Structural and Optical Properties of Ca 0.9 Cu 0.01 WO 4 Solid Solution Synthesized by Sonochemistry Method at Room Temperature

In this work, we report the room-temperature synthesis of pure calcium tungstate (CaWO ) and copper-doped calcium tungstate solid solution (Ca Cu WO ) by using a sonochemistry method. These materials were structurally characterized by X-ray diffraction (XRD) and Raman spectroscopy. The obtained XRD...

Full description

Saved in:
Bibliographic Details
Published inInorganic chemistry Vol. 59; no. 9; pp. 6039 - 6046
Main Authors Nobre, Francisco Xavier, Nogueira, Içamira Costa, Souza, Giancarlo da Silva, Matos, José Milton Elias de, Couceiro, Paulo Rogério da Costa, Brito, Walter Ricardo, de la Cruz, Javier Pérez, Leyet Ruiz, Yurimiler
Format Journal Article
LanguageEnglish
Published United States 04.05.2020
Online AccessGet full text

Cover

Loading…
More Information
Summary:In this work, we report the room-temperature synthesis of pure calcium tungstate (CaWO ) and copper-doped calcium tungstate solid solution (Ca Cu WO ) by using a sonochemistry method. These materials were structurally characterized by X-ray diffraction (XRD) and Raman spectroscopy. The obtained XRD patterns were submitted to a Rietveld refinement showing, in both materials, a tetragonal phase with space group and point group of 4 and , respectively. Microscopy images of both materials, obtained by field emission scanning electron microscopy, showed spherical agglomerated structures composed by spherical nanoparticles, while calcium and tungstate elements were identified by energy-dispersive X-ray spectroscopy for pure calcium tungstate and copper, calcium, and tungstate for Ca Cu WO solid solution. The decrease of optical band gap ( ) from 4.0 eV (CaWO ) to 3.45 eV (Ca Cu WO ) confirmed the substitution of calcium atoms for copper atoms in the clusters [CaO ]. Maximum photoluminescence (PL) emission was shifted from 522 nm in the pure CaWO to 475 nm in the Ca Cu WO solid solution. Consequently, there was an increase of PL emissions intensity in the blue and green regions of the visible spectrum, due to electronic transitions between the orbitals O 2p, Cu 3d, and W 5d.
ISSN:0020-1669
1520-510X
DOI:10.1021/acs.inorgchem.0c00019