4.6 Article

2D-on-2D core-shell Co3(PO4)2 stacked micropetals@Co2Mo3O8 nanosheets and binder-free 2D CNT-Ti3C2TX-MXene electrodes for high-energy solid-state flexible supercapacitors

Journal

JOURNAL OF MATERIALS CHEMISTRY A
Volume 9, Issue 46, Pages 26135-26148

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ta07919k

Keywords

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Funding

  1. Brain Pool Program through the National Research Foundation of Korea (NRF) - Ministry of Science and ICT [2020H1D3A1A04105926]
  2. National Research Foundation of Korea (NRF) - Korea government (MIST) [NRF-2019R1A2C2090443]
  3. Nano-materials Technology Development Program [NRF-2017M3A7B4041987]
  4. Korea Electric Power Corporation [R19XO01-23]
  5. Technology Innovation Program - Ministry of Trade, Industry & Energy (MOTIE, Korea) [20013621]
  6. National Research Foundation of Korea [2020H1D3A1A04105926] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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This study proposed a method to overcome the inferior performance of conventional electrodes in supercapacitors by assembling hybrid SC cells with porous and stable 2D core-shell positive electrodes and carbon/pseudocapacitive composite negative electrodes. The assembled hybrid solid-state SCs showed exceptional cycling stability and energy storage performance, providing a reference for next-generation energy storage devices.
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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