RESUMEN
Due to their photon up-converting capability, lanthanide ions are ideal candidates dopants for semiconductors for developing visible light-driven photocatalytic activity. Of particular relevance, the low luminescence efficiency of Ln-based nanoparticles is one of the main factors that limits their further applications. Carbon, which is present on the surface of all TiO2 photocatalysts, can be responsible for luminescence quenching processes and, thus, decreasing the photocatalytic activity of TiO2. This article presents a systematic experimental and theoretical study of the effects of carbon on the photocatalytic performance of Ho3+-modified TiO2. Ho3+-TiO2 photocatalysts modified with various carbon contents (from 0.5 to 20â¯mol.%) were successfully prepared using a simple hydrothermal method. As-obtained samples were characterized by UV-Vis diffuse reflectance spectroscopy (DRS/UV-Vis), X-ray diffraction (XRD), X-ray photoelectron emission spectroscopy (XPS), N2 adsorption measurements, photoluminescent spectroscopy (PL), field-emission scanning electron microscopy (FE-SEM) and scanning transmission microscopy (STEM). The photodegradation efficiency of phenol was estimated for visible light (λâ¯>â¯420â¯nm and λâ¯>â¯455â¯nm). The XPS and XRD analyses and theoretical calculations revealed that the substitutional doping of holmium and carbon in the TiO2 anatase structure resulted in the appearance of a new sub-band-gap. Changes in the material texture, BET surface area and pore volume can be easily controlled via carbon content in samples. Doping of the Ho3+-TiO2 photocatalysts with carbon resulted in quenching of the emission of Ho3+ and, thus, the photodegradation of phenol, was observed in samples containing smaller amounts of carbon. Sixty minutes of irradiation resulted in 89% of phenol degradation under visible light (λâ¯>â¯420â¯nm).
RESUMEN
Novel visible light responsive materials for water splitting are essential for the efficient conversion of solar energy into hydrogen bond energy. Among other semiconductors, gadolinium orthovanadate has appropriate conduction and valence band edges positioned to split water molecules and a narrow band gap that allows the use of visible light for hydrogen generation. Thus, we present here that hydrogen evolution under visible light (λ > 420 nm) could be accomplished using hierarchical 3D GdVO4 particles, obtained by a simple, one pot hydrothermal synthesis. We found that applying various reaction components, such as EDTA-Na2 and EDTA, and adjusting the pH of the solution allow one to tune the shape of GdVO4 (such as short nanowires, long nanowires, short nanorods, long nanorods, nanoparticles and spheres - all having a tetragonal crystal structure) as well as optical and photocatalytic properties. The highest ability to photocatalytically split methanol solution into hydrogen under UV-Vis irradiation was detected for the long nanowire sample (42 µmol h-1), having almost 11 times higher efficiency in comparison with the weakest sample - short nanowires. In addition, GdVO4 spheres generated H2 more than 2 times (5.75 µmol h-1) in comparison with the short nanorod sample (2.5 µmol h-1) under visible light excitation. Photostable in three-hour work cycles, long nanowires and spheres were even able to generate hydrogen from pure water, reaching values of 17 and 3 µmol under UV-Vis and Vis light, respectively.
RESUMEN
CdS quantum dot-decorated KNbO3 composite photocatalysts co-modified with Bi2S3 QDs were designed and synthesized by a combination of the hydrothermal method with a linker-assisted adsorption route, using starch and thioglycolic acid as capping agents, which facilitated the attachment of modifiers to the surface of potassium niobate. The quantum dots were successfully deposited onto the surface of the perovskite-type KNbO3 with a good dispersion and a stable heterostructure was formed. The as-prepared photocatalysts were subsequently characterized by UV-Vis diffuse reflectance spectroscopy (DRS), X-ray diffraction (XRD), scanning electron microscopy (SEM), scanning transmission electron microscopy (STEM), Fourier transform infrared spectroscopy (FT-IR), Brunauer-Emmett-Teller (BET) specific surface area, X-ray photoelectron spectroscopy (XPS) and photoluminescence (PL) emission spectroscopy. The obtained KNbO3-based composites showed greatly improved photocatalytic performance for the degradation of phenol in the aqueous phase under visible light irradiation (λ > 420 nm) over pristine KNbO3. The highest photocatalytic performance and enhanced stability were observed for the ternary 30% CdS-5%Bi2S3 quantum dot-decorated KNbO3 composite, which could be related to the enhanced visible-light absorption ability, efficient charge separation in the three-level electron transfer heterojunction, improved stability and appropriate amounts of composite components. The formation of a surface layer of CdO decreased the visible light photoactivity of the CdS QD-decorated KNbO3 photocatalysts. The main phenol oxidation intermediates were benzoquinone, catechol, hydroquinone, and 1,2,4-benzenetriol, which underwent further photooxidation to form non-cyclic organic acids. Action spectral analysis proved the better photocatalytic activity of the ternary CdS/B2S3 QDs co-decorated KNbO3 composite compared to the binary CdS QDs decorated KNbO3 sample and revealed that irradiation ranging from 420 to 520 nm was responsible for the visible light photoactivity.
RESUMEN
Quantum dot (QD)-decorated semiconductor micro- and nanoparticles are a new class of functional nanomaterials that have attracted considerable interest for their unique structural, optical and electronic properties that result from the large surface-to-volume ratio and the quantum confinement effect. In addition, because of QDs' excellent light-harvesting capacity, unique photoinduced electron transfer, and up-conversion behaviour, semiconductor nanoparticles decorated with quantum dots have been used widely in photocatalytic applications for the degradation of organic pollutants in both the gas and aqueous phases. This review is a comprehensive overview of the recent progress in synthesis methods for quantum dots and quantum dot-decorated semiconductor composites with an emphasis on their composition, morphology and optical behaviour. Furthermore, various approaches used for the preparation of QD-based composites are discussed in detail with respect to visible and UV light-induced photoactivity. Finally, an outlook on future development is proposed with the goal of overcoming challenges and stimulating further research into this promising field.
RESUMEN
Nd-modified TiO2 photocatalysts have been obtained via hydrothermal (HT) and sol-hydrothermal (SHT) methods. The as-prepared samples were characterized by X-ray diffraction (XRD), BET surface area measurements, scanning electron microscopy (SEM), diffuse reflectance spectroscopy (DRS), luminescence spectroscopy and X-ray photoelectron spectroscopy (XPS). The photocatalytic activity of the synthesized samples was evaluated by the degradation of phenol in aqueous solution under irradiation with UV-vis (λ > 350 nm) and vis (λ > 420 nm) light, as well as by the degradation of gaseous toluene under irradiation with vis (λmax = 415 nm) light. It was found that Nd-modified TiO2 is an efficient photocatalyst for the degradation of phenol and toluene under visible light. XPS analysis revealed that the photocatalyst prepared via HT method contains a three-times higher amount of hydroxy groups at the surface layer and a two-times higher amount of surface defects than that obtained by the SHT method. The photocatalytic efficiency of phenol and toluene degradation under vis irradiation in the presence of 0.25% Nd-TiO2(HT) reached 0.62 and 3.36 µmol·dm-1·min-1, respectively. Photocatalytic activity tests in the presence of Nd-TiO2 and scavenger confirm that superoxide radicals were responsible for the visible light-induced degradation of the model pollutant in aqueous solution.