AI Article Synopsis

  • Nitrogen-doped multiwalled carbon nanotubes (N-MWCNTs) can enhance various energy devices like supercapacitors, batteries, and sensors due to their unique properties.
  • Researchers synthesized CuO@MnO and CuO@MnO/N-MWCNT composites using a specific hydrothermal method and characterized their structural properties through various techniques (like Raman spectroscopy and SEM).
  • The composite electrodes demonstrated a specific capacitance of ~184 F/g and excellent stability, retaining 98.5% capacity after 5000 charge-discharge cycles when tested under specific conditions.

Article Abstract

Nitrogen-doped multiwalled carbon nanotubes (N-MWCNTs) have been used to fabricate nanostructured materials for various energy devices, such as supercapacitors, sensors, batteries, and electrocatalysts. Nitrogen-doped carbon-based electrodes have been widely used to improve supercapacitor applications via various chemical approaches. Based on previous studies, CuO@MnO and CuO@MnO/N-MWCNT composites were synthesized using a sonication-supported hydrothermal reaction process to evaluate their supercapacitor properties. The structural and morphological properties of the synthesized composite materials were characterized via Raman spectroscopy, XRD, SEM, and SEM-EDX, and the morphological properties of the composite materials were confirmed by the nanostructured composite at the nanometer scale. The CuO@MnO and CuO@MnO/N-MWCNT composite electrodes were fabricated in a three-electrode configuration, and electrochemical analysis was performed via CV, GCD, and EIS. The composite electrodes exhibited the specific capacitance of ~ 184 F g at 0.5 A g in the presence of a 5 M KOH electrolyte for the three-electrode supercapacitor application. Furthermore, it exhibited significantly improved specific capacitances and excellent cycling stability up to 5000 GCD cycles, with a 98.5% capacity retention.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9489798PMC
http://dx.doi.org/10.1038/s41598-022-16863-3DOI Listing

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