Raj Karthik

Green synthesized gold nanoparticles decorated graphene oxide for sensitive determination of chloramphenicol in milk, powdered milk, honey and eye drops.

A simple and rapid green synthesis using Bischofia javanica Blume leaves as reducing agent was developed for the preparation of gold nanoparticles (AuNPs). AuNPs decorated graphene oxide (AuNPs/GO) was prepared and employed for the sensitive amperometric determination of chloramphenicol. The green biosynthesis requires less than 40s to reduce gold salts to AuNPs. The formations of AuNPs and AuNPs/GO were evaluated by scanning electron and atomic force microscopies, UV-Visible and energy dispersive X-ray spectroscopies, X-ray diffraction studies, and electrochemical methods. AuNPs/GO composite film modified electrode was fabricated and shown excellent electrocatalytic ability towards chloramphenicol. Under optimal conditions, the amperometric sensing platform has delivered wide linear range of 1.5-2.95μM, low detection limit of 0.25μM and high sensitivity of 3.81μAμM(-1)cm(-2). The developed sensor exhibited good repeatability and reproducibility, anti-interference ability and long-term storage stability. Practical feasibility of the sensor has been demonstrated in food samples (milk, powdered milk and honey) and pharmaceutical sample (eye drops). The green synthesized AuNPs/GO composite has great potential for analysis of food samples in food safety measures.

Fabrication of potato-like silver molybdate microstructures for photocatalytic degradation of chronic toxicity ciprofloxacin and highly selective electrochemical detection of H2O2.

In the present work, potato-like silver molybdate (Ag2MoO4) microstructures were synthesized through a simple hydrothermal method. The microstructures of Ag2MoO4 were characterized by various analytical and spectroscopic techniques such as XRD, FTIR, Raman, SEM, EDX and XPS. Interestingly, the as-prepared Ag2MoO4 showed excellent photocatalytic and electrocatalytic activity for the degradation of ciprofloxacin (CIP) and electrochemical detection of hydrogen peroxide (H2O2), respectively. The ultraviolet-visible (UV-Vis) spectroscopy results revealed that the potato-like Ag2MoO4 microstructures could offer a high photocatalytic activity towards the degradation of CIP under UV-light illumination, leads to rapid degradation within 40 min with a degradation rate of above 98%. In addition, the cyclic voltammetry (CV) and amperometry studies were realized that the electrochemical performance of Ag2MoO4 modified electrode toward H2O2 detection. Our H2O2 sensor shows a wide linear range and lower detection limit of 0.04–240 μM and 0.03 μM, respectively. The Ag2MoO4 modified electrode exhibits a high selectivity towards the detection of H2O2 in the presence of different biological interferences. These results suggested that the development of potato-like Ag2MoO4 microstructure could be an efficient photocatalyst as well as electrocatalyst in the potential application of environmental, biomedical and pharmaceutical samples.

A voltammetric determination of caffeic acid in red wines based on the nitrogen doped carbon modified glassy carbon electrode

We reported an electrochemical determination of caffeic acid (CA) based on the nitrogen doped carbon (NDC). The described sensor material was prepared by the flame synthesis method, which gave an excellent platform for the synthesis of carbon nanomaterials with the hetero atom dopant. The synthesized material was confirmed by various physical characterizations and it was further characterized by different electrochemical experiments. The NDC modified glassy carbon electrode (NDC/GCE) shows the superior electrocatalytic performance towards the determination of CA with the wide linear concentration range from 0.01 to 350 μM. It achieves the lowest detection limit of 0.0024 μM and the limit of quantification of 0.004 μM. The NDC/GCE-CA sensor reveals the good selectivity, stability, sensitivity and reproducibility which endorsed that the NDC is promising electrode for the determination of CA. In addition, NDC modified electrode is applied to the determination of CA in red wines and acquired good results.

Electrochemical properties of the acetaminophen on the screen printed carbon electrode towards the high performance practical sensor applications

Acetaminophen is a non-steroidal anti-inflammatory drug used as an antipyretic agent for the alternative to aspirin. Conversely, the overdoses of acetaminophen can cause hepatic toxicity and kidney damage. Hence, the determination of acetaminophen receives much more attention in biological samples and also in pharmaceutical formulations. Here, we report a rapid and sensitive detection of the acetaminophen based on the bare (unmodified) screen printed carbon electrode (BSPCE) and its electrochemistry was studied in various pHs. From the observed results, the mechanism of the electro-oxidation of acetaminophen was derived for various pHs. The acetaminophen is not stable in strong acidic and strong alkaline media, which is hydrolyzed and hydroxylated. However, it is stable in intermediate pHs due to the dimerization of acetaminophen. The kinetics of the acetaminophen oxidation was briefly studied and documented in the schemes. In addition, the surface morphology and disorders of BSPCE was probed by scanning electron microscope (SEM) and Raman spectroscopy. Moreover, the BSPCE determined the acetaminophen with the linear concentration ranging from 0.05 to 190μM and the lower detection limit of 0.013μM. Besides that it reveals the good recoveries towards the pharmaceutical samples and shows the excellent selectivity, sensitivity and stability. To the best of our knowledge, this is the better performance compare to the previously reported unmodified acetaminophen sensors.

A highly sensitive and selective electrochemical determination of non-steroidal prostate anti-cancer drug nilutamide based on f-MWCNT in tablet and human blood serum sample

A novel electrochemical sensor based on the functionalized multiwalled carbon nanotube (f-MWCNT) was successfully developed for the sensitive and selective determination of non-steroidal prostate anti-cancer drug nilutamide in tablet and blood serum samples. The f-MWCNT was prepared by the simple reflux method and characterized by the scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), Raman spectroscopy, X-ray powder diffraction (XRD) and fourier transform infrared spectroscopy (FT-IR). Interestingly, the f-MWCNT was exhibited a superior electrocatalytic activity towards the anti-cancer drug nilutamide when compared with pristine MWCNT and unmodified electrodes. Besides, the electrochemical sensor was revealed an excellent current response for the determination of nilutamide with wide linear ranges (0.01-21μM and 28-535μM), high sensitivity (11.023 and 1.412μA μM-1cm2) and very low detection limit (LOD) 0.2nM. The developed electrochemical sensor was showed an excellent selectivity even in the presence of electrochemically active biological substances and nitro aromatic compounds. Moreover, it manifested a good reproducibility and stability. In addition, the f-MWCNT modified glassy carbon electrode (GCE) sensor was successfully applied for the detection of nilutamide in tablet and blood serum sample.

Construction of novel Pd/CeO2/g-C3N4 nanocomposites as efficient visible-light photocatalysts for hexavalent chromium detoxification

In this study, we report a series of novel palladium nanoparticles (Pd) supported cerium oxide (CeO2)/graphitic carbon nitride (g-C3N4) nanocomposites, fabricated via the simple strategy, which were used for the detoxification of toxic hexavalent chromium to benign trivalent chromium under visible light irradiation. The synthesized Pd/CeO2/g-C3N4 nanocomposites were characterized by various tools including powder X-ray diffraction (PXRD), fourier transform infrared (FTIR), X-ray photoelectron spectroscopy (XPS), UV-vis diffuse reflectance spectra (DRS/UV-vis), high resolution transmission electron microscopy (HRTEM), and energy dispersive X-ray spectra (EDS). The wrapping with surface of graphitic carbon nitride nanosheets can efficiently promote the interface charge separation and transmission over the ternary photocatalyst, which was studied by photoluminescence spectra (PL) analysis and electrochemical impedance spectroscopy (EIS) spectra. The obtained 3% Pd/CeO2/g-C3N4 nanocomposite photocatalyst exhibit an excellent photocatalytic performance when compared to other single and composite counter parts. The 3% Pd/CeO2/g-C3N4 exhibits a strong synergistic effect which arises due to the interactions between palladium nanoparticles, CeO2 and graphitic carbon nitride resulting in the lower recombination of photo-induced charge carriers with enhanced photocatalytic activity. This work implies that the synergistic Pd/CeO2/g-C3N4 nanocomposites would be a new kind of high-efficiency visible-light-driven photocatalysts materials for the detoxification of public safety and security.

Rapid synthesis of ethyl cellulose supported platinum nanoparticles for the non-enzymatic determination of H2O2

Cellulose derivatives are one of the carbohydrate polymers which received a great interest in the construction of nanostructured materials. Particularly, the ethyl cellulose provides an enormous support to the metal nanoparticles. To the best of our knowledge, this is the first time report for the simple and rapid synthesis of ethyl cellulose (EC) supported platinum nanoparticles (PtNPs) for the determination of non-enzymatic hydrogen peroxide (H2O2). The PtNPs/EC composite was confirmed by various characterizations such as fourier transform infra-red spectra, energy dispersive X-ray spectra, field emission scanning electron microscope and cyclic voltammetry. Further, the PtNPs/EC composite modified glassy carbon electrode (GCE) was successfully determined the H2O2 with the linear concentration range from 0.05μM to 2.22mM and the lowest detection limit of 0.01μM. Moreover, the PtNPs/EC/GCE sensor electrode manifested an acceptable sensitivity, selectivity and reproducibility. In addition, we have determined the H2O2 in contact lens solution and human blood serum samples.

Novel hydrothermal synthesis of MoS2 nanocluster structure for sensitive electrochemical detection of human and environmental hazardous pollutant 4-aminophenol

Herein, we have demonstrated a new electrochemical sensor for trace level detection of environmentally hazardous 4-aminophenol (4-AP) using a glassy carbon electrode (GCE) modified with MoS2 nanoclusters. The MoS2 nanoclusters were fabricated by a simple hydrothermal treatment without using any other organic templates or surfactants. The formation of MoS2 nanoclusters was confirmed by X-ray diffraction, FT-infrared, Raman and energy dispersive X-ray spectroscopies, scanning electron and transmission electron microscopies and selected area electron diffraction studies. The MoS2 modified GCE (MoS2/GCE) shows good electrocatalytic activity towards the redox reaction of 4-AP by means of cyclic voltammetry and differential pulse voltammetry. The DPV detection of 4-AP using MoS2/GCE delivers excellent sensitivity with a low detection limit of 0.03 (±0.008) μM and good linearity in the range of 0.04–17 μM. The sensitivity of the developed electrode is 4.278 (±0.058) μA mM−1 cm−2. The developed sensor displayed good repeatability, reproducibility and selectivity. Moreover, the practical applicability of the MoS2/GCE is demonstrated in water samples which delivered satisfactory recoveries.

Phyto mediated biogenic synthesis of gold nanoparticles using Cerasus serrulata and its utility in detecting hydrazine, microbial activity and DFT studies

Green synthesis of Au-NPs using Cerasus serrulata (C. serrulata) leaves extract has emerged as a nontoxic and ecofriendly option, as compared to currently available chemical and/or physical methods and also Au-NPs act as both reducing and stabilizing agent. The developed Au-NPs were characterized with XRD, UV-visible spectroscopy, FTIR, SEM, TEM and chemical constituents of C. serrulata leaves extract after and before reduction of Au-NPs have been identified through GC-MS. TEM images confirmed that biosynthesized Au-NPs were spherical in shape and approximately in the range of 5-25 nm. The electrochemical results showed remarkable electrocatalytic activity of the Au-NPs-modified GC electrode in the detection of environmentally hazardous pollutant like hydrazine. The modified electrode exhibits a wide linear range 5 nM to 272 μM with low detection limit 0.05 μM. The fabricated sensor shows good selectivity towards other electroactive species as well. Thus the proposed sensor seems to be a potential candidate for developing a simple, rapid and cost-effective electrochemical sensor. The synthesized Au-NPs exhibited higher antibacterial activity against gram negative (Escherichia coli) than gram positive (Staphylococcus aureus) bacteria. DFT studies revealed that the coumarin (CM) present in the C. serrulata leaves extract demonstrated greater reducing and stabilizing properties compared to the properties of other compounds like butylhydroxytoluene (BHT) and hydrocoumarin (HCM) present in the extract.

Sonochemical Synthesis of Sulfur Doped Reduced Graphene Oxide Supported CuS Nanoparticles for the Non-Enzymatic Glucose Sensor Applications

Over the present material synthesis routes, the sonochemical route is highly efficient and comfortable way to produce nanostructured materials. In this way, the copper sulfide (CuS-covellite) and sulfur doped reduced graphene oxide (S-rGO) nanocomposite was prepared by sonochemical method. Interestingly, the structure of the as-prepared S-rGO/CuS was changed from the covellite to digenite phase. Herein, the S-rGO was act as a mild oxidizer and liable for the structural transformations. These structural changes are sequentially studied by various physicochemical characterizations such as Fourier transform infrared spectroscopy (FT-IR), Raman spectroscopy, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and Transmission electron microscopy (TEM). After scrupulous structural evaluations, the transformation of CuS phase was identified and documented. This oxidized CuS has an excellent electrocatalytic activity when compare to the bulk CuS. This S-rGO/CuS was further used for the determination of glucose and acquired good electrocatalytic performances. This S-rGO/CuS was exhibited a wide linear concentration range, 0.0001–3.88 mM and 3.88–20.17 mM, and a low-level detection limit of 32 nM. Moreover, we have validated the practicability of our developed glucose sensor in real biological samples.