journal article·2018-07-23Open access

Modified Coprecipitation Synthesis of Mesostructure-Controlled Li-Rich Layered Oxides for Minimizing Voltage Degradation

Minghao Zhang, Haodong Liu, Zhao Liu, Chengcheng Fang, Ying Shirley Meng

ACS Applied Energy Materials· Volume 1· Issue 7

Abstract

Modified carbonate coprecipitation synthesis without addition of chelating agent is introduced to obtain mesostructure-controlled Li-rich layered oxides. The designed mesostructure for target material Li1.2Ni0.2Mn0.6O2 has uniformly dispersed spherical secondary particles with size around 3 μm. These micrometer-sized particles consist of self-assembled crystallites with size of ∼150 nm. This unique design not only decreases the surface area compared with the sample with dispersive particles, but also increases overall structural mechanical stability compared with the sample with larger dense secondary particles as observed by transmission X-ray microscope. As a result, the voltage decay and capacity loss during long-term cycling have been minimized to a large extent. Our findings clearly demonstrate that mesostructure design of Li-rich layered oxides play a key role in optimizing this class of cathode materials. Surprisingly, the voltage fading issue can be partially mitigated by such an approach.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Ferroelectric and Piezoelectric Materials

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of NanoEngineering, University of California San Diego, La Jolla, California 92093, United States

Department of Materials Science and Engineering, Northwestern University, Evanston, Illinois 60208, United States

Funding

Vehicle Technologies Program

References (41)

Show source-provided references
1. 10.1021/acs.chemmater.6b0481510.1021/acs.chemmater.6b04815 ↗
2. 10.1038/s41467-017-02291-910.1038/s41467-017-02291-9 ↗
3. 10.1038/nchem.247110.1038/nchem.2471 ↗
4. 10.1038/nchem.252410.1038/nchem.2524 ↗
5. 10.1038/ncomms1210810.1038/ncomms12108 ↗
6. 10.1021/cm070389q10.1021/cm070389q ↗
7. 10.1016/j.jpowsour.2008.04.08610.1016/j.jpowsour.2008.04.086 ↗
8. 10.1016/j.jpowsour.2012.11.14410.1016/j.jpowsour.2012.11.144 ↗
9. 10.1149/2.034311jes10.1149/2.034311jes ↗
10. 10.1039/C5EE03573B10.1039/C5EE03573B ↗
11. 10.1002/aenm.20160002510.1002/aenm.201600025 ↗
12. 10.1021/nl500856810.1021/nl5008568 ↗
13. 10.1016/j.nanoen.2015.07.03110.1016/j.nanoen.2015.07.031 ↗
14. 10.1246/cl.2004.70410.1246/cl.2004.704 ↗
15. 10.1246/cl.2004.74810.1246/cl.2004.748 ↗
16. 10.1016/j.jpowsour.2006.07.06410.1016/j.jpowsour.2006.07.064 ↗
17. 10.1002/adma.20140254110.1002/adma.201402541 ↗
18. 10.1016/j.jpowsour.2014.08.06310.1016/j.jpowsour.2014.08.063 ↗
19. 10.1016/j.jpowsour.2007.10.06210.1016/j.jpowsour.2007.10.062 ↗
20. 10.1016/j.jpowsour.2014.10.01610.1016/j.jpowsour.2014.10.016 ↗
21. 10.1039/c1jm11077b10.1039/c1jm11077b ↗
22. 10.1021/nl502980k10.1021/nl502980k ↗
23. 10.1021/jacs.6b0393210.1021/jacs.6b03932 ↗
24. 10.1039/c3ta11716b10.1039/c3ta11716b ↗
25. 10.1021/acsami.5b0493210.1021/acsami.5b04932 ↗
26. 10.1063/1.370157910.1063/1.3701579 ↗
27. Natterer F. · 198610.1007/978-3-663-01409-6 ↗
28. 10.1016/j.elecom.2012.12.02110.1016/j.elecom.2012.12.021 ↗
29. 10.1039/b309834f10.1039/b309834f ↗
30. 10.1021/cm030299v10.1021/cm030299v ↗
31. 10.1039/c2ce06655f10.1039/c2ce06655f ↗
32. 10.1021/nl034472y10.1021/nl034472y ↗
33. 10.1680/bbn.12.0001410.1680/bbn.12.00014 ↗
34. 10.1002/aenm.20150214310.1002/aenm.201502143 ↗
35. 10.1021/ja062027+10.1021/ja062027+ ↗
36. 10.1016/j.jpowsour.2013.03.09410.1016/j.jpowsour.2013.03.094 ↗
37. 10.1038/ncomms1410110.1038/ncomms14101 ↗
38. 10.1039/C5TA04151A10.1039/C5TA04151A ↗
39. 10.1016/j.jpowsour.2009.09.07410.1016/j.jpowsour.2009.09.074 ↗
40. 10.1103/PhysRevLett.78.224810.1103/PhysRevLett.78.2248 ↗
41. 10.1016/j.electacta.2012.04.12010.1016/j.electacta.2012.04.120 ↗