Heterocations Synergistic Doping for Kinetically Enhanced and Structurally Stable LiMn 0.6 Fe 0.4 PO 4
Source abstract
Abstract
LiMn x Fe 1– x PO 4 (LMFP) is a promising olivine cathode material successor to LiFePO 4, offering a higher operating voltage platform for enhanced energy density. However, its commercial application is hindered by inherent poor kinetics. Herein, a dual-site doping strategy involving Na + and Co 2+ is proposed to synergistically enhance the ionic and electronic conductivity of LMFP. The codoped LMFP-Na-Co cathode delivers a specific capacity of 135.8 mAh/g at 1 C and exhibits outstanding cycling stability with 92.5% capacity retention after 200 cycles. Remarkably, it also maintains 90.2% capacity retention after 300 cycles even at 0 °C. Theoretical calculations reveal that Na + doping expands the one-dimensional lithium-ion diffusion channels, while Co 2+ doping elevates the intrinsic electronic conductivity and suppresses the Jahn–Teller distortion associated with Mn 3+, collectively lowering the Li + diffusion barrier and improving structural stability. This work demonstrates that Na + -Co 2+ dual-site doping is a highly promising strategy for developing high-performance LiMn x Fe 1– x PO 4 cathodes.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · Thermal Expansion and Ionic Conductivity · Advanced Battery Materials and Technologies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Materials and New Energy
South China Normal University
School of Physics and Wuhan National High Magnetic Field Center
Huazhong University of Science and Technology
College of Chemistry and Environmental Engineering
Shenzhen University
School of Psychiatry
North Sichuan Medical College
Funding
Science and Technology Foundation of Shenzhen City · Natural Science Foundation of Guangdong Province · Shenzhen University · National Natural Science Foundation of China (NSFC)
References (32)
Show source-provided references
1. 10.1021/acsami.9b2336710.1021/acsami.9b23367 ↗
2. 10.1016/j.pecs.2015.01.00210.1016/j.pecs.2015.01.002 ↗
3. 10.1021/am403991f10.1021/am403991f ↗
4. 10.1021/acsami.8b0273610.1021/acsami.8b02736 ↗
5. 10.3390/molecules2624764110.3390/molecules26247641 ↗
6. 10.1016/j.est.2019.10111610.1016/j.est.2019.101116 ↗
7. 10.1155/2019/563859010.1155/2019/5638590 ↗
8. 10.1016/j.est.2024.11255210.1016/j.est.2024.112552 ↗
9. 10.1021/acs.iecr.2c0430310.1021/acs.iecr.2c04303 ↗
10. 10.1016/j.jssc.2020.12129410.1016/j.jssc.2020.121294 ↗
11. 10.1039/C7TA00104E10.1039/C7TA00104E ↗
12. 10.1016/j.ceramint.2019.02.11210.1016/j.ceramint.2019.02.112 ↗
13. 10.1039/C5TA05358G10.1039/C5TA05358G ↗
14. 10.1016/j.elecom.2006.07.01410.1016/j.elecom.2006.07.014 ↗
15. 10.1016/j.jelechem.2022.11711710.1016/j.jelechem.2022.117117 ↗
16. 10.1016/j.jpowsour.2017.05.06710.1016/j.jpowsour.2017.05.067 ↗
17. 10.1016/j.ssi.2006.03.04710.1016/j.ssi.2006.03.047 ↗
18. 10.1021/acssuschemeng.8b0339010.1021/acssuschemeng.8b03390 ↗
19. 10.1016/j.jelechem.2022.11605910.1016/j.jelechem.2022.116059 ↗
20. 10.1002/anie.20241059010.1002/anie.202410590 ↗
21. 10.3390/batteries302001110.3390/batteries3020011 ↗
22. 10.1016/j.est.2023.10871010.1016/j.est.2023.108710 ↗
23. 10.1016/j.est.2023.10900610.1016/j.est.2023.109006 ↗
24. 10.1016/j.jelechem.2015.08.01210.1016/j.jelechem.2015.08.012 ↗
25. 10.1016/j.carbon.2022.02.03410.1016/j.carbon.2022.02.034 ↗
26. 10.1038/s41598-021-91881-110.1038/s41598-021-91881-1 ↗
27. 10.1016/j.electacta.2020.13767510.1016/j.electacta.2020.137675 ↗
28. 10.1039/C4TA05900J10.1039/C4TA05900J ↗
29. 10.1016/j.cej.2022.13998610.1016/j.cej.2022.139986 ↗
30. 10.1021/acsaem.5c0244210.1021/acsaem.5c02442 ↗
31. 10.1016/j.ensm.2023.10312510.1016/j.ensm.2023.103125 ↗
32. 10.1002/adma.20240545810.1002/adma.202405458 ↗