The increasing contamination of water by organic dyes causes water pollution in the enviroment. Factories discharge untreated effluents into nearby water courses adding to the existing water pollution; this poses a significant environmental challenge. Hence there is a pressing demand to develop efficient technology for wastewater treatment, and photocatalysis has emerged as an advanced oxidation process with a green chemical approach for such treatment. This study aims to synthesize montmorillonite/TiO2 (Mnt/TiO2) photocatalysts and clarify the effect of montmorillonite content on the photodegradation of the organic dye rhodamine B (RhB). Mnt/TiO2 was prepared by a chemical method with various mass ratios of mMnt:mTiO2 based on the cation exchange capacity (CEC) of Mnt. The physicochemical properties of the samples prepared were determined by the following methods: energy-dispersive X-ray spectroscopy (EDX), scanning electron microscopy (SEM), Brunauer–Emmett–Teller (BET), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FTIR). The photocatalytic degradation efficiency of the RhB solution of Mnt/TiO2 was investigated by UV-Vis spectroscopy under UVC irradiation. Liquid chromatography-mass spectrometry (LCMS) was used to identify the photocatalytic by-products. The results showed that the structure of the nanocomposites has a ‘house-of-cards’ form with TiO2 nanoparticles randomly distributed on the surface and sheets of clay minerals. The best mass ratio of mMnt:mTiO2 is 10:1, corresponding to a 10 ppm RhB solution decolorization efficiency of 91.5% in 210 min. In this study, Mnt/TiO2 successfully cleaved the dye chromophore structure and broke the RhB rings into small and broken-ring compounds.

As a photocatalyst with good prospects, TiO2 has the shortcomings of easy agglomeration and no catalytic performance under visible light. The purpose of the present study was to help solve these problems by employing muscovite as a carrier for N-doped TiO2 in a nanocomposite. The nanocomposites were prepared by a liquid precipitation-grinding method using muscovite as the matrix and urea as the nitrogen source. The crystal structures, chemical bonding, and micromorphology of the nanocomposites were analyzed by X-ray diffraction, infrared absorption spectrometry, and field emission scanning electron microscopy, respectively. Visible and ultraviolet (UV-Vis) light absorption of the nanocomposites was analyzed by solid ultraviolet diffuse reflectance spectroscopy. The photocatalytic effect of the nanocomposites was studied based on the degradation of rhodamine B (RhB) solution. The photocatalytic degradation product of RhB was detected by high-performance liquid chromatography-mass spectrometry, revealing that N-doping inhibits the growth of TiO2 nanoparticles. The photocatalytic performance of N-TiO2/muscovite composite nanomaterials decreased with increasing heat-treatment temperature. N-doped TiO2/muscovite nanocomposites that were heated at 400°C showed the best photocatalytic performance under visible-light illumination with an RhB degradation of 97%.

Rational construction of Z-scheme photocatalysts and exploration of the Z-scheme charge transfer mechanism have drawn much attention in the field of CO2 reduction because of its great potential to alleviate energy crisis and environmental problems. In this study, a series of Z-scheme CdS/BiOI composites were constructed by depositing CdS nanoparticles on the surface of BiOI nanosheets. The synthesized materials were characterized comprehensively, and their photoreduction CO2 activities were evaluated. The results show that the composites exhibit higher photoreduction CO2 activity under visible light irradiation (λ > 400 nm) than pure CdS and BiOI. The yields of CO and CH4 for the optimal composite after 3 h irradiation are 3.32 and 0.54 μmol/g, respectively. The improved photocatalytic activity is attributed to Z-scheme transfer mode of the photogenerated charges in the composites. The mechanism of CO2 reduction is proposed and verified experimentally.

AgBr-modified Bi2WO6 nanosheets were successfully synthesized using a CTAB-assisted hydrothermal method followed by a facile deposition–precipitation procedure. The as-prepared photocatalysts were characterized using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), UV-vis diffuse reflectance spectroscopy (DRS), Brunauer–Emmett–Teller (BET), and photoluminescence emission spectroscopy (PL). AgBr nanoparticles were found evenly distributed on the surface of the Bi2WO6 nanosheets. The AgBr/Bi2WO6 nanocomposite demonstrated enhanced pollutant decolorization efficiency in eliminating Rhodamine B (RhB), methyl orange (MO), and phenol aqueous solutions under simulated solar light irradiation. It has been noticed that the adsorption performance of both Bi2WO6 nanosheets and AgBr-modified Bi2WO6 nanosheets played a more important role in the decolorization of pollutants, such as RhB and MO, than their photocatalytic ability. The high adsorption efficiency of the photocatalysts was mainly attributed to the increased surface area and the exposed reactive facets of the materials.

C3N4/Bi2WO6 heterojunction photocatalysts were successfully synthesized using consecutive hydrothermal and calcination processes. These photocatalysts were characterized using x-ray diffraction, scanning electron microscopy, transmission electron microscopy, ultraviolet-visible diffuse reflectance spectroscopy, x-ray photoelectron spectroscopy, and photoluminescence measurements. The results of these measurements indicated that the Bi2WO6 nanoparticles were approximately 30–50 nm and uniformly distributed on the surface of C3N4 lamellar structures. The 20% C3N4/Bi2WO6 displayed enhanced visible-light absorption from 432 nm to 468 nm. Photocatalytic tests also revealed that the 20% C3N4/Bi2WO6 photocatalyst exhibited significantly enhanced photocatalytic activity compared to that of pure C3N4 and Bi2WO6 under irradiation by visible light (λ > 420 nm). Furthermore, the excellent photocatalytic efficiency of the 20% C3N4/Bi2WO6 photocatalyst was determined to be related to the formation of C3N4/Bi2WO6 heterojunctions, and their presence was found to be generally beneficial for the separation of photogenerated electron–hole pairs.

Bi2O2CO3/ZnWO4 composite photocatalysts have been successfully synthesized by a mixed calcination method after hydrothermal process. The catalysts were characterized by powder x-ray diffraction, scanning electron microscopy, transmission electron microscopy, high resolution transmission electron microscopy, x-ray photoelectron spectroscopy, and UV-vis diffuse reflectance spectrum. The results showed that the hierarchical Bi2O2CO3/ZnWO4 nanocomposites were obtained by mixed grinding calcination method and Bi2O2CO3 nanospheres grow on the primary ZnWO4 particles. The Bi2O2CO3/ZnWO4 composites exhibit higher photocatalytic activities compared to pure ZnWO4 and Bi2O2CO3 particles under UV light irradiation. Furthermore, the excellent photocatalytic efficiency of the Bi2O2CO3/ZnWO4 composite was deduced closely related to Bi2O2CO3/ZnWO4 heterojunctions whose presence is generally regarded to be a favorable factor for the separation of photogenerated electrons and holes.

In this article, we review our recent research efforts on the synthesis, crystallinity control, and photocatalysis of nanostructured titanium dioxide (TiO2) shells. First, we introduce several synthetic methods for preparing TiO2 shell structures using either template-free or template-assisted approaches. Several methods to change the structures from amorphous to crystalline and subsequently ways to enhance the crystallinity are then discussed, including those involving the “silica-protected calcination” and “partial etching and recalcination” strategies. We also discuss the photocatalytic applications of the TiO2 nanoshells and the methods for improving their catalytic activities. Finally, we conclude with a summary and our perspective on the further development of the nanostructured TiO2 shells. It is believed that more rational design and modification strategies such as well-controlled nonmetal doping, plasmonic metal decoration and the hybridization with other semiconducting materials will significantly enhance the photocatalytic efficiency of TiO2-based catalyst materials.

The crystal structure of Li2LaTa2O6N was determined from laboratory X-ray powder diffraction data (Cu Kα1) using the Rietveld method. The title compound is tetragonal with space group I4/mmm, Z=2, and unit-cell dimensions a=0.395 049(4) nm, c=1.850 97(3) nm, and V=0.288 869(6) nm3. The initial structural model was successfully derived by the direct methods and further refined by the Rietveld method, with the anisotropic atomic displacement parameters being assigned for all atoms. The final reliability indices were Rwp=5.73%, S=1.46, Rp=4.33%, RB=1.13%, and RF=0.53%. Li2LaTa2O6N has a layered perovskite structure similar to that of Li2LaTa2O7.

The crystal structure of Ag2GeO3 was determined from laboratory X-ray powder diffraction data (Cu Kα1) using the Rietveld method. The title compound is orthorhombic with space group P212121, Z=4, unit-cell dimensions a=0.463 09(1) nm, b=0.713 93(2) nm, and c=1.040 79(3) nm, and V=0.344 10(2) nm3 . The final reliability indices were Rwp=5.58%, S=1.26, Rp=4.20%, RB=0.67% , and RF=0.35% . The GeO4 tetrahedra form infinite chains of [Ge2O6] along the a axis, with two tetrahedra per identity period of 0.463 nm. Individual chains are connected by Ag atoms, one-half of which are almost linearly coordinated by two O atoms and the rest are coordinated by three O atoms. The relatively short Ag-Ag distances of 0.299 to 0.339 nm indicate Ag(I)-Ag(I) interaction. This compound is isostructural with Ag2SiO3.

Various porous titania photocatalysts are analyzed three-dimensionally in real space by electron tomography. Shapes and three-dimensional (3D) distributions of fine pores and silver (Ag) particles (2 nm in diameter) within the pores are successfully reconstructed from the 3D data. Electron tomography is applied for measuring the specific surface area of the porous structures including open and closed porosity. Calculated specific surface areas of 22.8 m2/g for a conventional sol-gel TiO2 sample and 366 m2/g for a highly porous TiO2 sample prepared using the Pluronic P-123 self-assembly process are compared with those measured by the general BET method. The real-space surface measurement indicates that the highly porous TiO2 produced by the present method using block copolymers has a greater number of effective reaction sites for the degradation of methylene blue. Electron tomography shows a great potential to contribute considerably to the nanostructural analysis and design of such catalyst materials for photocatalysis.

The purpose of this paper was to describe a method of preparing Fe-TiO2 supported on sepiolite fibers with sol-gel method and to discuss the feasibility of photocatalytic degradation of paper-making waste water with chemical oxygen depletion (CODcr) (Potassium dichromate method) as evaluation criterion of catalytic activity. As-fabricated catalysts consisted of TiO2 particles impregnated with iron and dispersed on the sepiolite fibers (S.F.s). The novel Fe-TiO2-sepiolite was characterized by specific surface area and pore size distribution measurements, scanning electron microscope (SEM), high resolution transmission electron microscope (HRTEM), X-ray diffraction (XRD) and Fourier transform Infrared spectrometer (FT-IR) etc. The effects of parameters such as the amount of Ti/sepiolite fibers, initial pH, H2O2, Fe-doped, concentration of waste water, etc. were studied in detail. The results indicated that the presence of sepiolite in the support preparation and its role as a matrix over which TiO2 particles were dispersed seem to play an important effect in the migration process of oxygen species through the support vacancies. On the basis of these properties, the most promising carriers to be used in a waste water treatment process were selected.