Fabrication of Bi2MoO6 nanoplates hybridized with g-C3N4 nanosheets as highly efficient visible light responsive heterojunction photocatalysts for Rhodamine B degradation

The Bi₂MoO₆/g-C₃N₄ heterojunction photocatalysts have been successfully fabricated using a simple liquid chemisorptions and thermal post-treatment. These nanostructured Bi₂MoO₆/g-C₃N₄ composites were extensively characterized by X-ray diffraction(XRD), field emission scanning electron microscopy (FESEM), transmission electron microscope (TEM), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FT-IR),UV–vis diffuse reflectance spectra (UV–vis DRS) and Photoluminescence (PL). The photocatalytic results show that 20 wt% Bi₂MoO₆/g-C₃N₄ sample exhibits efficient visible light activity and excellent photo-stability. The kinetic constant of RhB degradation over 20 wt% Bi₂MoO₆/g-C₃N₄ is about 5 and 2.5 times higher than that over pure Bi₂MoO₆ and g-C₃N₄ nanosheets, respectively. The enhanced photocatalytic performance is attributed to the construction of heterogeneous interface to promote photo-induced charge carrier pairs separation.     

Enhanced photo-induced charge separation and solar-driven photocatalytic activity of g-C3N4 decorated by SO42−

SO₄²⁻ decorated g-C₃N₄ with enhanced photocatalytic performance was prepared by a facile pore impregnating method using (NH₄)₂S₂O₈ solution. The photocatalysts were characterized by the Brunauer–Emmett–Teller (BET) method, X-ray diffraction (XRD), scanning electron microscopy (SEM), UV–vis diffuse reflectance spectroscopy (DRS), transmission electron microscopy (TEM), Fourier-transform infrared (FT-IR), X-ray photoelectron spectroscopy (XPS) and surface photovoltage (SPV) spectroscopy, respectively. The separation efficiency of photo-generated charge was investigated using benzoquinone as scavenger. The results demonstrate that sulfating of g-C₃N₄ increases the adsorption of rhodamine B on g-C₃N₄, the hydroxyl content and the separation efficiency of photo-generated charge. The photocatalytic activity of SO₄²⁻/g-C₃N₄ for decolorization of rhodamine B and methyl orange (MO) aqueous solution was evaluated. The result shows that loading of 6.0 wt% SO₄²⁻ results in the best photocatalytic activity under simulated solar irradiation and SO₄²⁻ play an important role in boosting the photocatalytic activity.     

Significant improvement of photocatalytic activity of porous graphitic-carbon nitride/bismuth oxybromide microspheres synthesized in an ionic liquid by microwave-assisted processing

Graphitic-carbon nitride/bismuth oxybromide (g-C₃N₄/BiOBr) porous microspheres have been successfully synthesized by a one-pot ethylene glycol (EG) assisted microwave process in the presence of 1-hexadecyl-3-methylimidazolium bromine ([C₁₆mim]Br). The as-prepared samples are characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDS) and UV–vis diffuse reflectance spectroscopy (DRS). During the reaction process, the ionic liquid acts not only as solvent and Br source but also as a template for fabrication of g-C₃N₄/BiOBr porous microspheres. In addition, the photocatalytic activity of the g-C₃N₄/BiOBr is evaluated by degrading Rhodamine B (RhB) and ciprofloxacin (CIP) under visible-light irradiation. It is found that 12.75 wt% g-C₃N₄/BiOBr microspheres exhibit higher photocatalytic activity than that of the as-prepared BiOBr. A possible photocatalytic mechanism based on the relative band positions of g-C₃N₄/BiOBr has been proposed.     

Highly efficient visible-light driven AgBr/Ag3PO4 hybrid photocatalysts with enhanced photocatalytic activity

Highly efficient visible-light-driven AgBr/Ag₃PO₄ hybrid photocatalysts with different mole ratios of AgBr were prepared via an in-situ anion-exchange method and characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), UV–vis diffuse reflectance spectroscopy (DRS) and photoluminescence (PL) technique. Under visible light irradiation (>420 nm), the AgBr/Ag₃PO₄ photocatalysts displayed the higher photocatalytic activity than pure Ag₃PO₄ and AgBr for the decolorization of acid orange 7 (AO 7). Among the hybrid photocatalysts, AgBr/Ag₃PO₄ with 60% of AgBr exhibited the highest photocatalytic activity for the decolorization of AO 7. X-ray photoelectron spectroscopy (XPS) results revealed that AgBr/Ag₃PO₄ readily transformed to be Ag@AgBr/Ag₃PO₄ system while the photocatalytic activity of AgBr/Ag₃PO₄ remained after 5 recycling runs. In addition, the quenching effects of different scavengers displayed that the reactive h⁺ and O₂^∙− play the major role in the AO 7 decolorization. The photocatalytic activity enhancement of AgBr/Ag₃PO₄ hybrids can be ascribed to the efficient separation of electron–hole pairs through a Z-scheme system composed of Ag₃PO₄, Ag and AgBr, in which Ag nanoparticles act as the charge separation center.     

Development of novel Ag modified BiOF squares/g-C3N4 composite for photocatalytic applications

A novel Ag modified BiOF/g-C₃N₄ (Ag-BiOF/g-C₃N₄) organic–inorganic hybrid photocatalysts have been synthesized by a facile solvothermal route. The photocatalyst was characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), UV–vis diffuse reflection spectroscopy (UV-DRS) and X-ray photoelectron spectroscopy (XPS). The photocatalytic studies reveals that the as-prepared Ag-BiOF/g-C₃N₄ photocatalyst exhibited significantly enhanced photocatalytic activity than the pure BiOF and BiOF/g-C₃N₄ photocatalysts toward degrading methylene blue (MB) under visible light irradiation. The heterostructured combination of Ag, g-C₃N₄ and BiOF micro squares provides synergistic photocatalytic performance through an efficient electron transport mechanism.     

Synthesis of micro-nano Ag3PO4/ZnFe2O4 with different organic additives and its enhanced photocatalytic activity under visible light irradiation

Several novel micro-nano Ag₃PO₄/ZnFe₂O₄ with excellent magnetic separation property and photocatalytic performance were successfully synthesized using different organic additives for the first time. In the composite, Ag₃PO₄ with flower-like, quadrangular prism and flake structures were obtained when the organic additive is hexadecyl trimethyl ammonium bromide (CTAB), sodium diethyldithiocarbamate (DDTC), or DL-malic acid (DLMA), respectively, while the ZnFe₂O₄ showed uniform spherical structure. From the results of the photocatalytic activity analysis, the Ag₃PO₄/ZnFe₂O₄ gained with the organic additive of DDTC showed the highest photocatalytic capability for 2, 4-dichlorophenol (2, 4-DCP) degradation under visible light irradiation compared with those of CTAB and DLMA as the additives. Moreover, the composition of the composite seriously influences the photocatalytic activity, and when the mass ratio of Ag₃PO₄ and ZnFe₂O₄ in the Ag₃PO₄/ZnFe₂O₄ (DITCH) is 9:1, the apparent photo degradation rate constant of 2, 4-DC is 0.0155 min⁻¹, which is 5.74 times of ZnFe₂O₄ (0.0027 min⁻¹) and 1.89 times of Ag₃PO₄ (0.0082 min⁻¹). Finally, the photocatalytic mechanism of Ag₃PO₄/ZnFe₂O₄ was discussed based on the heterojunction energy-band theory and Z-Scheme theory in detail.     

Synthesis and characterization of g-C3N4/BiFeO3 composites with an enhanced visible light photocatalytic activity

The novel visible light-induced g-C₃N₄/BiFeO₃ composites were successfully synthesized by introducing BiFeO₃ into polymeric g-C₃N₄. The structures and optical properties of composites were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), field-emission transmission electron microscope (TEM), UV–vis diffuse reflection spectroscopy (DRS), respectively. For the degradation of Rhodamine B (RhB), the g-C₃N₄/BiFeO₃ composites exhibited significantly higher visible light photocatalytic activity than that of a single semiconductor. The optimal percentage of doped g-C₃N₄ was 50%. Both photooxidation and photoreduction processes follow first order kinetics. In addition, the stability of the prepared photocatalyst in the photocatalytic process was also investigated. The enhanced photocatalytic performance could be due to the high separation efficiency of the photogenerated electron–holes pairs. The possible photocatalytic mechanism of g-C₃N₄/BiFeO₃ was proposed to guide the further improvement of their photocatalytic activity.     

Highly efficient photocatalytic treatment of mixed dyes wastewater via visible-light-driven AgI–Ag3PO4/MWCNTs

A high-performance photocatalyst of AgI–Ag₃PO₄/multi-walled carbon nanotubes (MWCNTs) was fabricated by chemical precipitation method using KI, K₂HPO₄ and AgNO₃ in the presence of MWCNTs. Its structure and physical properties were characterized by means of scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), transmission electron microscope (TEM), X-ray diffraction (XRD), UV–vis absorption spectra, X-ray photo-electron spectroscopy (XPS), photoluminescence spectra (PL) and photocurrent techniques. SEM, TEM and EDS analyses verified that AgI–Ag₃PO₄ is successfully loaded on MWCNTs. AgI–Ag₃PO₄/MWCNTs possess the absorption edge of red shift and small band gap energy, and could absorb more photons in the visible region. PL and photocurrent analyses illustrated that AgI–Ag₃PO₄/MWCNTs have the lowest emission peak intensity and the highest photoelectric current, compared with Ag₃PO₄, AgI and AgI–Ag₃PO₄. By using the photocatalytic degradation of mixed dyes wastewater of Orange II and ponceau 4R as a model reaction, the photocatalytic efficiencies of Ag₃PO₄, AgI, AgI–Ag₃PO₄ and AgI–Ag₃PO₄/MWCNTs were evaluated. The reaction results showed that AgI–Ag₃PO₄/MWCNTs have strong photocatalytic activity and excellent chemical stability in repeated and long-term applications. Therefore, the prepared AgI–Ag₃PO₄/MWCNTs could act as a high-performance catalyst for the photocatalytic degradation of mixed dyes wastewater and also suggested the promising applications.     

Optical and electrochemical gas sensing properties of yttrium–silver co-doped lithium iron phosphate thin films

The new sensing material, LiFe_0.995Y_0.0025Ag_0.0025PO₄ was synthesized using hydro-thermal methods, and characterized by X-ray diffraction, energy dispersive spectroscopy and X-ray photoelectron spectroscopy. The as prepared products were subsequently utilized in a self assembled optical waveguide gases testing apparatus and a WS-30A electro-chemical gas sensing apparatus for xylene detection. A glass optical waveguide gas sensor was fabricated by spin-coating a LiFe_0.995Y_0.0025Ag_0.0025PO₄ thin film on the surface of single-mode tin-diffused glass Optical Waveguide. The sensing elements for electro-chemical gas sensor were made by dip-coating a LiFe_0.995Y_0.0025Ag_0.0025PO₄ thin film on the surface of an alumina ceramic tube, assembled with platinum wire. The experimental results indicated that, at room temperature, LiFe_0.995Y_0.0025Ag_0.0025PO₄ thin film/tin-diffused optical waveguide sensing element exhibited higher response to xylene in the range of 0.1–100 ppm; at an optimum operating temperature (300 °C), the response (S_r) of LiFe_0.995Y_0.0025Ag_0.0025PO₄ to 100 ppm of xylene was 5.29, as measured by the WS-30A electro-chemical gases sensing apparatus.     

Ag3VO4/ZnO nanocomposites with an n–n heterojunction as novel visible-light-driven photocatalysts with highly enhanced activity

The present work demonstrates the preparation of Ag₃VO₄/ZnO nanocomposites with an n–n heterojunction, as novel visible-light-driven photocatalysts, with different mole fractions of silver vanadate. The preparation method is facile one-pot, large-scale, and low-temperature and does not require any post preparation treatments. The microstructure, morphology, purity, and electronic properties of the as-prepared samples were studied using X-ray diffraction, scanning electron microscopy, energy dispersive analysis of X-rays, UV–vis diffuse reflectance spectroscopy, Fourier transform-infrared spectroscopy, and photoluminescence techniques. Photocatalytic activity of the nanocomposites was examined by degradation of rhodamine B under visible-light irradiation. It was found that mole fraction of silver vanadate has a considerable influence on the photocatalytic activity. The nanocomposite with 0.218 mol fraction of Ag₃VO₄ exhibited the superior activity relative to the other compositions. Compared with the pure ZnO and Ag₃VO₄, the nanocomposite exhibited 10.5 and 1.6-fold enhancement, respectively, in the degradation rate constant. In addition, influence of the refluxing time, calcination temperature, and scavengers of reactive species on the degradation activity was investigated in detail and the results were discussed. Moreover, the nanocomposite was found to be a reusable photocatalyst.     

Solar photocatalytic activity of chemical solution-prepared barium tungstate nanostructures

Nanostructured barium tungstate (BaWO₄) as a solar photocatalyst has been successfully synthesized by a chemical solution method. The sample was characterized using X-ray diffraction analysis (XRD), scanning electron microscopy (SEM), and UV–vis diffuse reflectance spectroscopy. Then, the photocatalytic degradation of methylene blue (MB) in an aqueous medium was evaluated with nanostructured BaWO₄ under direct sunlight irradiation. The effects of the initial pH, and the catalyst dosage on the dye degradation were studied in order to achieve maximum degradation efficiency. The nanostructured BaWO₄ exhibited good photocatalytic activity for degradation of MB under sunlight irradiation at pH 10 after 3 h of irradiation. Also, the optimal catalyst loading of 25 mg/L obtained throughout the present study. The degradation of the dye followed the first-order reaction and the adsorption obeyed the Langmuir model.     

Fabrication of heterojunction SnO2/BiVO4 composites having enhanced visible light photocatalystic activity

SnO₂/BiVO₄ heterojunction composite photocatalysts with various mole ratios have been prepared via a simple hydrothermal method. The structure, composition and optical properties of the SnO₂/BiVO₄ composites were determined by X-ray diffraction (XRD), Raman spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM), Brunauer–Emmett–Teller (BET) surface analysis, X-ray photoelectron spectroscopy (XPS) and UV–vis diffuse reflectance spectroscopy (UV–vis DRS). Photocatalytic activities of the composites were evaluated by studying the degradation of methylene blue (MB) solutions under simulated visible light irradiation (500 W halogen tungsten lamp). The 3:7 mol ratio SnO₂/BiVO₄ composite exhibited the highest photocatalytic performance, leading to 72% decompositon of MB within 120 min of irradiation.     

Enhanced properties for visible-light-driven photocatalysis of Ag nanoparticle modified Bi2MoO6 nanoplates

The visible light driven Bi₂MoO₆ photocatalyst doped with different contents of Ag nanoparticles was successfully synthesized by a combination of hydrothermal and sonochemical methods. The as-synthesized samples were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning and transmission electron microscopy (SEM and TEM) and UV–visible spectroscopy to investigate crystalline structure, morphology, composition and photocatalytic properties. XRD patterns and TEM images of the samples revealed pure phase orthorhombic Bi₂MoO₆ nanoplates without any detection of Ag dopant due to its low concentration and very tiny particle size. TEM images showed that Ag nanoparticles with the size of 10–15 nm were dispersed randomly on the surface of Bi₂MoO₆. The XPS analysis of Ag/Bi₂MoO₆ nanocomposites revealed the presence of additional metallic Ag. Photocatalytic activities of the Ag/Bi₂MoO₆ nanocomposites were evaluated by determining the degradation of rhodamine B (RhB) under visible light radiation. In this research, the 10 wt% Ag/Bi₂MoO₆ nanocomposites showed the best photocatalytic activity. The results suggest that the dispersion of Ag nanoparticles on the surface of Bi₂MoO₆ significantly enhances its photocatalytic activity.     

Sol–gel-synthesized mesoporous-assembled TiO2–ZrO2 mixed oxide nanocrystals and their photocatalytic sensitized H2 production activity under visible light irradiation

The purpose of this work was to investigate, in the first study of its kind, hydrogen production by photocatalytic water splitting under visible light irradiation using Eosin Y-sensitized mesoporous-assembled TiO₂–ZrO₂ mixed oxide nanocrystal photocatalysts. The mesoporous-assembled TiO₂–ZrO₂ mixed oxide nanocrystals, with various TiO₂-to-ZrO₂ molar ratios, were synthesized by a sol–gel method with the aid of a structure-directing surfactant. The synthesized nanocrystals were characterized by thermogravimetric and derivative thermogravimetric analyzer, N₂ adsorption–desorption, X-ray diffraction, UV–visible spectroscopy, scanning electron microscope–energy-dispersive X-ray analyzer, and transmission electron microscope analyses. Parameters affecting the photocatalytic activity, including calcination conditions and phase composition, were mainly discussed. Experimental results showed that the incorporation of ZrO₂ with suitable contents could preserve the mesoporous-assembled structure of TiO₂ at high calcination temperatures and enhance its thermal stability significantly. Results of the photocatalytic-sensitized hydrogen production revealed that the TiO₂–ZrO₂ mixed oxide photocatalyst, with a TiO₂-to-ZrO₂ molar ratio of 95:5, calcined at 800 °C for 4 h, provided maximum photocatalytic hydrogen production activity. The optimized TiO₂–ZrO₂ mixed oxide photocatalyst can be considered as a potential photocatalyst for hydrogen production under solar light irradiation.     

Regeneration of novel visible-light-driven Ag/Ag3PO4@C3N4 hybrid materials and their high photocatalytic stability

Novel visible-light-driven Ag₃PO₄@C₃N₄PO₄ loaded with metal Ag were synthesised via an anion-exchange precipitation method and regenerated by H₂O₂ and NaNH₃HPO₄. The obtained Ag/Ag₃PO₄@C₃N₄ and regenerated Ag/Ag₃PO₄@C₃N₄ were characterised by XRD, XPS, SEM and UV–vis. The XRD and UV–vis results revealed that the crystal structure and light adsorption property of Ag/Ag₃PO₄@C₃N₄ were similar to that of regenerated Ag/Ag₃PO₄@C₃N₄. The XPS result showed that the metallic Ag⁰ deposited on the surface of Ag/Ag₃PO₄@C₃N₄ and regenerated Ag/Ag₃PO₄@C₃N₄. The Ag/Ag₃PO₄@C₃N₄ hybrids displayed remarkable photocatalytic activity and stability after regeneration. Compared with pure Ag₃PO₄ or C₃N₄, the Ag/Ag₃PO₄@C₃N₄ and regenerated Ag/Ag₃PO₄@C₃N₄ enhancement in the photodegradation rate towards methyl orange is observed over under visible light irradiation. The enhanced photocatalytic performance was attributed to the synergistic effect between Ag₃PO₄ and C₃N₄ and a small amount of Ag⁰ which suppresses the charge recombination during photocatalytic process. This work could provide new insights into the fabrication of high stability visible photocatalysts and facilitate their practical application in environment issues.     

Microwave hydrothermal synthesis of BiFeO3: Impact of different surfactants on the morphology and photocatalytic properties

Pure-phase BiFeO₃ catalysts with different morphologies were synthesized by microwave hydrothermal treatment at 200 °C with and without surfactant. The as-prepared catalysts were characterized by X-ray diffraction, scanning electron microscopy, and diffuse reflectance spectroscopy. Their photocatalytic properties were also explored. Ball-like (no surfactant), flower-like (EDTA), and honeycomb-like (polyvinylpyrrolidone) BiFeO₃ catalysts were obtained. Surfactant addition decreased the bandgap of BiFeO₃ catalysts. The specific surface area for ball-like, flower-like, and honeycomb-like BiFeO₃ catalysts was 7.48, 3.48, and 12.38 m²/g, and the rate of rhodamine B degradation under UV light was 49%, 61%, and 87%, respectively, at 4 h.     

Deposition of Fe3O4 on oxidized activated carbon by hydrazine reducing method for high performance supercapacitor

Oxidized activated carbon/Fe₃O₄ (AC/Fe₃O₄) composites for supercapacitor electrodes were synthesized by a reduction method. Poly(vinylpyrrolidone) was added as a dispersing agent for homogeneous deposition of Fe₃O₄ on AC. The obtained products were identified as AC/Fe₃O₄ by X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) analysis. Morphological characterization of AC/Fe₃O₄ was carried out by field emission scanning electron microscopy (FE-SEM); the results clearly showed the formation of Fe₃O₄ nanoparticles about 30 nm in diameter on AC. Moreover, by using N₂ adsorption/desorption isotherm analysis, we confirmed that surface areas and pore volumes decreased with increasing Fe₃O₄ content. We also carried out electrochemical characterization of AC and AC/Fe₃O₄ composites. Remarkably, we found that the value of specific capacitance increased significantly from 99.4 F g⁻¹ of raw AC to 202.6 F g⁻¹ of AC/Fe₃O₄ composites at 10 mV s⁻¹ of scan rate. This result can be ascribed to a synergistic effect of the combination of electrical double-layer capacitance and pseudo-capacitance properties. This research represents a valuable contribution to the application of supercapacitor electrodes in regard to cost effectiveness and simple fabrication.     

Synthesis and properties of Fe3O4/SiO2/TiO2 nanocomposites by hydrothermal synthetic method

Fe₃O₄/SiO₂/TiO₂ nanocomposites with well-defined core-shell structures were successfully prepared by a facile hydrothermal synthetic method for titania coating on Fe₃O₄/SiO₂ magnetic core. The as-prepared Fe₃O₄/SiO₂/TiO₂ composite particles were characterized by X-ray diffraction (XRD),transmission electron microscopy (TEM),Fourier transform infrared spectroscopy (FT-IR). The results showed that Fe₃O₄/SiO₂/TiO₂ was well crystallized at 140 °C with well-defined core-shell structures. Fe₃O₄/SiO₂/TiO₂ nanocomposites as well as pure TiO₂ showed good photocatalytic performance in the decolorization of methyl orange aqueous solution. Magnetic core coated by SiO₂ and TiO₂ layer still retained the good magnetic properties (Ms:3.04 emu g^-1) to facilitate catalyst recovery using external magnetic field.     

Power factor improvement of delafossite CuAlO2 by liquid-phase sintering with Ag2O addition

Thermoelectric delafossite (CuAlO₂)_1−x(Ag₂O)_x with 0<x<0.06 is prepared at three different sintering temperatures, 1323 K, 1373 K, and 1473 K. The samples are obtained from a mixture of CuO, Al₂O₃, and additive Ag₂O powders. The mixture is ground and then pressed with uniaxial pressure into pellets. Differential scanning calorimetry and X-ray diffraction spectroscopy show that the sintering temperature to synthesize delafossite CuAlO₂ with Ag₂O addition is below 1473 K. X-ray diffraction patterns show the major phase of delafossite 3R-CuAlO₂ along with a trace amount of 2H-CuAlO₂. A small amount of the Ag phase is present in the samples depending on the amount of Ag₂O addition and sintering temperature. Energy dispersive spectroscopy and backscattered electron image analyses show that the Ag phase is segregated around the grain boundary. Liquid-phase sintering is used to explain the growth mechanism. The CuAlO₂ samples with Ag₂O addition obviously exhibit enhanced bulk density, grain size, and electrical conductivity. The highest power factor (PF), obtained by CuAlO₂ with 2 at% of Ag₂O sintered at 1373 K, is 8.23×10⁻⁵ W/(m K²) at 873 K. Hence, our findings show an improvement for delafossite CuAlO₂ by Ag₂O addition.