Synthesis of Pr3+-doped WO3 particles: correlation between photoluminescent and photocatalytic properties.

The WO3 and WO3:Pr3+ particles were successfully synthesized by the co-precipitation method. The XRD analysis with Rietveld refinement revealed the formation of a monoclinic phase for WO3 and for doped samples, this result was later confirmed by Raman spectroscopy studies. The presence of Pr3+ in the WO3 crystalline lattice induced structural and optical changes in the particles, increasing the crystallite size, distorting the clusters (shortening of the W-O bonds), favoring the crystallinity and changing the optical gap. The predominant morphology of the particles of WO3 and WO3:Pr3+ obtained was nanocubes constituted by the superposition of plates of nanometric thicknesses. The photoluminescence of WO3 and WO3:Pr3+ was produced by the existence of surface defects in the particles. The increase in the concentration of Pr3+ promoted an increase in the intensity of PL, due to the increase in the rate of recombination of electron/hole charges. The WO3 sample exhibited emission in the white region due to the adjustment of simultaneous electronic transitions in the blue, green and red regions, characteristic of the broadband spectrum. The interval of the 2.65 eV gap band and the high efficiency in the separation of the photogenerated charges (e-/h+) with the low recombination rate contributed to the photocatalytic degradation of Crystal Violet (CV) by the catalyst. The WO3:4% Pr3+ sample showed the best photocatalytic efficiency, degrading 73% of the CV dye in 80 minutes. This result was associated with a reduction in particle size and density of oxygen vacancies on the material surface.

Photocatalytic degradation of methylene blue and dye mixture using indium-doped CaWO4 synthesized by sonochemical and microwave-assisted hydrothermal methods.

This study presents indium-doped calcium tungstate for the first time. The photocatalytic and photoluminescent properties of pure and In3+ doped samples were investigated. All pure and indium-doped calcium tungstate particles were synthesized for 30 minutes by two different methods: the sonochemical method (SM) and the microwave-assisted hydrothermal method. The nanoparticles were characterized by X-ray diffraction (XRD), field emission gun-scanning electron microscopy (SEM-FEG), UV-Visible spectroscopy, Brunauer-Emmett-Teller method, and zeta potential analysis. The diffractogram results confirmed the formation of scheelite crystalline structures without forming deleterious phases. The SEM-FEG images show the powder with irregular morphology and agglomerated as rods and kibes. For both methods, samples with 8% In3+ ions showed lower PL intensities with maximum peaks at 479 and 483 nm, suggesting lower e-/h+ pair recombination, which led these samples to present better photocatalytic performance. The photocatalytic activity was estimated from the degradation of the methylene blue (MB) dye under UV light and the sample stability was tested in 3 reuse cycles. The scavenger methodology indicated that h+ is the most active mechanism in the photocatalysis process. The degradation of the dye mixture (MB, MO, and RhB dyes) was also performed.

Correction: Synthesis and evaluation of photocatalytic and photoluminescent properties of Zn2+-doped Bi2WO6.

Correction for 'Synthesis and evaluation of photocatalytic and photoluminescent properties of Zn2+-doped Bi2WO6' by L. X. Lovisa, et al., Dalton Trans., 2022, https://doi.org/10.1039/d2dt03175b.

Synthesis and evaluation of photocatalytic and photoluminescent properties of Zn2+-doped Bi2WO6.

This study consists of the synthesis of zinc-doped Bi2WO6 obtained by the sonochemical method. The XRD results indicated that the samples showed an orthorhombic phase with the P21ab space group without the presence of secondary phases, demonstrating success in the doping process. The results of the photocatalytic tests under the photodegradation of methylene blue showed better performance for the pure sample with 80% degradation during 2 hours of exposure to radiation. The high rate of photogenerated charges accompanied by the low recombination rate of the pairs and e-/h+ were responsible for forming hydroxyl radicals, the predominant oxidative agent of the mechanism. The increase in Zn2+ concentration in the Bi2WO6 matrix promoted inhibition of the photocatalytic properties by the appearance of oxygen vacancies that acted as a charge recombination center. In contrast, photoluminescence was improved by doping with Zn2+. The Bi2WO6:8% Zn2+ sample showed the highest PL intensity. The characteristics of the emitted colors are modulated from the emission spectra and are quantified in terms of the photometric parameters: chromaticity coordinates (x, y), color reproduction index (CRI), luminous radiation efficiency (LER), and purity of color (%) of samples. The adjustment in the colors is promoted as a function of the increase in the Zn2+ concentration observing the transition from: yellow → orange → green. PL is favored by the effect of the dopant (Zn2+) in the matrix, which allows Bi2WO6:Zn2+ to be considered a promising candidate for applications in optical devices. In addition, Bi2WO6 constitutes a high performance photocatalyst for the degradation of methylene blue.

Structure, electronic properties, morphology evolution, and photocatalytic activity in PbMoO4 and Pb1-2xCaxSrxMoO4 (x = 0.1, 0.2, 0.3, 0.4 and 0.5) solid solutions.

In this work PbMoO4 and Pb1-2xCaxSrxMoO4 (x = 0.1, 0.2, 0.3, 0.4 and 0.5) solid solutions have been successfully prepared, for the first time, by a simple co-precipitation method and the as-synthesized samples were subjected to a water-based reflux treatment. Structural characterization of these samples was performed using X-ray diffraction with Rietveld refinement analysis and Raman spectroscopy. Their optical properties were investigated by UV-Vis absorption spectroscopy and PL emissions, and the photocatalytic activity of the as-synthesized samples for the degradation process of Rhodamine B has been demonstrated. The surface structure and morphologies were characterized by field emission scanning electron microscopy. To complement and rationalize the experimental results, the geometry, electronic structures, and morphologies of as-synthesized samples were characterized by first-principles quantum-mechanical calculations at the density functional theory level. By using Wulff construction, based on the values of the surface energies for the (001), (100), (110), (111), (011) and (112) surfaces, a complete map of the available morphologies for PbMoO4 was obtained and a good agreement between the experimental and theoretical predicted morphologies was found. The structural and electronic changes induced by the substitution of Pb by Ca and Sr allow us to find a relationship among morphology, the electron-transfer process at the exposed surfaces, optical properties, and photocatalytic activity. We believe that our results offer new insights regarding the local coordination of superficial Pb/Ca/Sr and Mo cations (i.e., clusters) on each exposed surface of the corresponding morphology, which dictate the photocatalytic activities of the as-synthesized samples, a field that has so far remained unexplored. The present study, which combines multiple experimental methods and first-principles calculations, provides a deep understanding of the local structures, bonding, morphologies, band gaps, and electronic and optical properties, and opens the door to exploit the electrical, optical and photocatalytic activity of this very promising family of materials.

Fast and simultaneous doping of Sr0.9-x-y-zCa0.1In2O4:(xEu3+, yTm3+, zTb3+) superstructure by ultrasonic spray pyrolysis.

In the present work, Sr0.9-x-y-zCa0.1In2O4:(xEu3+, yTm3+, zTb3+) particles were synthesized by the ultrasonic spray pyrolysis (USP) method to obtain a single-phase white phosphorus formed by six different cations in solution within the lattice (superstructure). The samples were also structurally and morphologically characterized by X-ray diffraction (XRD) techniques and by field emission scanning electron microscopy (FE-SEM). The photoluminescent behavior and the characteristics of the emitted colors were studied by the variation in the co-doping of the rare earth elements. The Sr0.9Ca0.1In2O4 sample showed a near blue color emission, but all co-doped samples showed emission in white with very close chromaticity coordinates to the standard white (x = 0.33 and y = 0.33). The Tm3+ → Tb3+ (ET1), Tm3+ → Eu3+ (ET2) and Tb3+ → Eu3+ (ET3) Energy Transfers were proposed and are considered necessary for adjusting and controlling the desired color properties.