Rhodium Nanoparticle Shape Dependence in the Reduction of NO by CO

The shape dependence of the catalytic reduction of nitric oxide by carbon monoxide on rhodium nanopolyhedra and nanocubes was studied from 230 to 270 degrees C. The nanocubes are found to exhibit higher turnover frequency and lower activation energy than the nanopolyhedra. These trends are compared to previous studies on Rh single crystals.Chemistry, PhysicalSCI(E)EI21ARTICLE3-4317-32213

Y-junction nanostructures of palladium: Enhanced electrocatalytic properties for fuel cell reactions

Here we demonstrate the utility of hierarchically designed alumina templates for the formation of palladium Y-junction nanostructures through a chemical vapor deposition route. These structures exhibit enhanced electrocatalytic activity for the oxidation of formic acid (up to 1020%) compared to that of platinum Y-junction nanostructures, which could be of immense relevance to portable fuel cell technology, since designing a better electrocatalyst for fuel cell reactions continues to be an important challenge. Apart from the obvious applications in fuel cell electrocatalysis, these Y-junction nanostructures could also act as promising candidates for room temperature hydrogen separation and more importantly as interconnects in molecular scale electronic devices. The present method of fabrication of Y-junction nanostructures using hierarchical alumina templates could be extended to other metallic/semiconducting systems facilitating more general opportunities for such hierarchical designs in nanoelectronics. (C) 200

Comparative study of the shape-dependent electrocatalytic activity of platinum multipods, discs, and hexagons: applications for fuel cells

We here demonstrate a remarkable potential-dependent morphological evolution of platinum mesostructures in the form of multipods, discs, and hexagons using a porous anodic alumina membrane (PAAM). These structures prepared potentiostatically at -0.7, -0.5 and -0.3 V, respectively, reveal unique shape-dependent electrocatalytic activity toward both formic acid and ethanol oxidation reactions. A comparison of the electrooxidation kinetics of these structures illustrates that hexagons show better performance toward formic acid oxidation whereas, for ethanol oxidation, multipods show significantly enhanced activity. Interestingly, the enhancement factor (R) for these mesostructures with respect to that of commercial platinized carbon toward formic acid oxidation ranges up to 2000% for hexagons whereas for multipods and disc they are about 700% and 300%, respectively. Similarly, for ethanol oxidation, the calculated value of R varies up to 600% for multipods while for disc and hexagons these values are 500% and 200%, respectively. These shape-dependent electrocatalytic activity of Pt mesostructures have been further correlated with XRD results. Thus, the present results demonstrate the importance of precise control of morphology by an electric field and their potential benefits especially for fuel cell applications since designing a better electrocatalyst for many fuel cell reactions continues to be an important challenge

Y-junction nanostructures of palladium: enhanced electrocatalytic properties for fuel cell reactions

Here we demonstrate the utility of hierarchically designed alumina templates for the formation of palladium Y-junction nanostructures through a chemical vapor deposition route. These structures exhibit enhanced electrocatalytic activity for the oxidation of formic acid (up to 1020%) compared to that of platinum Y-junction nanostructures, which could be of immense relevance to portable fuel cell technology, since designing a better electrocatalyst for fuel cell reactions continues to be an important challenge. Apart from the obvious applications in fuel cell electrocatalysis, these Y-junction nanostructures could also act as promising candidates for room temperature hydrogen separation and more importantly as interconnects in molecular scale electronic devices. The present method of fabrication of Y-junction nanostructures using hierarchical alumina templates could be extended to other metallic/semiconducting systems facilitating more general opportunities for such hierarchical designs in nanoelectronics

Synthesis of platinum Y-junction nanostructures using hierarchically designed alumina templates and their enhanced electrocatalytic activity for fuel-cell applications

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Highly resolved quantized double-layer charging of relatively larger dodecanethiol-passivated gold quantum dots

Monolayer-protected quantum dots (Q-dots) show multivalent redox property, popularly known as the quantized double-layer (QDL) charging phenomena. In this report, we demonstrate the QDL behavior of the larger-sized Au Q-dots (ca. 3.72 nm) protected with dodecanethiol using differential pulse voltammetry (DPV) and cyclic voltammetry (CV). The voltammetric results show that the QDL property is evident even for these larger-sized Q-dots as reflected by a large population of well-resolved charging events in a narrow potential range with an almost equidistant voltage (Δ V) spacing. The theoretical calculation of the variation of charging energy with size using the well-known concentric sphere capacitance model facilitates the understanding of electrochemical behavior of these sidelined larger-sized Au Q-dots. The calculated capacitance value is in well agreement with the experimentally obtained value of 1.6 aF

Template-assisted synthesis of ruthenium oxide nanoneedles: electrical and electrochemical properties

We here demonstrate the formation of bundles of RuO2 nanoneedles (ca. 100 nm diameter) by a template-assisted electrodeposition from aqueous RuCl3 solution under potentiostatic conditions at room temperature. Cyclic voltammetric measurements in 0.5 M H2SO4 show significantly higher redox-related charging behavior for the RuO2 nanoneedles compared to that of the commercial sample, which is also supported by the electrochemical impedance data. A comparison of the specific capacitance reveals a higher value for nanoneedles (3 F/g instead of 0.4 F/g for the bulk), which has been explained on the basis of enhanced reactivity. More interestingly, electrical transport measurements reveal a transition from metallic to semiconducting behavior especially at low-temperature caused by an impurity scattering mechanism. We anticipate that the present simple route for the fabrication of RuO2 nanostructures will be useful to exploit their potentials in various fields such as electrocatalysis, nanoelectronics, and more importantly for designing supercapacitors

Tuning the aspect ratio of silver nanostructures: the effect of solvent mole fraction and 4-aminothiophenol concentration

In this report, we study the role of solvent on controlling the aspect ratio of silver nanostructures during their growth. More specifically, a single-step preparation of different aspect ratio silver nanostructures (R, 1-100) is demonstrated in aqueous acetonitrile using 4-aminothiophenol (ATP) as a reducing as well as surface passivating agent, where the variation of the mole fraction of acetonitrile has a dramatic effect on the morphology. The combined effect of ATP concentration and solvent mole fraction on aspect ratio is investigated by UV-Visible Spectroscopy (UV-Vis), Transmission Electron Microscopy (TEM), Fourier Transform Infra-red Spectroscopy (FTIR) and X-ray Diffraction analysis (XRD). At lower values of mole fraction (i.e. 0.4), high aspect ratio silver nanorods are formed, whereas a mole fraction close to 1 gives no such nanostructures. In comparison, only spherical nanoparticles are formed when the mole fraction is close to 0. High aspect ratio silver nanorods are also favored by higher ATP concentration