Comparative Study of Crystallite Size from XRD and TEM Results for Pure and V2O5 Doped CdO-FePO4 Composite Nanopowders

Document Type : Regular Article

Authors

1 Department of Physics, Acharya Nagarjuna University, Nagarjuna Nagar, Guntur-522510, A.P., India. Department of Physics, P. B. Siddhartha College of Arts and Science, Vijayawada-520010, A.P., India

2 Department of Physics, Acharya Nagarjuna University, Nagarjuna Nagar, Guntur-522510, A.P., India. Department of Physics, Government Institute of Textile Technology, Guntur-522005, A.P., India

3 Department of Physics, Acharya Nagarjuna University, Nagarjuna Nagar, Guntur-522510, A.P., India

10.22036/pcr.2022.337333.2077

Abstract

CdO-FePO4 composite nanopowders (CNPs) with V2O5 ions as dopants are prepared by a sol-gel technique. The as-synthesized CNPs are characterized by peak profile analysis of powder X-ray diffraction (XRD) and Transmission electron microscopy (TEM). The powder XRD analysis reveals that the prepared products are crystalline with the cubic phase of CdO. The Debye-Scherrer’s method and Williamson-Hall (W-H) plot analysis are worn to find out the separate contributions of the size of the crystal lattice and microstrain on the peak broadening of prepared CNPs. The other relevant physical parameters like microstrain and dislocation density values are determined for all the XRD peaks related to the cubic phase of CdO between 10 and 80 degrees of 2-theta values. The morphological analysis and determination of mean crystallite size are done from TEM images. The estimated crystallite size values obtained from the XRD (W-H plot and Debye-Scherrer’s method) and TEM analysis revealed that the results are highly inter-correlated. The EDX spectra confirm the presence of elements Cd, Fe, P, V, and O in the prepared sample. FT-IR study exhibited functional groups related to phosphates and oxides.

Graphical Abstract

Comparative Study of Crystallite Size from XRD and TEM Results for Pure and V2O5 Doped CdO-FePO4 Composite Nanopowders

Keywords


  • Receive Date: 12 April 2022
  • Revise Date: 31 May 2022
  • Accept Date: 06 June 2022
  • First Publish Date: 19 June 2022