A Compact MXene Film with Folded Structure for Advanced Supercapacitor Electrode Material
Source abstract
Abstract
A Ti3C2Tx MXene film assembled by using conventional vacuum-assisted filtration has an outstanding volumetric performance due to its excellent pseudocapacitive and high density. However, the severely high energy and time consumption by vacuum-assisted filtration will limit its practical mass production as electrodes; meanwhile, the self-restacking of MXene nanosheets increases ion diffusion limitation, especially for thicker film electrodes. Herein, a simple strategy is employed to fabricate a compact and nanoporous MXene film with folded structure (CN-MX) by mechanically pressing a three-dimensional MXene aerogel, resulting in an increased packing density and electrical conductivity (8681 S m–1) while retaining sufficiently abundant ion-accessible active sites. In addition, the formed highly interconnected nanopore channels can facilitate more rapid ionic and electronic transport. When applied as additive-free electrodes for supercapacitors, the CN-MX delivers a comparable volumetric capacitance and much improved rate capability performance compared to the MXene film fabricated by vacuum-assisted filtration. More impressively, it can still exhibit an attractive volumetric capacitance even at practical levels of mass loading (above 10 mg cm–2). This study opens a feasible avenue forward toward commercial applications of MXene in portable and compact storage devices.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: MXene and MAX Phase Materials · Supercapacitor Materials and Fabrication · Advanced Sensor and Energy Harvesting Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
MIIT Key Laboratory of Critical Materials Technology for New Energy Conversion and Storage, School of Chemistry and Chemical Engineering, Harbin Institute of Technology, Harbin 150001, P. R. China
National Key Laboratory of Science and Technology on Advanced Composites in Special Environments, Harbin Institute of Technology, Harbin 150080, P. R. China
Funding
China Postdoctoral Science Foundation · National Natural Science Foundation of China
References (56)
Show source-provided references
1. 10.1002/adma.20110230610.1002/adma.201102306 ↗
2. 10.1021/acs.chemmater.7b0284710.1021/acs.chemmater.7b02847 ↗
3. 10.1038/natrevmats.2016.9810.1038/natrevmats.2016.98 ↗
4. 10.1038/nenergy.2017.10510.1038/nenergy.2017.105 ↗
5. 10.1038/s41586-018-0109-z10.1038/s41586-018-0109-z ↗
6. 10.1002/smll.20190208510.1002/smll.201902085 ↗
7. 10.1126/science.aag242110.1126/science.aag2421 ↗
8. 10.1016/j.cej.2018.11.05110.1016/j.cej.2018.11.051 ↗
9. 10.1002/adma.20170236710.1002/adma.201702367 ↗
10. 10.1021/acsnano.8b0099710.1021/acsnano.8b00997 ↗
11. 10.1016/j.cej.2019.12269610.1016/j.cej.2019.122696 ↗
12. 10.1016/j.joule.2018.09.01110.1016/j.joule.2018.09.011 ↗
13. 10.1002/adfm.20190519710.1002/adfm.201905197 ↗
14. 10.1021/acsnano.9b0160210.1021/acsnano.9b01602 ↗
15. 10.1002/adfm.20180681910.1002/adfm.201806819 ↗
16. 10.1021/acsnano.6b0841510.1021/acsnano.6b08415 ↗
17. 10.1002/advs.20180051810.1002/advs.201800518 ↗
18. 10.1016/j.nanoen.2018.05.02010.1016/j.nanoen.2018.05.020 ↗
19. 10.1038/s41467-017-02529-610.1038/s41467-017-02529-6 ↗
20. 10.1016/j.mattod.2019.05.01710.1016/j.mattod.2019.05.017 ↗
21. 10.1016/j.compscitech.2019.10775410.1016/j.compscitech.2019.107754 ↗
22. 10.1073/pnas.141421511110.1073/pnas.1414215111 ↗
23. 10.1002/adfm.20160035710.1002/adfm.201600357 ↗
24. 10.1021/acsnano.6b0524010.1021/acsnano.6b05240 ↗
25. 10.1002/adma.20170267810.1002/adma.201702678 ↗
26. 10.1021/acsnano.9b0639410.1021/acsnano.9b06394 ↗
27. 10.1002/adfm.20170126410.1002/adfm.201701264 ↗
28. 10.1002/adma.20140414010.1002/adma.201404140 ↗
29. 10.1039/C8TA05807E10.1039/C8TA05807E ↗
30. 10.1002/adma.20150470510.1002/adma.201504705 ↗
31. 10.1002/smll.20180378610.1002/smll.201803786 ↗
32. 10.1002/advs.20180075010.1002/advs.201800750 ↗
33. 10.1002/adma.20110469110.1002/adma.201104691 ↗
34. 10.1016/j.joule.2018.02.01810.1016/j.joule.2018.02.018 ↗
35. 10.1002/aelm.20160025510.1002/aelm.201600255 ↗
36. 10.1039/C8NR01550C10.1039/C8NR01550C ↗
37. 10.1021/acsnano.9b0461210.1021/acsnano.9b04612 ↗
38. 10.1126/sciadv.aat049110.1126/sciadv.aat0491 ↗
39. 10.1016/j.matt.2019.05.02010.1016/j.matt.2019.05.020 ↗
40. 10.1002/anie.20190613810.1002/anie.201906138 ↗
41. 10.1021/acsnano.8b0573910.1021/acsnano.8b05739 ↗
42. 10.1002/adfm.20190396010.1002/adfm.201903960 ↗
43. 10.1021/nn402272u10.1021/nn402272u ↗
44. 10.1002/aenm.20160018510.1002/aenm.201600185 ↗
45. 10.1039/C7TA04384H10.1039/C7TA04384H ↗
46. 10.1039/C5EE03109E10.1039/C5EE03109E ↗
47. 10.1002/adma.20170571310.1002/adma.201705713 ↗
48. 10.1038/nature1397010.1038/nature13970 ↗
49. 10.1002/adma.20150415110.1002/adma.201504151 ↗
50. 10.1021/nn301291610.1021/nn3012916 ↗
51. 10.1039/C5TA03113C10.1039/C5TA03113C ↗
52. 10.1126/science.aam585210.1126/science.aam5852 ↗
53. 10.1021/acs.nanolett.6b0403510.1021/acs.nanolett.6b04035 ↗
54. 10.1039/C6TA01406B10.1039/C6TA01406B ↗
55. 10.1016/j.electacta.2015.10.01610.1016/j.electacta.2015.10.016 ↗
56. 10.1039/C5TA03113C10.1039/C5TA03113C ↗