Nanocomposite Of Nanoparticles Research Articles

The catalytic performance of CuFe2O4@CQD nanocomposite as a high-perform heterogeneous nanocatalyst in nitroaniline group reduction

In this study, we fabricated an economical, non-toxic, and convenient magnetic nanocomposite of CuFe2O4 nanoparticles (NPs)/carbon quantum dots (CQDs) of citric acid via the co-precipitation method. Afterward, obtained magnetic nanocomposite was used as a nanocatalyst to reduce the ortho-nitroaniline (o-NA) and para-nitroaniline (p-NA) using a reducer agent of sodium borohydride (NaBH4). To investigate the functional groups, crystallite, structure, morphology, and nanoparticle size of the prepared nanocomposite, FT-IR, XRD, TEM, BET, and SEM were employed. The catalytic performance of the nanocatalyst was experimentally evaluated based on the ultraviolet–visible absorbance to assess the reduction of o-NA and p-NA. The acquired outcomes illustrated that the prepared heterogeneous catalyst significantly enhanced the reduction of o-NA and p-NA substrates. The analysis of the absorption showed a remarkable decrease for ortho-NA and para-NA at λmax = 415 nm in 27 s and λmax = 380 nm in 8 s, respectively. The constant rate (kapp) of ortho-NA and para-NA at the stated λmax was 8.39 × 10–2 s−1 and 5.48 × 10–1 s−1. The most highlighted result of this work was that the CuFe2O4@CQD nanocomposite fabricated from citric acid performed better than absolute CuFe2O4 NPs, since nanocomposite containing CQDs had a more significant impact than copper ferrite NPs.

Biomass-assisted fabrication of rGO-AuNPs as surface-enhanced Raman scattering substrates for in-situ monitoring methylene blue degradation

Reduced graphene oxide-gold nanoparticles nanocomposites (rGO-AuNPs) with high surface-enhanced Raman scattering (SERS) activity was created by biomass-assisted green synthesis with Lilium casa blanca petals biomass for the first time, and its application for methylene blue (MB) degradation was explored through in-situ monitoring. Lilium casa blanca petals biomass was used as a reducing agent to reduce GO and chloroauric acid successively when carrying out rGO-AuNPs in-situ synthesis while it also acted as a capping agent. The produced rGO had oxygen-containing functional groups which had an outstanding performance in enhancing the SERS effect. Characterization results confirmed that the AuNPs were grafted onto the rGO sheet, and the mechanism study showed that total flavonoids in Lilium casa blanca petals biomass were the main biological compounds involved in the reduction. rGO-AuNPs had a high Raman enhancement factor (EF) which could reach 3.88 × 107. The synthesized nanocomposite also had a good catalytic activity that could be employed as catalyst in MB degradation, and it could complete degradation within 15min. The reaction rate increased linearly with the amount of rGO-AuNPs, and the degradation could be in-situ monitored both by UV and SERS.

Novel development of zinc oxide–coated carbon nanoparticles from pineapple leaves using sol gel method for optimal adsorption of Cu2+ and reuse in latent fingerprint application

This study underlines a latest approach of preparing nitrogen carbon nanoparticles fused on zinc oxide nanoparticle nanocomposite (N-CNPs/ZnONP nanocomposite) for the uptake of copper ions (Cu2+) from wastewater using a sol gel method. The metal loaded adsorbent was then applied in the latent fingerprint application. N-CNPs/ZnONP nanocomposite proved to be a good sorbent for the optimal adsorption of Cu2+ at pH 8 and 1.0 g/L dosage. Langmuir isotherm best fitted the process with the maximum adsorption capacity of 285.71 mg/g that was superior to most values reported in other studies for the removal of Cu2+. At 25 °C, the adsorption was spontaneous and endothermic. Furthermore, Cu2+-N-CNPs/ZnONP nanocomposite revealed to be sensitive and selective for latent fingerprint (LFP) identification on a variety of porous surfaces. As a result, it is an excellent identifying chemical for latent fingerprint recognition in forensic science.Graphical

One-pot microwave synthesis of chitosan-stabilized silver nanoparticles entrapped polyethylene oxide nanofibers, with their intrinsic antibacterial and antioxidant potency for wound healing

Different physical and chemical techniques could be used to prepare chitosan/Silver nanoparticle (CHS/AgNPs) nanocomposite. The microwave heating reactor was rationally adopted as a benign tool for preparing CHS/AgNPs owing to less energy consumption and shorter time required for completing the nucleation and growth particles. UV–Vis, FTIR, and XRD, provided conclusive evidence of the AgNPs creation, while TEM micrographs elucidated that the size was spherical (20 nm). CHS/AgNPs were embedded in polyethylene oxide (PEO) nanofiber via electrospinning, and their biological properties, cytotoxicity evaluation, antioxidant, and antibacterial activity assays were investigated. The generated nanofibers have mean diameters of 130.9 ± 9.5, 168.7 ± 18.8, and 186.8 ± 8.19 nm for PEO, PEO/ CHS, and PEO/ CHS (AgNPs), respectively. Because of the tiny AgNPs particle size loaded in PEO/CHS (AgNPs) fabricated nanofiber, good antibacterial activity with ZOI against E. coli was 51.2 ± 3.2, and S. aureus was 47.2 ± 2.1 for PEO/ CHS (AgNPs) nanofibers. Non-toxicity was observed against Human Skin Fibroblast and Keratinocytes cell lines (>93.5 %), which justifies its great antibacterial potential to remove or prevent infection in wounds with fewer adverse effects.

Graphene‐Oxide‐Coated, Polypyrrole‐Supported, Nano Zerovalent Iron Nanocomposites for Adsorption of Hexavalent Chromium from Wastewater

AbstractThe hexavalent chromium in water is extremely toxic to most living organisms and can cause many diseases. In this work, we developed Polypyrrole (PPy), Polypyrrole/graphene oxide (PPy/GO) nanocomposite, and Polypyrrole/graphene oxide/zerovalent iron nanoparticles (PPy/GO/n‐ZVI) nanocomposite for adsorption of Cr (VI) from water. PPy/GO nanocomposite showed the highest Cr (VI) removal capacity for 10 % (weight) loading of GO. PPy/GO/n‐ZVI nanocomposite showed the highest Cr (VI) adsorption capacity for 50 % iron nanoparticle loading. Chemical kinetics data showed that Cr (VI) adsorption occurred with pseudo‐second‐order. The maximum adsorption capacity (qmax) was found to be 64.29 mg/g, 129.09 mg/g, and 171.04 mg/g on PPy, PPy/GO nanocomposite, and PPy/GO/n‐ZVI nanocomposite respectively. The thermodynamic study showed a positive value of ΔS, and a negative value of ΔG indicated rise in the disorder at the adsorbate‐adsorbent interface and spontaneous nature of Cr (VI) adsorption. ΔH was close to 21 kJ/mole indicating adsorption process occurred via physisorption. The recycling of the adsorbent was carried out by washing with sodium hydroxide and Cr (VI) removal efficiency decreased by around twenty % in the fifth cycle. The present study suggests that the PPy/GO/n‐ZVI nanocomposite is an environment‐friendly magnetic material and provides a simple, low‐cost strategy for the adsorption of Cr (VI) from wastewater.

Silver Nanoparticles for Fluorescent Nanocomposites by High-Pressure Magnetron Sputtering

We report on the formation of silver nanoparticles by gas aggregation in a reaction chamber at room temperature. The size distribution of nanoparticles deposited on a silicon substrate for various lengths of an aggregation (high-pressure) chamber was investigated by atomic force microscopy. Nanoparticles were characterized by scanning and transmission electron microscopy and spectral ellipsometry. The physical shape of the nanoparticles and its distribution was correlated with their optical properties. Metal-dielectric nanocomposites were deposited employing simultaneous deposition of Ag NPs via high-pressure magnetron sputtering and the dielectric matrix was deposited via thermal evaporation. Pure and Eu-, Er-, and Yb-doped lithium fluoride was used as the dielectric host matrix. Optical transmittance of lithium fluoride containing silver nanoparticles was measured and their theoretical absorption cross-section calculated. The nanoparticles were also embedded in Eu3+-doped downshifting and Er3+- and Yb3+-doped up-conversion materials to study their influence on emission spectra. Spectra of identical layers with and without nanoparticles were compared. Their transmittance at various annealing temperatures is also presented.

Chitosan/luminol/AgNPs nanocomposite for electrochemiluminescent determination of prostate-specific antigen.

Agreen, environmentally friendly protocol was developed for ultrasensitive and highly specific recognition of prostate-specific antigen (PSA) based on the ECL effect of luminol supported by chitosan-silver nanoparticles (CS/AgNPs) nanocomposites. The transducing surface was fabricated through two consecutive electrodeposition steps of gold nanoparticles (AuNPs) and chitosan (CS)-AgNPs-luminol electrochemiluminophore onto the glassy carbon electrode. In addition to anappropriate desirable biocompatibility, theelectrochemical synthesis presents low-cost preparation and ultrafast determination opportunity. AgNPs play a linking role to attach luminol, as an ECL agent to the CS support via donor-acceptor bonds between Ag atoms with NH groups of luminol and CS. Also, AgNPs can amplify the ECL intensity as a consequence of their excellent specific surface area and conductivity. To enhance the performance of the nanobiosensor, AuNPs were also used due totheir high-specific surface area and excellent affinity toward amine groups of CS. Based on this high-performance analysis strategy, ultrasensitive screening of PSA was attained with a desirable limit of detection of 0.6 ng mL-1 and a broad linear range between 1 pg mL-1 and 10 ng⋅mL-1 (R2=0.994). Approximately, the same results were recorded for the analysis of the unprocessed serum samples of patients with prostate cancer at different stages. This research provided significant insight into electrografting methods to construct ECL transducers for clinical monitoring of PSA and other tumor biomarkers in the clinical setting.

Ag nanoparticles anchored reduced graphene oxide sheets@nickel oxide nanoflakes nanocomposites for enhanced capacitive performance of supercapacitors

In this work, ternary nanocomposite of silver nanoparticles embedded on the surface of few layered reduced graphene oxide coated nickel oxide (Ag-rGO@NiO) was successfully fabricated as electrode material for high performance supercapacitor applications. NiO nanoflakes was prepared by hydrothermal route while coating of few layered rGO and subsequent silver anchoring was done by chemical methodology. The morphological analysis by scanning electron microscopy and transmission electron microscopy showed NiO nanoflakes coated by rGO/distributed on rGO substrate with scattered Ag nanoparticles. The elemental composition and distribution was confirmed by energy-dispersive X-ray (EDX) and Raman spectroscopy. The electrochemical measurements showed that the fabricated electrode of Ag-rGO@NiO is suitable electrode material and can enhance the capacitive performance of supercapacitors due to its high capacitive value (1230 Fg−1) in contrast to the binary rGO@NiO (337.5 F g−1) and bare NiO flakes (145 F g−1) at current density of 1 A g−1. The enhancement in the capacitive value of Ag-rGO@NiO composite was mainly attributed to the highly conductive rGO sheets and Ag nanoparticles where rGO sheets provided conductive path and Ag created new channels for the electron transfer. Furthermore, it also showed excellent cyclic stability as it retained 88.5 % of its initial capacitive value even after 3000 cycles as well as showed excellent energy density of (27.33 Wh kg−1) at power density (200.073 W kg−1).

An ultrasensitive electrochemical immunosensor for CA72-4 based on a signal amplification strategy of MoS2 nanoflower-supported Au nanoparticles

Accurate detection of cancer antigen 72-4 (CA72-4), a tumor-associated glycoprotein, is of great significance for gastric cancer diagnosis and immunotherapy monitoring. Modification of noble metal nanoparticles on transition metal dichalcogenides can significantly enhance functions, such as electron transport. Molybdenum disulfide gold nanoparticles nanocomposites (MoS2-Au NPs) were prepared in this study and a series of characterization studies were carried out. In addition, a label-free, highly sensitive electrochemical immunosensor molybdenum disulfide -Au nanoparticles/Glassy carbon electrode (MoS2-Au NPs/GCE) was also prepared and used for the detection of CA72-4. The electrochemical performance of the immunosensor was characterized by electrochemical techniques, such as cyclic voltammetry (CV), differential pulse voltammetry (DPV), and electrochemical impedance spectroscopy (EIS). The results indicated that better MoS2-Au NPs nanomaterials have been synthesized, and the prepared electrochemical immunosensor, MoS2-Au NPs/GCE, showed excellent electrochemical performance. The sensor exhibited high detection sensitivity under optimal conditions, including an incubation time of 30 min, an incubation temperature of 25 °C, and a pH of 7.0. The electrochemical immunosensor also had a low detection limit of 2.0 × 10−5 U/mL (S/N = 3) in a concentration range of 0.001–200 U/mL, with good selectivity, stability, and repeatability. In conclusion, this study provided a theoretical basis for the highly sensitive detection of tumor markers in clinical biological samples.

Structural, morphological, and electrochemical studies of Mg2SiO4-Pr6O11 nanocomposite for energy storage applications

Owing to not only the high demand in the development of new materials for the energy storage applications but also the high abundance of magnesium orthosilicate (Mg2SiO4) belonging to olivine group of minerals in Earth, magnesium orthosilicate (called as MOS) nanoparticle and magnesium orthosilicate–praseodymium oxide (Mg2SiO4–Pr6O11) (MOS-PO) nanocomposite have been chosen to explore mainly their electrochemical characteristics. The MOS nanoparticle and MOS-PO nanocomposite were synthesized using sol-gel method. The characterization techniques such as x-ray diffraction (XRD), Scanning Electron Microscopy (SEM), energy dispersive x-ray (EDX) spectroscopy, Zeta potential analyzer, and Cyclic Voltammetry (CV) were used to investigate the structural, morphological, and electrochemical properties of the prepared samples. Using Scherrer’s equation, phase identification was performed for the samples of MOS nanoparticle and MOS-PO nanocomposite with crystallite sizes 43 nm and 52 nm, respectively. The respective average particle sizes of 39 nm and 50 nm were observed for MOS nanoparticle and MOS-PO nanocomposite, using SEM images, and these values along with the images revealed the formation of spherical nanoparticles along with some agglomerates. The Zeta potential of the samples was calculated to analyze the stability of the nanoparticles. The electrochemical characterization was performed using the sample coated Mg foil as the working electrode and 0.5 M of KOH solution as the electrolyte, with the help of cyclic voltametric technique. The CV analysis was conducted ranging from 1.5 to −1.5 V at various scan rates of 25, 50, 100, 200, and 300 mVs−1. For MOS-PO nanocomposite, the maximum specific capacitance of 1812 Fg−1 was observed at a scan rate of 25 mVs−1. The results showed the possibility of the usage of MOS-PO nanocomposite material in the application of energy storage devices.

Comparison of nanocomposite dispersion and distribution for several melt mixers

Breakup (dispersion) and distribution of nanoparticles are the chief hurdles towards taking advantage of nanoparticles in polymer nanocomposites for reinforcement, flame retardancy, conductivity, chromaticity, and other properties. Microscopy is often used to quantify mixing, but it has a limited field of view, does not average over bulk samples, and fails to address nano-particle hierarchical structures. Ultra-small-angle X-ray scattering (USAXS) can provide a macroscopic statistical average of nanoscale dispersion (breakup) and emergent hierarchical structure, as well as the distribution on the nanoscale. This work compares several common mixer geometries for carbon black-polystyrene nanocomposites. Two twin-screw extruder geometries, typical for industrial processing of melt blends, are compared with a laboratory-scale single screw extruder and a Banbury mixer. It is found that for a given mixer, nanoscale distribution increases following a van der Waals function using accumulated strain as an analogue for temperature while macroscopic distribution/dispersion, using microscopy, does not follow this dependency. Breakup and aggregation in dispersive mixing follow expected behavior on the nanoscale. Across these drastically different mixing geometries an unexpected dependency is observed for nanoscale distributive mixing (both nano and macroscopic) as a function of accumulated strain that may reflect a transition from distributive turbulent to dispersive laminar mixing as the mixing gap is reduced.

Exploring the optical properties of MnO2 nanoparticles doped PVP for optoelectronics devices

Numerous applications for optical technologies used the nanocomposites. The purpose of this work is to create novel kinds of polymer nanocomposites and analyze their optical characteristics. The polyvinyl pyrrolidone (PVP)/ manganese oxide nanoparticle (MnO2NPs) nanocomposites were created. Various content of PVA and MnO2 NPs were fabricated. The optical characteristics of these nanocomposites were examined. The results demonstrate that the absorbance, coefficient of absorption, index of refractive, coefficient of extinction, dielectric constant and conductivity of PVP are raise with arise of the MnO2NPs content. The transmittance and gap of energy are reduced with a rise of the MnO2NPs content. The results illustrated the PVP/MnO2nanostructures may be utilized in different photonics and optics fields.

Designing of a magnetically recoverable (Ce+3, +4/Fe+2. Fe+3) oxide@ 2D g-C3N4 surface for enhanced photo-Fenton catalytic degradation of Bismarck-Brown R and Congo red dyes: kinetics, optical properties,and mechanistic pathway studies

ABSTRACT Co-precipitation-assisted hydrothermal synthesis was employed to synthesize Fe3O4/CeO2 nanohybrids over 2D g-C3N4 (CF@GCN) for photo-Fenton catalytic degradation of Bismarck brown R (BBR) and Congo Red (CR) dyes. Initially, Fe loading was deployed in CF@GCN with different sets of molar ratios of Fe against the 1 mole of Ce (Ce: Fe=1:0.2-1). Among different sets, the one with 0.8 moles of Fe against the 1 mole of Ce (C1F0.8@GCN) performed excellently for BBR and CR dye degradation via aiding in the photo-Fenton process. Morphological, structural, compositional, and electronic states of the final nanocomposite were evaluated using powder X-ray diffraction, transmission electron microscopy/high-resolution transmission electron microscopy, selected area electron diffraction, energy dispersive X-ray spectroscopy, and X-ray photoelectron spectroscopy. BET analysis of the final nanocomposite showed an excellent surface area of 56.76 m2g−1, allowing for effective degradation. UV–vis spectrophotometry, UV-DRS, and PL (photoluminescence) techniques were performed to monitor the optical properties of the final nanocomposite. Taulc’s plots estimated the band gaps of catalysts, and the final nanocomposite’s band gap was 2.2 eV, which was key for capturing photons from the light source and functioning the degradation process. Further, operating parameters such as catalyst dose, dye concertation, pH, H2O2 dose, and contact time studies were done with the final nanocomposite. C1F0.8@GCN degraded BBR up to 94.5 % within 30 minutes with a first-order rate constant of 0.09747 min−1 and CR dye up to 97.7 % within 45 minutes with a first-order rate constant of 0.07391 min−1. All results supported a nanocomposite of Fe3O4 nanoparticles and CeO2 nanorods grown over 2D g-C3N4 sheets. As predicted, composing Fe3O4 sped up catalyst recovery. Also, the final nanocomposite’s dye degradation rate was consistent till the 6th run. So, the study proposes a cost-effective plan for dealing with organic water contaminants like hazardous dyes.

Antimicrobial waterborne acrylic paint by the additive of graphene nanosheets/silver nanocomposite

In this work, the use of the nanocomposite of silver nanoparticles (NPs) and reduced graphene oxide (RGO), Ag-RGO, as a promising antibacterial agent to water-based acrylic paints has been investigated. The hybrid nanomaterial represented a strong antibacterial activity against two bacteria strains of Gram-negative of Escherichia coli (E. coli) and Gram-positive of methicillin-resistant Staphylococcus aureus (S. aureus). To prepare the antibacterial paint, 190 ppm Ag-RGO was added to the paint under sonication. By increasing the concentration of Ag-RGO in paint, the inhibition efficiency increased. The atomic force microscopy images showed that after 24 h incubation of E. coli and S. aureus bacteria with the antibacterial paint, their lengths decrease and degrade. The antibacterial activity of antibacterial paint against S. aureus was greater than that of E. coli. Also, the antibacterial activity of Ag NPs, RGO, and Ag-RGO was investigated. Among these nanomaterials, Ag-RGO has the highest antibacterial property so that its value of minimum inhibitory concentration for both E. coli and S. aureus is the same as 230 ppm. The minimum bactericidal concentration values for Ag-RGO was measured as 330 and 280 ppm for E. coli and S. aureus, respectively.

Wearable Noninvasive Glucose Sensor Based on CuxO NFs/Cu NPs Nanocomposites.

Designing highly active material to fabricate a high-performance noninvasive wearable glucose sensor was of great importance for diabetes monitoring. In this work, we developed CuxO nanoflakes (NFs)/Cu nanoparticles (NPs) nanocomposites to serve as the sensing materials for noninvasive sweat-based wearable glucose sensors. We involve CuCl2 to enhance the oxidation of Cu NPs to generate Cu2O/CuO NFs on the surface. Due to more active sites endowed by the CuxO NFs, the as-prepared sample exhibited high sensitivity (779 μA mM-1 cm-2) for noninvasive wearable sweat sensing. Combined with a low detection limit (79.1 nM), high selectivity and the durability of bending and twisting, the CuxO NFs/Cu NPs-based sensor can detect the glucose level change of sweat in daily life. Such a high-performance wearable sensor fabricated by a convenient method provides a facile way to design copper oxide nanomaterials for noninvasive wearable glucose sensors.

Application of Cotton Swab–Ag Composite as Flexible Surface-Enhanced Raman Scattering Substrate for DMMP Detection

It is both important and required to quickly and accurately detect chemical warfare agents, such as the highly toxic nerve agent sarin. Surface-enhanced Raman scattering (SERS) has received considerable attention due to its rapid results, high sensitivity, non-destructive data acquisition, and unique spectroscopic fingerprint. In this work, we successfully prepared SERS cotton swabs (CSs) for the detection of the sarin simulant agent dimethyl methyl phosphonate (DMMP) by anchoring N1-(3-trimethoxysilylpropyl) diethylenetriamine (ATS)/silver nanoparticle (AgNP) nanocomposites on CSs using ATS as the stabilizer and coupling agent. Simultaneously, the binding mode and reaction mechanics between the AgNP, ATS, and CS were confirmed by XPS. The modified CSs exhibited good uniformity, stability, and adsorption capability for SERS measurements, enabling the adsorption and detection of DMMP residue from an irregular surface via a simple swabbing process, with a detection limit of 1 g/L. The relative standard deviations (RSDs) of RSD710 = 5.6% had high reproducibility. In this research, the fabrication method could easily be extended to other cellulose compounds, such as natural fibers and paper. Furthermore, the versatile SERS CSs can be used for the on-site detection of DMMP, particularly in civil and defense applications, to guarantee food security and the health of the population.

PROLIFIC FABRICATION OF LANTHANUM OXIDE WITH GRAPHITIC CARBON/GRAPHENE OXIDE FOR ENHANCING PHOTOCATALYTIC DEGRADATION OF CARBOFURAN FROM AQUEOUS SOLUTION

Carbofuran insecticide is one of the most widely used low-cost carbamate pesticides because it effectively controls pests in agriculture fields and gardens. This study provides experimental results of the photocatalytic detoxification of Carbamate in wastewater using graphitic carbon nitride/GO/La2O3 nanocomposite nanoparticles. Calcination and hydrothermal technique were used to produce g-C3N4/GO/La2O3 nanocomposite. Furthermore, the photocatalytic detoxification of Carbofuran was investigated by numerous factors such as catalyst concentrations, irradiation period, and pH. According to the observation, the photo detoxification efficiency of Carbofuran pesticides rises as time increases. According to this study, g-C3N4/GO/La2O3 nanocomposite outperformed pure forms of g-C3N4, g-C3N4/GO, g-C3N4/La2O3 in degrading Carbofuran up to 80% and photo catalytically making it a potential alternative for wastewater treatment.

An electrochemical immunosensor for an alpha-fetoprotein cancer biomarker on a carbon black/palladium hybrid nanoparticles platform.

The early detection of cancer is a key step in cancer survival. Thus, there is a need to develop low-cost technologies, such as electrochemical immunosensor technologies, for timely screening and diagnostics. The discovery of alpha-feto protein (AFP) as a tumour-associated antigen lends AFP as a biomarker for cancer detection and monitoring. Thus, immunosensors can be developed to target AFP in cancer diagnostics. Hence, we report the application of a hybrid nanocomposite of carbon black nanoparticles (CBNPs) and palladium nanoparticles (PdNPs) as a platform for the electrochemical immunosensing of cancer biomarkers. The hybrid carbon-metal nanomaterials were immobilised by using the drop-drying and electrodeposition technique on a glassy carbon electrode, followed by the immobilisation of the anti-AFP to fabricate an immunosensor. The nanoparticles were characterised with electron microscopy, voltammetry, and electrochemical impedance spectroscopy (EIS). Square wave voltammetry (SWV) and EIS were used to study the immunosensor signal toward the bio-recognition of the AFP cancer biomarker. The hybrid nanoparticles enhanced the immunosensor performance. A linear detection range from 0.005 to 1000 ng mL-1 with low detection limits of 0.0039 ng mL-1 and 0.0131 ng mL-1 were calculated for SWV and EIS, respectively. The immunosensor demonstrated good stability, reproducibility, and selectivity. Its real-life application potential was tested with detection in human serum matrix.

Green synthesis of silver@graphene oxide nanocomposite for antibacterial, cytotoxicity assessment, and hydrogen peroxide electro-sensing

The nanocomposite of graphene oxide and silver nanoparticles with uniform particle distribution was successfully green synthesized for bioactive assessment and hydrogen peroxoide electro-sensing application.

A novel strategy for dramatically improving catalytic performance for light-driven thermocatalytic CO2 reduction with CH4 on Ru/MgO: the CO2 molecular fencing effect promoted by photoactivation

A novel strategy of CO2 molecular fencing effect promoted by photoactivation via preparing a nanocomposite of Ru nanoparticles supported on MgO is developed to significantly enhance fuel production rates and light-to-fuel efficiency, and completely prohibit coking for photothermocatalytic DRM.