ZrxCo0.8−xNi0.2−xFe2O4-graphene nanocomposite for enhanced structural,dielectric and visible light photocatalytic applications

Zirconium doped nickel cobalt ferrite (Zr_xCo_0.8−xNi_0.2−xFe₂O₄) nanoparticles and Zr_xCo_0.8−xNi_0.2−xFe₂O₄-graphene nanocomposites were synthesized by a cheap and facile co-precipitation method. Annealing was done at 750 °C for 6.5 h. Spinel cubic structure of prepared nanoparticles was confirmed by X-ray powder diffraction (XRD) technique. Crystalline size of nanoparticles was observed in the range of 18–27 nm. Graphene was synthesized by Hummer's method. Formation of rGO was confirmed by UV-visible spectroscopy (UV-vis) and XRD. Zr_xCo_0.8−xNi_0.2−xFe₂O₄-graphene nanocomposites were prepared by ultra-sonication route. Grain size of nanoparticles and dispersion of nanoparticles between rGO layers was determined by Scanning electron microscopy (SEM). In application studies of nanoparticles and their nanocomposites, photocatalytic efficiency of nanoparticles under visible light irradiation was observed by degradation of methylene blue. Charge transfer resistance was measured by electrochemical impedance spectroscopy (EIS) and the variation in dc electrical resistivity was analyzed by room temperature current voltage characteristics (I-V). Dielectric constant was also evaluated in frequency range from 1 MHz to 3 GHz. All these investigations confirmed the possible utilization of these materials for a variety of applications such as visible light photocatalysis, high frequency devices fabrication etc.     

Magnetically recyclable Ni1-xCdxCeyFe2-yO4-rGO nanocomposite photocatalyst for visible light driven photocatalysis

In this study, a magnetically recyclable Ni_1-xCd_xCe_yFe_2-yO₄-rGO (x, y = 0.05) (NCCF-rGO) nanocomposite photocatalyst has been prepared by following a facile in-situ co-precipitation method combined with ultra-sonication means. The as-synthesized magnetically separable NCCF-rGO nanocomposite photocatalyst efficiently degrades methylene blue (MB) dye in comparison to bare Ni_1-xCd_xCe_yFe_2-yO₄ (x, y = 0.05) (NCCF) nanoparticles (NPs) under visible light irradiation. The photo-degradation rate of MB with NCCF-rGO was ~9 times higher than NCCF nanoparticles (NPs). This enhanced photocatalytic performance of NCCF-rGO photocatalyst was due to the presence of reduced graphene oxide, which greatly help in production of photoactive species by reducing the rate of electro-hole pair recombination. The role of photoactive species that were responsible for the photocatalytic degradation of methylene blue has also been investigated. The as-synthesized NCCF-rGO photocatalyst expressed superb chemical stability and photocatalytic activity even after seven cycle runs. Moreover, the NCCF-rGO nanocomposite worked at all pH values and showed good acid resistance. In particular, the as-synthesized NCCF-rGO photocatalyst could be collected for the next cycle run by simply applying an external magnetic field. Hence, the NCCF-rGO nanocomposite could have potential use in organic dyes contained wastewater treatment.     

Effect of Nb substitution on magnetic,ferroelectric and photocatalytic properties of Bi0.95Sm0.05Fe1-xNbxO3 (0 ≤ x ≤ 0.1) nanoparticles

The single phase Bi_0.95Sm_0.05Fe_1-xNb_xO₃ (0 ≤ x ≤ 0.1) nanoparticles were synthesized by the sol-gel route, and the effect of Nb substitution on their magnetic, ferroelectric and photocatalytic properties were studied. X-ray diffractometry confirms a phase transformation from rhombohedral to orthorhombic with an increase in Nb substitution. The grain size decreases significantly, and the morphology of grains becomes homogeneous with the increase of Nb concentration. The maximum remnant magnetization (0.014 emu/g), coercivity (565 Oe) and polarization (0.592 μC/cm²) are observed in Bi_0.95Sm_0.05Fe_0.9Nb_0.1O₃. It has been observed that the energy band gap has been slightly reduced from 2.14 to 2.03 eV with Nb substitution, indicating an improvement of photocatalytic activity. The methylene blue degradation is used to represent the photocatalytic ability of Bi_0.95Sm_0.05Fe_1-xNb_xO₃ nanoparticles. The highest degradation efficiency (~74%) of methylene blue is obtained in Bi_0.95Sm_0.05Fe_0.93Nb_0.07O₃, which is much higher than that of Bi_0.95Sm_0.05FeO₃ (~51%) and can be attributed to the optimum particle size and the smallest energy band gap.     

Co-substituted Mg–Zn spinel nanocrystalline ferrites: Synthesis,characterization and evaluation of catalytic degradation efficiency for colored and colorless compounds

In this investigation, cobalt substituted Magnesium–Zinc ferrites were successfully synthesized by using the co-precipitation technique. The prepared spinel ferrites were characterized by using Scanning electron microscopy (SEM), Ultraviolet–Visible analysis, X-ray powder diffractometer (XRD) and Fourier-transform infrared spectroscopy (FTIR). Confirmation of formation of a single-phase spinel structure was assessed by the XRD and FTIR. Crystallite size, evaluated from X-ray analysis, of MZF, MZF1, MZF2, MZF3 is 9.72 nm, 7.21 nm, 8.49 nm and 8.30 nm respectively. Cluster formation and agglomeration of powdered samples of Co substituted Mg–Zn ferrites were represented through the SEM images. The optical bandgap range was calculated from the Ultraviolet–Visible spectrum. The photocatalytic activity was assessed through the photodegradation of coloured and colourless pollutants under sunlight. This paper focuses on the photocatalytic degradation of harmful compounds like benzimidazole and methylene blue. The photocatalytic activity of Mg–Zn ferrites as a photocatalyst was enhanced by the substitution of cobalt in it. Especially, MZF3 with the highest cobalt content gave the maximum photodegradation of methylene blue. Hence, we conclude that Mg_0.5Zn_0.5Co_xFe₂O₄ works as a potential catalyst in wastewater treatment.     

Nano Ca–Mg–Zn ferrites as tuneable photocatalyst for UV light-induced degradation of rhodamine B dye and antimicrobial behavior for water purification

We report the synthesis of Ca-doped Mg–Zn ferrite Mg_0.4Zn_(0.6-x)Ca_xFe₂O₄ nanomaterials with x = 0, 0.1, 0.2, 0.3, 0.4, 0.5, and 0.6 through citrate precursor approach and their structural, morphological, optical, photocatalytic, and antimicrobial properties were systematically studied. The prepared nanoferrites's cubic spinel structure with an average crystallite size of 15–38 nm was evaluated by the XRD examination. The spherical morphology of these ferrite nanoparticles was seen from scanning electron microscopy (SEM). The observed bands at 560 cm⁻¹ and 406 cm⁻¹ in the FTIR spectra confirmed the spinel structure of the synthesized nanoferrite. The optical study confirmed an optical band gap of 1.60 eV–1.86 eV. The photocatalysis was done for the degradation of rhodamine B dye solution under UV light. All the synthesized nano ferrites displayed a promising antimicrobial potential upon Candida albicans fungi. Mg_0.4Zn_0.1Ca_0.5Fe₂O₄ nanoparticles have a better photocatalytic response (99.5%) for the degradation of rhodamine B dye and show superior antimicrobial activity (96.1%) for the inhibition of Candida albicans fungi.     

Structural,spectral, dielectric and photocatalytic studies of Zr-Ni doped MnFe2O4 co-precipitated nanoparticles

In this study the Mn_1–2xZr_xFe_2−yNi_yO₄ nanoparticles fabricated by co-precipitation technique were investigated. Thermo-gravimetric analysis (TGA) exhibited the annealing temperature of the nanoparticles ~990 °C. Cubic spinel structure of Mn_1–2xZr_xFe_2−yNi_yO₄ nanoparticles was confirmed by X-ray diffraction (XRD) and Fourier transform infrared (FTIR) analysis. Crystallite size was calculated by XRD data and found in the range of 32–58 nm. Photocatalytic activity of Mn_0.92Zr_0.04Fe_1.88Ni_0.12O₄/graphene nanocomposites was tested by degrading methylene blue (MB) under visible light irradiation. The MB was almost completely degraded in the presence of Mn_0.92Zr_0.04Fe_1.88Ni_0.12O₄-graphene nanocomposites under visible light irradiation. Dielectric parameters were also investigated in the frequency range 1×10⁶–3×10⁹ Hz. An overall decrease in the values of dielectric constant, dielectric loss and tangent loss was observed on account of the substitution of Zr and Ni with Mn and Fe cations.     

Nanocrystalline transition metal oxides and their composites with reduced graphene oxide and carbon nanotubes for photocatalytic applications

Transition metal oxide nanoparticles (CuO, ZnO & Fe₂O₃) and mixed metal oxides CuO. ZnO.Fe₂O₃ were fabricated by facile co-precipitation approach for photocatalytic treatment of organic dyes. The structural features, phase purity, crystallite size and morphology of individual and mixed metal oxides were analysed by X-rays diffraction patterns (XRD) and scanning electron microscopic (SEM) analysis. Electrical behaviour of CuO, ZnO, Fe₂O₃ and mixed metal oxides CuO. ZnO.Fe₂O₃ was explored by current-voltage (I-V) measurements. Functional groups present in the synthesized metal oxides were investigated by Fourier transform infrared spectroscopy (FTIR) which ensures the existence of M-O functional groups in the samples. The optical bandgap analysis was carried out by UV–visible spectroscopic technique which revealed that the blend of three different transition metal oxides reduced the bandgap energy of mixed metal oxides. The reason behind this reduced bandgap energy is formation of new electronic state which arises due to the metal-oxygen interactions. Moreover, the nanocomposites of CuO.ZnO.Fe₂O₃ with reduced graphene oxide (rGO) and carbon nanotubes (CNTs) were prepared to study the effect of the carbonaceous materials on the rate of photodegradation. These carbonaceous nanomaterials have plethora properties which can bring advancement in sector of photocatalytic treatment of wastewater. The photocatalytic experiments were performed using methylene blue (MB) as standard dye for comparative study of metal oxides and their composites with rGO and CNTs. The percentage degradation of methylene blue (MB) by nanocomposite CuO.ZnO.Fe₂O₃/rGO is 87% which is prominent among all samples. This result ascribed the photocatalytic aspects of reduced graphene oxide along with mixed metal oxides.     

Photoluminescent and antimicrobial properties of silver-doped indium hydroxide synthesized by one-step microwave-assisted hydrothermal method

Silver-doped indium hydroxide In_(1-x)(OH)₃:_xAg (with x = 0, 1, 2, 4, and 8 mol%) of Ag nanoparticles were synthesized by the microwave-assisted hydrothermal (MAH) method at 140°C for 30 minutes. These nanoparticles were characterized by X-ray diffraction (XRD), fourier transformed infrared (FT-IR) spectroscopy, and optical diffuse reflectance. Photoluminescence (PL) spectra were acquired with a 350 nm beam of a krypton ion laser as an excitation source. The antibacterial activities of the samples were evaluated against gram negative Escherichia coli bacteria and gram positive Staphylococcus aureus bacteria using the disc diffusion method. The results showed that all diffraction peaks present in XRD patterns could be indexed to the cubic lattice related to the In(OH)₃ phase. Broadband photoluminescence behavior in visible range spectra was observed for all samples with a maximum peak centered in the blue and green regions. The antibacterial activities showed that In_(1-x)(OH)₃: _xAg nanoparticles have a promising bactericide that can be used for deactivating microbes.     

Visible light active Cu-doped iron oxide for photocatalytic treatment of methylene blue

In recent work, pure α-Fe₂O₃ (F-1) and series of 5% Cu doped Fe₂O₃ (CF-5) , 10% Cu doped Fe₂O₃ (CF-10) and 15% Cu doped Fe₂O₃ (CF-15) nanoparticles by facile chemical coprecipitation method were synthesized to study the effect of concentration of doping for photocatalytic activity. As prepared F-1, CF-5, CF-10, CF-15 nanoparticles were subjected to X-ray diffraction (XRD) and Fourier transform infra-red (FTIR) techniques to analyse the structural and functional groups features. These characterization techniques confirmed the successful doping of Cu ²⁺ ions in α-Fe₂O₃. The crystallite size of synthesized samples was calculated by Scherrer formula. Gradually decline in crystallite size from 18 to 15 nm was observed for undoped to doped samples. Scanning electron microscopic (SEM) analysis expressed that doping of Cu reduced the aggregation of particles and enhanced the surface area of nanoparticles. UV–Visible spectroscopic analysis of synthesized samples was used to calculate the bandgap energy of F-1, CF-5, CF-10, CF-15 nanoparticles i.e., 2.0, 1.7, 1.5, 1.4eV respectively. Narrowing bandgap energy of doped hematite supported to perform excellent photocatalytic activity. Maximum degradation of methylene blue was recorded via CF-10 within 140 min. Higher degradation rate of methylene blue by optimal concentration of CF-10 is due to effective electron trapping ability of photocatalyst.     

Effect of Fe2+/Fe3+ ratio on photocatalytic activities of Zn1-xFexO nanoparticles fabricated by the auto combustion method

Zn_1-xFe_xO nanoparticles with Fe doping content from 0 % to 6 % were fabricated by a facile auto combustion method. SEM, XRD, PL and XPS were carried out to characterize the morphologies, structures, optical properties and surface chemical states of the samples. The photocatalytic properties were also investigated toward Methyl Orange (MO) degradation. It was found that the maximum photocatalytic activity was obtained by 4 % Fe-doped ZnO nanoparticles, which was ascribed to the highest ratio of Fe²⁺/Fe³⁺. The experimental results and DFT calculations indicated that Fe could effectively affect the photocatalytic activity of ZnO nanoparticles, dependent on Fe²⁺/Fe³⁺ ratio and doping contents. Furthermore, a conceivable mechanism of band gap structure and carrier transfer of Fe²⁺/Fe³⁺ co-existed Zn_1-xFe_xO was proposed according to experimental analyses and theory calculations.     

Evaluation of biosynthesized nickel oxide nanoparticles from Clerodendrum phlomidis: A promising photocatalyst for methylene blue and acid blue dyes degradation

In the present investigation, nickel oxide nanoparticles (NiO) were biosynthesized utilizing an extract of Clerodendrum phlomidis leaves. Their size, phase study, and shape were investigated using a variety of research methods. In addition, we assessed the photocatalytic effects of NiO nanoparticles on the degradation of methylene blue (MB) and acid blue (AB) dyes. Throughout the research process, we found that these nanoparticles had extraordinary potential for photocatalysis when exposed to UV light. This is a 100% environmentally friendly method that makes no use of any harmful or poisonous solvents. High-resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy, and ultraviolet–visible spectroscopy (UV–Vis) were used to analyze the biosynthesized NiO nanoparticles. The catalytic activity of the newly synthesized nanoparticles was evaluated by seeing how well they degraded dyes called methylene (MB) and acid blue (AB). Following the first-order reaction, kinetics was the photocatalytic effectiveness against the methylene blue (MB) and acid blue (AB) dyes, both of which exhibited a maximum degradation efficiency of 92% and 63%. Because of this, the biosynthesized NiO nanoparticles synthesized utilizing the extract of Clerodendrum phlomidis leaves have the potential to be used in photocatalytic applications.     

Facile mechano-chemical synthesis and enhanced photocatalytic performance of Cu2ZnSnS4 nanopowder

In the present study, Cu₂ZnSnS₄ (CZTS) powder was synthesized by the mechano-chemical method from its elemental constituents. X-ray diffraction (XRD), Energy-dispersive X-ray spectroscopy (EDS), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy and diffusion reflectance spectroscopy (DRS) were used for characterization of structural, morphological and optical properties. XRD result confirmed that a highly crystalline CZTS phase corresponding to the kesterite structure was formed after 50 h ball milling. Raman analysis confirmed the existence of single phase CZTS without any other phases. FESEM and TEM images reveal the irregular CZTS nanoparticles with an average size of 90 nm. The elemental mapping of the CZTS nanopowder showed the uniform distribution in agreement with the stoichiometry. DRS result showed a band gap value of 1.53 eV. XPS result revealed the oxidation states as Cu⁺, Zn²⁺, Sn⁴⁺ and S²⁻. The photocatalytic activity of CZTS has been investigated through photodegradation of methylene blue (MB) and methyl orange (MO) dyes solution with different concentrations under visible light irradiation. Although the CZTS decomposed MO only 81% until 210 min, the MB solution was completely photodegraded after 100 min. A kinetic study by Langmuir-Hinshelwood (L-H) model indicated about 3.7 times faster degradation of MB than MO and also higher adsorption capacity for MB by CZTS. Furthermore, the prepared CZTS was reusable and can be repeatedly used for the removal of dyes from aqueous solutions.     

One-step preparation of size-defined aggregates of TiO2 nanocrystals with tuning of their phase and composition

One-step route based on the thermal decomposition of the double salt (NH₄)₂TiO(SO₄)₂ (ammonium titanyl sulfate, ATS) is presented to prepare size-defined aggregates of Ti-based nanoparticles with structural hierarchy. The component of Ti-based networks is tunable from anatase/rutile TiO₂, nitrogen-doped TiO₂, TiN_xO_1−x, to TiN depending on the atmospheres and reaction temperatures. The as-prepared Ti-based powders were characterized by X-ray diffraction analysis (XRD), transmission electron microscopy (TEM), UV–vis diffuse reflectance spectra (DRS), and BET surface area techniques. It is found that TiO₂ in the predominant rutile phase could be achieved by the thermal decomposition of ATS in flowing Ar gas. Furthermore, the nitrogen-doped TiO₂, TiN_xO_1−x solid solution and TiN were prepared by the thermal decomposition of ATS in flowing NH₃ gas by varying the temperatures. The network of anatase TiO₂ with a specific surface area up to 64 m² g⁻¹ contains large mesopores with a mean diameter of ca. 15 nm, and the large pore size allows more accessible surface and interface available for the photocatalytic degradation of large-molecule dyes. The photocatalytic activity of the prepared TiO₂ and nitrogen-doped TiO₂ under UV–vis light irradiation is compared to Degussa P-25 using the photocatalytic degradation of methylene blue (MB) as a model reaction. The anatase TiO₂ nanoparticles derived from one-step route show the highly efficient photocatalytic activity for the degradation of MB in comparison with Degussa P-25. The presence of large-sized rutile in the TiO₂ powder decreases the specific surface area and thus the powder exhibits a lower photocatalytic activity.     

Facile Synthesis of ZSM-5/TiO2/Ni Novel Nanocomposite for the Efficient Photocatalytic Degradation of Methylene Blue Dye

It is critical to develop an appropriate dye degrading technique to preserve the natural environment and human health owing to the dangerous water pollution caused by effluent dyes. So, in this work, a ZSM-5/TiO₂/Ni photocatalyst was synthesized as a novel composite and used for degrading methylene blue dye in the solution. The sol–gel approach was used to immobilize titanium dioxide nanoparticles on the ZSM-5 surface, and the resulting photocatalyst was then modified using nickel nanoparticles to improve its photocatalytic performance. The nanocomposite was characterized using different tools such as FE-SEM, EDX, XRD, FT-IR, TGA, and UV–Vis spectrophotometer. The XRD confirmed that the synthesized composite has the characteristic TiO₂ peaks. FE-SEM images of ZSM-5 exhibited rough, uneven, and jagged surfaces. A distinct shift in the morphology of the surface resulted when titanium dioxide was fully immobilized on the surface of ZSM-5. Shape complexity and surface roughness of the particles are elevated in the case of the ZSM-5/TiO₂/Ni nanocomposite. The maximum % degradation of 50 mL of 15 mg/L of methylene blue dye is 99.17% and achieved at pH?=?8, irradiation time?=?140 min, and photocatalyst dosage?=?0.05 g. The synthesized composite can be regenerated and reused several times without losing its efficacy.

     

Ternary Ag@SrTiO3@CNT plasmonic nanocomposites for the efficient photodegradation of organic dyes under the visible light irradiation

In this research, carbon nanotube (CNT)-modified plasmonic silver-strontium titanate (Ag@ SrTiO₃) nanocomposites for the degradation of the organic dye were prepared by the sol-gel method. The characterization of all products was carried out using the X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), N₂ adsorption-desorption test (BET), field emission-scanning electron microscopy (FESEM), transmission electron microscopy (TEM), UV–visible diffuse reflectance spectroscopy (DRS), photoluminescence (PL) spectroscopy, electrochemical impedance spectroscopy (EIS), and transient photocurrent (TPC) studies. It was found that the incorporation of Ag in and introducing CNT into the SrTiO₃ nanoparticles reduced the crystallite size to 21 nm and the band gap energy to 2.7 eV. The Reduced PL peak intensity, increased photocurrent value, and reduced charge transfer resistance approved that the Ag@SrTiO₃@CNT nanocomposite had a greater charge transfer efficiency than other samples. The optimal dosage of the photocatalyst, for the complete degradation of 5 ppm of the methylene blue (MB) solution after 30 min of the visible light irradiation, was decided as 0.5 g/L. Besides, in the experimental environment, the Ag@SrTiO₃@CNT sample illustrated the most significant photocatalytic performance of the degradation of methyl orange (MO) and Rhodamine B (RhB) dyes. The detailed mechanism and kinetics of the degradation procedure were clarified. Finally, the prepared system displayed increased stability and reusability in the entire cyclic degradation experiment.     

Preparation of CdS/TiO2 nanotube arrays and the enhanced photocatalytic property

In this paper, a series of CdS/TiO₂ NTs have been synthesized by SILAR method. The as-prepared CdS/TiO₂ NTs have been analyzed by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), energy dispersive spectrometer (EDS), and ultraviolet–visible (UV–vis). And their photocatalytic activities have been investigated on the degradation of methylene blue under simulated solar light irradiation. XRD results indicate that TiO₂ NTs were anatase phase, CdS nanoparticles were hexagonal phase. FESEM results indicate that low deposition concentration can keep the nanotubular structures. UV–vis results indicate that CdS can be used to improve the absorbing capability of TiO₂ NTs for visible light, and the content of CdS affects the band gap. Photocatalytic results indicate that CdS nanoparticles are conducive to improve the photocatalytic efficiency of TiO₂ NTs, and the highest degradation rate can reach 93.8%. And the photocatalytic mechanism of CdS/TiO₂ NTs to methylene blue is also described.     

A novel method for the synthesis of Fe3O4 nanoparticles/CdS nanowires heterostructure nanocomposite and uses in photodegradation of methylene blue

We report here a simple, efficient, practical, and novel method for the preparation of Fe₃O₄ nanoparticles (NPs)/CdS nanowires. The CdS nanowire/Fe₃O₄ NP reported here was characterized by transmission electron microscopy (TEM), X-ray Diffraction (XRD), vibrating sample magnetometer (VSM), and energy-dispersive X-ray. Cadmium diethyl dithiophosphate has been used as a 3 in 1 precursor (cadmium, sulfur, and ligand source) for the synthesis of high-quality one-dimensional Fe₃O₄ NPs/CdS nanowires using a simple hydrothermal method in the presence of Fe₃O₄ NPs in water. Photocatalytic activity studies show that the nanocomposite has good photocatalytic activity toward the photodegradation of methylene blue in an aqueous solution.     

Photocatalytic performance of Fe-substituted ZnAl2O4 powders under sunlight irradiation on degradation of industrial dyes

Using the sol–gel auto combustion method with diethanolamine (DEA) as fuel, a sequence of iron-substituted zinc aluminates, ZnFe_xAl_2-xO₄ powders, including variable Fe³⁺ ion concentrations (0 ≤ x ≤ 2) were effectively prepared. X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), transmission electron microscopy (TEM), scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), the Brunauer–Emmett–Teller (BET) method, UV–visible diffuse reflectance spectroscopy (UV-DRS), and vibrating sample magnetometer (VSM) were employed to examine the structures, chemical bonds, morphologies, composition, surface area, and optical properties as well as the magnetic behavior of the obtained samples. A single-phase spinel structure was obtained for the calcined aluminate powders with different interplanar spacing and crystallite sizes, as revealed by the classification results. The bandgap energy (E_g) of adapted aluminates was in the range of 2.04-3.14 eV, identified as being much lower compared to the pure sample (5.60 eV). Thus, Fe³⁺-substituted ZnAl₂O₄ samples could be successfully photoexcited using both ultraviolet and visible light, as suggested by the results. Examination of how the four main pollutant types decay when irradiated by sunlight was carried out to assess the samples and establish photocatalytic activity. These contaminants included rhodamine B (RhB), methylene blue (MB), methyl orange (MO), and methyl red (MR). The performance of photocatalytic degradation reached 98% after 150 min for all optimal samples of organic dyes. Besides, each of the altered photocatalysts could be recycled and displayed high stability. The S-shaped curve of ferrimagnetism can result in those samples as found by the magnetic measurements, though pure ZnAl₂O₄ displays diamagnetic characteristics. The adapted samples show intense improvement in the remanent magnetization (M_r) when compared to pure ZnAl₂O₄, signifying that magnetic photocatalyst recovery by applying an external magnetic field is easy. Thus, these results offer a convincing sign that ZnAl₂O₄ powders replaced by Fe³⁺ could provide the ability to aid in the ecologically friendly collection of solar energy.     

Surface tuning of the photoelectrochemical properties of oblique angle co-sputtered ZnxFeyO films by Fe concentration

Complex three-dimensional nanosheet structure of Zn_xFe_yO was prepared by highly stable co-sputtering oblique angle deposition. Scanning electron microscopy was employed to observe surface morphology evolution of Zn_xFe_yO with different Fe concentrations. X-ray diffraction was employed to analyze compositions of ZnO, ZnFe₂O₄, and ZnFe₂O₄/Fe₂O₃ with Fe doping. Furthermore, specific nanostructures of Zn_xFe_yO decreased band gap and increased visible-light absorption ability. The ZnFe₂O₄/Fe₂O₃ sample exhibited higher photocatalytic efficiency than those of other films for the degradation of methylene blue. Addition of Fe led to the enhancement of photoelectrochemical properties of ZnFe₂O₄/Fe₂O₃ compared to pure ZnO and Fe₂O₃, and photocurrent response of ZnFe₂O₄/Fe₂O₃ was ~10 times than that of pure ZnO at constant potential of −0.2 V (vs. Ag/AgCl).     

Cost effective synthesis of CuxBi2-xSe3 photocatalysts by sol-gel method and their enhanced photodegradation and antibacterial activities

A simple sol-gel approach was used to synthesize Cu doped Bismuth Selenide nanoparticles denoted as Cu_xBi_2-xSe₃ (x = 0.1, 0.2), in order to comprehend the effect of Cu-dopant on the photocatalytic and antibacterial activity of Bismuth Selenide. The structural properties of prepared samples were investigated by the XRD technique and results showed the formation of hexagonal Cu_xBi_2-xSe₃ (x = 0.1, 0.2). The average crystallite size of Cu_xBi_2-xSe₃ was found to increase from 39 nm to 42 nm with the increase in the concentration of Cu ions. Atomic force microscopy (AFM) was used to confirm the morphology and particle size of prepared samples. Photoluminescence (PL) studies revealed the decrease in band gap from 1.66 eV to 1.61 eV for Cu_0.1Bi_1.9Se₃ and Cu_0.2Bi_1.8Se₃, respectively. The Raman spectra of Cu_xBi_2-xSe₃ (x = 0.1, 0.2) showed two vibrational modes at 130 cm^?1 and 170 cm^?1. The photocatalytic performance of prepared nanoparticles was evaluated by the removal of methyl blue (MB) and malachite green (MG), under natural sunlight. Cu doped Bismuth Selenide Cu_0.2Bi_1.8Se₃ exhibited higher photocatalytic activity as compared to Cu_0.1Bi_1.9Se₃ and undoped Bismuth Selenide with the 97% and 99% degradation of MB and MG, respectively. Hence, Cu doping proved an efficient way to enhance the photocatalytic response of Bismuth Selenide. Through the antibacterial activity, it was further disclosed that the Cu doped samples had better inhibition zones than undoped Bismuth Selenide. The maximum inhibition zone (29 mm) was observed at optimum doping concentration for Cu_0.2Bi_1.8Se₃. From the results, it can be deduced that Cu_0.2Bi_1.8Se₃ can be as effective photocatalytic and antibacterial agent to treat water pollution.