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H W Sheng

Publications and source records attributed to H W Sheng.

5 recordsLinked to original sources

Atomic packing and short-to-medium-range order in metallic glasses.

Unlike the well-defined long-range order that characterizes crystalline metals, the atomic arrangements in amorphous alloys remain mysterious at present. Despite intense research activity on metallic glasses and relentless pursuit of their structural description, the details of how the atoms are packed in amorphous metals are generally far less understood than for the case of network-forming glasses. Here we use a combination of state-of-the-art experimental and computational techniques to resolve the atomic-level structure of amorphous alloys. By analysing a range of model binary systems that involve different chemistry and atomic size ratios, we elucidate the different types of short-range order as well as the nature of the medium-range order. Our findings provide a reality check for the atomic structural models proposed over the years, and have implications for understanding the nature, forming ability and properties of metallic glasses.

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Atomic packing of the inherent structure of simple liquids.

We report a universal inherent packing structure underlying the simple liquids, the normalized distribution functions of which are independent of temperature and density. The inherent packing state, carrying the maximized configurational entropy, has intrinsic connections with the maximally random jammed state of hard spheres.

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Icosahedral short-range order in amorphous alloys.

We have characterized the icosahedral short-range order in amorphous solids using local environment probes. Such topological local order is pronounced even in an amorphous alloy that does not form quasicrystalline phases upon crystallization, as demonstrated by the extended x-ray absorption fine structure and x-ray absorption near-edge structure of a Ni-Ag amorphous alloy analyzed through reverse Monte Carlo simulations.

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Homogeneity of a supersaturated solid solution.

Extended x-ray absorption fine structures, small-angle x-ray scattering, and atomistic model calculations have been employed to probe the homogeneity of the fcc solution created in Ag-Cu, a classical system demonstrating the extension of solubility across the entire miscibility gap through rapid quenching. Our results reveal that in many cases the supersaturated solutions formed have decomposition features on the scale of 1 nm. Conventional diffraction methods are inadequate in determining the level of supersaturation or the uniformity of such solid solution alloys.

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Amorphous structures in the immiscible Ag-Ni system.

Vapor quenching in the phase-separating Ag-Ni system creates alloys that appear homogeneously amorphous under conventional probes. However, an atomic-level structural analysis based on extended x-ray absorption fine structures in combination with reverse Monte Carlo and molecular dynamics simulations demonstrates that these new phases are characterized by nonuniform, spinodal-like structures on an extremely fine scale. This heterogeneous nature of the structure is directly responsible for the unexpectedly low heat (and temperature) of crystallization observed in calorimetric measurements.

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