Carbon Textile Decorated with Pseudocapacitive VC/VxOy for High‐Performance Flexible Supercapacitors
Source abstract
Abstract
Abstract It is demonstrated that, via V2O5 coating by low temperature atomic layer deposition and subsequent pyrolysis, ubiquitous cotton textile can readily turn into high‐surface‐area carbon textile fully decorated with pseudocapacitive VxOy/VC widely usable as electrodes of high‐performance supercapacitor. It is found that carbothermic reduction of V2O5 (C + V2O5 → C′ + VC + CO/CO2(g)) leads to chemical/mechanical activation of carbon textile, thereby producing high‐surface‐area conductive carbon textile. In addition, sequential phase transformation and carbide formation (V2O5 → VxOy → VC) occurred by carbothermic reduction trigger decoration of the carbon textile with redox‐active VxOy/VC. Thanks to the synergistic effect of electrical double layer and pseudocapacitance, the supercapacitors made of the hybrid carbon textile exhibit far better energy density (over 30‐fold increase) with excellent cycling stability than the carbon textile simply undergone pyrolysis. The method can open up a promising and facile way to synthesize hybrid electrode materials for electrochemical energy storages possessing advantages of both electrical double layer and pseudocapacitive material.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Supercapacitor Materials and Fabrication · Advanced battery technologies research · Electrocatalysts for Energy Conversion
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Nanomechanics Korea Institute of Machinery and Materials (KIMM) 156 Gajeongbuk‐ro Yuseong‐gu Daejeon 34103 South Korea
Nano Mechatronics Korea University of Science and Technology (UST) 217 Gajeong‐ro Yuseong‐gu Daejeon 34113 South Korea
Funding
Ministry of Science, ICT and Future Planning · National Research Council of Science and Technology · Korea Institute of Machinery and Materials
References (40)
Show source-provided references
1. 10.1126/science.124962510.1126/science.1249625 ↗
2. 10.1149/2.F08081IF10.1149/2.F08081IF ↗
3. 10.1016/j.rser.2015.12.24910.1016/j.rser.2015.12.249 ↗
4. 10.1039/C1CS15060J10.1039/C1CS15060J ↗
5. 10.1038/nmat229710.1038/nmat2297 ↗
6. 10.1002/cssc.20110057110.1002/cssc.201100571 ↗
7. 10.1021/acsnano.6b0660810.1021/acsnano.6b06608 ↗
8. 10.1126/science.121674410.1126/science.1216744 ↗
9. 10.1016/j.jpowsour.2012.01.02810.1016/j.jpowsour.2012.01.028 ↗
10. 10.1002/advs.20150028610.1002/advs.201500286 ↗
11. 10.1038/ncomms754410.1038/ncomms7544 ↗
12. 10.1021/acs.jpclett.5b0086810.1021/acs.jpclett.5b00868 ↗
13. 10.1002/ese3.5010.1002/ese3.50 ↗
14. 10.1021/nn203085j10.1021/nn203085j ↗
15. 10.1038/ncomms293210.1038/ncomms2932 ↗
16. 10.1002/adma.20130350310.1002/adma.201303503 ↗
17. 10.1021/cm504801r10.1021/cm504801r ↗
18. 10.1039/C4TA04431B10.1039/C4TA04431B ↗
19. 10.1039/c2ee21110f10.1039/c2ee21110f ↗
20. 10.1038/ncomms343110.1038/ncomms3431 ↗
21. 10.1038/ncomms1158610.1038/ncomms11586 ↗
22. 10.1016/j.jpowsour.2016.08.03910.1016/j.jpowsour.2016.08.039 ↗
23. 10.1007/s10853-010-5123-y10.1007/s10853-010-5123-y ↗
24. 10.1134/S107042721501006110.1134/S1070427215010061 ↗
25. 10.1039/b003593i10.1039/b003593i ↗
26. 10.1016/j.elspec.2004.03.00410.1016/j.elspec.2004.03.004 ↗
27. 10.1039/C6TA08900C10.1039/C6TA08900C ↗
28. 10.1039/C4CC08896D10.1039/C4CC08896D ↗
29. 10.1039/C4RA13707H10.1039/C4RA13707H ↗
30. 10.1016/j.jmps.2009.06.00210.1016/j.jmps.2009.06.002 ↗
31. 10.1039/c0sm00401d10.1039/c0sm00401d ↗
32. 10.1016/j.ssc.2006.01.02610.1016/j.ssc.2006.01.026 ↗
33. 10.1002/adfm.20100260310.1002/adfm.201002603 ↗
34. 10.1039/C4TA03731F10.1039/C4TA03731F ↗
35. 10.1039/C4TA04062G10.1039/C4TA04062G ↗
36. 10.1016/j.jcis.2013.11.08610.1016/j.jcis.2013.11.086 ↗
37. 10.1126/science.113219510.1126/science.1132195 ↗
38. 10.1002/adma.20130475610.1002/adma.201304756 ↗
39. 10.1021/nn306044d10.1021/nn306044d ↗
40. 10.1002/adma.20120341010.1002/adma.201203410 ↗