journal article·2016-09-01Open access

Determination of the mechanism and extent of surface degradation in Ni-based cathode materials after repeated electrochemical cycling

Sooyeon Hwang, Se Young Kim, Kyung Yoon Chung, Eric A. Stach, Seung Min Kim, Wonyoung Chang

APL Materials· Volume 4· Issue 9

Abstract

We take advantage of scanning transmission electron microscopy and electron energy loss spectroscopy to investigate the changes in near-surface electronic structure and quantify the degree of local degradation of Ni-based cathode materials with the layered structure (LiNi0.8Mn0.1Co0.1O2 and LiNi0.4Mn0.3Co0.3O2) after 20 cycles of delithiation and lithiation. Reduction of transition metals occurs in the near-surface region of cathode materials: Mn is the major element to be reduced in the case of relatively Mn-rich composition, while reduction of Ni ions is dominant in Ni-rich materials. The valences of Ni and Mn ions are complementary, i.e., when one is reduced, the other is oxidized in order to maintain charge neutrality. The depth of degradation zone is found to be much deeper in Ni-rich materials. This comparative analysis provides important insights needed for the devising of new cathode materials with high capacity as well as long lifetime.
Source: crossref · 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

Korea Institute of Science and Technology (KIST) 1 Center for Energy Convergence, , Seoul 02792, South Korea

Brookhaven National Laboratory 2 Center for Functional Nanomaterials, , Upton, New York 11973, USA

Institute of Advanced Composite Materials, KIST 3 Carbon Composite Materials Research Centre, , Wanju-gun 55324, South Korea

Funding

Korea Institute of Science and Technology · Brookhaven National Laboratory

References (26)

Show source-provided references
1. Nature · 2008 · 451 · 65210.1038/451652a ↗
2. Science · 2011 · 334 · 92810.1126/science.1212741 ↗
3. Adv. Energy Mater. · 2014 · 4 · 130078710.1002/aenm.201300787 ↗
4. ChemSusChem · 2015 · 8 · 341410.1002/cssc.201501041 ↗
5. J. Power Sources · 2012 · 207 · 13410.1016/j.jpowsour.2012.01.122 ↗
6. Nat. Commun. · 2014 · 5 · 352910.1038/ncomms4529 ↗
7. J. Electrochem. Soc. · 2007 · 154 · A100510.1149/1.2776160 ↗
8. Appl. Phys. Lett. · 2014 · 105 · 10390110.1063/1.4895336 ↗
9. J. Power Sources · 2015 · 275 · 9910.1016/j.jpowsour.2014.10.197 ↗
10. ACS Appl. Mater. Interfaces · 2014 · 6 · 1582210.1021/am5030726 ↗
11. J. Mater. Chem. A · 2015 · 3 · 1059210.1039/C5TA00929D ↗
12. Chem. Mater. · 2015 · 27 · 539310.1021/acs.chemmater.5b02016 ↗
13. J. Electrochem. Soc. · 2009 · 156 · A37110.1149/1.3076137 ↗
14. J. Power Sources · 2011 · 196 · 772110.1016/j.jpowsour.2011.05.017 ↗
15. J. Phys. Chem. B · 2003 · 107 · 288710.1021/jp026484y ↗
16. Phys. Rev. B · 2004 · 69 · 23510310.1103/PhysRevB.69.235103 ↗
17. Energy Environ. Sci. · 2011 · 4 · 222310.1039/c1ee01131f ↗
18. Chem. Mater. · 2013 · 25 · 231910.1021/cm4009392 ↗
19. Ultramicroscopy · 2006 · 106 · 28410.1016/j.ultramic.2005.09.002 ↗
20. Micron · 2000 · 31 · 57110.1016/S0968-4328(99)00139-0 ↗
21. J. Phys. Chem. B · 2005 · 109 · 1074910.1021/jp050486b ↗
22. Chem. Mater. · 2015 · 27 · 604410.1021/acs.chemmater.5b02457 ↗
23. J. Electrochem. Soc. · 2015 · 162 · A248310.1149/2.0101514jes ↗
24. Nano Lett. · 2015 · 15 · 51410.1021/nl5038598 ↗
25. Nano Lett. · 2013 · 13 · 385710.1021/nl4019275 ↗
26. J. Electrochem. Soc. · 1998 · 145 · 364710.1149/1.1838857 ↗