Suppression of Monoclinic Phase Transitions of O3-Type Cathodes Based on Electronic Delocalization for Na-Ion Batteries
Source abstract
Abstract
As high capacity cathodes, O3-type Na-based oxides always suffer from a series of monoclinic transitions upon sodiation/desodiation, mainly caused by Na+/vacancy ordering and Jahn-Teller (J-T) distortion, leading to rapid structural degradation and serious performance fading. Herein, a simple modulation strategy is proposed to address this issue based on refrainment of electron localization in expectation to alleviate the charge ordering and change of electronic structure, which always lead to Na+/vacancy ordering and J-T distortion, respectively. According to density functional theory calculations, Fe3+ with slightly larger radius is introduced into NaNi0.5Mn0.5O2 with the intention of enlarging transition metal layers and facilitating electronic delocalization. The obtained NaFe0.3Ni0.35Mn0.35O2 exhibits a reversible phase transition of O3hex-P3hex without any monoclinic transitions in striking contrast with the complicated phase transitions (O3hex-O'3mon-P3hex-P'3mon-P3'hex) of NaNi0.5Mn0.5O2, thus excellently improving the capacity retention with a high rate kinetic. In addition, the strategy is also effective to enhance the air stability, proved by direct observation of atomic-scale ABF-STEM for the first time.
Source: europepmc · Quality: candidate unverified · Source record ↗
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
Fujian Provincial Key Laboratory of Quantum Manipulation and New Energy Materials College of Physics and Energy, Fujian Normal University, Fuzhou 350117, China
Fujian Provincial Collaborative Innovation Center for Optoelectronic Semiconductors and Efficient Devices, Xiamen, 361005, China
University of Chinese Academy of Sciences, Beijing 100049, China
Funding
Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China
References (37)
Show source-provided references
1. 10.1021/acsami.8b1631910.1021/acsami.8b16319 ↗
2. 10.1038/s41586-018-0015-410.1038/s41586-018-0015-4 ↗
3. 10.1021/acsami.8b0389810.1021/acsami.8b03898 ↗
4. 10.1038/nmat482110.1038/nmat4821 ↗
5. 10.1021/am405970s10.1021/am405970s ↗
6. 10.1002/adfm.20170171810.1002/adfm.201701718 ↗
7. 10.1021/acsami.8b1051910.1021/acsami.8b10519 ↗
8. 10.1002/anie.20170437310.1002/anie.201704373 ↗
9. 10.1021/acsami.8b1160910.1021/acsami.8b11609 ↗
10. 10.1021/acsenergylett.8b0060910.1021/acsenergylett.8b00609 ↗
11. 10.1002/aenm.20170322310.1002/aenm.201703223 ↗
12. 10.1002/smll.20170367110.1002/smll.201703671 ↗
13. 10.1002/aenm.20160037710.1002/aenm.201600377 ↗
14. 10.1002/anie.20141037610.1002/anie.201410376 ↗
15. 10.1039/c3ee40847g10.1039/c3ee40847g ↗
16. 10.1039/C6EE01807F10.1039/C6EE01807F ↗
17. 10.1021/acsami.8b0061410.1021/acsami.8b00614 ↗
18. 10.1002/aenm.20140045810.1002/aenm.201400458 ↗
19. 10.1021/cr500192f10.1021/cr500192f ↗
20. 10.1038/nmat396410.1038/nmat3964 ↗
21. 10.1149/2.023302jes10.1149/2.023302jes ↗
22. 10.1016/j.jpowsour.2014.02.04810.1016/j.jpowsour.2014.02.048 ↗
23. 10.1016/j.nanoen.2018.09.02810.1016/j.nanoen.2018.09.028 ↗
24. 10.1103/PhysRevB.71.13411110.1103/PhysRevB.71.134111 ↗
25. 10.1039/C6EE01750A10.1039/C6EE01750A ↗
26. 10.1002/aenm.20180205710.1002/aenm.201802057 ↗
27. 10.1021/acsami.5b0059410.1021/acsami.5b00594 ↗
28. 10.1039/C8CP00715B10.1039/C8CP00715B ↗
29. 10.1021/acs.inorgchem.7b0200610.1021/acs.inorgchem.7b02006 ↗
30. 10.1039/C6RA25409H10.1039/C6RA25409H ↗
31. 10.1016/j.chempr.2018.05.01810.1016/j.chempr.2018.05.018 ↗
32. 10.1021/jacs.7b0517610.1021/jacs.7b05176 ↗
33. 10.1039/C6TA07589D10.1039/C6TA07589D ↗
34. 10.1021/ic300357d10.1021/ic300357d ↗
35. 10.1149/1.151300110.1149/1.1513001 ↗
36. 10.1002/adfm.20160129210.1002/adfm.201601292 ↗
37. 10.1002/aenm.20170018910.1002/aenm.201700189 ↗