In the present study, typical ZnO microcrystals exhibiting the wurtzite hexagonal crystal structure were produced successfully, characterized by a high degree of crystallinity, via hydrothermal processing at 120, 150 and 180 °C, assisted by N-cetyl-N,N,N-trimethylammonium (CTAB). The samples were characterised by XRD, Raman and infrared, FE-SEM, UV-Vis by diffuse reflectance and photoluminescence (PL). The experimental results confirm that all hydrothermally synthesised ZnO samples were crystallised into a wurtzite hexagonal structure. The ZnO crystals exhibit the morphology of hexagonal columns in the absence and double hexagonal columns in the presence of CTAB. The length and average diameter of the microstructures decrease with increasing processing temperature. It is evident that all the synthesised samples present very similar profiles and band positions in the PL emission spectra, with an emission band in the violet range at approximately 400 nm, a small peak in the UV range at approximately 380 nm, and highly superposed and intense emission bands between 440 and 750 nm (blue to red emission), with a maximum at approximately 610 nm. Furthermore, a nucleation and growth model was proposed to explain the formation of ZnO microcrystals, based on the experimental conditions, that were preferably grown in the [001] direction. In addition, the ZnO exhibited excellent performance in the photocatalytic degradation of rhodamine B (RhB) and methyl orange (MO), achieving 97% and 99% photodegradation of RhB and MO, respectively, when ZnO obtained at 120 °C, in the absence of CTAB, was used as catalyst.

Barium praseodymium tungstate (Ba_1-xPr_2x/3)WO₄ crystals with (x = 0, 0.01, and 0.02) were prepared by the coprecipitation method. These crystals were structurally characterized by X-ray diffraction (XRD), Rietveld refinements, Fourier-transform Raman (FT-Raman) and Fourier-transform infrared (FT-IR) spectroscopies. The shape and size of these crystals were observed by field emission scanning electron microcopy (FE-SEM). Their optical properties were investigated by ultraviolet visible (UV-vis) absorption and photoluminescence (PL) measurements. Moreover, we have studied the photocatalytic (PC) activity of crystals for degradation of rhodamine B (RhB) dye. XRD patterns, Rietveld refinements data, FT-Raman and FT-IR spectroscopies indicate that all crystals exhibit a tetragonal structure without deleterious phases. FT-Raman spectra exhibited 13 Raman-active modes in a range from 50 to 1000 cm⁻¹, while FT-IR spectra have 8 infrared active modes in a range from 200 to 1050 cm⁻¹. FE-SEM images showed different shapes (bonbon-, spindle-, rice- and flake-like) as well as a reduction in the crystal size with an increase in Pr³⁺ ions. A possible growth process was proposed for these crystals. UV-vis absorption measurements revealed a decrease in optical band gap values with an increase of Pr³⁺ into the matrix. An intense green PL emission was noted for (Ba_1-xPr_2x/3)WO₄ crystals (x = 0), while crystals with (x = 0.01 and 0.02) produced a reduction in the wide band PL emission and the narrow band PL emission which is related to f–f transitions from Pr³⁺ ions. High photocatalytic efficiency was verified for the bonbon-like BaWO₄ crystals as a catalyst in the degradation of the RhB dye after 25 min under UV-light. Finally, we discuss possible mechanisms for PL and PC properties of these crystals.