journal article·2016

Enhancement on the Cycling Stability of the Layered Ni-Rich Oxide Cathode by In-Situ Fabricating Nano-Thickness Cation-Mixing Layers

Jun Yang, Yongyao Xia

Publisher page

Abstract

The layered Ni-rich oxide cathode (LiNi 0.8 Co 0.1 Mn 0.1 O 2 ) has been significantly attractive due to its large reversible capacity (200 mAh g −1 ). However, the layered Ni-rich oxide cathode suffers from a tremendous structural degradation during long-term cycling, causing the drastic rise of electrode impedance and deterioration of the capacity retention. In this paper, we develop a novel and facile approach to stabilize its structure by per-cycling of the layered Ni-rich oxide cathode at high voltage of 4.5 V (vs Li/Li + ). The nano-thickness cation-mixing layers with Fm-3m structure were in-situ formed on the layered Ni-rich oxide LiNi 0.8 Co 0.1 Mn 0.1 O 2 cathode by the surface structural transition from rhombohedral phase to cubic phase. The as-prepared LiNi 0.8 Co 0.1 Mn 0.1 O 2 cathode coated with the nano-thickness cation-mixing layers shows superior cycling life at a cutoff voltage of 4.3 V, and it keeps a capacity retention of 83% after 500 cycles, which could be attributed to that the nano-thickness cation-mixing layers stabilize the structure of LiNi 0.8 Co 0.1 Mn 0.1 O 2 during long-term cycling.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Supercapacitor Materials and Fabrication

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

References (32)

Show source-provided references
1. 10.1038/3510464410.1038/35104644 ↗
2. 10.1038/451652a10.1038/451652a ↗
3. 10.1021/cr020731c10.1021/cr020731c ↗
4. 10.1016/j.electacta.2013.11.18610.1016/j.electacta.2013.11.186 ↗
5. 10.1021/nn305065u10.1021/nn305065u ↗
6. 10.1016/S0378-7753(01)00700-510.1016/S0378-7753(01)00700-5 ↗
7. 10.1016/j.jpowsour.2011.05.01710.1016/j.jpowsour.2011.05.017 ↗
8. 10.1002/adfm.20120069310.1002/adfm.201200693 ↗
9. 10.1021/cm403332s10.1021/cm403332s ↗
10. 10.1021/cm201452q10.1021/cm201452q ↗
11. 10.1063/1.489533610.1063/1.4895336 ↗
12. 10.1002/aenm.20130078710.1002/aenm.201300787 ↗
13. 10.1149/1.307613710.1149/1.3076137 ↗
14. 10.1021/nl304558t10.1021/nl304558t ↗
15. 10.1021/acs.nanolett.5b0004510.1021/acs.nanolett.5b00045 ↗
16. 10.1002/anie.20140926210.1002/anie.201409262 ↗
17. 10.1016/j.electacta.2014.06.07910.1016/j.electacta.2014.06.079 ↗
18. 10.1021/acsami.5b0078810.1021/acsami.5b00788 ↗
19. 10.1021/am503278f10.1021/am503278f ↗
20. 10.1021/acsami.5b0064510.1021/acsami.5b00645 ↗
21. 10.1016/S0013-4686(99)00402-810.1016/S0013-4686(99)00402-8 ↗
22. 10.1021/acsami.5b0993810.1021/acsami.5b09938 ↗
23. 10.1016/j.electacta.2015.12.08010.1016/j.electacta.2015.12.080 ↗
24. 10.1149/1.195492710.1149/1.1954927 ↗
25. 10.1039/c0jm01971b10.1039/c0jm01971b ↗
26. 10.1149/2.005207jes10.1149/2.005207jes ↗
27. 10.1016/S0167-2738(99)00334-310.1016/S0167-2738(99)00334-3 ↗
28. 10.1016/S0167-2738(00)00699-810.1016/S0167-2738(00)00699-8 ↗
29. 10.1016/S0378-7753(00)00653-410.1016/S0378-7753(00)00653-4 ↗
30. 10.1016/j.jpowsour.2007.06.09210.1016/j.jpowsour.2007.06.092 ↗
31. 10.1149/1.298872910.1149/1.2988729 ↗
32. 10.1016/j.elecom.2013.04.01510.1016/j.elecom.2013.04.015 ↗