4.6 Article

In situ nanoarchitecturing of conjugated polyamide network-derived carbon cathodes toward high energy-power Zn-ion capacitors

期刊

JOURNAL OF MATERIALS CHEMISTRY A
卷 10, 期 2, 页码 611-621

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ta07350h

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资金

  1. National Natural Science Foundation of China [21875165, 51772216, 21905207, 22172111]
  2. Science and Technology Commission of Shanghai Municipality, China [20ZR1460300, 14DZ2261100]
  3. Zhejiang Provincial Natural Science Foundation of China [LY19B010003]
  4. Fundamental Research Funds for the Central Universities
  5. Large Equipment Test Foundation of Tongji University

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Zn-ion hybrid capacitors with O/N-decorated porous carbon cathodes demonstrated large capacity, ultrahigh energy density, excellent power output, and remarkable capacity retention, offering valuable insights into the fabrication of high-performance carbon cathodes for practical Zn-based energy storage in the future.
Zn-ion hybrid capacitors, with a large-capacity Zn anode (battery-type) integrated with a capacitive cathode, hold great potential to relieve the unsatisfactory energy-to-power ratio of aqueous supercapacitors. The research into cathode design is expected to bridge the capacity gap between the two electrodes without sacrificing the inherent power/cycling superiorities but is still in its infancy. In this work, robust O/N-decorated porous carbon cathodes were derived by the in situ calcination of conjugated polyamides, wherein the solvent-guided strategy was applied to shape the carbon nanoarchitecture for the activation of Zn storage sites. After optimizing the solvent-precursor interactions, the packed particle architecture (C-DMF) ultimately exposed ample electrosorption platform up to 1656 m(2) g(-1), and O/N dopants (15.77 wt%) promoted interfacial Zn adsorption by lowering the energy barrier for C-O-Zn bonding. Further experimental evaluations revealed that the C=O species on the robust C-DMF framework tended to boost reversible chemical adsorption to form C-O-Zn bondings while maintaining durable charge transfer, which minimized capacity loss even at high rates. As a result, the aqueous C-DMF//Zn capacitor achieved a large capacity of 180 mA h g(-1), an ultrahigh energy density of 106.7 W h kg(-1) and an excellent power output of 13.4 kW kg(-1), as well as 91.1% capacity retention over 300 000 cycles. This design strategy gives an appealing insight into the subtle fabrication of high-performance carbon cathodes and highlights their applicability towards practical Zn-based energy storage in the future.

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