Ptychography is a coherent diffraction imaging technique that measures diffraction patterns at many overlapping points on a sample and then uses an algorithm to reconstruct amplitude and phase images of the object and probe. Here, we report imaging, spectroscopy and linear dichroism ptychographic measurements at the carbon K-edge. This progress was achieved with a new generation of scientific Complementary Metal Oxide Semiconductor (sCMOS) X-ray cameras with an uncoated image sensor which has fast image transfer and high quantum efficiency at the carbon K-edge. Reconstructed amplitude and phase contrast images, C 1s spectral stacks, and X-ray linear dichroism of carbon nanotubes at the carbon K-edge were measured with ptychography. Ptychography and conventional Scanning Transmission X-ray Microscopy (STXM) are compared using results acquired from the same area. Relative to STXM, ptychography provides both improved spatial resolution and improved image quality. We used defocus ptychography, with an X-ray beam spot size of 1.0 micron, in order to reduce radiation damage and carbon deposition. Comparable spatial resolution was achieved to that of ptychography performed with a focused beam. Ptychography at the carbon K-edge offers unique opportunities to perform high resolution spectromicroscopy on organic materials important in medicine, biology, environmental science and energy materials.

Solid dosage forms such as tablets are extensively used in drug administration for their simplicity and large-scale manufacturing capabilities. High-resolution X-ray tomography is one of the most valuable non-destructive techniques to investigate the internal structure of the tablets for drug product development as well as for a cost effective production process. In this work, we review the recent developments in high-resolution X-ray microtomography and its application towards different tablet characterizations. The increased availability of powerful laboratory instrumentation, as well as the advent of high brilliance and coherent 3rd generation synchrotron light sources, combined with advanced data processing techniques, are driving the application of X-ray microtomography forward as an indispensable tool in the pharmaceutical industry.

The control of emergent magnetic monopoles for the generation of monopole currents in artificial spin ice is essential for their use in nanomagnet-based device applications. Here we present a scheme to inject monopole currents into an artificial square ice at specific locations, which provides a means to control the propagation of the generated emergent monopole currents. Specifically, we modify an artificial square ice by populating two of its edges with different vertex configurations consisting of two, three, and four nanomagnets meeting at a common point. After setting an initial state with a global magnetic field, injection of monopoles occurs at one of the edges where the vertices have higher switching probability. We experimentally observe this vertex-specific nucleation of emergent magnetic monopoles using x-ray photoemission electron microscopy. Additionally, we demonstrate that a lateral shift in the reversal of the magnets, leading to the formation of large domains, is consistent with theoretical simulations incorporating higher-order contributions in the magnetic Hamiltonian. Finally, we find a strong correlation between the location of emergent monopole injection and the film thickness, which is a result of the switching probability associated with the different vertex configurations.

Understanding chemical reactivity and magnetism of 3d transition metal nanoparticles is of fundamental interest for applications in fields ranging from spintronics to catalysis. Here, we present an atomistic picture of the early stage of the oxidation mechanism and its impact on the magnetism of Co nanoparticles. Our experiments reveal a two-step process characterized by (i) the initial formation of small CoO crystallites across the nanoparticle surface, until their coalescence leads to structural completion of the oxide shell passivating the metallic core; (ii) progressive conversion of the CoO shell to Co₃O₄ and void formation due to the nanoscale Kirkendall effect. The Co nanoparticles remain highly reactive toward oxygen during phase (i), demonstrating the absence of a pressure gap whereby a low reactivity at low pressures is postulated. Our results provide an important benchmark for the development of theoretical models for the chemical reactivity in catalysis and magnetism during metal oxidation at the nanoscale.

Spectro-ptychography offers improved spatial resolution and additional phase spectral information relative to that provided by scanning transmission X-ray microscopes. However, carrying out ptychography at the lower range of soft X-ray energies (e.g. below 200 eV to 600 eV) on samples with weakly scattering signals can be challenging. Here, results of soft X-ray spectro-ptychography at energies as low as 180 eV are presented, and its capabilities are illustrated with results from permalloy nanorods (Fe 2p), carbon nanotubes (C 1s) and boron nitride bamboo nanostructures (B 1s, N 1s). The optimization of low-energy X-ray spectro-ptychography is described and important challenges associated with measurement approaches, reconstruction algorithms and their effects on the reconstructed images are discussed. A method for evaluating the increase in radiation dose when using overlapping sampling is presented.