Li4Ti5O12−TiO2 Composite Coated on Carbon Foam as Anode Material for Lithium Ion Capacitors: Evaluation of Rate Performance and Self‐Discharge
Source abstract
Abstract
Abstract Li4Ti5O12‐TiO2 (LTO‐TO) composite is coated on carbon foam (CF) for anode of lithium ion capacitors (LICs). The resulting CF@LTO‐TO electrodes with varied mass loadings of LTO‐TO exhibit much improved rate performance compared to pristine LTO electrode. Specifically, asymmetric LICs based on activated carbon cathode and CF@LTO‐TO anode (AC//CF@LTO‐TO) with 25 wt% of LTO‐TO delivers a specific capacity of 65 mAh g−1 at 300 C. In addition, the self‐discharge rates of the LICs are evaluated. It is found that AC//CF@LTO‐TO LIC with 45 wt% of LTO‐TO shows much reduced self‐discharge rate (open circuit voltage drops from 2.5 to 1.1 V in 144 hours) relative to AC//CF@LTO‐TO with different LTO‐TO mass loadings. The results of this study suggest that the introduction of TO in LTO anode can affect both the rate performance and the self‐discharge behavior, which may be due to the fast faradaic reaction kinetic of TO and the rich LTO‐TO grain boundary interfaces.
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Research context
OpenAlex topics: Advancements in Battery Materials · Supercapacitor Materials and Fabrication · Advanced Battery Materials and Technologies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
CAS Center for Excellence in Nanoscience Beijing Institute of Nanoenergy and Nanosystems Chinese Academy of Sciences Beijing 100083 China
School of Nanoscience and Technology University of Chinese Academy of Sciences Beijing 100049 China
Center on Nanoenergy Research School of Physical Science and Technology Guangxi University Nanning Guangxi 530004 China
References (43)
Show source-provided references
1. 10.1038/451652a10.1038/451652a ↗
2. 10.1038/nmat229710.1038/nmat2297 ↗
3. 10.1021/cm901452z10.1021/cm901452z ↗
4. 10.1002/adma.20090171010.1002/adma.200901710 ↗
5. 10.1002/adma.20100358710.1002/adma.201003587 ↗
6. 10.1039/c1ee01598b10.1039/c1ee01598b ↗
7. 10.1002/aenm.20130081610.1002/aenm.201300816 ↗
8. 10.1002/smll.20190246610.1002/smll.201902466 ↗
9. 10.1016/j.cej.2018.09.18610.1016/j.cej.2018.09.186 ↗
10. 10.1016/j.cej.2018.09.16310.1016/j.cej.2018.09.163 ↗
11. 10.1039/C8TA10513H10.1039/C8TA10513H ↗
12. 10.1016/j.nanoen.2015.04.01110.1016/j.nanoen.2015.04.011 ↗
13. 10.1039/c3ee40509e10.1039/c3ee40509e ↗
14. 10.1016/j.cej.2017.08.07010.1016/j.cej.2017.08.070 ↗
15. 10.1149/1.138355310.1149/1.1383553 ↗
16. 10.1002/fuce.20100004110.1002/fuce.201000041 ↗
17. 10.1039/c2ee21675b10.1039/c2ee21675b ↗
18. 10.1021/acs.chemrev.8b0011610.1021/acs.chemrev.8b00116 ↗
19. 10.1039/C4CS00266K10.1039/C4CS00266K ↗
20. 10.1021/cr500091510.1021/cr5000915 ↗
21. 10.1039/c3ra23466e10.1039/c3ra23466e ↗
22. 10.1016/j.electacta.2012.03.15110.1016/j.electacta.2012.03.151 ↗
23. Wang H. · Adv. Mater. · 2017 · 29
24. 10.1016/j.jelechem.2019.11338610.1016/j.jelechem.2019.113386 ↗
25. 10.1021/acsami.9b0345410.1021/acsami.9b03454 ↗
26. 10.1039/C9NR07091E10.1039/C9NR07091E ↗
27. 10.1149/1.352798310.1149/1.3527983 ↗
28. 10.1149/1.205005310.1149/1.2050053 ↗
29. 10.1149/1.204859210.1149/1.2048592 ↗
30. 10.1016/S0167-2738(99)00095-810.1016/S0167-2738(99)00095-8 ↗
31. 10.1149/1.134452310.1149/1.1344523 ↗
32. 10.1007/s10008-016-3433-y10.1007/s10008-016-3433-y ↗
33. 10.1021/ja902423e10.1021/ja902423e ↗
34. 10.1021/acsnano.6b0047910.1021/acsnano.6b00479 ↗
35. 10.1002/aenm.20130029410.1002/aenm.201300294 ↗
36. 10.1021/nn900150y10.1021/nn900150y ↗
37. 10.1039/C7RA09343H10.1039/C7RA09343H ↗
38. 10.1039/C5RA12397F10.1039/C5RA12397F ↗
39. 10.1073/pnas.121007210910.1073/pnas.1210072109 ↗
40. 10.1016/j.jpowsour.2015.02.07910.1016/j.jpowsour.2015.02.079 ↗
41. 10.1021/am505756810.1021/am5057568 ↗
42. 10.1016/j.nanoen.2014.06.03210.1016/j.nanoen.2014.06.032 ↗
43. 10.1016/j.jallcom.2016.08.05910.1016/j.jallcom.2016.08.059 ↗