Sodium Alginate: A Water-Processable Binder in High-Voltage Cathode Formulations
Source abstract
Abstract
Binders are electrochemically inactive electrode components. However, their chemical and physical nature greatly affects battery performance and plays a key role in electrode integrity and interface reactivity. The binders thus have a strong impact on battery capacity retention and cycle life. Water-processable binders would make the electrode preparation process cheap and environmentally friendly and provide a viable alternative to polyvinylidene difluoride (PVdF). Here we report the use of sodium alginate (SA) as binder for LiNi 0.5 Mn 1.5 O 4 (LNMO), one of the most promising cathode materials for high-voltage and high-energy LIBs. We demonstrate that electrodes with high mass loading containing SA have excellent specific discharge capacity (120 mAh g −1 at C/3 and 100 mAh g −1 at 5C) with negligible overpotentials in conventional electrolyte based on ethylene carbonate (EC): dimethyl carbonate (DMC) and 1 M LiPF 6 , where the reactivity of LNMO is known to negatively affect stability. The electrodes with SA also show a good stability over subsequent cycles of charge and discharge at 1C with capacity retention of 95% and 86% with respect to the initial cycles at the 100th and 200th cycle.
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.
References (42)
Show source-provided references
1. Pillot C. , Lithium-Ion Battery Market Expansion Beyond Consumer and Automotive, AABC 2015 January 26–29 Mainz, Germany. http://www.avicenne.com/articles_energy.php (last access 07/07/16).
2. 10.1149/2.0211514jes10.1149/2.0211514jes ↗
3. 10.1039/c1ee01598b10.1039/c1ee01598b ↗
4. 10.1021/jz101542210.1021/jz1015422 ↗
5. 10.1016/j.jpowsour.2013.11.10310.1016/j.jpowsour.2013.11.103 ↗
6. 10.1149/2.0111514jes10.1149/2.0111514jes ↗
7. 10.1016/j.ssi.2015.02.00610.1016/j.ssi.2015.02.006 ↗
8. 10.1021/cr500003w10.1021/cr500003w ↗
9. 10.1021/cr020738u10.1021/cr020738u ↗
10. 10.1039/C4CP02475C10.1039/C4CP02475C ↗
11. 10.1002/polb.2009910.1002/polb.20099 ↗
12. 10.1021/jp201691g10.1021/jp201691g ↗
13. 10.1149/1.201228710.1149/1.2012287 ↗
14. 10.1149/1.217707110.1149/1.2177071 ↗
15. 10.1016/j.jpowsour.2011.04.04310.1016/j.jpowsour.2011.04.043 ↗
16. 10.1149/1.308626210.1149/1.3086262 ↗
17. 10.1016/j.electacta.2010.01.01110.1016/j.electacta.2010.01.011 ↗
18. 10.1021/am100871y10.1021/am100871y ↗
19. 10.1016/j.jpowsour.2013.08.05110.1016/j.jpowsour.2013.08.051 ↗
20. 10.1016/j.jpowsour.2008.10.04010.1016/j.jpowsour.2008.10.040 ↗
21. 10.1039/c2jm34964g10.1039/c2jm34964g ↗
22. 10.1016/j.jpowsour.2010.09.08010.1016/j.jpowsour.2010.09.080 ↗
23. 10.1149/1.197921410.1149/1.1979214 ↗
24. 10.1149/1.239872510.1149/1.2398725 ↗
25. 10.1016/j.elecom.2007.10.00110.1016/j.elecom.2007.10.001 ↗
26. 10.1149/2.0131514jes10.1149/2.0131514jes ↗
27. 10.1149/1.329197610.1149/1.3291976 ↗
28. 10.1016/j.jpowsour.2013.10.01810.1016/j.jpowsour.2013.10.018 ↗
29. 10.1016/j.jpowsour.2012.10.03310.1016/j.jpowsour.2012.10.033 ↗
30. 10.1016/j.electacta.2011.11.09410.1016/j.electacta.2011.11.094 ↗
31. 10.1016/j.jpowsour.2011.04.03010.1016/j.jpowsour.2011.04.030 ↗
32. 10.1126/science.120915010.1126/science.1209150 ↗
33. 10.1039/c3ta13514d10.1039/c3ta13514d ↗
34. 10.1039/c2jm31583a10.1039/c2jm31583a ↗
35. 10.1016/j.apsusc.2015.08.04610.1016/j.apsusc.2015.08.046 ↗
36. 10.1016/j.jpowsour.2008.08.04310.1016/j.jpowsour.2008.08.043 ↗
37. 10.1002/cphc.20140005210.1002/cphc.201400052 ↗
38. 10.1016/j.jpowsour.2005.07.00910.1016/j.jpowsour.2005.07.009 ↗
39. 10.1149/2.0921510jes10.1149/2.0921510jes ↗
40. 10.1002/(SICI)1097-4628(19970822)65:8<1517::AID-APP9>3.0.CO;2-J10.1002/(SICI)1097-4628(19970822)65:8<1517::AID-APP9>3.0.CO;2-J ↗
41. 10.1149/07301.0249ecst10.1149/07301.0249ecst ↗
42. 10.1149/1.139388610.1149/1.1393886 ↗