Journal article
Effects of sulfate modification of stoichiometric and lithium-rich LiNiO<sub>2</sub> cathode materials
- Abstract:
- Lithium nickel oxide, LiNiO2, has attracted considerable interest as a high energy cathode for next generation lithium ion batteries. Nevertheless, shortcomings such as significant cycling capacity decay and low stability in ambient atmosphere have hindered its practical application, and consequently most work has focused on the more stable Mn and Co doped analogues Li(Ni,Mn,Co)O2. Here, we report an investigation of an alternative strategy, sulfate modification, in the LiNiO2 (LNO) system. We show that improved performance can be achieved, attributed to the dual effect of a low level of bulk doping and the presence of a self-passivation Li2SO4 layer formed beyond the solid solution limit. Ab initio simulations suggest that the behavior is similar to that of other high valent dopants such as W and Mo. These dual effects contribute to the improved air stability and enhanced electrochemical performance for the sulfate modified lithium-rich LNO, leading to high initial capacities (~245 mAhg-1 at 25 mA/g, and ~205 mAhg-1 at 100 mA/g) and better capacity retention. Overall, the results show that polyanion modification represents an excellent alternative low cost strategy to improve the performance of lithium nickel oxide cathode materials
- Publication status:
- Published
- Peer review status:
- Peer reviewed
Actions
Access Document
- Files:
-
-
(Preview, Version of record, pdf, 3.8MB, Terms of use)
-
- Publisher copy:
- 10.1039/d4ta00284a
Authors
- Publisher:
- Royal Society of Chemistry
- Journal:
- Journal of Materials Chemistry A: materials for energy and sustainability More from this journal
- Volume:
- 12
- Issue:
- 19
- Pages:
- 11390-11402
- Publication date:
- 2024-05-14
- DOI:
- EISSN:
-
2050-7496
- ISSN:
-
2050-7488
- Language:
-
English
- Keywords:
- Pubs id:
-
1991147
- Local pid:
-
pubs:1991147
- Source identifiers:
-
W4393955014
- Deposit date:
-
2026-01-27
- ARK identifier:
This ORA record was generated from metadata provided by an external service. It has not been edited by the ORA Team.
Terms of use
- Copyright date:
- 2024
- Licence:
- CC Attribution (CC BY)
If you are the owner of this record, you can report an update to it here: Report update to this record