Morphology Of Nanoparticles Research Articles

Superhydrophobic and antibacterial larch wood prepared by PEI controlled growth of conical ZnO nanopillar

The natural antibacterial performance of cicada wings inspired the morphology design and application of zinc oxide (ZnO) nanoparticles on wood surfaces to enhance combined antibacterial function. The commonly interior used larch wood was chosen as base material and firstly pre-treated with ultrasonic-hydrothermal method, the deposition of ZnO nanoparticles with different morphologies was controlled by polyethyleneimine (PEI) concentration during the crystal growth, and the analysis of surface characteristics and antibacterial efficacy was fully tested. Scanning Electron Microscopy (SEM) observations revealed that the addition of PEI altered the morphology of ZnO nanoparticles on the wood surface. ZnO structures without PEI exhibited hexagonal prismatic shapes. As the PEI concentration increased, the particle size of ZnO decreased. When 6 mmol/L of PEI was added, ZnO transformed into a conical structure. Contact angle measurements confirmed the preparation of superhydrophobic ZnO, which exhibited self-cleaning properties. The antibacterial circle method test results showed that superhydrophobic ZnO wood prepared with 6 mmol/L of PEI exhibited superior antibacterial properties, with higher activity against Staphylococcus aureus compared to Escherichia coli. Overall, the study demonstrates a promising approach to developing polyfunctional and effective antibacterial wood surfaces inspired by natural cicada wings nanostructures.

Curcumin-loaded lignin nanoparticles: Exploring sonication effects on drug loading and particle properties for future biomedical use

The present study investigates the effects of sonication and cross-linker (oxalic acid) concentration on drug loading and the properties of curcumin-loaded lignin nanoparticles. Selected samples were further assessed for their toxicity and antioxidant potential using the eukaryotic model organism Saccharomyces cerevisiae. Transmission electron microscopy analyses revealed the formation of spherical nanoparticles with diameters in the range of 39–49 nm. Differential scanning calorimetry experiments confirmed the encapsulation of curcumin. Factorial experimental design analyses indicated that sonication time, wave amplitude, cross-linker concentration, and their interactions significantly influenced both ζ-potential – from (−37.0 ± 1.7) mV to (−48.4 ± 0.6) mV – and curcumin loading – from (3.70 ± 0.32) % to (7.10 ± 0.57) %. These parameters are critical for biomedical applications as they relate to the clearance of nanoparticles from the human bloodstream and drug dosage optimization. Although sonication has been previously reported for the preparation of lignin nanoparticles, this study represents the first documented instance of manipulating drug loading by controlled sonication parameters. While none of the investigated factors significantly affected the mean particle diameter, observations from TEM micrographs suggest that cross-linker concentration and wave amplitude notably influence nanoparticle morphology. Moreover, the curcumin-loaded nanoparticles exhibited non-toxicity toward Saccharomyces cerevisiae and demonstrated the ability to enhance yeast cell tolerance to H2O2-induced oxidative stress, underscoring their antioxidant potential. Therefore, this research significantly contributes to the scientific understanding of how the control of sonication parameters and cross-linkers can modulate the properties of curcumin-loaded lignin nanoparticles for future biomedical applications.

The effect of ZnO nanoparticles morphology on the barrier and antibacterial properties of hybrid ZnO/graphene oxide/montmorillonite coatings for flexible packaging

The need for eco-friendly packaging solutions is continuously increasing, with several materials being investigated to develop functional coatings able to contrast food degradation due to oxidation and bacterial growth. In this work, ZnO nanoparticles (NPs) with various morphology and size from spherical to hexagonal, dots-like and platelets-like shape, were synthesized. Hybrid coatings constituted by ZnO NPs, graphene oxide (GO) and montmorillonite (MMT) were applied onto flexible polyethylene (PE) in order to exploit the 2D nanomaterials self-assembly ability and gas barrier properties and to synergistically combine these functionalities with the antibacterial activity of ZnO. The effect of ZnO NPs morphology and the ZnO/GO/MMT relative content was explored to obtain nanostructured coatings with optimized functionality. Results evidence a correlation between oxygen permeability and microbial proliferation, allowing to reach 88 % of reduction of PE oxygen permeability and about 60 % inhibition towards Gram-positive (i.e. Weizmannia coagulans) and Gram-negative (i.e. Escherichia coli) microorganisms.

Stimuli-responsive nanoparticles from RAFT dispersion polymerization-induced self-assembly (PISA) of N-phenylacrylamide copolymerized with a boronic acid-substituted derivative

Boronic acid (BA) moieties confer a variety of stimuli-response properties upon polymers. PISA is the most efficient technique for the preparation of core–shell nanoparticles (NPs), however aqueous dispersion PISA of free BA-containing monomers is complicated by the formation of the boroxine anhydride at the hydrophobic core. In the present work, dispersion reversible addition-fragmentation chain transfer (RAFT) copolymerization of a free BA-containing derivative of N-phenylacrylamide yields NP morphologies which are different to those formed from the equivalent PISA homopolymerization without BA. Depending on conditions, PISA results in spheres, rods, and worms with colloidal stability improved by using a higher fraction of the non-stimuli responsive monomer to give large compound micelles. Post-polymerization stimuli-response from the resultant PISA dispersion through hydrolysis of boroxine-rich copolymer NPs by dilution with the aqueous dispersion solvent or with water yields micron-sized worms, lamellae, and vesicles. Self-assembly to higher order morphologies is driven by the extent of hydrolysis. The resultant free BA-containing NPs becoming smaller and spherical upon basification and glucose addition.

Structural, Magnetic and Electrochemical Properties of Nickel Manganese Ferrite (NixMn1-xFe2O4) Nanoparticles Prepared via Coprecipitation Method

In current work, the co-precipitation approach was effectively used to synthesize NixMn1-xFe2O4 nanoparticles. Thermal stability of the nickel manganese ferrite nanoparticle was observed at temperatures above 390 ºC by TG/DTA analysis. XRD investigation revealed the cubic structure of the synthesized NixMn1-xFe2O4 nanoparticles. The average crystallite size of synthesized nanoparticles determined via Scherrer’s equation, increases linearly with calcination temperature and nickel concentration. The FTIR spectra showed the existence of stretching vibrations of metal oxide, which are ascribed to the formation of nickel manganese ferrite nanoparticles. The surface morphology of NixMn1-xFe2O4 nanoparticles, as observed using FESEM, exhibited a spherical shape. The EDX spectrum indicates the occurrence of Ni, Fe, Mn and O in the synthesized nickel manganese ferrite nanoparticles. The average size of the crystallites, as determined by XRD, closely matches the analysis conducted using HRTEM. The magnetic properties of NixMn1-xFe2O4 nanoparticles were analyzed using VSM. Nickel manganese ferrite nanoparticles exhibit increasing saturation magnetization and coercivity values as nickel concentration increases, indicating soft ferrimagnetic properties and making it appropriate for high-density recording devices. The cyclic voltammetry investigation of Ni0.7Mn0.3Fe2O4 sample, calcinated at 600 ºC, reveals a significant specific capacitance of 590 F g–1 at a scan rate of 2 mV s–1, suggesting its potential use in supercapacitors.

Green synthesis of NiO and NiO@graphene oxide nanomaterials using Elettaria cardamomum leaves: Structural and electrochemical studies

An eco-friendly synthetic route was developed for the formation of nickel oxide (NiOaq and NiOet) nanoparticles (NPs) by treating Ni(NO3)2.6H2O with aqueous/ethanolic extracts of Elettaria cardamomum leaves; the same reaction was performed in the presence of graphene oxide (GO) to produce NiOaq@GO and NiOet@GO nanocomposites (NCs), respectively. The NMs were characterized by XRD, FT-IR, SEM, EDX, UV–visible spectroscopy, and TGA-DSC analysis. They were also subjected to electrochemical investigations and photocatalytic degradation of crystal violet (CV) dye. XRD analysis revealed the average crystallite sizes of 8.84–14.07 nm with a face-centered cubic form of NiO NPs and a hexagonal structure of their nanocomposites with GO. FT-IR spectroscopy confirmed the presence of Ni-O vibrations at 443-436 cm−1. SEM images confirmed the spherical morphology of NiO NPs while NiOaq@GO NCs contained randomly aggregated, thin, and wrinkled graphene sheets. NiOaq and NiOet have shown particle sizes of 27.7–30.63 nm which were decreased to 19.33–26.39 nm in their respective NiOaq@GO and NiOet@GO NCs. EDX spectra verified the homogeneous distribution of elements (Ni, O, C) on the surface of the particles. The synthesized NCs have shown smaller band gaps (NiOaq@GO = 3.74 eV; NiOet@GO = 3.34 eV) as compared to their respective NPs (NiOaq = 5.0 eV; NiOet = 3.89 eV). TGA/DSC data was used to find the thermal stabilities, glass transition temperatures, and enthalpies. Cyclic voltammetry measurements exhibited distinct oxidation and reduction peaks. NCs exhibited better potential as electrode materials for supercapacitor applications as compared to their respective NPs. NiOet@GO exhibited the best electrochemical performance and photocatalytic degradation efficiency of CV dye. After 120 min exposure to sunlight, the degradation coefficient of CV was observed to be 82.93, 86.34, 89.99, 90.27 and 81.65 % in the presence of NiOaq, NiOet, NiOaq@GO, NiOet@GO and GO, respectively.

EFFECT OF ANNEALING DURATION ON PHOTOCATALYTIC PROPERTIES OF LaFeO3 PEROVSKITE

In this paper, the effect of the annealing duration on the photocatalytic properties of lanthanum ferrite perovskite synthesized by the hydrothermal method is investigated. Lanthanum ferrite was chosen as the object of study due to its high activity under the influence of visible light. During the experiments, the structural changes occurring in the material during annealing during 2, 4 and 6 hours were studied. The main attention was paid to the analysis of the morphology of nanoparticles, phase composition, crystallinity, absorption spectra and photocatalytic activity. The results show that an increase in the annealing time leads to an improvement in the crystal structure, an increase in the size of crystallites and a higher level of oxygenation. The optimal annealing time to achieve maximum photocatalytic activity was determined to be 6 hours. The work confirms the prospects of using long-term annealing to improve the photocatalytic properties of perovskite-based materials.

Secondary-explosion modification study on gaseous detonation synthesis of Fe@C nanoparticles

To enhance the graphitization degree of Fe@C nanoparticles synthesized via gaseous detonation, this study employed ferrocene as the precursor and hydrogen–oxygen mixed gas as the explosion source to investigate the effects of secondary-explosion on the phase composition, morphology, and magnetic properties of carbon-encapsulated iron nanoparticles. The results show that after the secondary-explosion, the phase composition of Fe@C nanoparticles changes significantly, with partial oxidation of iron carbide/iron to FeO. The morphology remains largely unchanged, with particle sizes between 20–40 nm, but the crystallinity of both the metal core and carbon layer improves markedly, and lattice fringes become more distinct. The saturation magnetization(Ms) and residual magnetization(Mr) of Fe@C nanoparticles decrease by 56.7 % and 69 %, respectively, while the coercivity force shows little change.

Visible-light induced effective and sustainable remediation of nitro organics pollutants using Pd-doped ZnO nanocatalyst

Nitroaromatic compounds represent a class of highly toxic pollutants discharged into aquatic environments by various industrial activities, posing significant threats to ecological integrity and human health due to their persistent and hazardous nature. In this study, Pd-doped ZnO nanoparticles were investigated as a potential solution for the degradation of nitro organics, offering heightened photocatalytic efficacy and prolonged stability. The synthesis of Pd-doped ZnO NPs was achieved via the hydrothermal method, with subsequent analysis through XRD spectra and XPS confirming successful Pd doping within the ZnO matrix. Characterization through FESEM and HRTEM unveiled the heterogeneous morphologies of both undoped and Pd-doped ZnO nanoparticles. Additionally, UV–vis and PL spectroscopy provided insights into the optical properties, chemical bonding, and defect structures of the synthesized Pd-doped ZnO NPs. Pd doping induces a redshift in ZnO’s absorption spectra, reducing the bandgap from 3.12 to 2.94 eV as Pd concentration rises from 0 to 0.2 wt.%. The photocatalytic degradation, following pseudo-first-order kinetics, achieved 90% nitrobenzene abatement (200 µg/L, pH 7) under visible light within 320 min with a catalyst loading of 16 µg/mL. The photocatalytic efficacy of 0.08 wt% Pd-doped ZnO (k = 0.058 min⁻1) exhibited a 25-fold enhancement compared to bare ZnO (k = 3.1 × 10–4 min-1). Subsequent quenching and ESR experiments identified hydroxyl radicals (OH•) as the predominant active species in the degradation mechanism. Mass spectrometry analysis unveiled potential breakdown intermediates, illuminating a plausible degradation pathway. The investigated Pd-doped ZnO nanoparticles demonstrated reusability for up to five successive treatment cycles, offering a sustainable solution to nitro organics contamination challenges.

Antimicrobial gelatin-based films with cinnamaldehyde and ZnO nanoparticles for sustainable food packaging

Cinnamaldehyde (CIN), a harmless bioactive chemical, is used in bio-based packaging films for its antibacterial and antioxidant properties. However, high amounts can change food flavor and odor. Thus, ZnO nanoparticles (NPs) as a supplementary antimicrobial agent are added to gelatin film with CIN. The CIN/ZnO interactions are the main topic of this investigation. FTIR-Attenuated Total Reflection (ATR), X-ray diffraction (XRD), and scanning electron microscopy (SEM) were utilized to investigate CIN/ZnO@gelatin films. Transmission electron microscope (TEM) images revealed nanospheres morphology of ZnO NPs, with particle sizes ranging from 12 to 22 nm. ZnO NPs integration increased the overall activation energy of CIN/ZnO@gelatin by 11.94%. The incorporation of ZnO NPs into the CIN@gelatin film significantly reduced water vapour permeability (WVP) of the CIN/ZnO@gelatin film by 12.07% and the oxygen permeability (OP) by 86.86%. The water sorption isotherms of CIN/ZnO@gelatin were described using Guggenheim-Anderson-de Boer (GAB) model. The incorporation of ZnO NPs into the CIN@gelatin film reduced monolayer moisture content (M0) by 35.79% and significantly decreased the solubility of CIN/ZnO@gelatin by 15.15%. The inclusion of ZnO into CIN@gelatin film significantly decreased tensile strength of CIN/ZnO@gelatin by 13.32% and Young`s modulus by 18.33% and enhanced elongation at break by 11.27%. The incorporation of ZnO NPs into the CIN@gelatin film caused a significant decrease of antioxidant activity of CIN/ZnO@gelatin film by 9.09%. The most susceptible organisms to the CIN/ZnO@gelatin film included Candida albicans, Helicobacter pylori, and Micrococcus leutus. The inhibition zone produced by the CIN/ZnO@gelatin film versus Micrococcus leutus was 25.0 mm, which was comparable to the inhibition zone created by antibacterial gentamicin (23.33 mm) and cell viability assessment revealed that ZnO/CIN@gelatin (96.8 ± 0.1%) showed great performance as potent biocompatible active packaging material.

Chitosan Coupled Silver Nanoparticles Electrocatalyst Synthesis and Characterization

This study sought to find a suitable technique for synthesizing and characterizing silver nanoparticles due to its applications in various fields such as nanotechnology and medical. The synthesized silver nanoparticles were characterized using SEM microscopy, FT-IR and UV-Vis spectroscopy. The maximum absorbance from the UV-Vis spectrophotometer showed the formation of silver nanoparticles with λ max of 418 nm. The FTIR analysis envisaged a strong symmetrical stretching at 1400 cm-1 to 1200 cm-1 with the major peaks recorded at 1390 cm-1 and 1380 cm-1, indicating the presence of nitro components in the sample. The signal at 1658 cm−1 corresponded to the amide (C=O) bonds stretching vibrations, at 1089 cm−1 C-O-C bonds and at 564 cm−1 plane with bends NH, plane-out and bends C−O. C-H stretching vibrational signal was noted at 2927 cm−1, and a broader band at 3426 cm−1 with an overlap between the O−H stretching vibration and N−H stretching vibration of the oligosaccharide applied in the capping. The concentration of chitosan on transmittance was done using 0.5%, 1.0%, 1.5% and 2.0% solutions with the results from FT-IR showing elaborate intensity at 2.0 % chitosan capping and the least at 0.5 %. Scanning microscope validated characterized silver nanoparticles morphology at 500nm. The results obtained from SEM depicted a size range of 100 nm with resolutions between 0.5 to 4 nm

Characterization and applications of iron oxide nanoparticles synthesized from Phyllanthus emblica fruit extract

Nanotechnology is a treasure trove of diversified themes which are endowed with broad applications. Herein, iron oxide (Fe2O3) nanoparticles were synthesized using Phyllanthus emblica aqueous fruit extract. The UV-Visible spectrum exhibited a surface plasmon resonance peak at 295nm. Fourier Transform Infrared Spectroscopy provided insight into the functional groups responsible for capping. X-ray diffraction analysis authenticated the crystalline nature of nanoparticles, while energy dispersive X-ray spectroscopy divulged that iron and oxygen comprised 54% of the nanoparticles’ weight. Scanning electron microscopy established irregular morphology and agglomeration of nanoparticles. The Fe2O3 nanoparticles validated potent antimicrobial activity against 11 bacterial and 1 fungal isolates. The biggest zone of inhibition (23mm) was measured against S. enterica, whereas the smallest zone of inhibition (12mm) was documented against C. albicans and E. coli. The values for minimum inhibitory concentration ranged between 10 and 15μg/ml for all microbes. Nevertheless, no synergy was exhibited by the nanoparticles with any of the selected antibiotics (Fractional Inhibitory Concentration Index > 1). The photocatalytic dye degradation capability of Fe2O3 nanoparticles was assessed and the observations implied a significant increase in degradation of methyl red although, not of methylene blue. Furthermore, the nanoparticles were in possession of substantial antioxidant (34–38%) and anti-inflammatory (31–38%) capacities. Consequent upon the robust activities of P. emblica-mediated nanoparticles, these can be scrutinized for biomedical and environmental implementations in future.

The impact of varying EDTA dosage on the flower-like morphology and thermoelectric properties of Ce-doped Bi2Te₃

Thermoelectric materials have significant applications in energy utilization and environmental protection. The effect of different EDTA (ethylenediaminetetraacetic acid) dosages on the flower-like morphology and thermoelectric properties of Ce-doped Bi2Te3 nanoparticles were investigated. The Ce-doped Bi2Te3 nanoparticles were sucessfully prepared via the hydrothermal method, and the influence of EDTA dosage on the morphology, structure, and thermoelectric properties of the materials was analyzed. The experimental results showed that an appropriate amount of EDTA can promote the formation of a flower-like morphology in Ce-doped Bi2Te3 nanomaterials and enhance their thermoelectric properties. The ZT values of the x = 0.15 sample made by the better flower-like morphology of nanopowders are all around 1, which reach 1.15 at 398 K. This work demonstrates the synergistic effects of combining nanostructure engineering and chemical doping strategies for thermoelectric performance enhancement.

Why Colloidal Syntheses of Bimetallic Nanoparticles Cannot be Generalized.

Introducing one general synthesis to form bimetallic nanoparticles (NPs) could accelerate the discovery of NPs for promising energy applications. Although colloidal syntheses can provide precise structural and morphological control of bimetallic NPs, the complex chemical nature of multicomponent syntheses challenges the realization of such synthetic simplicity. Common synthetic issues are frequently ascribed to the variation in metal ion precursor reactivities and complex chemical interactions between the different metal surfaces and capping agents employed. However, no systematic studies have shown how these factors compete to ultimately assign the factor limiting the mixing and formation of bimetallic NPs. Here, we provide a parametric investigation of how the intrinsic standard reduction potentials (E0red) of the metal ions and cocapping agents influence the formation of bimetallic AuCu, AuPd, and PdCu NPs. Using a combination of in situ X-ray total scattering along with transmission electron microscopy and nuclear magnetic resonance spectroscopy, we illustrate the multifunctional role of the cocapping agents through interactions with both the metal ion precursors and NP surfaces to stabilize metastable structures. Additionally, we demonstrate how system-specific side reactions and the local metal ion coordination environment can be used to selectively tune the formation kinetics, structure, and morphology of bimetallic NPs. Ultimately, these insights show that the chemical interactions rather than the intrinsic E0red are responsible for the formation of bimetallic NPs. Broadly, these insights should aid the synthetic design of tailored multimetallic NPs.

Photocatalytic activity of self-heterojunctioned intermediate phases in HCl protonated and HNO3 deconjugated g-C3N4 nanostructures

This research involved the different acid-treatment conditions of graphitic carbon nitride and its modified nanostructures through thermal polycondensation of urea at various temperatures. X-ray diffraction patterns revealed that processing at a lower temperature than 500 °C resulted in melem and its derivatives, indicating incomplete transformation of urea to g-C3N4. However, treatment at higher temperatures and the HCl acid treatment led to the formation and expansion of g-C3N4 networks, as evidenced by notable differences in peak intensities observed in their Fourier-transform infrared and Raman spectra. Scanning electron microscopy analysis illustrated a transition from the granular morphology of melamine to the layered structure characteristic of g-C3N4. The nanoparticle morphology observed in the HNO3 acid treatment sample was attributed to the deconjugation of nanosheets through the highly oxidative acid medium. The most suitable photocatalytic activity for Methylene Blue (MB) degradation under UV and visible light illumination was observed for the samples prepared at 550 °C and HCl post-processed nanostructures. It is proposed that the enhanced photocatalytic activity observed in these samples is most likely attributed to the reduced recombination of photogenerated charge carriers facilitated by heterojunctions formed between different intermediate phases. These findings highlight the potential of modified g-C3N4 and its derivatives as promising photocatalytic materials for water purification applications.

Simulation-Guided Preparation of Copper Chalcogenide Nanoparticle-Based Transparent Photothermal Coating with Enhanced Deicing Performance.

In this investigation, transparent photothermal coatings utilizing plasmonic copper chalcogenide (Cu2-xS) nanoparticles were designed and fabricated for the deicing of glass surfaces. Cu2-xS nanoparticles, chosen for their high near-infrared (NIR) absorption and efficient photothermal conversion, were analyzed via finite difference time domain (FDTD) simulations to optimize nanoparticle morphology, thus avoiding costly trial-and-error synthesis. FDTD simulations determined that Cu2-xS nanorods (Cu-NRs) with an optimal aspect ratio of 2.2 had superior NIR absorption. Guided by FDTD simulations, the composite coating composed of Cu-NRs in clear acrylic resin paint was brush-coated to glass, achieving 62.4% visual transmittance and over 95% NIR absorbance. Photothermal conversion tests exhibited a significant temperature increase, with the coating reaching 65 °C under NIR irradiation within 6 min. The dynamic deicing process of ice beads on the coating at -20 °C completed within 220s, in contrast to the frozen state on glass coated with clear acrylic resin paint. Furthermore, heat transfer simulations in COMSOL illustrated melting initiation at the ice-coating interface and subsequent progression through the ice layer. This simulation-driven synthesis method and photothermal testing offer a design framework for the fabrication of photothermal deicing coatings with applications for automobiles, buildings, and aircraft in cold environments.

Sol-gel hydrothermal synthesis of lead-free BT nanoparticles for enhanced dielectric properties in PVDF nanocomposites

In the present work BaTiO3 nanoparticles (NPs) with different sizes from 150 to 400 nm were prepared by sol–gel hydrothermal method at a temperature lower than 220 °C, and were used as nanofiller for PVDF composites with a loading from 10 to 25 vol%. The morphology of the BT NPs was analyzed by Scanning Electron Microscopy (SEM), and the structural composition was studied by Raman spectroscopy and X-ray diffraction (XRD). The hydrothermal temperature was found to control both the size as well as the phase composition of the BT NPs.The PVDF/BT nanocomposites exhibit enhanced dielectric permittivity and reduced loss tangent, especially with 20 vol% NPs, which contributes to the improvement of the ferroelectric properties. The inclusion of BT in PVDF matrix enhances also the crystallinity of PVDF by acting as a nucleating agent, which further increases the stiffness of the composite. However, at higher volume loading, the reverse tendency was observed with a huge decrease in the PVDF crystallinity at 25 vol%. The simulated PE loop was also investigated for the different loadings mentioned above using an Ising type model based on a 2D lattice and solved by monte-Carlo metropolis method. The results are in good agreement with the experimental results for the polarization hysteresis loops.

Evaluation of antioxidant, catalytic and antidiabetic activity of Phaseolus vulgaris (French green bean) mediated nickel oxide and copper doped nickel oxide bimetallic nanoparticles

In this study, nickel oxide nanoparticles (NPs) and copper doped NiO bimetallic nanoparticles (Cu@NiO BMNPs) were synthesized using Phaseolus vulgaris extracts as reducing and stabilizing agents by sol gel methods. The chemical and physical properties of synthesized NiO NPs and Cu@NiO BMNPs were confirmed by various techniques, like UV Visible spectrophotometer (UV–Vis), Fourier transform infrared spectroscopy (FTIR), Scanning Electron Microscope (SEM), Energy Dispersive X-ray (EDX), Transmission Electron Microscope (TEM) and X-ray diffraction (XRD) analysis. The optical properties of both NPs observed by UV–Vis analysis with well-defined peak and band gap value 3.2 eV & 2.62 eV. FTIR analysis confirmed the presence of functional group of NPs with fruits extract. The morphology of NPs was confirmed by SEM and TEM analysis as polygonal, rod and spherical shape. The elements present in NPs were confirmed by EDX analysis. The crystalline size calculated based on the XRD analysis was 49.78 nm and 53.66 nm for NiO and Cu@ NiO NPs respectively which were found to be slightly smaller than particle size determined from SEM and TEM micrograph. Antioxidant activity of NPs was examined using 2,2-Diphenyl-1-picrylhydrazyl (DPPH) scavenging radicals, Catalytic activities were screened by the degradation of Methylene blue (MB) and by the inhibition of alpha-amylase enzyme, antidiabetic activity of NPs were evaluated using acarbose as standard drug. The Cu@NiO BMNPs showed 77.60 % antioxidant, 76.98 % photocatalytic and 88.86 % antidiabetic activity, which were found to be more as compared to NiO NPs. The NiO and Cu@NiO BMNPs were synthesized for the first-time using P. vulgaris extracts. This study clearly showed that P. vulgaris extracts mediated mono- and bimetallic NPs were more stable and biocompatible than their respective bulk particles.

Promising ferroelectric and piezoelectric response of Cr-doped ZnO nanofiller-incorporated PVDF flexible and laminated nanocomposite system.

Cr3+-doped ZnO (CZ) nanoparticles are prepared using hydrothermal and co-precipitation techniques. The desired crystallographic phase of the nanoparticles is confirmed using X-ray diffraction study. Rod-shaped and spherical morphologies of CZ nanoparticles prepared using hydrothermal and co-precipitation techniques were confirmed through FESEM observation. Each type of nanoparticle was taken separately in PVDF to understand the characteristic properties, such as dielectric, piezoelectric, and ferroelectric properties of the resultant CZ-PVDF nanocomposite films. All the nanocomposite films comprising rod-shaped or spherical CZ nanoparticles show butterfly loops with a low leakage current density of 10-5 A m-2 at a maximum electric field of 100 kV m-2 under J-E measurement. These findings suggest that the polarization property of CZ-PVDF nanocomposite films can be obtained at a high external electric field without causing electric breakdown in the samples. Dielectric permittivity as a function of temperature increases with an increase in the loading percentage of both rod-shaped or spherical CZ nanofillers in PVDF. Polarization response also improves with an increase in the loading percentage of CZ nanofillers in PVDF. In particular, the rod-shaped CZ nanofillers in PVDF with a higher loading percentage (CZHP2) result in a maximum polarization of (10 ± 0.29) × 10-4 μC cm-2, remanent polarization of (2 ± 0.04) × 10-4 μC cm-2, and coercive field of (10 ± 0.1) kV cm-1 at a maximum electric field of 50 kV cm-1. The CZHP2 nanocomposite film has a piezoelectric coefficient (d33) of (25 ± 0.24) pC N-1 and a power density of 1278.90 W m-3. These results indicate that the nanocomposite films have potential application in piezoelectric energy harvesters, offering a possible solution to the energy issue faced by modern society.

Revealing the surface structure and morphology evolution of Co nanoparticle supported on ZrO2 surfaces

The optimization of structure-dependent activity of supported metal catalysts has driven the dynamic determination of the morphology of Co nanoparticles on ZrO2 using atomic-level simulations. Density functional theory (DFT) calculations combined with ab initio molecular dynamics (AIMD) simulations were used to investigate the surface structure, nucleation mechanism and morphology evolution of Con clusters supported on different ZrO2 facets. As the size of the Con (n = 1–5) cluster increases, the competition between Co-Co bonding and the interaction of Con clusters with the ZrO2 surface further promotes the nucleation of larger clusters. Co atoms prefer to nucleate into large clusters on both c-ZrO2(111) and t-ZrO2(101) surfaces, but this behavior is unfavorable on the m-ZrO2(-111) surface. The analysis of electric properties suggests that the types of hybrid orbitals and the number of electron transfer accounts for the difference in energies of Con clusters on ZrO2 surfaces. Further, the AIMD simulations verified the stable structure of small Co5 cluster obtained by DFT, and predicted the morphology of large Co13 clusters on ZrO2 surfaces under realistic reaction conditions, consistent with the experimental SAM images. Our work provides an intuitive understanding of structure and morphology evolution of catalysts for the targeted design of catalysts to achieve the desired activity and explore more reaction possibilities.