Highly Rate Capable Nanoflower-like NiSe and WO3@PPy Composite Electrode Materials toward High Energy Density Flexible All-Solid-State Asymmetric Supercapacitor
Source abstract
Abstract
An advanced novel all-solid-state asymmetric supercapacitor (ASC) device of high energy and power densities is designed on the basis of the nanoflower-like NiSe as the positive electrode and WO3@PPy composite as the negative one. The porous NiSe was prepared by facile selenization of predesigned NiO nanoflowers, and the WO3@PPy composite was synthesized through in situ oxidative polymerization of pyrrole in the presence of dispersed WO3 nanosticks which, in turn, was produced by a simple sulfate-assisted hydrothermal method. When tested as a supercapacitor positive electrode in the three-electrode system, the NiSe exhibits an appreciably higher specific capacitance of 1274 F g–1 at 2 A g–1 than that of the NiO nanoflower (774 F g–1). Again, as the negative electrode, the WO3@PPy composite also shows excellent electrochemical properties with a higher specific capacitance (586 F g–1 at 2 A g–1) than those of either of its components (WO3: 402 F g–1 and PPy: 224 F g–1). Based on these properties of the respective electrodes, a flexible ASC device was designed and fabricated by assembling the NiSe as the positive electrode with WO3@PPy composite as the negative electrode. The NiSe//WO3@PPy solid-state ASC with an extended potential window of 1.25 V demonstrates an admirable energy density of 37.3 Wh kg–1 at a power density of 1249 W kg–1 at 2 A g–1 along with outstanding long-term cycling stability that retains 91% of the initial capacitance even after 5000 charging and discharging cycles. All these results reveal the proficiency of the ASC device as a high-performance energy storage system for next-generation portable electronics.
Source: openalex_inverted_index · 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
Materials Science Centre, Indian Institute of Technology Kharagpur, Kharagpur 721302, West Bengal, India
Funding
Indian Institute of Technology Kharagpur
References (47)
Show source-provided references
1. 10.1002/smll.20170097910.1002/smll.201700979 ↗
2. 10.1016/j.electacta.2017.08.08410.1016/j.electacta.2017.08.084 ↗
3. 10.1007/s11581-017-2428-810.1007/s11581-017-2428-8 ↗
4. 10.1021/acssuschemeng.7b0072910.1021/acssuschemeng.7b00729 ↗
5. 10.1039/C7TA03004E10.1039/C7TA03004E ↗
6. 10.1016/j.cej.2017.08.07810.1016/j.cej.2017.08.078 ↗
7. 10.1039/C6TA08331E10.1039/C6TA08331E ↗
8. 10.1002/adfm.20180088610.1002/adfm.201800886 ↗
9. 10.1002/celc.20150028510.1002/celc.201500285 ↗
10. 10.1016/j.jpowsour.2010.09.07810.1016/j.jpowsour.2010.09.078 ↗
11. 10.1039/C6TA04258A10.1039/C6TA04258A ↗
12. 10.1039/C5TA05523G10.1039/C5TA05523G ↗
13. 10.1002/aenm.20160273310.1002/aenm.201602733 ↗
14. 10.1016/j.jpowsour.2016.08.09710.1016/j.jpowsour.2016.08.097 ↗
15. 10.1002/adma.20160416710.1002/adma.201604167 ↗
16. 10.1039/C6TA10179H10.1039/C6TA10179H ↗
17. 10.1038/ncomms769410.1038/ncomms7694 ↗
18. 10.1039/C6RA06909F10.1039/C6RA06909F ↗
19. 10.1002/celc.20170103310.1002/celc.201701033 ↗
20. 10.1002/smll.20140234010.1002/smll.201402340 ↗
21. 10.1039/C8NR02311E10.1039/C8NR02311E ↗
22. 10.1016/j.jpowsour.2018.05.02010.1016/j.jpowsour.2018.05.020 ↗
23. 10.1016/j.electacta.2016.12.06610.1016/j.electacta.2016.12.066 ↗
24. 10.1016/j.jallcom.2017.01.22610.1016/j.jallcom.2017.01.226 ↗
25. 10.1016/j.colsurfa.2015.06.04010.1016/j.colsurfa.2015.06.040 ↗
26. 10.1039/C5CC00965K10.1039/C5CC00965K ↗
27. 10.1021/nl400378j10.1021/nl400378j ↗
28. 10.1002/adma.20140462210.1002/adma.201404622 ↗
29. 10.1039/C8TA05976D10.1039/C8TA05976D ↗
30. 10.1016/j.matlet.2016.06.06510.1016/j.matlet.2016.06.065 ↗
31. 10.1039/C0JM02316G10.1039/C0JM02316G ↗
32. 10.1016/j.jpowsour.2012.11.08810.1016/j.jpowsour.2012.11.088 ↗
33. 10.1039/c3ta13859c10.1039/c3ta13859c ↗
34. 10.1039/c0jm03749d10.1039/c0jm03749d ↗
35. 10.1021/acsami.5b0409410.1021/acsami.5b04094 ↗
36. 10.1021/acsami.8b1938610.1021/acsami.8b19386 ↗
37. 10.1016/j.jechem.2017.09.02310.1016/j.jechem.2017.09.023 ↗
38. 10.1016/j.ensm.2017.03.00510.1016/j.ensm.2017.03.005 ↗
39. 10.1039/C7TA05134D10.1039/C7TA05134D ↗
40. 10.1007/s11814-014-0323-910.1007/s11814-014-0323-9 ↗
41. 10.1149/1.205613010.1149/1.2056130 ↗
42. 10.1016/0379-6779(94)90073-610.1016/0379-6779(94)90073-6 ↗
43. 10.1016/j.jpowsour.2011.01.07310.1016/j.jpowsour.2011.01.073 ↗
44. 10.1002/cphc.20140262510.1002/cphc.201402625 ↗
45. 10.1155/2014/81312010.1155/2014/813120 ↗
46. 10.1016/j.electacta.2019.01.00710.1016/j.electacta.2019.01.007 ↗
47. 10.1016/j.ensm.2017.07.00610.1016/j.ensm.2017.07.006 ↗