The atomic structure of metallic glasses has been a long-standing scientific problem. Unlike crystalline metals, where long-range ordering is established by periodic stacking of fundamental building blocks known as unit cells, a metallic glass has no long-range translational or orientational order, although some degrees of short- and medium-range order do exist. Previous studies have identified solute- (minority atom)-centred clusters as the fundamental building blocks or short-range order in metallic glasses. Idealized cluster packing schemes, such as efficient cluster packing on a cubic lattice and icosahedral packing as in a quasicrystal, have been proposed and provided first insights on the medium-range order in metallic glasses. However, these packing schemes break down beyond a length scale of a few clusters. Here, on the basis of neutron and X-ray diffraction experiments, we propose a new packing scheme-self-similar packing of atomic clusters. We show that the medium-range order has the characteristics of a fractal network with a dimension of 2.31, and is described by a power-law correlation function over the medium-range length scale. Our finding provides a new perspective of order in disordered materials and has broad implications for understanding their structure-property relationship, particularly those involving a change in length scales.

The engineering materials diffractometer, VULCAN, at the Spallation Neutron Source began commissioning on June 26, 2009. This instrument is designed for materials science and engineering studies. In situ lattice strain measurements of a model metallic material under monotonic tensile load have been performed on VULCAN. The tensile load was applied under two different strain rates, and neutron diffraction measurements were carried out in both high-intensity and high-resolution modes. These experiments demonstrated VULCAN's in situ study capability of deformation behaviors even during the early phases of commissioning.

We report an in-situ neutron diffraction study of a large format pouch battery cell. The succession of Li-Graphite intercalation phases was fully captured under an 1C charge-discharge condition (i.e., charge to full capacity in 1 hour). However, the lithiation and dilithiation pathways are distinctively different and, unlike in slowing charging experiments with which the Li-Graphite phase diagram was established, no LiC24 phase was found during charge at 1C rate. Approximately 75 mol. % of the graphite converts to LiC6 at full charge, and a lattice dilation as large as 4% was observed during a charge-discharge cycle. Our work demonstrates the potential of in-situ, time and spatially resolved neutron diffraction study of the dynamic chemical and structural changes in “real-world” batteries under realistic cycling conditions, which should provide microscopic insights on degradation and the important role of diffusion kinetics in energy storage materials.

A four‐circle neutron diffractometer with a new multi‐wafer 331 Si monochromator has been installed and commissioned on a thermal beamline at the High Flux Isotope Reactor at Oak Ridge National Laboratory. The instrument is well suited to studies of nuclear and magnetic structures as a function of composition and temperature, resolving symmetry changes (lattice distortions and local structural changes), mapping the evolution of complex magnetic phases, determining hydrogen bonding, analyzing nuclear and spin densities, mapping diffuse scattering, and exploring fiber diffraction. Three incident wavelengths are available, 1.000, 1.536 and 2.540 Å, with intensities of 2.5 × 106, 2.2 × 107 and 8.0 × 106 neutrons cm−2 s−1, respectively. Either high‐resolution or high‐intensity modes are possible by horizontal bending of the monochromator. With increased bending of the monochromator, the incident flux on the sample passes through a maximum, increasing by ×2.0 for 1.000 Å, by ×3.5 for 1.536 Å and by ×3.5 for 2.540 Å, as compared to the flat condition. The flux increases because the lattice strain in the silicon crystals increases. The ω‐scan peak width increases with monochromator curvature and this width versus scattering angle flattens. Given these effects, the monochromator bending can be adjusted to deliver high intensity primarily for crystal structure refinements or high resolution for resolving symmetry changes. In addition to the traditional step‐scanning mode, a more efficient continuous‐scanning mode was developed, and both these are implemented through a LabView‐based control program, i.e. a modified version of the SPICE software package. A 4 K closed‐cycle helium refrigerator is permanently mounted on the χ‐circle of the goniometer to provide temperature control between 4 and 450 K.

The rapid solidification and subsequent thermal cycles that material is subjected to during additive manufacturing (AM) of a component result in a buildup of residual stresses, which lead to part distortion, and negatively impact the component's mechanical properties. We present a method for using neutron diffraction to validate thermomechanical models developed to predict the residual stresses in Inconel 625 walls fabricated by laser-based directed energy deposition. Residual stress calculations from neutron diffraction measurements depend strongly on the determination of stress-free lattice spacings. After measurement of stressed lattice spacings in Inconel 625 walls, reference samples were obtained by extracting thin slices from the walls and cutting comb-type slits into these slices. Reference lattice spacings were measured in these