UV Vis Diffuse Reflectance Spectroscopy Research Articles

Facile synthesis and characterization of zinc molybdate (ZnMoO4) nanosheets for electrochemical supercapacitor application

Abstract This study explores the synthesis and characterization of zinc molybdate (ZnMoO4) nanosheets with emphasis on their potential application for energy storage devices particularly supercapacitors. The synthesis of ZnMoO4 nanosheets was done through co-precipitation followed by examination of their structure, morphology, optical, thermal behaviour and electrochemical performance by various characterization techniques. X-ray diffraction (XRD) analysis confirmed that the formation of monoclinic ZnMoO4 phase with the average crystallite size 17.93 nm. Scanning electron microscopy (SEM) and Transmission electron microscopy (TEM) revealed that this material had nanosheets-like structure which helps to increase ion transport and surface area; these two factors are essential for enhancing the material’s supercapacitor efficacy. The semiconductor characteristics were determined using UV–Visible diffuse reflectance spectroscopy (UV-DRS) which indicated a band gap energy of 4.2 eV. Fourier transform infrared (FTIR) analysis confirmed that the presence of Zn–O and Mo–O bonds in their crystal lattice. Thermogravimetric analysis (TGA) showed that the ZnMoO4 nanosheets had thermal stability since they experienced only a slight mass loss of 2.57 % up to 800 °C. Cyclic voltammetry (CV) and galvanostatic charge-discharge (GCD) tests were undertaken to find out the specific capacitance and the value is 618 F g⁻1 at a current density of 1 A g⁻1.

Achieving High Photocatalytic NOx Removal Activity Using a Bi/BiOBr/TiO2 Composite Photocatalyst.

Fossil fuel combustion generates nitrogen oxides (NO + NO2 = NOx), which pose threats to the environment and human health. Although commercial products containing titanium dioxide (TiO2) can remedy NOx pollution by photocatalysis, they only function in the ultraviolet (UV). On the other hand, bismuth oxybromide (BiOBr) is active in the visible. BiOBr is stable, affordable, and non-toxic, making it an appealing alternative. In addition, nanoparticulate Bi metal can further enhance visible light absorption through its surface plasmon properties and charge carrier lifetime by spatially separating charge. In this study, to enhance the visible-light activity of TiO2-based photocatalysts for NOx pollution, a composite of Bi-decorated BiOBr/TiO2 was synthesized using a solvothermal method across varying the Ti/Bi atomic ratio (0.2, 2.2, 4.4, and 6.6), and synthesis duration (6h, 12h, and 18h). The photocatalytic performance of the synthesised composites for NO gas removal was investigated using an adapted ISO method (22197-1:2016). Analysis showed that the preferential growth of the (010) crystal facet in BiOBr and the presence of Bi metal both play an important role in the superior photocatalytic activity seen in our Bi-decorated BiOBr/TiO2 composite. The composites were characterised using X-ray diffraction (XRD), attenuated total reflectance - Fourier transform infrared spectroscopy (ATR-FTIR), high-resolution scanning electron microscopy (HRSEM), UV-Vis diffuse reflectance (DRS) spectroscopy, transmission electron microscopy (TEM), scanning transmission electron microscopy (STEM), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, Brunauer-Emmett-Teller (BET) analysis, thermogravimetric analysis (TGA), and diffuse reflectance transient absorption spectroscopy (DR-TAS). Our research shows that the Bi/BiOBr-TiO2 composite synthesised through the 12-hour solvothermal method with a Ti/Bi atomic ratio of 4.4 exhibits the highest photocatalytic performance towards both NO and NO2 oxidation; with 32.8% and 54.9% NO removal and 15.1% and 29.5% NO2 under visible and UV lamps, respectively.

Visible light sensitive BiVO4–TiO2 nanocomposites for photocatalytic dye degradation

Abstract The hydrothermal approach was used to prepare visible light active BiVO4–TiO2 nanosheet composites in varying molar ratios. The photoluminescence (PL) spectrum, X-ray photoelectron spectroscopy (XPS), UV-Visible Diffuse Reflectance Spectroscopy (DRS), Transmission electroscopy (TEM), Brunauer-Emmett-Teller (BET) and field emission scanning electron microscopy (FESEM), were used to analyze the photocatalysts and composites. Photocatalytic activity of BiVO4–TiO2 composites was investigated by decolorizing methylene blue. Out of four different molar ratio BiVO4–TiO2 composites with a molar ratio of 3:1 BiVO4 TiO2 composite showed enhanced photocatalytic activity which is further proved by photoluminescence investigation of coumarin and Scavenger test. The DRS of BiVO4 TiO2 composite showed red shift in optical absorption. The enhanced photocatalytic activity is due to minimizing electron hole recombination by making composite with TiO2.

Different metal-doped NiO nanoparticles for sunlight-mediated degradation of low-density polyethylene microplastic films.

Due to the widespread use and incorrect handling of plastics, we need to find a practical and effective way to eliminate plastic waste from the environment. Different metal-doped nickel oxide (DMD-NiO) nanoparticles (NPs) were synthesized using a sol-gel technique and were used to degrade low-density polyethylene (LDPE) microplastic (MP) films when exposed to sunlight. The optical and structural properties of sol-gel method synthesized materials were investigated using a variety of characterization methods (Fourier transform infrared (FT-IR), UV-vis diffuse reflectance spectroscopy (UV-vis DRS), X-ray diffractometer (XRD) analysis, X-ray photoelectron spectroscopy (XPS), high-resolution transmission electron microscopy (HR-TEM), scanning electron microscopy (SEM) with energy dispersive X-ray (EDX) analysis, and thermogravimetric analysis (TGA). Degradation study results suggest that the photocatalytic activity of DMD-NiO-LDPE nanocomposites (NCs) films was greater than that of pure LDPE and undoped NiO-LDPE films. Because of their increased optical absorption and efficient suppression of photo-produced charge carriers' recombination, the DMD-NiO NPs showed higher photocatalytic degradation of LDPE films. Thus, LDPE films with 2% wt Fe-NiO (iron-doped nickel oxide) nanomaterials showed a degradation of around 38.16% among DMD-NiO-LDPE NCs films under visible light over a short period of 30 days (240 h). The formation of carbonyl groups in the degradation product of LDPE was confirmed by Fourier transform infrared (FT-IR) analysis. When compared to the original LDPE film, the Fe-NiO-LDPE NCs films showed a significant decrease in crystallinity and carbonyl indexes, as much as 8.4% lower. The current project proposes the development of eco-friendly photocatalysts using a sol-gel technique for combating MP pollution in the environment.

La-supported SnO2–CaO composite catalysts for efficient malachite green degradation under UV–vis light

This study presents the development and optimization of La@SnO2–CaO composite catalysts for efficient photocatalytic degradation of malachite green dye in aqueous solutions under UV–vis light irradiation. The catalysts were prepared via conventional incipient-wetness impregnation and thoroughly characterized using advanced analytical techniques, including X-ray diffraction, Fourier transform infrared spectroscopy, UV–vis diffuse reflectance spectroscopy, N2 adsorption–desorption analysis, and scanning electron microscopy. To optimize photodegradation efficiency, the effects of three independent factors were systematically investigated using response surface methodology: Temperature, pH, and Sn/Ca molar ratio. Our results reveal optimal conditions for maximum dye degradation: pH 7, Sn/Ca molar ratio of 0.33, and a process time of 35 min, resulting in a maximum photodegradation efficiency of 98.80% for malachite green dye. Notably, visible light exhibited a more pronounced effect on dye degradation compared to UV light over time, with visible light achieving 25% greater dye removal after 60 min of illumination. Furthermore, the catalyst showed excellent recyclability, retaining 85% of its initial activity after five consecutive cycles. These findings contribute significantly to the development of sustainable methods for dye removal from wastewater and highlight the potential of La@SnO2–CaO composite catalysts in environmental remediation processes, particularly in treating textile industry effluents.

Phytomediated synthesis of WO3 nanoparticles using Solanum lycopersicum fruit extract for enhanced photocatalytic activity of 2,4-dichlorophenol

ABSTRACT In the present study, bio-citric acid/tungsten oxide (WO3) (BCAWO) nanoparticles (NPs) were prepared by using Solanum lycopersicum fruit extract as a reducing as well as a capping agent. The photocatalysts were characterized by UV–vis diffuse reflection spectroscopy, powder X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectrometry (EDS), high-resolution transmission electron microscopy, and photoluminescence spectroscopy techniques. Diffraction peaks in the XRD spectrum were identified as the crystal planes of crystalline tungsten oxide. The BCAWO had an average size of 23.14 nm. For W–O bonds, the Fourier transform infrared spectrum displays the vibrational peak at 671.23 cm−1. A prominent absorption band was observed at 268 nm, indicating the 1.2 eV bandgap. Under xenon (Xe) lamp irradiation, the synthesized BCAWO nanoparticles showed notable photocatalytic degradation of 2,4-dichlorophenol (2,4-DCP), with a degradation rate of 96%. With BCAWO concentrations of 2.5 g/L, pH of 4, reaction period of 180 min, and 2,4 DCP concentration of 10 mg/L, the degradation of 2,4-DCP had the highest efficacy, 96%. The degradation of phenols in wastewater may be facilitated by using the green WO3 nanoparticles as a photocatalyst, according to the results.

Isothermal conversion of methane to methanol over Cu-CHA using different oxidants

Methane oxidation to methanol in cyclic processes using CuO-zeolites has traditionally employed O2 and N2O as oxidants. This study explores the use of Cu-CHA zeolite, demonstrating that CO2 can substitute O2 in an isothermal reaction at 400 °C, analogous to previous findings using Cu-MAZ. The use of in situ UV-Vis diffuse reflectance spectroscopy (UV-Vis DRS) and density functional theory (DFT) theoretical calculations identified the formation of a binuclear copper hydroxide complex, Z-[CuOH-HOCu]2+-Z, on the Cu-CHA. Initial treatment using CO2 led to marginally superior catalytic activity, compared to the use of O2 alone, indicating the stability of the Z-[CuOH-HOCu]2+-Z complex against self-reduction at 400 °C. In subsequent cycles, activation with O2 facilitated the oxidation of adsorbed methanol, yielding water and reconstituting the active sites. Conversely, activation with CO2 led to the partial desorption of methanol, precluding water production and subsequent catalyst regeneration. The findings suggested that both O2 and CO2 activations necessitated a post-reaction water extraction step, followed by thermal treatment to replenish the active sites. Importantly, the results indicated that CO2 could be used as a viable alternative oxidant to O2 in this catalytic process, potentially enhancing the sustainability of industrial methanol production.

NH4Ca[B5O7(OH)4] H2O: A Biaxial Mixed‐Cation Pentaborate with Moderate Birefringence

AbstractAmmonium‐calcium mixed‐cation pentaborate NH4Ca[B5O7(OH)4]·H2O has been synthesized for the first time. Single‐crystal X‐ray diffraction analysis reveals that it crystallizes in the triclinic space group P‐1 with lattice parameters a = 6.7042(3) Å, b = 7.1859(3) Å, c = 10.7447(4) Å, α = 100.304(3), β = 97.774(3), γ = 96.972(3). The structure is characterized by 1D boron–oxygen chains composed of [B5O7(OH)4]3− polyanions that are further interspaced by Ca2+, NH4+ cations, along with lattice water molecules. The phase purity and thermal stability of the as‐synthesized sample were confirmed by XPRD and TG‐DSC analyses. Experimental UV–vis diffuse reflectance spectroscopy coupled with Urbach fitting indicates a direct bandgap of 4.50 eV, contrasting with theoretical calculations that suggest an indirect bandgap of 5.53 eV. Additionally, both theoretical computation and polarized light experimental test indicate that NH4Ca[B5O7(OH)4]·H2O exhibits moderate birefringence.

Facile one-pot synthesis of photoresponsive Cu1.8S and CuInS2 nanostructures aided by Cu-pyrimidylthiolate molecular precursor

Copper-based binary and ternary sulfides have attracted significant attention due to their excellent photo-physical properties, making them highly promising for high-performance energy harvesting and storage devices. This study focuses on the synthesis and structural characterization of an air-stable hexanuclear Cu-pyrimidylthiolate cluster complex which serves as an efficient single-source precursor for the preparation of Cu1.8S nanocrystals. Furthermore, coupling the molecular precursor with suitable indium source resulted in a facile one-pot pathway for the preparation of technologically important, copper-based ternary CuInS₂, nanocrystals. The crystal structure, phase purity, and compositions of the nanostructures were confirmed using PXRD, XPS, EDS, and area elemental mapping. Electron microscopic studies revealed the formation of polygonal and hexagonal morphology with varied size in Cu1.8S and CuInS₂ nanocrystals respectively. UV-Vis diffuse reflectance spectroscopy showed a slight blue shift in the band gap of the nanostructures compared to their bulk counterparts which can be attributed to quantum confinement or surface lattice distortion effects. The band gap of the pristine nanocrystals along with high photocurrent and stable photo-switching characteristics suggest that they can serve as suitable electrode material for optoelectronic and photodetector devices.

Physical and enhanced photocatalytic MO dye degradation behaviour of Zn doped β-Ga2O3 microrods

This work explored the effects of Zn doping on the structural, micrographic, optical and photocatalytic behaviour of gallium oxide (β-Ga2O3) microrods. The X-ray diffractogram (XRD) and Raman spectral analyses confirmed the monoclinic structure of β-Ga2O3, with a shift to lower angles in the XRD pattern indicating Zn incorporation into the Ga2O3 lattice. The Scanning electron microscopy (SEM) images revealed a rod-like shape, with the diameter decreasing from 604 nm to 573 nm with Zn doping. Further analysis using TEM, HR-TEM, SAED, EDX, and elemental mapping confirmed the shape, crystallinity, crystal structure, and elemental distribution. The interplanar spacings were measured as 0.4 and 0.2 nm, corresponding to the (002) and (−311) planes of β-Ga2O3. UV–Vis diffuse reflectance spectroscopy (UV–Vis DRS) showed a slight shift in the absorption edge, while photoluminescence (PL) analysis demonstrated strong UV and weak visible light emission. Photocatalytic results revealed a high efficiency of dye degradation,(i.e) 98 % (20 ppm) and 89 % (30 ppm) against methyl orange (MO) dye aqueous solution over 150 min, with a rate constant of 0.02/min and 0.01/min, respectively for 1.5 wt% Zn doping. This suggests that the Zn-doped material holds promise as a photocatalyst for wastewater treatment applications.

Anodic Synthesis of Highly Ordered TiO2 Nanotube Arrays: Role of Electrolyte Composition on the Structural, Morphological, Optical, and Photo-electrochemical Properties

The fluoride species present in two different anodizing electrolytes were used to produce TiO2 nanotube arrays (TiO2 NTAs) by simultaneous anodic reaction and chemical dissolution. In this investigation, two different electrolytes were used for the preparation; [Eth-TiO2 NAs: 95 ml ethylene glycol+0.5% NH4F+5 ml DI water] and [Gly-TiO2 NAs: 75 ml glycerine+0.5% NH4F+25 ml DI water]. The effects of the prepared electrolytes used in the synthesis of TiO2 nanotube arrays on structural element composition, morphology, and optical properties are the focus of this study and are characterized by X-ray diffraction (XRD), scanning electron microscopy field emission (FE-SEM), energy-dispersive X-ray spectroscopy (EDX) and UV-vis diffusion reflection spectroscopy (DRS), respectively. The photoelectrochemical properties of TiO2 NTAs prepared in different electrolytes were investigated. The photoelectrochemical performance of TiO2 NTAs in Na2SO3 (0.1 M) and Na2S (0.1) was examined under the light of 100 mW/cm2 from a xenon lamp. Comparing the photoelectrochemical (PEC) results of both electrolytes, we find that Eth-TiO2 NTAs contribute a wide surface area resulting in an enhanced PEC response. TiO2 NTs, which were prepared with Eth-TiO2 NTAs, exhibited the highest photocurrent density, 0.326 mA cm–2, and photoconversion efficiency (0.22%).

Synthesis and characterization of zinc-doped hematite nanoparticles for photocatalytic applications and their electronic structure studies by density functional theory

Hematite nanoparticles doped with 1, 3 and 5 % Zn (all % are in molar) were prepared using mechanical alloying. Morphological and phase structure studies using scanning electron microscopy and X-ray diffraction showed nanoparticles possessing a semi-spherical shape and particle size of <50 nm crystallized in rhombohedral structure. The lattice parameters of hematite increased upon Zn doping. The energy-dispersive X-ray and Fourier-transform infrared results demonstrated that Zn was successfully incorporated. The optical behavior of nanoparticles was examined by UV–Vis diffuse reflectance spectroscopy and revealed that Zn doping increased the absorption intensity in the visible light region and decreased the band gap from 1.95 (hematite) to 1.83 eV (3 % Zn). Methylene blue dye degradation by the 3 % Zn sample proved doubling of the photocatalytic activity due to electronic structure modification upon Zn doping. First principles studies using density functional theory performed to investigate the effect of Zn on the electronic band structure of hematite showed that Zn doping caused band gap reduction, causing formation of new energy states, mainly above the valence band. Eventually, the enhancement of Urbach energy and reduction of effective mass, respectively accountable for increasing the relaxation time and mobility of charge carriers, were considered the two main mechanisms regarding the increased photocatalytic behavior of hematite by Zn doping.

Visible Light-driven Effective Photocatalytic Degradation of the Persistent Organic Pollutant Using Cobalt-doped Strontium Titanate

Residual antibiotics in natural aquatic environments pose a critical threat to humans and other organisms. However, most sewage treatment plants fail to remove them. Photocatalytic nanomaterials can efficiently destroy these persistent organic pollutants in wastewater. In this study, we developed a series of cobalt-doped SrTiO3 (Co-STO) catalysts with different doping amounts (3, 5, 7, and 9 wt%) for the effective photocatalytic degradation of ciprofloxacin (CIP). The nanostructures were characterized using X-ray diffraction, field-emission scanning electron microscopy with energy dispersive X-ray analysis, transmission electron microscopy, X-ray photoelectron spectroscopy, UV-visible diffuse reflectance spectroscopy, and Brunauer–Emmett–Teller N2 adsorption isotherms. The Co-STO particles have a mesoporous diameter of ~30.8 nm, and the Co-doped nanostructures have a rhombohedral hopper-like shape. Co-doping decreased the bandgap of pure STO from 3.61 to 3.42 eV, which enabled it to absorb visible light. Among the catalysts, 7 wt% Co-STO showed the highest CIP degradation activity (90.6%) during 120 min of visible-light irradiation. Radical scavenging experiments revealed that superoxide (O2 •-) is the primary reactive species during degradation. These Co-doped nanostructures have potential applications in the remediation of hazardous pollutants in pharmaceutical wastewater. Moreover, the crystal and energy band structure, density of states, and Bader charge of these molecules were analyzed.

Photocatalytic reduction of nitroarene derivatives by impressive visible-light active Co3O4-QDs/Mn3O4 nanocomposite

A visible light active Co3O4-quantum dots (QDs)/Mn3O4 nanocomposite was successfully synthesized by a straightforward precipitation approach. Notably, the formation of Mn3O4 nanosheets in composite structure was evidenced by different physicochemical techniques especially transmission electron microscopy (TEM), energy dispersive X-ray (EDX) and N2 sorption analyses, which indicated the uniform distribution of Co3O4-QDs with small size of around 5 nm on the surface of Mn3O4 nanosheets along with the enhancement of specific surface area for final composite. Also, the persistence of Co3O4-QDs during nanocomposite synthesis was analyzed by X-ray diffraction (XRD), FT-IR and TEM techniques. The diffuse reflectance UV–Vis and electrochemical impedance spectroscopies revealed the reduction of band gap energy and enhanced charge separation efficiency for Co3O4-QDs/Mn3O4 nanocomposite, respectively, which consequently led to improved photocatalytic response in comparison with bare Co3O4-QDs and Mn3O4 nanosheets. The as-prepared nanocomposite exhibited excellent photocatalytic activity in the reduction of a wide range of substituted nitroarenes with the yields of higher than 80 % relative to the corresponding arylamines, using N2H4·H2O as the hydrogen source and ethanol as green solvent at 25 °C and ambient pressure under visible light illumination. The synergistic effect could improve the production of active hydrogen atoms, therefore, the reasons for this transformation over the prepared nanocomposite under benign conditions are fully discussed. Furthermore, the nanocomposite could be easily recycled without decay in photocatalytic activity for at least five successive cycles.

Zeolitic imidazolate framework-67/barium zirconate titanate nanocomposite, Part I: Synthesis, characterization, and boosted photocatalytic activity

Using BaTi0.85Zr0.15O3/ZIF-67 (BTZ/ZIF-67) nanocomposite, tetracycline (TC) was photodegraded. Characterization of the samples was carried out using a variety of techniques, including XRD, FESEM-EDS (Field Emission Scanning Electron Microscopy – Energy Dispersive X-ray Spectroscopy), FT-IR (Fourier Transform Infra-Red), TEM (Transmission Electron Microscopy), BET (Brunauer-Emmett-Teller), BJH (Barrett-Joyner-Halenda), PL (Photoluminescence), TG-DTG (Thermogravimetry and Derivative Thermogravimetry), and UV–Vis DRS (Diffuse Reflectance Spectroscopy). BTZ/ZIF-67 nano-composites were synthesized using a one-step co-precipitation method. BTZ (30 %wt)/ZIF-67 showed the most impressive photocatalytic ability among the binary photocatalysts. Averaging the crystallite sizes of the nanocomposite samples identified by Scherrer and Williamson-Hall methods was 43.3 nm and 65.0 nm, respectively. The pHpzc values of samples of BTZ and BTZ (30 %wt)/ZIF-67 were approximately 6.7 and 10.0, respectively. Using the proposed method, we measured 357, 414, and 377 nm absorption edges for ZIF-67, BTZ, and BTZ (30 %wt)/ZIF-67 samples, which correspond to 3.47, 2.99, and 3.28 eV bandgap energies, respectively. The specific surface areas of BTZ, ZIF-67, and BTZ (30 %wt)/ZIF-67 nanocomposite are 122.15, 1218, and 1509 m2g−1, respectively. Under optimum conditions (0.8 g/L of the catalyst, CTC: 30 mg/L, and a pH 5), 89.5 % of total organic carbon (TOC) was removed within 180 min. Compared to BTZ photocatalyst, the BTZ (30 %wt)/ZIF-67 nanocomposite has a significantly larger surface area, thus enhancing photocatalytic activity. A synergistic effect was observed in the photodegradation of TC under Hg-lamp irradiation with the proposed BTZ/ZIF-67 composite. It is possible to alter the photocatalytic activity of the catalyst by changing the BTZ (30 %wt)/ZIF-67 ratio.

Nanocasting synthesis of mesoporous CeO2 particle abrasives from mesoporous SiO2 hard templates for enhanced chemical mechanical polishing performance

Mesoporous abrasive particles exhibit superior chemical mechanical polishing/planarization (CMP) performance, as compared with the corresponding bulk materials. Nevertheless, the lack of control over the shape and particle size or distribution extremely restricts the development of mesoporous abrasives and their potential applications. To overwhelm these drawbacks, pure and ytterbium-doped mesoporous ceria (mCeO2 and mCeYbO2) spheres with well-defined morphology and good uniformity were synthesized via a straightforward nanocasting strategy using high-quality mesoporous silica spheres as hard templates and metal nitrates as precursors. The resulting samples were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, selected area electron diffraction, X-ray photoelectron spectroscopy, Raman spectroscopy, UV–vis diffuse reflectance spectroscopy, photoluminescence spectroscopy, Zeta potential, and N2 adsorption-desorption measurements. The as-prepared mCeO2 and mCeYbO2 products exhibited enriched surface defects (trivalent Ce, vacancy oxygen, hydroxyls) and polycrystalline porous frameworks with a surface area of up to 160 m2/g and pore size of 4–7 nm. Benefiting from these synergistic attributes, the flexible and defective particle abrasives enabled significant improvements in both surface quality and removal efficiency during oxide-CMP, as compared to commercial CeO2. A possible CMP mechanism was proposed on the basis of the physical contact state, adsorption and adhesion behavior, as well as tribochemical interaction occurred at CeO2–SiO2 interfaces. This work demonstrates highly promising abrasive materials advancement combining architecture and defect engineering towards high-performance oxide-CMP.

Competent CuS QDs@Fe MIL101 heterojunction for Sunlight-driven degradation of pharmaceutical contaminants from wastewater

In this study, we introduce an advanced photocatalyst developed by integrating copper sulfide quantum dots (CuS QDs) with an iron-based metal–organic framework (MOF), specifically Fe MIL101. The resulting CuS QDs@Fe MIL101 photocatalyst is engineered to efficiently degrade meloxicam (MLX) under simulated sunlight. The heterojunctions were generated by incorporating different concentrations of CuS QDs (5 %, 10 %, 15 %, 20 %, and 50 %) into the Fe MIL101 MOF matrix using the microwave-assisted hydrothermal method. The results of the XRD and the TEM studies confirmed the formation of the heterojunctions, which maintain the structural integrity of both CuS QDs and Fe MIL101. The BET measurements indicated a decrease in surface area upon CuS QDs incorporation, attributed to porés blockage and structural modifications. UV–Vis diffuse reflectance spectroscopy (DRS) revealed a redshift in absorption edges as CuS QDs content increased, enhancing visible light absorption. Photoluminescence (PL) investigations revealed that the 15 % CuS QDs@Fe MIL101 heterojunction had an effective charge separation and low recombination rates. The zeta potential analysis revealed a negative surface charge, indicating an overall electronegative characteristic. The photocatalytic performance, assessed through the degradation of MLX, demonstrated that the 15 % CuS QDs@Fe MIL101 heterojunction achieved the maximum degradation efficiency, reaching 96 % after 45 min of irradiation at a dosage of 0.1 g/L. This exceptional performance is attributed to potent charge separation, improving visible light absorption, high surface area and adsorption capacity. Various scavengers were used to investigate the roles of different reactive species, revealing holes as the predominant active species in the photocatalytic degradation process. These results highlight the potential of 15 % CuS QDs@Fe MIL101 heterojunctions as efficient photocatalyst for environmental remediation from pharmaceutical pollutants under simulated sunlight. These findings highlight the potential for application of CuS QDs@Fe MIL101 in real-world wastewater treatment systems, particularly in addressing pharmaceutical contaminants like meloxicam in industrial effluents.

Enhanced band gap energy of one-pot mechano-synthesized Ag3PO4 for Orange G photodegradation under visible light irradiation: An in-depth experimental and DFT studies

The present study highlights the efficiency of Ag3PO4 photocatalyst with a band gap of 2.25 eV, synthesized by a green and one-pot simple mechanochemical method, towards photodegradation of orange G under visible irradiation. The phase structure, morphology, and optical properties of mechano-synthesized Ag3PO4 were investigated using X-ray diffraction, Scanning Electron Microscopy, Thermogravimetric Analysis, Fourier Transform Infrared, the Brunauer-Emmet-Teller surface area, and UV–vis diffuse reflectance spectroscopy. DFT calculations were also conducted for band gap energy prediction. The photocatalytic activity of the sample was evaluated using a central composite design for surface response methodology (CCD-RSM) to determine the optimal conditions for Orange G (OG) removal. The photocatalytic activity of Ag3PO4 was approximately 93 % within 20 min of reaction under irradiation for 24.6 mg/L and 11 mg/L of Ag3PO4 and Orange G, respectively. Trapping experiments confirmed that peroxides and hydroxyl radicals are the dominant active species in the photodegradation process.

Exploring the structural, morphology, optical and magnetic properties of ZnCoxMn(2-x)O4 prepared using hydrothermal method

Here we report the structural and physical property of ZnCoxMn(2-x)O4 (x = 0, 0.1 and 0.2) materials. The hierarchical ZnCoxMn2-xO4 (x = 0, 0.1 and 0.2) have been successfully synthesized by hydrothermal method. The surface of the ZnCoxMn(2-x)O4 varies according to its composition which is investigated. The absorption and band gap of the material were measured by UV-Vis diffuse reflectance spectroscopy (DRS) in the range of 200 – 800 nm. It was observed that the band gap gets decreased from the parent compound. The room temperature photoluminescence emission spectra of ZnCoxMn(2-x)O4 (x = 0,0.1 and 0.2) has been investigated. The magnetic property of material shows an antiferromagnetic nature. Further, X-ray photoelectron spectroscopy analysis confirms the substitution of Co on Mn site.

Understanding of the effect of concentration of green polysaccharide-based TiO2 for photoelectrochemical, photocatalytic, and antibacterial properties

Composites formed by TiO2/babassu mesocarp were synthesized by the sol-gel method with a percentage variation of 3 % and 5 % (w/v) called 3BBT and 5BBT, respectively. The materials were characterized by X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM), UV–Vis Diffuse Reflectance Spectroscopy, and surface area was calculated by the Brunauer–Emmett–Teller method (BET). Electrochemical studies were carried out, and photocurrent data was obtained as a function of the variation in gallic acid concentration and applied potential. The photocatalytic efficiency of the material was investigated by the degradation of the Methylene Blue (MB) dye under light. The antimicrobial activity of the materials was tested on Gram-positive and Gram-negative strains. XRD showed that the composites obtained are in the anatase crystallographic phase, and the increase in the percentage of babassu mesocarp influenced the reduction of peak intensity and crystallite size. The microscopy showed a more porous aspect of the 3BBT material and a denser aspect of the 5BBT material. It was confirmed by textural characterizations, which showed reduced pore volume and specific surface area of 5BBT compared to 3BBT. Increasing the percentage of polysaccharides caused a reduction in the band gap energy of TiO2 (Eg = 2.90 eV and Eg = 2.47 eV for 3BBT and 5BBT, respectively). The electrochemical study showed that the composites could detect gallic acid, providing increased sensitivity according to the increased applied photocurrent. They also showed good precision for the photoelectrochemical measurements, as verified in the repeatability test (2.66 % and 3.68 % RPD for 3BBT and 5BBT, respectively). The 3BBT showed greater photocatalytic capacity, discoloring 63.4 % of the MB dye in 120 min under light and electrons are the main species involved in photocatalytic activity demonstrated by 3BBT. Antibacterial tests indicated that the 5BBT material exhibits a greater capacity to inhibit E. coli and S. aureus bacteria.