Synthesis and surface engineering of Ag chalcogenide quantum dots for near-infrared biophotonic applications.

Quantum dots (QDs), a novel category of semiconductor materials, exhibit extraordinary capabilities in tuning optical characteristics. Their emergence in biophotonics has been noteworthy, particularly in bio-imaging, biosensing, and theranostics applications. Although conventional QDs such as PbS, CdSe, CdS, and HgTe have garnered attention for their promising features, the presence of heavy metals in these QDs poses significant challenges for biological use. To address these concerns, the development of Ag chalcogenide QDs has gained prominence owing to their near-infrared emission and exceptionally low toxicity, rendering them suitable for biological applications. This review explores recent advancements in Ag chalcogenide QDs, focusing on their synthesis methodologies, surface chemistry modifications, and wide-ranging applications in biomedicine. Additionally, it identifies future directions in material science, highlighting the potential of these innovative QDs in revolutionizing the field.

Zn-MOF decorated bio activated carbon for photocatalytic degradation, oxygen evolution and reduction catalysis.

An emerging global necessity for alternative resources combined with maximum catalytic efficiency, low cost, and eco-friendly composite remains a hotspot in the scientific society. Hereby, a novel protocol is approached to design a heterostructure of Zinc MOF decorated on the surface of 2D activated carbon (AC) through a simplistic approach. To begin with, analytical, morphological and spectroscopical studies were performed to identify the functional moieties, cruciate-flower like morphology and oxidative state of atoms present in the composite Zn-MOF @AC. The photocatalytic material aids in degrading both cationic and anionic dye in a UV (254 nm) irradiated environment at a rate of 86.4% and 77.5% within 90 mins. Subsequently, the hybrid materials are coated on the carbon substrate to evaluate the catalytic activity using oxygen evolution and reduction reaction process. The mechanical insight for the catalytic activity relies on the electronic transitions of atoms on the edges of the sheets ascribing to d-d energy levels between the interfacial electron movement. Our composite exhibits an overpotential of 0.7 V and a Tafel slope of 70 mV/dec for the oxygen reduction reaction. This study proposes an alternate approach for developing MOF decorated carbon-based composites for photocatalytic degradability and energy necessity.

TriMOF synergized on the surface of activated carbon produced from pineapple leaves for the environmental pollutant reduction and oxygen evolution process.

Facile and modest synthesis of significantly effective and less-cost catalysts for environmental pollutant degradation and oxygen evolution holds substantial potential in environmental and energy fields. Hereby, Trimetallic organic frameworks (TriMOF) consisting of Fe, Co, and Zn synergized on the surface of activated carbon (AC) from pineapple leaves tend to show exponential catalytic activity due to the more excellent ionic conductivity, catalytic stability and multiple active sites provided by different metal precursors. Furthermore, the developed nanocomposite was coated on the stainless-steel electrode substrate at room temperature, delivering greater electrocatalytic surface area and numerous active sites. The oxidation reaction kinetics drives the catalytic reduction of 4-nitrophenol to 4-aminophenol with a minimal time of 12 min @ >97 % efficiency. Furthermore, on electrocatalytic oxidation of water splitting process due to the presence of multiple metallic, active sites, the overpotential is at 370 mV having Tafel slope of 40 mV/dec and electrochemically active surface area of is 9.9 mF/cm2. This superior catalytic reduction of 4-nitrophenol and electrocatalytic water oxidation process is attributed to the developed composite's active centre and conductivity.

Green synthesized carbon quantum dots from maple tree leaves for biosensing of Cesium and electrocatalytic oxidation of glycerol.

Carbon quantum dots (CQDs) synthesized from biological sources play a significant role in biomedical and environmental applications, including bioimaging, biosensing, metal ions detection and electrocatalytic oxidations. Herein, we synthesized blue-emitting carbon quantum dots using maple tree leaves via a one-step hydrothermal process to detect Cesium ions selectively. The synthesized CQDs' functional group composition, morphology, and pH stability was analytical and morphologically investigated. The maple leaves derived carbon quantum dots (M-CQDs) exhibited blue fluorescence, and their sizes ranged from 1 to 10 nm. They exhibited emission at 445 nm upon excitation at 360 nm. M-CQDs PL intensity was highly stable for about 100 d without any changes and confirmed that the as-prepared CQDs could be used as a probe for Cesium ion sensing. M-CQDs were effectively used as Cesium sensing probes based on the electron transfer process and simultaneously used as a catalyst for glycerol electrooxidation. The PL intensity of M-CQDs was quenched while adding the varies concentration of Cesium ions in the linear range from 100 µM to 100 nM with the detection limit of (LOD) 160 nM, simultaneously electrocatalytic oxidation of glycerol showed an onset potential of 1.32 V at a current density of 10 mA/cm2.

Tuning the interfacial electronic transitions of bi-dimensional nanocomposites (pGO/ZnO) towards photocatalytic degradation and energy application.

The two-dimensional carbonaceous nanocomposites tend to have extreme capacitance and catalysis activity because of their surface tunability of oxygenated moieties aiding in photocatalytic degradation. Herewith, we performed microwave-assisted alkaline treatment of graphene oxide sheets to attain defective sites on the graphitic surface by altering microwave parameters. The synergism of zinc oxide (ZnO) on the graphitic surface impacts electronic transitions paving paths for vacant oxygen sites to promote photocatalytic degradation and catalytic activity. The photocatalytic efficiency of the synthesized material for the degradation of rhodamine B (RhB) because of its susceptibility in industrial effluents, and the degradation rate was estimated to be around 87.5% within a short span of 30 min by utilizing UV irradiation. Concomitantly, the pGO/ZnO coated substrate exhibits a specific capacity of 561.7 mAh/g and incredible coulombic efficiency illustrating pseudocapacitive nature. Furthermore, on subjecting the composite modified electrode to oxygen evolution catalysis due to the vacant sites located at the lattice edges attributing to the d-d coulombic interaction within the local electron clouds possessing a low overpotential of 205 mV with a Tafel slope of 84 mV/dec. This modest approach boosts an eco-friendly composite to develop photocatalytic degradability and bifunctional catalytic activity for futuristic necessity.

Detection of white spot syndrome virus in seafood samples using a magnetosome-based impedimetric biosensor.

White spot syndrome virus (WSSV) is a significant threat to the aquaculture sector, causing mortality among crabs and shrimps. Currently available diagnostic tests for WSSV are not rapid or cost-effective, and a new detection method is therefore needed. This study demonstrates the development of a biosensor by functionalization of magnetosomes with VP28-specific antibodies to detect WSSV in seafood. The magnetosomes (1 and 2 mg/ml) were conjugated with VP28 antibody (0.025-10 ng/µl), as confirmed by spectroscopy. The magnetosome-antibody conjugate was used to detect the VP28 antigen. The binding of antigen to the magnetosome-antibody complex resulted in a change in absorbance. The magnetosome-antibody-antigen complex was then concentrated and brought near a screen-printed carbon electrode by applying an external magnetic field, and the antigen concentration was determined using impedance measurements. The VP28 antigen (0.025 ng/µl) bound more efficiently to the magnetosome-VP28 antibody complex (0.025 ng/µl) than to the VP28 antibody (0.1 ng/µl) alone. The same assay was repeated to detect the VP28 antigen (0.01 ng/µl) in WSSV-infected seafood samples using the magnetosome-VP28 antibody complex (0.025 ng/µl). The WSSV in the seafood sample was also drawn toward the electrode due to the action of magnetosomes controlled by the external magnetic field and detected using impedance measurement. The presence of WSSV in seafood samples was verified by Western blot and RT-PCR. Cross-reactivity assays with other viruses confirmed the specificity of the magnetosome-based biosensor. The results indicate that the use of the magnetosome-based biosensor is a sensitive, specific, and rapid way to detect WSSV in seafood samples.

Well-Designed Au Nanorod-Doped Cu2O Core-Shell Nanocube-Embedded Reduced Graphene Oxide Composite for Efficient Removal of a Water Pollutant Dye.

To ensure environmental safety, the removal of organic pollutants has gained increasing attention globally. We have synthesized uniform Au nanorod (NR)-doped Cu2O core-shell nanocubes (CSNCs) via a seed-mediated route embedded on the surface of rGO sheets. The Au NRs@Cu2O/rGO nanocomposite was characterized using various techniques such as transmission electron microscopy (TEM), atomic force microscopy (AFM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and Fourier-transform infrared (FT-IR) and Raman spectroscopies. The scanning TEM-energy-dispersive spectroscopy (STEM-EDS) elemental mapping of the AuNRs@Cu2O/rGO nanocomposite indicates that the Au NR (40 nm) is fully covered with the Cu2O particles (∼145 nm) as a shell. N2 gas sorption analysis shows that the specific surface area of the composite is 205.5 m2/g with a mesoporous character. Moreover, incorporation of Au NRs@Cu2O CSNCs increases the nanogaps around the nanoparticles and suppresses the stacking/bundling of rGO, which significantly influences the pore size and increase the surface area. A batch adsorption experiment was carried out under various parameters, such as the effect of pH, contact time, temperature, initial dye concentration, and adsorbent dosage, for the removal of methylene blue (MB) in aqueous solution. The high surface area and mesoporosity can cause the adsorption capacity to reach equilibrium within 20 min with a 99.8% removal efficiency. Both kinetic and isotherm data were obtained and fitted very well with the pseudo-second-order kinetic and Langmuir isotherm model. The Langmuir isotherm revealed an excellent dye sorption capacity of 243.9 mg/g at 298 K. Moreover, after five adsorption cycles, the dye removal efficiency decreased from 99 to 86%. This novel route paves a new path for heterogeneous adsorbent synthesis, which is useful for catalysis and electrochemical applications.

Analytical insights of COVID-19 pandemic.

Coronavirus disease-19 (COVID-19) is caused by the severe acute respiratory syndrome coronavirus 2 (2019-nCoV or SARS-CoV-2). Genomic analysis has revealed that bat and pangolin coronaviruses are phylogenetically related to SARS-CoV-2. The actual origin and passage history of the virus are unknown, but human-human transmission of the virus has been confirmed. Several diagnostic techniques have been developed to detect COVID-19 in this prevailing pandemic period. In this review, we provide an overview of SARS-CoV-2 and other coronaviruses. The origin, structure, current diagnostic techniques, such as molecular assays based on oligonucleotides, immunoassay-based detection, nanomaterial-based biosensing, and distinctive sample based detection are also discussed. Furthermore, our review highlights the admissible treatment strategies for COVID-19 and future perspectives on the development of biosensing techniques and vaccines for the diagnosis and prevention of the disease, respectively.

Magnetosome-anti-Salmonella antibody complex based biosensor for the detection of Salmonella typhimurium.

Epidemic Salmonellosis contracted through the consumption of contaminated food substances is a global concern. Thus, simple and effective diagnostic methods are needed. Magnetosome-based biosensors are gaining attention because of their promising features. Here, we developed a biosensor employing a magnetosome-anti-Salmonella antibody complex to detect lipopolysaccharide (somatic "O" antigen) and Salmonella typhimurium in real samples. Magnetosome was extracted from Magnetospirillum sp. RJS1 and characterized by microscopy. The magnetosome samples (1 and 2 mg/mL) were directly conjugated to anti-Salmonella antibody (0.8-200 µg/mL) and confirmed by spectroscopy and zeta potential. The concentrations of magnetosome, antibody and lipopolysaccharide were optimized by ELISA. The 2 mg/mL-0.8 µg/mL magnetosome-antibody complex was optimal for detecting lipopolysaccharide (0.001 µg/mL). Our assay is a cost-effective (60%) and sensitive (50%) method in detection of lipopolysaccharide. The optimized magnetosome-antibody complex was applied to an electrode surface and stabilized using an external magnetic field. Increased resistance confirmed the detection of lipopolysaccharide (at 0.001-0.1 µg/mL) using impedance spectroscopy. Significantly, the R2 value was 0.960. Then, the developed prototype biosensor was applied to food and water samples. ELISA confirmed the presence of lipopolysaccharide in homogenized infected samples and cross reactivity assays confirmed the specificity of the biosensor. Further, the biosensor showed low detection limit (101 CFU/mL) in water and milk sample demonstrating its sensitivity. Regression coefficient of 0.974 in water and 0.982 in milk was obtained. The magnetosome-antibody complex captured 90% of the S. typhimurium in real samples which was also confirmed in FE-SEM. Thus, the developed biosensor is selective, specific, rapid and sensitive for detection of S. typhimurium.

Development of magnetosomes-based biosensor for the detection of Listeria monocytogenes from food sample.

Listeriosis through contaminated food is one of the leading causes of premature deaths in pregnant women and new born babies. Here, the authors have developed a magnetosomes-based biosensor for the rapid, sensitive, specific and cost-effective detection of Listeria monocytogenes from food sample. Magnetosomes were extracted from Magnetospirillum sp. RJS1 and then directly bound to anti-Listeriolysin antibody (0.25-1 µg/ml), confirmed in spectroscopy. Listeriolysin (LLO) protein (0.01-7 µg/ml) was optimised in enzyme-linked immunosorbent assay. Magnetosomes was conjugated with LLO antibody (0.25 µg/ml) in optimum concentration to detect LLO protein (0.01 µg/ml). Magnetosomes-LLO antibody complex was 25% cost effective. The magnetosomes-LLO antibody complex was directly stabilised on screen printed electrode using external magnet. The significant increase in resistance (RCT value) on the electrode surface with increase in concentration of LLO protein was confirmed in impedance spectroscopy. The L. monocytogenes contaminated milk and water sample were processed and extracted LLO protein was detected in the biosensor. The specificity of the biosensor was confirmed in cross-reactivity assay with other food pathogens. The detection limit of 101 Cfu/ml in both water and milk sample manifests the sensitive nature of the biosensor. The capture efficiency and field emission scanning electron microscopy confirmed positive interaction of Listeria cells with magnetosomes-antibody complex.