Probing pharmaceutically important amino acids L-isoleucine and L-tyrosine Solubilities: Unraveling the solvation thermodynamics in diverse mixed solvent systems.

The study specifically investigates the solubilities of L-isoleucine and L-tyrosine in water-mixed solvent systems (DMF, DMSO, and ACN), exploring the behaviour of amino acids in complex environments. The experimental methods prioritize meticulous solvent purification to ensure reliable results. The work explores solubility data, uncovering temperature-dependent trends and intricate interactions influencing solubility in the chosen mixed solvent systems. The study emphasizes the impact of thermodynamic properties, solvent-solvent interactions, and amino acid structure on solubility patterns. The broader implications highlight the relevance of understanding amino acid behaviour in diverse solvent environments, offering potential applications in cosmetics and pharmaceutical industries. The distinct solubility patterns contribute valuable insights, enhancing on the understanding of the solution stability and interactions of L-isoleucine and L-tyrosine in different solvent systems. In conclusion, work suggests the enhanced utilization of L-isoleucine and L-tyrosine in various industries, driven by a profound understanding of their solubility in mixed solvent systems. The research expands our knowledge of amino acid behaviour, paving the way for advancements in industries relying on protein-based products and technologies.

Photo/electro catalytic green hydrogen production promoted by Ga modified Co0.6Cu0.4Fe2O4 nano catalysts.

The current work concentrates on the fabrication of Ga doped Co0.6Cu0.4Fe2O4 nanocatalysts via sol-gel auto-combustion (SGA) for the production of green and sustainable source of energy i.e., hydrogen through photocatalytic and electrocatalytic routes. Single-phased cubic crystal structure with Fd3m geometry was observed through XRD patterns. FESEM images show the aggregated and spherical shaped grains with distinct grain boundaries and average grain size of 1.04 and 1.39 µm for the Co0.6Cu0.4Fe2O4, and Co0.6Cu0.4Ga0.02Fe1.98O4 nanomaterials. Soft magnetic behaviour with a coercivity (Hc) and saturation magnetization (Ms) of 235.32-357.26 Oe and 54.65-61.11 emu/g was obtained for the produced nanomaterials. The estimation of photocatalytic nature for generating H2 was conducted using the sacrificial agents i.e., 0.128 M Na2S and 0.079 M Na2SO3. The analysis focused on measuring the maximum H2 generation was achieved by photocatalysts throughout three consecutive 4-h cycles. Out of all compositions, Co0.6Cu0.4Ga0.02Fe1.98O4 nanomaterial have the highest photocatalytic activity of 16.71 mmol gcat-1. However, the electrocatalytic behaviour of prepared Co0.6Cu0.4GaxFe2-xO4 (x = 0.00-0.03) electrocatalysts were determined for HER (Hydrogen evolution reaction) reaction. The overpotential values of Co0.6Cu0.4Fe2O4, Co0.6Cu0.4Ga0.01Fe1.99O4, Co0.6Cu0.4Ga0.02Fe1.98O4, and Co0.6Cu0.4Ga0.03Fe1.97O4 catalysts at 10 mA cm-2 were -0.81, -0.85, -1.03, and 1.21 V, correspondingly. Thus, at cathode current density of 10 mA/cm-2, an elevation in overpotential was noted, which indicates that the undoped Co0.6Cu0.4Fe2O4 (x = 0.00) electrocatalyst have remarkable electrocatalytic HER activity. Consequently, owing to photo/electro catalytic water splitting traits, the prepared catalysts are highly efficient for the green hydrogen generation.

A sustainable approach for fluoride treatment using coconut fiber cellulose as an adsorbent.

In developing countries like India, an economically viable and ecologically approachable strategy is required to safeguard the drinking water. Excessive fluoride intake through drinking water can lead to dental fluorosis, skeletal fluorosis, or both. The present study has been under with an objective to investigate the feasibility of using cellulose derived from coconut fiber as an adsorbent under varying pH conditions for fluoride elimination from water. The assessment of equilibrium concentration of metal ions using adsorption isotherms is an integral part of the study. This present finding indicates the considerable effect of variation of adsorbent dosages on the fluoride removal efficiency under constant temperature conditions of 25 ± 2 °C with a contact period of 24 h. It is pertinent to mention that maximum adsorption of 88% has been observed with a pH value of 6 with 6 h time duration with fluoride dosage of 50 mg/L. The equilibrium concentration dwindled to 0.4 mg/L at fluoride concentration of 20 mg/L. The Langmuir model designates the adsorption capacity value of 2.15 mg/L with initial fluoride concentration of 0.21 mg/g with R2 value of 0.660. Similarly, the adsorption capacity using Freundlich isotherms is found to be 0.58 L/g and 0.59 L/g with fluoride concentration of 1.84 mg/L and 2.15 mg/L respectively. The results from the present study confirm that coconut fiber possesses appropriate sorption capabilities of fluoride ion but is a pH dependent phenomenon. The outcomes of the study indicate the possible use of cellulose extracted from waste coconut fiber as a low-cost fluoride adsorbent. The present study can be well implemented on real scale systems as it will be beneficial economically as well as environmentally.

Exploring solubility and energetics: Dissolution of biologically important l-threonine in diverse aqueous organic mixtures across the temperature range of 288.15 K to 308.15 K.

This research provides a thorough investigation into the solubility behavior and solution thermodynamics of l-threonine in significant organic solvent systems. The work was done on measuring the actual solubility and subsequently calculating overall transfer solvation free energetics (∆Genergetic0i) and transfer entropies (∆St0i) at a temperature of 298.15 K. These measurements were performed as l-threonine transitioned from water to different water-organic mixed solvents systems. The saturated solubilities of l-threonine were determined using the 'gravimetric method' at five equidistant temperatures namely 288.15 K, 293.15 K, 298.15 K, 303.15 K and 308.15 K. By analyzing the data on solubility, we further obtained the different energies involved in solvation related issues. In the case of single solvents, the nature of solubility of l-threonine was observed like: dimethylsulfoxide (DMSO) < acetonitrile (ACN) < N, N-dimethylformamide (DMF) < ethylene glycol (EG) < water (H2O), irrespective of the experimental conditions. Specifically, at 298.15 K, the solubilities of l-threonine in single solvents were found to be as follows: 0.8220 mol per kg of water, 0.3101 mol per kg of EG, 0.1337 mol per kg of DMF, 0.1107 mol per kg DMSO and 0.1188 mol per kg of ACN. This research critically examines the relationship between the experimental saturated solubility of l-threonine and the complex properties influencing its solvation energy in diverse aqueous organic solvent systems.

Symbiotic MoO3-SrTiO3 Heterostructured Nanocatalysts for Sustainable Hydrogen Energy: Combined Experimental and Theoretical Simulations.

Highly efficient Z-scheme MoO3-SrTiO3 heterostructured nanocatalytic systems were engineered via a sol-gel chemical route and exploited in green H2 energy synthesis via overall water splitting. The optical and electronic investigations corroborated the enhancement of the optoelectronic properties of SrTiO3 after the incorporation of MoO3. Emergence of the interfacial charge transfer between SrTiO3 and MoO3 is the driving force, which synergistically triggered the catalytic efficiency of MoO3-SrTiO3 heterostructures. The substitution of Ti4+ by Mo6+ ions led to the suppression of Ti3+ mid-gap states, as the potential involved in the Mo6+/Mo5+ reduction is higher than that in Ti4+/Ti3+. Theoretical studies were employed in order to comprehend the mechanism behind the advancement in the catalytic activity of MoO3-SrTiO3 porous heterostructures, which also possessed a higher surface area. 2% MoO3-SrTiO3 exhibited the optimum catalytic response toward H2 evolution via photochemical, electrochemical, and photo-electrochemical water splitting. 2% MoO3-SrTiO3 evolved H2 at the fourfold higher rate than SrTiO3 with phenomenal 16.06% AQY during photochemical water splitting and photo-degraded MB dye at nearly 88% against the 42% degradation in SrTiO3-led photocatalysis. Electrochemical and photo-electrochemical investigations also manifested the superiority of 2% MoO3-SrTiO3 toward HER, as it exhibited accelerated current and photocurrent densities of 25.02 and 27.45 mA/cm2, respectively, at the 1 V potential. EIS studies demonstrated the improved charge separation efficiency of MoO3-SrTiO3 heterostructures. This work highlights the multi-dimensional approach of obtaining green H2 energy as the sustainable energy source using MoO3@SrTiO3 heterostructures.

Magnetically recoverable sol-gel auto-combustion developed Ni1-xCuxDyyFe2-yO4 magnetic nanoparticles for photocatalytic, electrocatalytic, and antibacterial applications.

Copper and dysprosium doped NiFe2O4 magnetic nanomaterials, Ni1-xCuxDyyFe2-yO4 (x = y = 0.00, 0.01, 0.02, 0.03), was prepared by utilizing sol-gel auto-combustion approach to inspect the photodegradation of methylene blue (MB) pollutant and also, to perform the electrocatalytic water splitting and antibacterial studies. The XRD analysis reveal the growth of a single-phase spinel cubic structure for produced nanomaterials. The magnetic traits show an increasing trend in saturation magnetization (Ms) from 40.71 to 47.90 emu/g along with a decreasing behaviour of coercivity from 158.09 to 156.34 Oe at lower and higher Cu and Dy doping content (x = 0.0-0.01). The study of optical band gap values of copper and dysprosium-doped nickel nanomaterials decreased from 1.71 to 1.52 eV. This will increase the photocatalytic degradation of methylene blue pollutant from 88.57% to 93.67% under natural sunlight, respectively. These findings clearly show that under natural sunlight irradiation for 60 min, the produced N4 photocatalyst displays the greatest photocatalytic activity with a maximum removal percentage of 93.67%. The electrocatalytic characteristics of produced magnetic nanomaterials for both HER and OER were examined with a Calomel electrode taking as a reference in a 0.5 N H2SO4 and 0.1 N KOH electrolyte. The N4 electrode demonstrated considerable 10 and 0.024 mA/cm2 of current density, with onset potentials of 0.99 and 1.5 V for HER and OER and also, have tafel slopes of 58.04 and 295 mV/dec, respectively. The antibacterial activity for produced magnetic nanomaterials was examined against various bacteria (Bacillus subtilis, Staphylococcus aureus, S. typhi, and P. aeruginosa) in which N3 sample produced significant inhibition zone against gram-positive bacteria (Bacillus subtilis and Staphylococcus aureus) but no zone of inhibition against gram-negative bacteria (S. typhi and P. aeruginosa). With all these superior traits, the produced magnetic nanomaterials are highly valuable for the wastewater remediation, hydrogen evolution, and biological applications.

Influences of Partial Destruction of Ti-MOFs on Photo(electro)catalytic H2 Evolution by Dominating Role of Charge Carrier Trapping over Surface Area.

The design of water-stable photo and electrocatalysts of metal-organic frameworks (MOFs) for its promising catalytic applications at long-term irradiations or persisted current loads is extremely necessary but still remains as challenging. A limited number of reports on Ti-MOF-based catalysts for water splitting are only available to explain and understand the correlation between the nature of materials and MOFs array. Herein, spherical Ti-MOFs and corresponding partially annealed hollow core-shell Ti-MOFs (Ti-MOF/D) are designed and the correlation with their photo(electro)catalytic water splitting performance is evaluated. The switchable valence state of Ti for the Ti-MOF as a function of molecular bonding is the possible reason behind the observed photocatalytic hydrogen generation and light-harvesting ability of the system. Besides, the defect state, solid core-shell mesoporous structure, and active sites of Ti-MOF help to trap the charge carriers and the reduction of the recombination process. This phenomenon is absent for hollow core-shells Ti-MOF/D spheres due to the rigid TiO2 outer surface although there is a contradiction in surface area with Ti-MOF. Considering the diversity of Ti-MOF and Ti-MOF/D, further novel research can be designed using this way to manipulate their properties as per the requirements.

Metal-Organic Precursor Synthesis, Structural Characterization, and Multiferroic Properties of GdFeO3 Nanoparticles.

GdFeO3 nanoparticles were fabricated by a facile metal-organic precursor method using citric acid as a complexing agent. The phase purity and structural analysis by powder X-ray diffraction and FTIR studies indicates that the material is highly crystalline with an orthorhombic structure. Electron microscopic (TEM and SEM) studies of rare earth ferrites reveal worm-shaped nanoparticles with an average grain size of 95 nm. The high-resolution TEM study provides an insightful image, which shows an interplanar spacing of approximately 0.12 nm that corresponds to the (112) crystalline plane. A high surface area of 231.5 m2 g-1 has been achieved with a mesoporous texture, which in turn gives a high dielectric constant. Well-defined hysteresis is obtained with a saturation magnetization of 17.5 emu g-1, remanent magnetization of 3.9 emu g-1, and coercive field of -446 Oe. Room-temperature ferroelectricity in GdFeO3 nanoparticles has been found for the first time with no leaky current and hence may be used in multistate memory devices.

Self-Assembled Interwoven Nanohierarchitectures of NaNbO3 and NaNb1-x Ta x O3 (0.05 ≤ x ≤ 0.20): Synthesis, Structural Characterization, Photocatalytic Applications, and Dielectric Properties.

Dependence on fossil fuels for energy purposes leads to the global energy crises due to the nonrenewable nature and high CO2 production for environmental pollution. Therefore, new ways of nanocatalysis for environmental remediation and sustainable energy resources are being explored. Herein, we report a facile surfactant free, low temperature, and environmentally benign hydrothermal route for development of pure and (5, 10, 15, and 20 mol %) Ta-doped horizontally and vertically interwoven NaNbO3 nanohierarchitecture photocatalysts. To the best of our knowledge, such a type of hierarchical structure of NaNbO3 has never been reported before, and changes in the microstructure of these nanoarchitectures on Ta-doping has also been examined for the first time. As-synthesized nanostructures were characterized by different techniques including X-ray diffraction analysis, electron microscopic studies, X-ray photoelectron spectroscopic studies, etc. Ta-doping considerably affects the microstructure of the nanohierarchitectures of NaNbO3, which was analyzed by FESEM analysis. The UV-visible diffused reflectance spectroscopy study shows considerable change in the band gap of as-synthesized nanostructures and was found to be ranging from 2.8 to 3.5 eV in pure and different mole % Ta-doped NaNbO3. With an increase in dopant concentration, the surface area increases and was equal to 5.8, 6.8, 7.0, 9.2, and 9.7 m2/g for pure and 5, 10, 15, and 20 mol % Ta-doped NaNbO3, respectively. Photocatalytic activity toward the degradation of methylene blue dye and H2 evolution reaction shows the highest activity (89% dye removal and 21.4 mmol g-1 catalyst H2 evolution) for the 10 mol % NaNbO3 nanostructure which was attributed to a change in the conduction band maximum of the material. At 100 °C and 500 kHz, the dielectric constants of pure and 5, 10, 15, and 20 mol % Ta-doped NaNbO3 were found to be 111, 510, 491, 488, and 187, respectively. The current study provides the rational insight into the design of nanohierarchitectures and how microstructure affects different properties of the material upon doping.

Chemical fabrication, structural characterization and photocatalytic water splitting application of Sr-doped SnO2nanoparticles.

Semiconductor photocatalysis has gained considerable attention in recent years due to their enabling nature to convert solar energy into fuels of renewable hydrocarbon. However, many of them suffer from some drawbacks like the inability to visible light irradiation and wide band gaps. Herein, we have synthesized monophasic strontium (Sr) doped SnO2nanoparticles by a cost-effective and environmental friendly hydrothermal method. As-synthesized nanoparticles showed rutile crystalline structure with irregular and rough cubical shape and no other elemental impurities. Sr-doped SnO2nanoparticles show a constant decrease in bandgap with increasing dopant concentration, which is estimated for excellent photocatalytic activity. The photocatalytic water splitting of as-prepared Sr-doped SnO2nanoparticles for H2generation shows a large influence of the increasing dopant concentration related to the narrowing bandgap on H2generation rate. Hence, the tunable bandgap with adjusted dopant concentration indicates that band gap tuning through doping for produced nanostructures may open up a new opportunities for photocatalytic and other optoelectronic applications.

Modified, Solvothermally Derived Cr-doped SnO2 Nanostructures for Enhanced Photocatalytic and Electrochemical Water-Splitting Applications.

Cr-doped SnO2 nanostructures with a dopant concentration ranging from 1 to 5% have been successfully prepared using low-temperature modified solvothermal synthesis. The as-prepared nanoparticles showed a rutile tetragonal structure with a rough undefined morphology having no other elemental impurities. The particle shape and size, band gap, and specific surface area of the samples were investigated by scanning electron microscopy, transmission electron microscopy (TEM), high-resolution TEM, UV-visible diffused reflectance spectroscopy, and Brunauer-Emmett-Teller surface area studies. The optical band gap was found in the range of 3.23-3.67 eV and the specific surface area was in the range of 108-225 m2/g, which contributes to the significantly enhanced photocatalytic and electrochemical performance. Photocatalytic H2 generation of as-prepared Cr-doped SnO2 nanostructures showed improved effect of the increasing dopant concentration with narrowing of the band gap. Electrochemical water-splitting studies also stressed upon the superiority of Cr-doped SnO2 nanostructures over pristine SnO2 toward hydrogen evolution reaction and oxygen evolution reaction responses.

Utilization of Phyllanthus emblica fruit stone as a Potential Biomaterial for Sustainable Remediation of Lead and Cadmium Ions from Aqueous Solutions

In the present work, an effort has been made to utilize Phyllanthus emblica (PE) fruit stone as a potential biomaterial for the sustainable remediation of noxious heavy metals viz. Pb(II) and Cd(II) from the aqueous solution using adsorption methodology. Further, to elucidate the adsorption potential of Phyllanthus emblica fruit stone (PEFS), effective parameters, such as contact time, initial metal concentration, temperature, etc., were investigated and optimized using a simple batch adsorption method. It was observed that 80% removal for both the heavy metal ions was carried out within 60 min of contact time at an optimized pH 6. Moreover, the thermodynamic parameters results indicated that the adsorption process in the present study was endothermic, spontaneous, and feasible in nature. The positive value of entropy further reflects the high adsorbent-adsorbate interaction. Thus, based on the findings obtained, it can be concluded that the biosorbent may be considered a potential material for the remediation of these noxious impurities and can further be applied or extrapolated to other impurities.

B-doped SnO2 nanoparticles: a new insight into the photocatalytic hydrogen generation by water splitting and degradation of dyes.

Boron-doped SnO2 (B:SnO2) has been synthesized via a facile wet chemical method to deal with increasing energy demand and environment-related issues. Powder XRD confirmed the rutile phase of the synthesized B:SnO2 nanoparticles. Energy dispersive X-ray analysis and elemental mapping confirmed 1% B doping into SnO2 lattice. A red shift was observed during the analysis of Raman and FTIR spectral data. The bands in FTIR and Raman spectra confirmed the in-plane and bridging oxygen vacancies in SnO2 lattice introduced due to B doping. These nanoparticles showed proficiency in photocatalytic hydrogen generation and degradation of crystal violet (CV) and rhodamine B (RhB) dyes. The degradation of CV and RhB dyes in the presence of B:SnO2 NPs and ethane-1,2-diaminetetracetic acid (EDTA) was found to be 83 and ~ 100%, respectively. To escalate the efficiency of dye degradation, the experiment was performed with different sacrificial agents (EDTA, methanol, and triethanolamine). The maximum hydrogen production rate (63.6184 µmol g-1 h-1) was observed for B:SnO2 along with Pd as co-catalyst, and methanol and EDTA solution as sacrificial agents.

Rare earth doped metal oxide nanoparticles for photocatalysis: a perspective.

Metal oxides are well-known materials that have been considered as the prominent photocatalysts. Photocatalysis is a promising way to address the environmental issues which are caused by fossil fuel the combustion and industrial pollutants. Lot of efforts such as doping of metal oxides with metals, non-metals have been made to enhance their photocatalytic activity. More specifically, in this review we have discussed detailed synthesis procedures of rare earth doped metal oxides performed in the past decades. The advantage of doping metal oxides with rare earth metals is that they readily combine with functional groups due to the 4f vacant orbitals. Moreover, doping rare earth metals causes absorbance shift to the visible region of the electromagnetic spectrum which results to show prominent photocatalysis in this region. The effect of rare earth doping on different parameters of metal oxides such as band gap and charge carrier recombination rate has been made in great details. In perspective section, we have given a brief description about how researchers can improve the photocatalytic efficiencies of different metal oxides in coming future. The strategies and outcomes outlined in this review are expected to stimulate the search for a whole new set of rare earth doped metal oxides for efficient photocatalytic applications.

Magnetic Nanoparticles-A Multifunctional Potential Agent for Diagnosis and Therapy.

Magnetic nanoparticles gained considerable attention in last few years due to their remarkable properties. Superparamaganetism, non-toxicity, biocompatibility, chemical inertness, and environmental friendliness are some of the properties that make iron oxide nanoparticles (IONPs) an ideal choice for biomedical applications. Along with being easily tuneable and a tailored surface for conjugation of IONPs, their physio-chemical and biological properties can also be varied by modifying the basic parameters for synthesis that enhances the additional possibilities for designing novel magnetic nanomaterial for theranostic applications. This review highlights the synthesis, surface modification, and different applications of IONPs for diagnosis, imaging, and therapy. Furthermore, it also represents the recent report on the application of IONPs as enzyme mimetic compounds and a contrasting agent, and its significance in the field as an anticancer and antimicrobial agent.

Fabrication of GaN nano-towers based self-powered UV photodetector.

The fabrication of unique taper-ended GaN-Nanotowers structure based highly efficient ultraviolet photodetector is demonstrated. Hexagonally stacked, single crystalline GaN nanocolumnar structure (nanotowers) grown on AlN buffer layer exhibits higher photocurrent generation due to high quality nanotowers morphology and increased surface/volume ratio which significantly enhances its responsivity upon ultraviolet exposure leading to outstanding performance from the developed detection device. The fabricated detector display low dark current (~ 12 nA), high ILight/IDark ratio (> 104), fast time-correlated transient response (~ 433 µs) upon ultraviolet (325 nm) illumination. A high photoresponsivity of 2.47 A/W is achieved in self-powered mode of operation. The reason behind such high performance could be attributed to built-in electric field developed from a difference in Schottky barrier heights will be discussed in detail. While in photoconductive mode, the responsivity is observed to be 35.4 A/W @ - 3 V along with very high external quantum efficiency (~ 104%), lower noise equivalent power (~ 10-13 WHz-1/2) and excellent UV-Vis selectivity. Nanotower structure with lower strain and dislocations as well as reduced trap states cumulatively contributed to augmented performance from the device. The utilization of these GaN-Nanotower structures can potentially be useful towards the fabrication of energy-efficient ultraviolet photodetectors.

Self-assembled chitosan polymer intercalating peptide functionalized gold nanoparticles as nanoprobe for efficient imaging of urokinase plasminogen activator receptor in cancer diagnostics.

Targeting cell surface receptors for specific drug delivery in cancer has garnered lot of attention. Urokinase plasminogen activator receptor (uPAR), a surface biomarker, is overexpressed on many tumours including breast, colorectal, prostate, and ovarian cancers. Binding of growth factor domain (GFD) of urokinase plasminogen activator (uPA) with uPAR lead to its close conformation, and allow somatomedin B domain (SMB) of vitronectin binding by allosteric modulation. In-silico docking of uPAR with GFD and SMB peptides was performed to identify potential binding affinity. Herein, we report fluorescently labeled peptide functionalized AuNPs with a mixed self-assembled monolayer of intercalating chitosan polymer for efficient targeting and imaging of uPAR-positive cells. The biophysical characterization of nanoconjugates and uPAR-specific targeting was assessed by FACS, cell adhesion, and fluorescence imaging. AuNPs/chitosan/GFD+SMB peptides showed higher uptake as compared to AuNPs/chitosan/GFD, and AuNPs/chitosan/SMB that can be utilized as a tool for molecular targeting and imaging in metastasis.

Silver-Decorated Cobalt Ferrite Nanoparticles Anchored onto the Graphene Sheets as Electrode Materials for Electrochemical and Photocatalytic Applications.

The present work describes the synthesis of Ag-CoFe2O4/rGO nanocomposite as a photocatalyst through the hydrothermal process by the attachment of silver and cobalt ferrite (CoFe2O4) nanoparticles on the surface of reduced graphene oxide. The effect of Ag and reduced graphene oxide (rGO) on the structure, optical, magnetic, photocatalytic, and electrochemical performance of the CoFe2O4 is systematically explored through various analytical techniques. The analyses of the observed outcomes reveal that the graphene sheets are exfoliated and decorated with well-dispersed Ag and CoFe2O4 nanoparticles. UV-vis spectra indicate a gradual shift in the absorption edge toward the higher wavelength with the addition of Ag ions, which signifies variation in the energy gap of the samples. Photoluminescence results divulge that graphene can decline the electron-hole recombination rate and improve the photocatalytic activity of the Ag-CoFe2O4/rGO nanocomposite. In this context, the Ag-CoFe2O4/rGO sample presents good catalytic activity as compared to the CoFe2O4 and Ag-CoFe2O4 photocatalysts for the degradation of methylene blue (MB) dye and suggests that the rGO plays a vital role in the Ag-CoFe2O4/rGO nanocomposite. The deterioration rate of the samples is found to be in the order of CoFe2O4(78.03%) < Ag-CoFe2O4(83.04%) < Ag-CoFe2O4/rGO(93.25%) in 100 min for MB dye, respectively, under visible-light irradiation. The room-temperature ferromagnetic behavior of the samples is confirmed by the M-H hysteresis loop measurements. Overall, the Ag-CoFe2O4/rGO nanocomposite promises to be a strong magnetic photocatalyst for contaminated wastewater treatment. The electrochemical performance of all of the samples was examined by the cyclic voltammetry (CV) that exhibits a superior rate performance and cycle stability of the Ag-CoFe2O4/rGO nanocomposite as compared to the other samples.

Quenching Assisted Reverse Micellar Synthesis and Electrical Properties of High Surface Area BiFeO3 Nanoparticles.

Multiferroic compounds are prime important materials for future electronic and magnetic devices and overcome the fundamental limits of conventional materials. In present work, we reported the preparation of purely one phase of nano-sized BiFeO3 compound by microemulsion micellar method for the first time by employing rapid quenching of sample at 500 °C, that is the main driving force to get the pure phase of BiFeO3 nanoparticles at low temperature method. The nanoparticles that we obtained were almost uniform with sphere shaped and these prepare nanoparticles possess high surface. The increase in permittivity in the form of dielectric constants were reported that depends on temperature and frequency that supports the ferroelectric nature and was further confirmed by the ferroelectric loops even at the room temperature has been found in theses prepared nanoparticles.