The best photocatalytic properties for monoclinic ZnWO₄nanocrystals are related to the surface energy and the types of clusters formed on their surface.

CaWO₄:Eu³⁺ microcrystals (with 0, 1, 2 and 4 mol% Eu³⁺) were synthesized by a co-precipitation (CP) method and grown in a microwave-assisted hydrothermal (MAH) system at 130 °C for 30 min. X-ray diffraction (XRD), Rietveld refinement, X-ray absorption near edge spectroscopy (XANES), Fourier-transform Raman (FT-Raman) and Fourier-transform infrared (FT-IR) spectroscopy indicated that all of the microcrystals have a scheelite-type tetragonal structure without deleterious phases. Structural refinement data were employed to model the [CaO₈], [EuO₈] and [WO₄] clusters. XANES spectra confirmed that the presence of deltahedral [EuO₈] clusters promotes small distortions of neighbouring tetrahedral [WO₄] clusters in a global tetragonal lattice. Field emission scanning electron microcopy (FE-SEM) images revealed that the replacement of Ca²⁺ by Eu³⁺ ions changed the particles' shapes, resulting in the different morphologies of the microcrystals. UV-vis diffuse reflectance spectra indicated a reduction in the optical band gap with the replacement of Ca²⁺ by Eu³⁺ ions. The photoluminescence (PL) properties of the Eu³⁺ ions in CaWO₄ were studied as well as the chromaticity coordinates and lifetimes of these compounds.

Europium doped silver tungstates α-Ag_2−3xEu_xWO₄(x= 0, 0.0025, 0.005, 0.0075 and 0.01 mol) were synthesized by the coprecipitation method at 90 °C for 30 minutes. PL spectra showed a broad band related to the [WO₆] group and characteristic narrow peaks due to the f–f transitions of Eu³⁺as a result of efficient energy transfer from the matrix.