Enhanced High Voltage Stability of Spinel‐Type Structured LiNi0.5Mn1.5O4 Electrodes: Targeted Octahedral Crystal Site Modification
Source abstract
Abstract
Abstract High‐voltage spinel‐type structured LiNi0.5Mn1.5O4 (LNMO) shows promise as a next‐generation high‐energy‐density lithium‐ion battery cathode material, however, capacity decay on extended cycling hinders its widespread adoption, underscoring an urgent need for further development. In this work, we introduce Zn at octahedral 16c crystal sites in LNMO with Fd m space group to improve rate capability and reduce the rapid capacity decay otherwise experienced during extended cycling. The current work resolves the detailed influence of isolated modification at octahedral 16c crystal sites, unveiling the mechanism for these performance improvements. We show that occupation of Zn at previously empty 16c sites prevents the migration of Ni/Mn to adjacent 16c sites, eliminating transformation to a rock‐salt type structured Ni0.25Mn0.75O2 phase above 4.8 V, preventing structure degradation and suppressing voltage polarization. This study provides insights into the fundamental structure‐function relationship of the LNMO battery cathode, pointing to pathways for the crystal structure engineering of materials with superior performance.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · Ferroelectric and Piezoelectric Materials · Dielectric properties of ceramics
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Chemical Engineering The University of Adelaide Adelaide SA 5005 Australia
Australian Synchrotron, Australian Nuclear Science and Technology Organisation Melbourne VIC Australia
Faculty of Engineering Institute for Superconducting & Electronic Materials University of Wollongong Wollongong NSW Australia
Australian Centre for Neutron Scattering, Australian Nuclear Science and Technology Organisation Sydney NSW Australia
Funding
Australian Research Council
References (31)
Show source-provided references
1.
2. 10.1038/s41560-019-0513-010.1038/s41560-019-0513-0 ↗
3. 10.1021/acsenergylett.7b0013010.1021/acsenergylett.7b00130 ↗
4.
5. 10.1039/D0TA02812F10.1039/D0TA02812F ↗
6. 10.1039/D3TA01777J10.1039/D3TA01777J ↗
7. 10.1039/c3ee42981d10.1039/c3ee42981d ↗
8.
9. 10.1016/j.jpowsour.2013.07.11410.1016/j.jpowsour.2013.07.114 ↗
10. 10.1002/smll.20210689810.1002/smll.202106898 ↗
11.
12. 10.3389/fenrg.2018.0008910.3389/fenrg.2018.00089 ↗
13. 10.1002/adma.20190452810.1002/adma.201904528 ↗
14.
15. 10.1016/j.mtcomm.2020.10100310.1016/j.mtcomm.2020.101003 ↗
16. 10.1016/j.jallcom.2017.07.20210.1016/j.jallcom.2017.07.202 ↗
17.
18. 10.1002/anie.20200145410.1002/anie.202001454 ↗
19. 10.1002/adma.20210141310.1002/adma.202101413 ↗
20. 10.1002/anie.20220196910.1002/anie.202201969 ↗
21. 10.1016/j.chempr.2018.04.02010.1016/j.chempr.2018.04.020 ↗
22. 10.1107/S056773947600155110.1107/S0567739476001551 ↗
23. 10.1021/cm503972a10.1021/cm503972a ↗
24. 10.1002/adma.20170376410.1002/adma.201703764 ↗
25.
26. 10.1002/aenm.20120006810.1002/aenm.201200068 ↗
27. 10.1021/acs.jpcc.6b1074310.1021/acs.jpcc.6b10743 ↗
28. 10.1021/cm035050s10.1021/cm035050s ↗
29. 10.1016/j.jpowsour.2014.01.08910.1016/j.jpowsour.2014.01.089 ↗
30. 10.1021/acssuschemeng.2c0171110.1021/acssuschemeng.2c01711 ↗
31. 10.1002/anie.20221380610.1002/anie.202213806 ↗