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article · Microscopy Research and Technique

Enhanced Electrochemical Performance of Highly Porous <scp>CeO<sub>2</sub></scp>‐Doped Zr Nanoparticles for Supercapacitor Applications

202411 citationsOpen accessUniversity of South Africa

Abstract

The aim of this work was to develop an ultrasonic-assisted synthesis method for the fabrication of CeO<sub>2</sub>-doped Zr nanoparticles that would improve the performance of supercapacitor electrodes. This method, which eliminates the need for high-temperature calcination, involves embedding CeO<sub>2</sub> into Zr nanoparticles through 1 hr (CeO<sub>2</sub>-Zr-1) and 2 hrs (CeO<sub>2</sub>-Zr-2) of ultrasonic irradiation, resulting in the formation of nanostructures with significant improvements in their electrochemical properties. Through physicochemical analysis, we observed that the CeO<sub>2</sub>-doped Zr nanoparticles, particularly those treated for 2 hrs (CeO<sub>2</sub>-Zr-2), exhibit superior crystalline phase purity, optimal chemical surface composition, minimal agglomeration with particle sizes below 50 nm, and an impressive average surface area of 178 m<sup>2</sup>/g. Compared to the 1 hr irradiation samples (CeO<sub>2</sub>-Zr-1) and undoped CeO<sub>2</sub> nanoparticles, the (CeO<sub>2</sub>-Zr-2) electrodes demonstrated a remarkable capacitance of 198 Fg<sup>-1</sup> at a current density of 1 A/g while maintaining ~94.9% of their capacity after 3750 cycles. This indicates not only good reversibility but also exceptional stability. In (CeO<sub>2</sub>-Zr-2) samples, the nanospherical structure achieved through ultrasonic synthesis is responsible for the enhanced capacitive behavior and stability, along with the synergistic effects caused by Zr doping, which improves the CeO<sub>2</sub> nanoparticle conductivity to a significant extent. Surface areas of the electrodes are larger due to the combination of these two materials, which contribute to their superior performance.

Research topics

  • Supercapacitor Materials and Fabrication
  • Electrocatalysts for Energy Conversion
  • Catalytic Processes in Materials Science

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DOI: 10.1002/jemt.24728

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