2D-on-2D core-shell Co-3(PO4)(2) stacked micropetals@Co2Mo3O8 nanosheets and binder-free 2D CNT-Ti3C2TX-MXene electrodes for high-energy solid-state flexible supercapacitors
- Authors
- Patil, Amar M.; Chodankar, Nilesh R.; Jung, Euigeol; Roy, Sanjib; Dubal, Deepak P.; Guan, Guoqing; Han, Young-Kyu; Jun, Seong Chan
- Issue Date
- 30-Nov-2021
- Publisher
- ROYAL SOC CHEMISTRY
- Citation
- JOURNAL OF MATERIALS CHEMISTRY A, v.9, no.46, pp 26135 - 26148
- Pages
- 14
- Indexed
- SCIE
SCOPUS
- Journal Title
- JOURNAL OF MATERIALS CHEMISTRY A
- Volume
- 9
- Number
- 46
- Start Page
- 26135
- End Page
- 26148
- URI
- https://scholarworks.dongguk.edu/handle/sw.dongguk/4154
- DOI
- 10.1039/d1ta07919k
- ISSN
- 2050-7488
2050-7496
- Abstract
- The structural instability and sluggish kinetics of conventional positive electrodes with the lower capacitance of carbon-based negative electrodes result in an inferior performance for state-of-art supercapacitors (SCs). A general yet sustainable approach is proposed here to overcome this hitch by assembling hybrid SC cells utilising porous and stable 2D-on-2D core-shell and carbon/pseudocapacitive composite electrodes. Porous Co-3(PO4)(2) transparent stacked micropetals (TSMs) were synthesised and decorated with Co2Mo3O8 nanosheets (NSs) (Co-3(PO4)(2)@Co2Mo3O8) forming a 2D-on-2D core-shell positive electrode, which was combined with a 2D carbon nanotube/MXene (CNT-Ti3C2TX) composite negative electrode. The core-shell electrode achieved a specific capacity of 184.7 mA h g(-1) (738 mF cm(-2)) and cycling stability of 95.6% over 15 000 charge/discharge cycles. The CNT-Ti3C2TX electrode exhibited a remarkable areal capacitance of 187.5 mF cm(-2) and cycling stability of 93.1%. Consequently, the assembled unique hybrid solid-state SCs delivered an exceptional volumetric capacitance of 7.9 F cm(-3) and a specific energy of 74.06 W h kg(-1) (2.47 mW h cm(-3)) at a specific power and cycling stability of 1.13 kW kg(-1) and 93.2%, respectively. Overall, the techniques and electrode materials presented in this study can serve as a reference to produce a range of electrode materials for next-generation energy storage devices.
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Collections - College of Engineering > Department of Energy and Materials Engineering > 1. Journal Articles

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