2644 research outputs found

    Bio-inspired catalyst compositions for enhanced oxygen reduction using nanostructured Pt electrocatalysts in polymer electrolyte fuel cells

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    Composites of Nafion with a class of bio-molecules viz., plant hormones, are explored as potential polymer electrolytes for improving the proton transport inside the catalyst layer of a H2/O2 fuel cell. Specifically, four nitrogenous plant hormones, two each from the class of auxins and cytokinins have been investigated, following preliminary characterization of the composite dispersions and membranes. Interestingly, the use of indole-3-acetic acid (an auxin) in the catalyst layer reveals a 30% enhancement in Pt catalyst utilization and improved fuel cell performance by 150 mW /cm2. The effect of these bio-molecules on the kinetic and mass transport parameters has been analyzed systematically using a combination of electrochemical and spectroscopic techniques

    Artificially Designed Membranes Using Phosphonated Multiwall Carbon Nanotube-Polybenzimidazole Composites for Polymer Electrolyte Fuel Cells

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    The ability of phosphonated carbon nanotubes to offer an unprecedented approach to tune both proton conductivity and mechanical stability of hybrid polymer electrolytes based on the polybenzimidazole membrane is demonstrated for fuel cell applications. The covalent attachment between the amino group of the 2-aminoethylphosphonic acid precursor and CNTs has been confirmed by NMR and IR experiments, while EDAX analysis indicates that one out of every 20 carbon atoms in the CNT is functionalized. Proton conductivity of the composite membrane shows a remarkable 50% improvement in performance, while a maximum power density of 780 and 600mWcm-2 is obtained for the composite and pristine membranes, respectively. Finally, the ultimate strength determined for the composite and pristine membranes is 100 and 65 MPa, respectively, demonstrating the superiority of the composite. This study opens up a newstrategy to systematically tune the properties of polymer electrolytes for special applications by using appropriately functionalized CNTs

    Influence of plane wave cut-off on structural and electronic properties in Sn-BEA and Ti-BEA zeolite water molecule interaction

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    Periodic systems are best described by the pseudo-potential methods. However, the accuracy of its description depends on the cut-off of plane wave basis. This is much more critical in the case of weak interactions, where a clear understanding on the influence of plane wave cut-off on the structural and electronic properties is not readily available in the literature. In the present work, we have taken a metal substituted beta zeolite–H2O complex for understanding this objective. Our studies show that while a lower cut-off of 500 eV is sufficient for the convergence of the structural parameters, description of energy-dependent properties necessitates a high cut-off value

    Voltammetric behavior of perfluorocarboxylic acids and their corresponding ethyl esters on glassy carbon electrode: surface effects

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    Voltammetric responses of trifluoroacetic acid, perfluorobutyric acid, perfluorohexanoic acid, and perfluorooctanoic acid (PFOA) were studied in acetonitrile/tetra-nbutylammonium perchlorate medium on glassy carbon electrode. All the four acids gave two voltammetric waves. PFOA exhibits blocking effects. In the presence of excess water, the first cathodic peak current increases, and the second peak disappeared. Very small quantity of triethylamine (TEA; 1–2 mM) was found to be effective in suppressing the first cathodic peak. Both the peak current and peak potential values were sensitive to water and TEA content. The ester derivatives of all the four perfluorocarboxylic acids (PFCAs), however, gave well-defined cathodic reduction peak around −2.3 V. This peak appears to be the best choice for quantitative estimation of PFCAs

    Preparation and Characterization of Ceria-Based Electrolytes for Intermediate Temperature Solid Oxide Fuel Cells (IT-SOFC)

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    Solid-oxide fuel cells (SOFCs) can be used for clean, efficient and environment-friendly energy conversion with a variety of fuels at high temperature (1273 K). The high temperature operation accelerates unwanted reactions and creates materials challenges; so, intermediate-temperature SOFCs (IT-SOFCs) have been developed. Reduction of the operating temperature (between 873-1073 K) requires solid electrolyte materials with higher conductivities. In this study, partially substituted ceria as solid electrolyte is experimented systematically for use in solid oxide fuel cells operating below 1073 K (intermediate temperature range). Nine compositions namely, CeO2, Ce0.95Gd0.05O2-δ (CGO9505), Ce0.90Gd0.10O2-δ (CGO9010), Ce0.85Gd0.15O2-δ (CGO8515), Ce0.80Gd0.20O2-δ (CGO8020), Ce0.95Sm0.05O2-δ (SDC9505), Ce0.90Sm0.10O2-δ (SDC9010), Ce0.85Sm0.15O2-δ (SDC8515) and Ce0.80Sm0.20O2-δ (SDC8020) were synthesized by Glycine Nitrate (GN) combustion technique and investigated. The physical properties and the other relevant features of the data obtained are analyzed with a view to use these alternate electrolyte materials in IT-SOFC

    Studies on development of electroless Ni–B bath for corrosion resistance and wear resistance applications

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    Electroless deposition process has undergone numerous changes to meet the challenging needs for a variety of industrial applications ever since the invention of the process during 1947. Among the various metals that can be electrolessly plated, electroless nickel has proved its supremacy for producing coatings with high corrosion resistance, hardness, wear resistance and uniformity. Electroless nickel can be deposited from a variety of baths and the coating properties depends upon the type of reducing agents and other deposition conditions. Electroless nickel–boron coatings have received considerable interest nowadays because of the superior hardness, corrosion and wear resistance characteristics. In this paper, the authors have reported on the development of a biodegradable electroless Ni–B bath and evaluated its characteristic properties. The influence of bath constituents, temperature and pH on the rate of deposition was studied. Scanning electron microscopy, X-ray diffraction, X-ray fluorescence spectroscopy and atomic absorption spectroscopy techniques were employed to find out the deposit morphology and boron content in the deposits. The hardness and wear resistance of the deposits were evaluated in the as deposited and heat treated conditions. The influence of sodium hypophosphite as reducing agent on the Ni–B deposit has also been studied. The use of nickel methane sulphonate as the metal ion source increases the bath lifetime without adversely affecting the deposit qualities. Annealing the Ni–B deposit at 400uC for one hour resulted in an increase in the hardness and thereby the wear resistance. The corrosion resistance of as plated electroless Ni–B deposit is higher than the heat treated deposits. Also, the corrosion resistance is highly enhanced by the incorporation of phosphorous to the nickel–boron alloy coating

    Synthesis of Rh–carbon nanotube based heterostructures and their enhanced field emission characteristics

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    Selective decoration of Rh nanospheres on acid functionalized carbon nanotubes has been demonstrated using Al as a sacrificial substrate. Remarkable field emission has been observed for this heterostructure as a high current density of 170 muA / cm2 is generated at an ultra-low threshold of 300 V/ mu m, compared to much smaller values for Rh nanospheres and carbon nanotubes separately

    Removal of NO3– from Drinking Water by Electrocoagulation – An Alternate Approach

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    The present study provides an electrocoagulation method, for the removal of NO3 – from drinking water using magnesium as the anode and cathode. The experiments are carried out as a function of pH, temperature, and current density. The results show that the maximum removal efficiency of 95.8% was achieved at a current density of 0.25 A/dm2, at a pH of 7.0. The adsorption of NO3 – preferably fitting the Langmuir adsorption isotherm suggests monolayer coverage of the adsorbed molecules. The adsorption process follows a second-order kinetics model. Thermodynamic studies show that the adsorption was exothermic and spontaneous in nature

    Molecularly Imprinted Electrochemical Sensors

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    In this review, the applications of molecularly imprinted polymer (MIP) materials in the area of electrochemical sensors have been explored. The designs of the MIPs containing different polymers, their preparation and their immobilization on the transducer surface have been discussed. Further, the employment of various transducers containing the MIPs based on different electrochemical techniques for determining analytes has been assessed. In addition, the general protocols for getting the electrochemical signal based on the binding ability of analyte with the MIPs have been given. The review ends with describing scope and limitations of the above electrochemical based MIP sensors

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