Understanding Electrolyte Decomposition of Graphite/NCM811 Cells at Elevated Operating Voltage
Source abstract
Abstract
Cells containing LiNi x Co y Mn 1-x-y O 2 (NCM) materials with very high nickel content suffer from cathode material degradation upon cycling, especially when operating these cells at higher voltage. While the cathode particle degradation is a problem other issues contribute to electrochemical performance loss. Graphite/LiNi 0.8 Co 0.1 Mn 0.1 O 2 cells have been cycled to different upper cutoff voltages and investigated with electrochemical impedance spectroscopy (EIS), gas analysis with online electrochemical mass spectroscopy (OEMS), nuclear magnetic resonance (NMR) spectroscopy, gas chromatography with MS (GCMS) and inductively coupled plasma MS (ICP-MS). Increased gas evolution was observed when the upper cutoff voltage was increased from 4.2 to 4.6 V. An increase in O 2 evolution upon cycling as well as an increase of CO 2 upon increasing the voltage, have been observed. More electrolyte decomposition products are observed on the anode for cells cycled to higher voltage. An increased amount of nickel has been detected on the graphite electrode in accordance with an increased reaction of the cathode surface with the electrolyte leading to transition metal dissolution. Finally, an increase in carbonate solvent transesterification products has been observed.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · Advanced Battery Technologies Research · Advanced Battery Materials and Technologies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (35)
Show source-provided references
1. 10.1149/2.0351701jes10.1149/2.0351701jes ↗
2. 10.1016/j.jpowsour.2013.01.06310.1016/j.jpowsour.2013.01.063 ↗
3. 10.1021/acsenergylett.6b0059410.1021/acsenergylett.6b00594 ↗
4. 10.1002/aenm.20170202810.1002/aenm.201702028 ↗
5. 10.1016/j.ensm.2016.10.00710.1016/j.ensm.2016.10.007 ↗
6. 10.1016/j.apenergy.2017.03.07410.1016/j.apenergy.2017.03.074 ↗
7. 10.1021/cm303096e10.1021/cm303096e ↗
8. 10.1021/acs.jpcc.8b0784810.1021/acs.jpcc.8b07848 ↗
9. 10.1021/acs.jpclett.7b0192710.1021/acs.jpclett.7b01927 ↗
10. 10.1016/j.mattod.2017.11.00110.1016/j.mattod.2017.11.001 ↗
11. 10.1149/2.0021707jes10.1149/2.0021707jes ↗
12. 10.1016/j.jpowsour.2015.12.01310.1016/j.jpowsour.2015.12.013 ↗
13. 10.1149/2.0951603jes10.1149/2.0951603jes ↗
14. 10.1149/2.117406jes10.1149/2.117406jes ↗
15. 10.1149/2.042303jes10.1149/2.042303jes ↗
16. 10.1016/j.jpowsour.2016.09.07110.1016/j.jpowsour.2016.09.071 ↗
17. 10.1016/j.jpowsour.2010.09.12110.1016/j.jpowsour.2010.09.121 ↗
18. 10.1016/S0167-2738(00)00644-510.1016/S0167-2738(00)00644-5 ↗
19. 10.1149/2.0081701jes10.1149/2.0081701jes ↗
20. 10.1149/2.1151605jes10.1149/2.1151605jes ↗
21. 10.1149/2.1001712jes10.1149/2.1001712jes ↗
22. 10.1149/2.1261811jes10.1149/2.1261811jes ↗
23. 10.1149/1.200898710.1149/1.2008987 ↗
24. 10.1016/j.jpowsour.2005.02.02110.1016/j.jpowsour.2005.02.021 ↗
25. 10.1149/1.203451710.1149/1.2034517 ↗
26. 10.1149/2.0191701jes10.1149/2.0191701jes ↗
27. 10.1016/S0378-7753(97)02635-910.1016/S0378-7753(97)02635-9 ↗
28. 10.1016/j.jpowsour.2014.07.05110.1016/j.jpowsour.2014.07.051 ↗
29. 10.1016/j.jpowsour.2008.11.03110.1016/j.jpowsour.2008.11.031 ↗
30. 10.1021/acs.jpcc.5b0007210.1021/acs.jpcc.5b00072 ↗
31. 10.1016/j.progsolidstchem.2014.04.00310.1016/j.progsolidstchem.2014.04.003 ↗
32. 10.1016/S0039-6028(97)00353-110.1016/S0039-6028(97)00353-1 ↗
33. 10.1039/C6TA08865A10.1039/C6TA08865A ↗
34. 10.1149/2.1151902jes10.1149/2.1151902jes ↗
35. 10.1021/acs.jpcc.7b0636310.1021/acs.jpcc.7b06363 ↗