A Cross-Linked Triphenylamine-Based Polymer Cathode Material with Dual Anion-Cation Reversible Insertion for Lithium Ion Battery
Source abstract
Abstract
A cross-linked triphenylamine polymer poly[N,N'-bis(4-diphenylaminophenyl) naphthalene-1,4,5,8-tetracarboxylic diimide] cathode material with dual anion-cation reversible insertion is polymerized from monomer N,N'-bis(4-diphenylaminophenyl) naphthalene-1,4,5,8-tetracarboxylic diimide by chemical oxidative polymerization, which has a very low solubility in common organic solvents and electrolytes. The triphenylamine unit in the polymer can reversibly dope/dedope the PF 6 − anion, while the naphthalimide unit can reversibly insert/extract the lithium cation. The lithium ion half-cells with the polymer as a cathode and the lithium foil as an anode are assembled and the electrochemical properties are tested. For comparison, the electrochemical properties of monomer are studied. Thanks to its cross-linked network structure, the electrochemical performance of polymer is much better than that of its monomer. The polymer has excellent cycle performance, the initial discharge specific capacity is 140 mAh g −1 , which is close to its theoretical specific capacity, and the capacity can still be maintained at 125 mAh g −1 after 100 cycles, suggesting that this polymer is a potential cathode material for lithium ion batteries.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Conducting polymers and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (34)
Show source-provided references
1. 10.1039/C7TA08413G10.1039/C7TA08413G ↗
2. 10.1016/S0378-7753(01)00728-510.1016/S0378-7753(01)00728-5 ↗
3. 10.1021/ja905325610.1021/ja9053256 ↗
4. 10.1021/acsami.8b0513210.1021/acsami.8b05132 ↗
5. 10.1149/2.0911906jes10.1149/2.0911906jes ↗
6. 10.1002/ange.20160782010.1002/ange.201607820 ↗
7. 10.1149/2.0131809jes10.1149/2.0131809jes ↗
8. 10.1039/C6TA01069E10.1039/C6TA01069E ↗
9. 10.1016/j.electacta.2017.09.11910.1016/j.electacta.2017.09.119 ↗
10. 10.1149/2.0831807jes10.1149/2.0831807jes ↗
11. 10.1039/C8TA11230D10.1039/C8TA11230D ↗
12. 10.1149/2.1011702jes10.1149/2.1011702jes ↗
13. 10.1039/C4RA15976D10.1039/C4RA15976D ↗
14. 10.1016/j.jpowsour.2007.02.04310.1016/j.jpowsour.2007.02.043 ↗
15. 10.1149/2.0631807jes10.1149/2.0631807jes ↗
16. 10.1021/acsami.7b1825210.1021/acsami.7b18252 ↗
17. 10.1002/macp.20170052410.1002/macp.201700524 ↗
18. 10.1039/C6TA10127E10.1039/C6TA10127E ↗
19. 10.1002/aenm.20170198810.1002/aenm.201701988 ↗
20. 10.1039/C8NJ04765K10.1039/C8NJ04765K ↗
21. 10.1016/j.electacta.2018.07.06210.1016/j.electacta.2018.07.062 ↗
22. 10.1016/j.jpowsour.2007.10.08610.1016/j.jpowsour.2007.10.086 ↗
23. 10.1039/C4RA14401E10.1039/C4RA14401E ↗
24. 10.1002/ange.20180659610.1002/ange.201806596 ↗
25. 10.1021/cm504678610.1021/cm5046786 ↗
26. 10.1021/acs.chemmater.8b0130410.1021/acs.chemmater.8b01304 ↗
27. 10.1149/2.0391811jes10.1149/2.0391811jes ↗
28. 10.1021/acsami.6b0759110.1021/acsami.6b07591 ↗
29. 10.1016/j.orgel.2014.10.05010.1016/j.orgel.2014.10.050 ↗
30. 10.1016/j.dyepig.2017.05.03110.1016/j.dyepig.2017.05.031 ↗
31. 10.1016/j.energy.2017.12.14410.1016/j.energy.2017.12.144 ↗
32. 10.1016/j.jpowsour.2005.01.00610.1016/j.jpowsour.2005.01.006 ↗
33. 10.1016/j.jpowsour.2013.11.02910.1016/j.jpowsour.2013.11.029 ↗
34. 10.1002/anie.20100243910.1002/anie.201002439 ↗