journal article·2019-09-04

Surficial Structure Retention Mechanism for LiNi0.8Co0.15Al0.05O2 in a Full Gradient Cathode

Chaodeng Liu, Guoqin Cao, Zhihao Wu, Junhua Hu, Haoyang Wang, Guosheng Shao

ACS Applied Materials & Interfaces· Volume 11· Issue 35
Publisher page

Abstract

A LiNi0.8Co0.15Al0.05O2 (NCA) solid battery was assembled by coupling an NCA cathode with a polyvinylidene fluoride (PVDF)/Li6.75La3Z1.75Ta0.25O12 (LLZTO) composite polymer electrolyte and a Li anode. A NiO-like phase transition is regarded as the reason for interface impedance, which leads to drastic capacity fading during cycling. A gradient cathode with excessive addition of Li6.75La3Zr1.75Ta0.25O12 was fabricated at the cathode/electrolyte interface to overcome the increased impedance. Using high-resolution transmission electron microscopy and electron energy loss spectra, the formation of a unique localized cation migration (LCM) region was confirmed on the NCA surface. The formation of an LCM region hindered further distortion and enhanced the capacity retention of the spinel lattice.
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

School of Materials Science and Engineering, Zhengzhou University, Zhengzhou 450001, China

State Center for International Cooperation on Designer Low-carbon & Environmental Materials (CDLCEM), Zhengzhou University, 100 Kexue Avenue, Zhengzhou 450001, China

Funding

Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China · Henan Province

References (35)

Show source-provided references
1. 10.1002/adma.20170570210.1002/adma.201705702 ↗
2. 10.1016/j.ssi.2015.02.01410.1016/j.ssi.2015.02.014 ↗
3. 10.1002/aenm.20170265710.1002/aenm.201702657 ↗
4. 10.1021/acs.nanolett.7b0022110.1021/acs.nanolett.7b00221 ↗
5. 10.1016/j.electacta.2016.10.05210.1016/j.electacta.2016.10.052 ↗
6. 10.1016/j.jallcom.2018.12.12110.1016/j.jallcom.2018.12.121 ↗
7. 10.1016/j.jallcom.2017.12.02110.1016/j.jallcom.2017.12.021 ↗
8. 10.1016/j.apsusc.2017.11.07910.1016/j.apsusc.2017.11.079 ↗
9. 10.1002/smll.20170180210.1002/smll.201701802 ↗
10. 10.1021/cm403332s10.1021/cm403332s ↗
11. 10.1016/j.elecom.2006.06.00510.1016/j.elecom.2006.06.005 ↗
12. 10.1149/1.161329110.1149/1.1613291 ↗
13. 10.1149/1.312638510.1149/1.3126385 ↗
14. 10.1016/j.jpowsour.2016.07.00810.1016/j.jpowsour.2016.07.008 ↗
15. 10.1016/j.jpowsour.2017.11.02010.1016/j.jpowsour.2017.11.020 ↗
16. 10.1016/j.jpowsour.2011.03.09010.1016/j.jpowsour.2011.03.090 ↗
17. 10.1016/j.jpowsour.2013.10.00510.1016/j.jpowsour.2013.10.005 ↗
18. 10.1016/j.jpowsour.2016.02.08810.1016/j.jpowsour.2016.02.088 ↗
19. 10.1016/S1388-2481(99)00046-610.1016/S1388-2481(99)00046-6 ↗
20. 10.1016/j.ensm.2018.09.00310.1016/j.ensm.2018.09.003 ↗
21. 10.1073/pnas.160042211310.1073/pnas.1600422113 ↗
22. 10.1021/acsami.5b0993810.1021/acsami.5b09938 ↗
23. 10.1016/0167-2738(93)90317-V10.1016/0167-2738(93)90317-V ↗
24. 10.1149/1.277616010.1149/1.2776160 ↗
25. 10.1149/2.0841613jes10.1149/2.0841613jes ↗
26. 10.1021/nl304558t10.1021/nl304558t ↗
27. 10.1149/2.073207jes10.1149/2.073207jes ↗
28. 10.1149/1.354484310.1149/1.3544843 ↗
29. 10.1149/1.217182810.1149/1.2171828 ↗
30. 10.1149/1.233699410.1149/1.2336994 ↗
31. 10.1021/acsenergylett.8b0149010.1021/acsenergylett.8b01490 ↗
32. 10.1126/sciadv.aar601810.1126/sciadv.aar6018 ↗
33. 10.1039/C8EE00239H10.1039/C8EE00239H ↗
34. 10.1002/adfm.20180882510.1002/adfm.201808825 ↗
35. 10.1021/acsnano.8b0731910.1021/acsnano.8b07319 ↗