Abstract

The investigation deals with the synthesis and characterization of praseodymium doped ceria (PDC) nanoparticles by citrate nitrate auto-combustion method. The as prepared PDC powders were calcined at 700 °C, and then dense cylindrical electrolyte bodies were fabricated by uni-axial compression followed by sintering at 1200 °C. The PDC nanocrystals and compacts were subjected to characterization studies such as X-ray diffraction, scanning and transmission electron microscopy, elemental analysis, Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy and electrochemical analyses. The crystal structure of PDC was found to be a cubic fluorite system by X-ray diffraction analysis (XRD). The surface morphologies and the grain distributions of the calcined nanoparticles and sintered bodies were studied by scanning electron microscopy (SEM). The grain size of the sintered material was found to be in the range from 100 nm to 500 nm. Transmission electron microscopic (TEM) images revealed the presence of polyhedral, sphere-like shape of the nanoparticles with a size range 10–25 nm. The symmetric stretching mode of the Ce–O was obtained at 555 cm−1 in the FTIR spectrum. The Raman active mode for the PDC was obtained at 457 cm−1. The presence of oxygen vacancies was confirmed from the weaker absorption band observed at 560 cm−1 in the Raman spectrum. The change in current density with increasing sweep scan potential was studied by cyclic voltammetry (CV) analysis. The specific capacitance range of the PDC was calculated as 20–72.4 Fg−1.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.