We demonstrate a hard-x-ray microscope that does not use a lens and is not limited to a small field of view or an object of finite size. The method does not suffer any of the physical constraints, convergence problems, or defocus ambiguities that often arise in conventional phase-retrieval diffractive imaging techniques. Calculation times are about a thousand times shorter than in current iterative algorithms. We need no a priori knowledge about the object, which can be a transmission function with both modulus and phase components. The technique has revolutionary implications for x-ray imaging of all classes of specimen.

We examine the spectral dependence in the visible frequency range of the polarization rotation of two-dimensional gratings consisting of chiral gold nanostructures with subwavelength features. The gratings, which do not diffract, are shown to exhibit giant specific rotation ($\sim {10}^4°/\mathrm{mm}$) of polarization in direct transmission at normal incidence. The rotation is the same for light incident on the front and back sides of the sample. Such reciprocity indicates three dimensionality of the structure arising from the asymmetry of light-plasmon coupling at the air-metal and substrate-metal interfaces. The structures thus enable polarization control with quasi-two-dimensional planar objects. However, in contradiction with recently suggested interpretation of experiments on larger scale but otherwise similar structures, the observed polarization phenomena violate neither reciprocity nor time-reversal symmetry.

Single-cell level measurements are necessary to characterize the intrinsic biological variability in a population of cells. In this study, we demonstrate that, with the microarrays for mass spectrometry platform, we are able to observe this variability. We monitor environmentally (2-deoxy- d -glucose) and genetically (ΔPFK2) perturbed Saccharomyces cerevisiae cells at the single-cell, few-cell, and population levels. Correlation plots between metabolites from the glycolytic pathway, as well as with the observed ATP/ADP ratio as a measure of cellular energy charge, give biological insight that is not accessible from population-level metabolomic data.

A method for the fabrication of ultrahigh-resolution Fresnel zone plate lenses for x-ray microscopy is demonstrated. It is based on the deposition of a zone plate material (Ir) onto the sidewalls of a prepatterned template structure (Si) using an atomic layer deposition technique. This results in a doubling of the effective zone density, thus improving the achievable resolution of x-ray microscopes. Test structures with lines and spaces down to 15 nm were resolved in a scanning transmission x-ray microscope at 1 keV photon energy.