26 research outputs found

    On the apparently fixed dispersion of size distributions

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    Probability density functions (PDF) of statistical distributions of cluster sizes N, where N is the number of particles in the cluster, often seem to have less freedom than expected from considering the number of degrees of freedom at the clusters' source. The full width at half maximum appears to be comparable to the average . Such a hidden symmetry is intriguing theoretically and practically impairs size selection towards narrow distributions. However, reviewing the example of Helium cluster beams demonstrates that the origin of the apparent fixing is the assumption that the distributions should be log-normal or exponential and the subsequent use of these functions to fit the data in n = ln(N) log-space. This demands more care when using parametric statistics. Alternatives to the traditionally employed fitting functions are discussed.Comment: 15 pages, preprint, to appear in Journal of Computational and Theoretical Nanoscienc

    The rate sensitivity and plastic deformation of nanocrystalline tantalum films at nanoscale

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    Nanoindentation creep and loading rate change tests were employed to examine the rate sensitivity (m) and hardness of nanocrystalline tetragonal Ta films. Experimental results suggested that the m increased with the decrease of feature scale, such as grain size and indent depth. The magnitude of m is much less than the corresponding grain boundary (GB) sliding deformation with m of 0.5. Hardness softening behavior was observed for smaller grain size, which supports the GB sliding mechanism. The rate-controlling deformation was interpreted by the GB-mediated processes involving atomic diffusion and the generation of dislocation at GB

    Preparation of Pt–GO composites with high-number-density Pt nanoparticles dispersed uniformly on GO nanosheets

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    Pt–GO composites with high-number-density Pt nanoparticles dispersed uniformly on GO nanosheets were prepared using ethylene glycol as reducer at 180 °C. The nanoparticles had an average size of 12 nm with corners and edges on their surfaces. The composites had electrochemically active surface area of 31.7 m2 g−1 with a ratio (If/Ir=0.96) of the forward anodic peak current (If) to the reverse anodic peak current (Ir) in cyclic voltammetry curves, which is much higher than those of the reported Pt nanodendrites/reduced graphene oxide composites

    冰纳米晶体热力学参量的尺度和维度效应

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    The rate sensitivity and plastic deformation of nanocrystalline tantalum films at nanoscale

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    <p>Abstract</p> <p>Nanoindentation creep and loading rate change tests were employed to examine the rate sensitivity (<it>m</it>) and hardness of nanocrystalline tetragonal Ta films. Experimental results suggested that the <it>m </it>increased with the decrease of feature scale, such as grain size and indent depth. The magnitude of <it>m </it>is much less than the corresponding grain boundary (GB) sliding deformation with <it>m </it>of 0.5. Hardness softening behavior was observed for smaller grain size, which supports the GB sliding mechanism. The rate-controlling deformation was interpreted by the GB-mediated processes involving atomic diffusion and the generation of dislocation at GB.</p

    Electro Polymerization of Polypyrrole Coatings Doped with Different Proton Acids for Corrosion Protection of 304 Stainless Steel

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    Polypyrrole (PPY) coatings doped with sulphuric, oxalic and phosphoric acid were prepared on 304 stainless steel (304SS) by electropolymerization. Surface morphology and anti-corrosive performance of the polymer film was investigated by scanning electron microscope and electrochemical tests. The results indicate that the phosphoric acid doped PPY coating has a compact and smooth surface which shifts the Ecorr of 304SS towards to more positive value, while the jcorr was dropped from 10.4 to 0.88 μA cm−2. Long-term immersion test shows that the PPY coating doped with phosphoric acid provides better and durable corrosion resistance in comparison with the PPY coatings doped with the sulphuric and oxalic acids
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