Bistacked Titanium Carbide (MXene) Anodes for Hybrid Sodium-Ion Capacitors
Source abstract
Abstract
Two-dimensional transition-metal carbides (MXenes) have shown great promise as electrode materials for high-rate pseudocapacitive energy storage. In this study, we report on the fabrication of bistacked two-dimensional titanium carbide electrodes which are free of binder, conductive additives, and current-collector. This MXene electrode is capable of reversible electrochemical storage of sodium ions with good cycling stability and rate capability. A prototype hybrid Na-ion capacitor was assembled by combining the bistacked MXene anode with an activated carbon cathode, which showed an energy density of 39 Wh/kg (including the total weight of bistacked MXene and activated carbon, 6 mg/cm) at 1C rate and maintained up to 60% of its performance at a 60C rate, in the operating voltage window of 3.4 V. This study opens new avenues for developing self-standing binder and additive-free MXene electrodes for metal-ion batteries and capacitors.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: MXene and MAX Phase Materials · Supercapacitor Materials and Fabrication · Advancements in Battery Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
A. J. Drexel Nanomaterials Institute and Department of Materials Science and Engineering, Drexel University, Philadelphia, Pennsylvania 19104, United States
Materials Science and Engineering, King Abdullah University of Science and Technology (KAUST), Thuwal 23955-6900, Saudi Arabia
Funding
King Abdullah University of Science and Technology
References (46)
Show source-provided references
1. 10.1038/451652a10.1038/451652a ↗
2. 10.1021/cr100290v10.1021/cr100290v ↗
3. 10.1109/TIE.2010.207641410.1109/TIE.2010.2076414 ↗
4. Nazri G.-A. · 2004
5. 10.1038/nchem.68010.1038/nchem.680 ↗
6. 10.1038/nenergy.2016.7010.1038/nenergy.2016.70 ↗
7. 10.1038/nmat229710.1038/nmat2297 ↗
8. 10.1126/science.124962510.1126/science.1249625 ↗
9. 10.1039/c3ee44164d10.1039/c3ee44164d ↗
10. 10.1021/acsnano.8b0191410.1021/acsnano.8b01914 ↗
11. 10.1021/jp044252o10.1021/jp044252o ↗
12. 10.1021/cm049649j10.1021/cm049649j ↗
13. 10.1038/nmat261210.1038/nmat2612 ↗
14. 10.1149/2.040405jes10.1149/2.040405jes ↗
15. 10.1038/natrevmats.2016.9810.1038/natrevmats.2016.98 ↗
16. 10.1002/adma.20110230610.1002/adma.201102306 ↗
17. 10.1038/nature1397010.1038/nature13970 ↗
18. 10.1126/science.124148810.1126/science.1241488 ↗
19. 10.1002/adma.20130413810.1002/adma.201304138 ↗
20. 10.1021/acs.chemmater.7b0284710.1021/acs.chemmater.7b02847 ↗
21. Barsoum M. W. · 201310.1002/9783527654581 ↗
22. 10.1038/nenergy.2017.10510.1038/nenergy.2017.105 ↗
23. 10.1021/nn503921j10.1021/nn503921j ↗
24. 10.1021/acsnano.7b0535010.1021/acsnano.7b05350 ↗
25. 10.1038/ncomms754410.1038/ncomms7544 ↗
26. 10.1021/acsnano.5b0695810.1021/acsnano.5b06958 ↗
27. 10.1038/s41586-018-0109-z10.1038/s41586-018-0109-z ↗
28. 10.1021/acsnano.6b0766810.1021/acsnano.6b07668 ↗
29. 10.1021/acs.jpclett.5b0086810.1021/acs.jpclett.5b00868 ↗
30. 10.1016/j.nanoen.2016.06.00510.1016/j.nanoen.2016.06.005 ↗
31. 10.1002/adma.20170209310.1002/adma.201702093 ↗
32. 10.1016/j.ensm.2017.12.00610.1016/j.ensm.2017.12.006 ↗
33. 10.1126/science.121300310.1126/science.1213003 ↗
34. 10.1039/C6EE01807F10.1039/C6EE01807F ↗
35. 10.1016/S1388-2481(01)00244-210.1016/S1388-2481(01)00244-2 ↗
36. 10.1021/jp074464w10.1021/jp074464w ↗
37. 10.1021/nn505501v10.1021/nn505501v ↗
38. 10.1039/C6EE01717G10.1039/C6EE01717G ↗
39. 10.1149/2.0151514jes10.1149/2.0151514jes ↗
40. 10.1039/C8EE00546J10.1039/C8EE00546J ↗
41. 10.1039/c2ee21675b10.1039/c2ee21675b ↗
42. 10.1016/j.electacta.2013.10.11310.1016/j.electacta.2013.10.113 ↗
43. 10.1021/am300385r10.1021/am300385r ↗
44. 10.1002/adfm.20150243310.1002/adfm.201502433 ↗
45. 10.1021/nn300920e10.1021/nn300920e ↗
46. 10.1002/aenm.20170276910.1002/aenm.201702769 ↗