A Highly Sensitive Luminescent Upconversion Nanosensor for Turn-On Detection of As3.

A luminescent nanoprobe (NP), MnO2-modified Er3+/Yb3+-codoped Ag2MoO4 upconversion nanoparticles (UCNPs; cod-AMO-3/MnO2), was constructed for rapid, sensitive, and selective "turn-on" detection of trace As3+. Herein, two kinds of luminescent NPs were developed based on luminescence resonance energy transfer (LRET) between cod-AMO-3 as the energy donor and MnO2 as the energy acceptor. By using MnO2 as the matrix in cod-AMO-3/MnO2 fluorometric assay, the upconversion luminescence (UCL) intensity (IUCL) of the cod-AMO-3 probe was quenched significantly through LRET, illustrating MnO2 as an efficient quencher for UCL. With the addition of As3+, a stable bidentate binuclear (BB) corner-sharing bridged complex (As5+-MnO2) was probably formed, which alters the surface of the upconversion NP, leading to gradual separation between UCNPs and MnO2 and subsequent recovery of IUCL. Interestingly, it possessed superior sensitivity, reaction kinetics, and also high selectivity toward As3+ in aqueous solution. Our optimized cod-AMO-3/MnO2 nanocomposite (NComp) demonstrated a linear range of 0-150 ppb and an ultrasensitive detection limit of 0.028 ppb for As3+, which is extremely below the regulatory level, signifying the promising practical usage of this system. To the best of our knowledge, such a surface-modified Ln3+-codoped Ag-based nanosensor being applied for As3+ detection probably has not been reported yet, and it is rather unexplored. In a nutshell, the ability to monitor the As3+ concentration may enable the rational design of a convenient platform for a diverse range of environmental monitoring applications.

Fluorescent carbon nanoparticles obtained from charcoal via green methods and their application for sensing Fe3+ in an aqueous medium.

Two green methods (microwave and hydrothermal) were employed for the preparation of water dispersible fluorescent carbon nanoparticles (CNPs) from activated charcoal. Microwave and hydrothermally synthesized carbon nanoparticles, (MW-CNPs) and (HT-CNPs), respectively were characterized by microscopic and spectroscopic techniques. A detailed study of their fluorescence characteristics was made. MW-CNPs and HT-CNPs were tested for metal ion selectivity in aqueous medium. MW-CNPs showed selectivity for Fe3+ among the tested metal ions and important studies such as for interference, linear range and limit of detection were carried out. The application of MW-CNPs for detection of Fe3+ in water was demonstrated.

Electrochemical loading of TEM grids used for the study of potential dependent morphology of polyaniline nanofibres.

An electrochemical method for loading electroactive materials over the TEM grid is reported. The protocol has been demonstrated using polyaniline as an example. The electroactive polymer was directly deposited over the Au TEM grid, used as working electrode in a 3 electrode electrochemical cell. The undisturbed as-deposited morphologies under the influence of various counter ions and ex situ electrochemical states have been studied and compared. Contrary to behaviour in bulk the individual polyaniline fibre was found thinner at anodic potentials. The movement of counter ions as a function of the electrochemical state of the polymer was studied using STEM-EDX elemental mapping.

Polymer-graphite composite: a versatile use and throw plastic chip electrode.

We report an efficient plastic chip electrode (PCE) fabricated from a composite of graphite and poly(methyl methacrylate) by a simple solution casting method and promoted as an economically inexpensive, multipurpose disposable electrode for various applications. The TEM images of the filler (graphite) show that the material consists of single, as well as multi-layers. Thus, the self-standing and arid electrodes prepared were characterized for their material properties such as, microscopy (SEM and AFM), as well as thermal properties (TGA), mechanical (tensile strength) and electrical properties. A set of physical parameters were derived from these characterizations for sustainability of these electrodes in harsh off-laboratory conditions. The utility of these mechanically stable, bulk-conducting and high surface area electrodes were demonstrated in various well understood electrochemical protocols, such as cyclic voltammetry, stripping voltammetry, electropolymerization, electrowinning and amperometric sensing. The voltammetry data were compared with the data recorded on a conventional glassy carbon electrode.

Correction: Highly active spherical amorphous MoS2: facile synthesis and application in photocatalytic degradation of rose bengal dye and hydrogenation of nitroarenes.

[This corrects the article DOI: 10.1039/C5RA19442C.].

Controlled assembly of cobalt embedded N-doped graphene nanosheets (Co@NGr) by pyrolysis of a mixed ligand Co(ii) MOF as a sacrificial template for high-performance electrocatalysts.

The development of high-efficiency and durable bifunctional electrocatalysts is an important and challenging topic in the area of energy storage/conversion. Herein, we prepared metallic cobalt nanoparticle decorated N-doped graphitic sheets (Co@NGr) by adopting facile pyrolysis of a mixed ligand cobalt-based MOF (CoMOF-2) as a sacrificial template displaying good OER and HER activity. The catalytic material harvested at three different pyrolytic temperatures was characterized by various analytical methods such as PXRD, SEM, TEM, Raman, and XPS analyses. The catalytic activity of the obtained hybrid composite materials towards oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) was studied. Co@NGr-900 was found to be an efficient bifunctional electrocatalyst and 10 mA cm-2 current density was afforded at an overpotential of 390 mV for OER and 340 mV for HER respectively. This study provides insight for the development of cost-effective nonprecious element-based electrocatalysts for water splitting which has relevance in energy storage and conversion. Catalytic performance is governed by the synergistic compositional effect of metallic cobalt/nitrogen-doping in the graphitic carbon increasing the electrical conductivity/active sites of the composite material.

Antimicrobial, antioxidant and anticancer activities of gold nanoparticles green synthesized using Mangifera indica seed aqueous extract.

In this study, gold nanoparticles (AuNPs) were synthesised using seed extract of mango (Mangifera indica) which is considered as waste and generally thrown away into the environment. The bioactive molecules in the seed act as reducing agent to synthesise AuNPs without using any external agent. The characterisation of green synthesised AuNPs was done using various spectroscopic techniques. Visual colour change from colourless to ruby red colour confirmed the formation of AuNPs which was further confirmed by maximum absorption peak at 550 nm by UV-spectra. Crystalline nature was confirmed by XRD technique while round, triangle and irregular shape and 19.45 nm size was confirmed by TEM and SAED analysis. FTIR analysis confirmed the presence of alcohol or phenol, carboxylic acid, ketones, amines, aromatic amines, aliphatic amines, alkyl halides and alkynes in M. indica seed which were responsible for the reduction of gold to AuNPs. The green synthesised AuNPs were evaluated for their antimicrobial, antioxidant and cytotoxic potential. They showed moderate antibacterial, cytotoxic and dose-dependent antioxidant activity. Seeds of M. indica instead of discarding can be successfully utilised for AuNPs synthesis which can be used as a natural source of antimicrobial, antioxidant and anticancer agent. Highlights Green synthesis of gold nanoparticles (AuNPs) from fruit (Mangifera indica) waste (seed). Characterisation using various spectroscopic techniques: UV-Vis spectroscopy, Zeta potential, FTIR, XRD and TEM analysis. Synthesized AuNPs were round, triangle and irregular in shape and 19.45 nm in size. Antimicrobial activity of AuNPs against 14 microorganisms. Antioxidant activity of AuNPs in terms of DPPH, SO and ABTS. Cytotoxic activity against HeLa, MCF-7 and fibroblast normal cell lines.

One pot solvent assisted syntheses of Ag3SbS3 nanocrystals and exploring their phase dependent electrochemical behavior toward oxygen reduction reaction and visible light induced methanol oxidation reaction.

A huge variety of silver based ternary sulfide semiconductors (SCs) have been considered for the sustainable advancement of renewable energy sources. Herein, we have synthesized two important classes of newly emerging semiconductor nanocrystals (NCs) Ag3SbS3 (SAS), i.e. hexagonal and monoclinic by simply tuning the solvent polarity, of which the second one has been synthesized in a phase pure NC for the first time by the thermal decomposition of silver and antimony based dithiocarbamate (∼N-CS2-M) complexes. Interestingly, these two systems exhibit two different semiconducting (SC) properties and band gaps; hexagonal SAS has a p type (Eg ∼ 1.65 eV) whereas monoclinic SAS has an n type (Eg ∼ 2.1 eV) character. For the first time ever we have designed a reducing working electrode (i.e. cathode) by modifying the rotating disc electrode (RDE) with hexagonal SAS that exhibits excellent electrochemical oxygen reduction reaction (ORR) activity (Eonset = 1.09 V vs. RHE and average number of electron transfer: 3.89) comparable to that of the highly expensive Pt/C (Eonset = 0.88 V vs. RHE and average number of electron transfer: 3.92). Density functional theory (DFT) investigation confirms the corroborations of experimental data with theoretical implications. In addition, the electrode fabricated from monoclinic SAS acts as an efficient photoanode which exhibits higher photoelectrochemical (PEC) methanol oxidation reaction (MOR) activity under illumination in alkaline medium compared to that of standard TiO2 grown on an indium tin oxide (ITO) coated glass slide. On illumination, the relative photocurrent density at the onset potential has been obtained to be 845 which is a very significant experimental output with respect to any other TiO2 or Pt@TiO2 based photocatalysts for this application. The physicochemical stability and reusability of both materials were supported by 50 hours of extended electrochemical chronoamperometric measurements and powder XRD and the TEM analyses after electrocatalysis. This study explores a possible pathway for designing simple and less expensive but catalytically efficient silver based ternary sulfide NC systems for developing an SC material to reduce the energy crisis in the near future.

Fluorescence characteristics of carbon nanoemitters derived from sucrose by green hydrothermal and microwave methods.

In this work, fluorescent carbon nanoparticles (CNPs) were prepared through two green methods i.e. microwave and hydrothermal, using sucrose as carbon precursor. Both of these methods have offered fluorescent CNPs as characterized by TEM, FTIR, zeta potential, absorbance and emission techniques. Excitation dependent emission spectra were exhibited by aqueous dispersion of these CNPs when they were subjected to different excitation wavelengths. The luminous characteristics of CNPs obtained from both of these methods were studied and compared. Their fluorescence stability in water and buffer was monitored for about three months. Influence of pH and various metal ions on emission spectra were investigated.

A novel amperometric biosensor for hydrogen peroxide and glucose based on cuprous sulfide nanoplates.

A facile, greener and template free route has been developed to produce cuprous sulfide (Cu2S) nanoplates (NPs) with average diameters of 70-150 nm, via one step solvothermal decomposition of a single-source precursor (SSP) Cu(ACDC)2 [ACDC = 2-aminocyclopentene-1-dithiocarboxylate] in the presence of ethylenediamine (EN) and triethylenetetramine (TETA) as structure orienting agents. The precursor complex and nanomaterials were thoroughly characterized by several common techniques and measurements, which give the composition and characteristics of the materials. Amperometric biosensors for hydrogen peroxide (H2O2) and glucose have been constructed by immobilizing the synthesized Cu2S NPs in glutaraldehyde on a glassy carbon (GC) electrode using a direct drop-coating method. The proposed sensor has displayed faster response, high and reproducible sensitivity (64.27 µA mM-1) with linear range of 10 µM to 3.75 mM, towards the electrochemical biosensing of H2O2 at -0.35 V (vs. Ag/AgCl). The sensor also showed high and reproducible sensitivity (61.67 µA mM-1) towards glucose determination with linear range of 10 µM to 3.1 mM. The anti-inference ability of electroactive molecules and favorable stability are some of the advantages of the proposed sensor. Finally, using the sensor we have determined the glucose concentration in a human blood serum sample. The results strongly demonstrate the usefulness of Cu2S NPs for biosensor design and other biological applications.