Suppressing the Voltage Decay Based on a Distinct Stacking Sequence of Oxygen Atoms for Li-Rich Cathode Materials
Source abstract
Abstract
Li-rich cathode materials possess a much higher theoretical energy density than all intercalated cathode materials currently reported and thus are considered as the most promising candidate for next-generation high-energy density Li-ion batteries. However, the rapid voltage decay and the irreversible phase transition of O3-type Li-rich cathode materials often lessen their actual energy density and limit their practical applications, and thus, effectively suppressing the voltage decay of Li-rich cathodes becomes the hotspot of the current research. Herein, the F-doped O2-type Li-rich cathode materials Li1.2Mn0.54Ni0.13Co0.13O2+δ−xFx (F-O2-LRO) are designed and prepared based on the P2-type sodium-ion cathode materials Na5/6Li1/4(Mn0.54Ni0.13Co0.13)3/4O2+δ (Na-LRO) by ion exchange. It has been found that the as-prepared F-O2-LRO exhibits excellent electrochemical performance, for example, a high discharge specific capacity of 280 mA h g–1 at 0.1 C with an initial Coulombic efficiency of 94.4%, which is obviously higher than the original LRO (77.2%). After 100 cycles, the F-O2-LRO cathode can still maintain a high capacity retention of 95% at a rate of 1 C, while the capacity retention of the original LRO is only 69.1% at the same current rate. Furthermore, the voltage difference (ΔV) of F-O2-LRO before and after cycling is only 0.268 V after 100 cycles at 1 C, which is less than that of the LRO cathode (0.681 V), indicating much lower polarization. Besides, even at a high current rate of 5 C, F-O2-LRO still displays a satisfactory discharge capacity of 210 mA h g–1 with a capacity retention of 90.1% after 100 cycles. Therefore, this work put forward a new strategy for the development and industrial application of Li-rich cathode materials in high-energy Li-ion batteries.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Advanced Battery Technologies Research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
National Base for International Science & Technology Cooperation, National Local Joint Engineering Laboratory for Key Materials of New Energy Storage Battery, Hunan Province Key Laboratory of Electrochemical Energy Storage & Conversion, School of Chemistry, Xiangtan University, Xiangtan 411105, China
School of Chemistry & Materials Engineering, Xinxiang University, Henan 453003, China
Funding
National Natural Science Foundation of China · Key Project of Strategic New Industry of Hunan Province
References (37)
Show source-provided references
1. 10.1039/d0ee01694b10.1039/d0ee01694b ↗
2. 10.1038/s41563-019-0572-410.1038/s41563-019-0572-4 ↗
3. 10.1002/aenm.20190426410.1002/aenm.201904264 ↗
4. 10.1002/aenm.20170239710.1002/aenm.201702397 ↗
5. 10.1126/science.121274110.1126/science.1212741 ↗
6. 10.1002/adma.20170557510.1002/adma.201705575 ↗
7. 10.1016/j.ensm.2019.10.02910.1016/j.ensm.2019.10.029 ↗
8. 10.1038/s41560-018-0097-010.1038/s41560-018-0097-0 ↗
9. 10.1038/natrevmats.2017.5710.1038/natrevmats.2017.57 ↗
10. 10.1038/natrevmats.2016.1310.1038/natrevmats.2016.13 ↗
11. 10.1016/j.jpowsour.2005.01.01910.1016/j.jpowsour.2005.01.019 ↗
12. 10.1021/acsnano.9b0596010.1021/acsnano.9b05960 ↗
13. 10.1039/c8ta04568b10.1039/c8ta04568b ↗
14. 10.1002/adma.20180175110.1002/adma.201801751 ↗
15. 10.1039/c7ee03122j10.1039/c7ee03122j ↗
16. 10.1002/aenm.20180210510.1002/aenm.201802105 ↗
17. 10.1021/acs.nanolett.0c0164010.1021/acs.nanolett.0c01640 ↗
18. 10.1021/acsaem.0c0043910.1021/acsaem.0c00439 ↗
19. 10.1016/j.ensm.2020.05.01310.1016/j.ensm.2020.05.013 ↗
20. 10.1021/jacs.0c0230210.1021/jacs.0c02302 ↗
21. 10.1021/acs.nanolett.8b0103610.1021/acs.nanolett.8b01036 ↗
22. 10.1021/acssuschemeng.7b0177310.1021/acssuschemeng.7b01773 ↗
23. 10.1002/aenm.20160128410.1002/aenm.201601284 ↗
24. 10.1039/c4ta05281a10.1039/c4ta05281a ↗
25. 10.1016/j.ensm.2018.06.01610.1016/j.ensm.2018.06.016 ↗
26. 10.1016/j.electacta.2016.02.21010.1016/j.electacta.2016.02.210 ↗
27. 10.1038/s41550-018-0544-710.1038/s41550-018-0544-7 ↗
28. 10.1016/j.cej.2017.10.05010.1016/j.cej.2017.10.050 ↗
29. 10.1039/c4ta00189c10.1039/c4ta00189c ↗
30. 10.1021/acsaem.0c0131510.1021/acsaem.0c01315 ↗
31. 10.1021/acsami.7b0880210.1021/acsami.7b08802 ↗
32. 10.1016/j.electacta.2017.10.11910.1016/j.electacta.2017.10.119 ↗
33. 10.1002/aenm.20170168210.1002/aenm.201701682 ↗
34. 10.1016/j.jpowsour.2015.02.08510.1016/j.jpowsour.2015.02.085 ↗
35. 10.1039/c6ta01878e10.1039/c6ta01878e ↗
36. 10.1039/c7ta05971j10.1039/c7ta05971j ↗
37. 10.1021/acsami.8b1631910.1021/acsami.8b16319 ↗