Electric-Field-Assisted Synthesis of Cu/MoS2 Nanostructures for Efficient Hydrogen Evolution Reaction.

Molybdenum sulfide-oxide (MoS2, MS) emerges as the prime electrocatalyst candidate demonstrating hydrogen evolution reaction (HER) activity comparable to platinum (Pt). This study presents a facile electrochemical approach for fabricating a hybrid copper (Cu)/MoS2 (CMS) nanostructure thin-film electrocatalyst directly onto nickel foam (NF) without a binder or template. The synthesized CMS nanostructures were characterized utilizing energy-dispersive X-ray spectroscopy (EDS), scanning electron microscopy (SEM), X-ray diffraction (XRD), and electrochemical methods. The XRD result revealed that the Cu metal coating on MS results in the creation of an extremely crystalline CMS nanostructure with a well-defined interface. The hybrid nanostructures demonstrated higher hydrogen production, attributed to the synergistic interplay of morphology and electron distribution at the interface. The nanostructures displayed a significantly low overpotential of -149 mV at 10 mA cm-2 and a Tafel slope of 117 mV dec-1, indicating enhanced catalytic activity compared to pristine MoS2.This research underscores the significant enhancement of the HER performance and conductivity achieved by CMS, showcasing its potential applications in renewable energy.

Croton macrostachyus Leaf Extract-Mediated Green Synthesis of ZnO Nanoparticles and ZnO/CuO Nanocomposites for the Enhanced Photodegradation of Methylene Blue Dye with the COMSOL Simulation Model.

The photodegradation of organic pollutants using metal oxide-based catalysts has drawn great attention as an effective method for wastewater treatment. In this study, zinc oxide nanoparticles (ZnO NPs) and zinc oxide/copper oxide nanocomposites (ZnO/CuO NCs) were fabricated using the leaf extract of Croton macrostachyus as a nontoxic, natural reducing and stabilizing agent. The synthesized samples were characterized by employing X-ray diffraction, microscopic, spectroscopic, and electrochemical methods. The results confirmed the successful synthesis of ZnO NPs and ZnO/CuO NCs with well-defined crystalline structures and morphologies. The prepared samples were tested for the photodegradation of methylene blue (MB) dye under visible light irradiation. Compared to ZnO NPs, ZnO/CuO NCs showed greatly improved photocatalytic performances, particularly with the sample prepared with the 20 mol % Cu precursor (97.02%). The enhancement could be related to the formed p-n heterojunction, which can suppress the recombination of charge carriers and extend the photoresponsive range. A theoretical study of the photocatalytic activity of ZnO/CuO NCs against MB dye degradation was also conducted by using COMSOL Multiphysics software. The results of the simulation are in reasonable agreement with those of the experiment. This study contributes to the development of sustainable and effective photocatalytic materials that are suitable for application in environmental remediation, particularly in the treatment of wastewater.

Green Synthesis of a CuO-ZnO Nanocomposite for Efficient Photodegradation of Methylene Blue and Reduction of 4-Nitrophenol.

CuO-ZnO nanocomposites (NCs) were synthesized using an aqueous extract of Verbascum sinaiticum Benth. (GH) plant. X-ray diffraction (XRD), spectroscopic, and microscopic methods were used to explore the crystallinity, optical properties, morphology, and other features of the CuO-ZnO samples. Furthermore, catalytic performances were investigated for methylene blue (MB) degradation and 4-nitrophenol (4-NP) reduction. According to the results, CuO-ZnO NCs with 20 wt % CuO showed enhanced photocatalytic activity against MB dye with a 0.017 min-1 rate constant compared to 0.0027 min-1 for ZnO nanoparticles (NPs). Similarly, a ratio constant of 5.925 min-1 g-1 4-NP reductions was achieved with CuO-ZnO NCs. The results signified enhanced performance of CuO-ZnO NCs relative to ZnO NPs. The enhancement could be due to the synergy between ZnO and CuO, resulting in improved absorption of visible light and reduced electron-hole (e-/h+) recombination rate. In addition, variations in the CuO content affected the performance of the CuO-ZnO NCs. Thus, the CuO-ZnO NCs prepared using V. sinaiticum Benth. extract could make the material a desirable catalyst for the elimination of organic pollutants.

Biogenic Synthesis of Cu-Doped ZnO Photocatalyst for the Removal of Organic Dye.

The Cu-doped ZnO photocatalysts were prepared with a green and coprecipitation approach by using water hyacinth (Eichhornia crassipes) aquatic plant extract. In the preparation process, different amount of copper precursors such as 1, 2, 3, 4, and 5% of molar ratio were added to zinc nitrate precursors and abbreviated as Cu-ZnO (1%), Cu-ZnO (2%), Cu-ZnO (3%), Cu-ZnO (4%), and Cu-ZnO (5%), respectively. The characterization of the obtained samples was carried out, and the removal of the methylene blue (MB) dye was examined. Out of all catalysts, Cu-ZnO (3%) had the best photocatalytic performance and 89% of the MB dye was degraded. However, the degradation performances of blank (without catalysts), ZnO, Cu-ZnO (1%), Cu-ZnO (2%), Cu-ZnO (4%), and Cu-ZnO (5%) catalysts were 6, 54, 69, 83, 80, and 73%, respectively. Therefore, the use of water hyacinth plant extract with the optimum amount of Cu added to ZnO during the preparation of the catalyst could have a promising application in the degradation of organic pollutants.

Citrus sinensis and Musa acuminata Peel Waste Extract Mediated Synthesis of TiO2/rGO Nanocomposites for Photocatalytic Degradation of Methylene Blue under Visible Light Irradiation.

Water pollution caused by various natural and artificial sources such as expansion of industrialization, rapid increment in population size, the threat of climate change, and development in urbanization takes a serious attention. Due to this fact, various protocols and techniques were adopted for the treatment of such polluted water. In the present findings, TiO2 nanoparticles (NPs) and TiO2/rGO nanocomposites (NCs) were synthesized using titanium tetra butoxide in the presence of Citrus sinensis (CS) and Musa acuminata (MA) peel waste extract as a capping, reducing, and stabilizing agent. The synthesized NPs and NCs were characterized using thermogravimetric-differential thermal analysis (TGA/DTA), X-ray diffraction (XRD), scanning electron microscope (SEM), high resolution transmission electron microscopy (HR-TEM), selected area electron diffraction (SAED) pattern, ultraviolet diffuse reflectance spectroscopy (UV-DRS), and Fourier transform infrared (FTIR) spectroscopy. The synthesized NPs and NCs were investigated as green alternative photocatalyst for the degradation of methylene blue (MB) dye under visible light irradiation. Thermal analysis results confirmed that the green synthesized TiO2 NPs were found to be too stable above 550°C. XRD analysis result showed that the average crystalline size of CS and MA mediated synthesized TiO2 NPs with various volume ratios was in the range of 7.3-27.3 nm and 13.4-22.4 nm, respectively. The average crystalline size of CS and MA peel extract template synthesized TiO2/rGO NCs was found to be in the range of 7.5-15.3 and 11.2-12.5 nm, respectively. The band gap energy was calculated to be in the range of 3.17-3.29 eV and 3.10-3.38 eV for the CS and MA mediated synthesized TiO2 NPs, respectively. E g of CS and MA peel extract template formed TiO2/rGO NCs was found to be in the range of 2.85-3.11 eV and 3.07-3.11 eV, respectively. SEM analysis proved that the various synthesized TiO2 NPs and TiO2/rGO NCs were spherical in shape and the absence of any other foreign materials confirmed the purity of the corresponding nanocatalysts. In addition, TEM, HRTEM, and SAED analysis confirmed that the structures of the synthesized nanocatalysts were spherical in shape and the catalysts were too crystalline and the result was found to fit with the XRD result. Among the synthesized various volume ratios of TiO2 nanocatalysts, high percentage of degradation (62% and 58.2%) was achieved using TiO2-2c and TiO2-2 m, respectively. Moreover, 94.28% and 94.25% of MB degradation were achieved in the presence of TiO2/rGO-1.5c and TiO2/rGO-1.5c nanocomposite photocatalysts, respectively.

Water hyacinth plant extract mediated green synthesis of Cr2O3/ZnO composite photocatalyst for the degradation of organic dye.

The Cr2O3/ZnO composite catalysts with varying the amount of chromium precursors abbreviated as 0.02CrZn, 0.04CrZn, 0.06CrZn, 0.08CrZn, 0.1CrZn, and fixed the amount of Zn precursor (0.1 M) were prepared by using water hyacinth (Eichhornia crassipes) extract as a template/capping agent. The prepared catalysts were characterized and the catalytic performances of the catalysts were also checked for the degradation of methylene blue (MB) dye. The photocatalytic MB dye degradation by 0.08CrZn catalyst was achieved and 85% of MB dye was degraded within 90 min irradiation time. However, 0.1CrZ, 0.06CrZ, 0.04CrZ, 0.02CrZ, ZnO, and Cr2O3 catalysts degrade only 80, 74, 79, 76, 52, and 74% of MB dye, respectively. The catalytic performances indicated that the addition of optimum amount of chromium precursor in the preparation of Cr2O3/ZnO composite catalysts with the aid of Eichhornia crassipes plant extract enhances the catalytic activities. This performance enhancement could be as a result of reducing the electron/hole pair separation and the porosity resulted from the plant extract in the catalyst system.

Use of Different Natural Products to Control Growth of Titanium Oxide Nanoparticles in Green Solvent Emulsion, Characterization, and Their Photocatalytic Application.

Water, one of the crucial and the pillar resources to every living thing, could be polluted day to day by different causes such as expansion in industrialization, rapid increment in population size, the threat of climate, and growth of urbanization. The existence of a number of organic dyes, detergents, and pesticides from industrial effluents could lead to severe diseases and even to the death of human beings. Currently, remediation of those hazardous organic contaminants using semiconductor metal oxide catalysts has received extensive attention in recent years. Among the numerous nanometal oxides, titanium oxide (TiO2) nanoparticles (NPs) have been well known as a significant photocatalytic material due to their suitable physiochemical behaviors such as stability, conductivity, high surface area to volume ratio, structure, and porosity nature at the nanoscale level. TiO2 semiconductor nanoparticles could be synthesized via several physiochemical approaches; among those, the biogenic technique is the most selective one which involves the synthesis of NPs using different templates. Biogenic synthesis of nanoparticles is an environmentally friendly protocol that involves the use of different parts and types of biogenic sources such as bacteria, fungi, yeast, virus, and green plants or the byproducts of their metabolism, which act as both reducing and stabilizing agents. TiO2 NPs obtained via the biogenic method provide a potential application for the degradation of organic dyes and other pollutants in wastewater. This method of synthesis of NPs has been given a great attention by researchers due to their nontoxicity, low cost, environmental friendliness, the usage of green solvents, and simplicity of the process. This review focuses on summarizing the synthesis of TiO2 NPs using various biogenic sources, characterization, and their photocatalytic applications for the degradation of different wastes and organic dyes from polluted water.

Enhanced photocatalytic and electrochemical performance of TiO2-Fe2O3 nanocomposite: Its applications in dye decolorization and as supercapacitors.

This work reveals a green combustion route for the synthesis of TiO2, Fe2O3 and TiO2-Fe2O3 nanocomposites as photocatalysts for decolorization of Titan Yellow (TY) and Methyl Orange (MO) dyes at room temperature in aqueous solution concentration of 20 ppm under UV-light irradiation. We observed that the TiO2-Fe2O3 nanocomposite shows superior photocatalytic activity for TY dye compared to pure TiO2 and Fe2O3. Rate constant (k) values of TiO2, Fe2O3 and TiO2-Fe2O3 for TY and MO are 0.0194, 0.0159, 0.04396 and 0.00931, 0.00772 0.0119 kmin-1 respectively. The surface area and pore volume of TiO2-Fe2O3 nanocomposite were found to be 71.56 m2/g and 0.076 cm3/g, respectively as revealed by BET studies. From the Barrett-Joyner-Halenda (BJH) plot, the mean pore diameter of TiO2-Fe2O3 nanoparticles was found to be 2.43 nm. Further, the TiO2-Fe2O3 nanocomposite showed good electrochemical behavior as an electrode material for supercapacitors when compared to pure TiO2 and Fe2O3 nanoparticles resulted in stable electrochemical performance with nearly 100% coulombic efficiency at a scan rate of 10 mV/s for 1000 cycles. Interestingly, the novelty of this work is that the designed supercapacitors showed stable electrochemical performance even at 1000th cycle, which might be useful for rechargeable supercapacitor applications. The electrochemical properties of the nanocomposites were compared by the data obtained by cyclic voltammograms, charge-discharge tests and electrochemical impedance spectroscopic studies. These results demonstrated that the TiO2-Fe2O3 nanocomposite showed stable performance compared to TiO2 and Fe2O3 nanoparticles at current density of 5 Ag-1.

N-Doped carbon dots with pH-sensitive emission, and their application to simultaneous fluorometric determination of iron(III) and copper(II).

Simultaneous fluorometric determination of iron(III) and copper(II) without the use of any masking agent or additional treatment is achieved by using N-doped carbon dots (NCDs). The NCDs were hydrothermally prepared, have strongest excitation/emission peaks at 320/406 nm and a 47% quantum yield. Excitation-tunable emission is found to depend on solution pH values. This supports the involvement of surface states in the origin of the excitation dependent nature. The NCDs were employed as a fluorescent probe for the simultaneous determination of Fe(III) with a linear response in the 3-60 µM concentration range and a 0.31 µM detection limit (LOD). The probe also responds linearly to Cu(II) in the 0.5-15 µM concentration range and with a 56 nM LOD. With the addition of Cu(II), the absorption spectra of NCDs presented a clear decrease in the intensity at 312 nm followed by an increase at 360 nm. This is not observed in the presence of Fe(III). The fluorescence lifetime of NCDs (5.8 ns) is reduced by Fe(III) but not by Cu(II). Thus, the two metal ions can be simultaneously detected without the need for any reagents. The probe was employed to quantify Fe(III) and Cu(II) in spiked water, serum, and urine samples. Graphical abstract Schematic representation of hydrothermal synthesis of highly fluorescent N-doped carbon dots with novel pH dependent emission and their application for the simultaneous determination of Cu(II) and Fe(III) with individual ion discrimination.