. 10.1039/C6TA08865A10.1039/C6TA08865A ↗
26. 10.1149/1.278929910.1149/1.2789299 ↗
27. 10.1002/aenm.20130026910.1002/aenm.201300269 ↗
28. 10.1021/cm900862v10.1021/cm900862v ↗
29. 10.1149/1.186199410.1149/1.1861994 ↗
30. 10.1149/1.139777110.1149/1.1397771 ↗
31. 10.1016/j.jelechem.2005.07.01110.1016/j.jelechem.2005.07.011 ↗
32. 10.1016/j.electacta.2004.06.02110.1016/j.electacta.2004.06.021 ↗
33. 10.1149/1.150563610.1149/1.1505636 ↗
34. 10.1149/1.176377110.1149/1.1763771 ↗
35. 10.1021/jp060152210.1021/jp0601522 ↗
36. 10.1021/acs.jpcc.7b0843310.1021/acs.jpcc.7b08433 ↗
37. 10.1016/j.electacta.2010.05.07210.1016/j.electacta.2010.05.072 ↗
38. 10.1149/1.342851510.1149/1.3428515 ↗
39. 10.1149/1.344775010.1149/1.3447750 ↗
40. 10.1016/j.jpowsour.2007.02.05510.1016/j.jpowsour.2007.02.055 ↗