Scanning transmission X-ray microscopy is a powerful method for mapping chemical phases in nano-materials. The point spread function (PSF) of a conventional zone-plate-based microscope limits the achievable spatial resolution and also results in spatially resolved spectra that do not accurately reflect the spatial heterogeneity of the samples when the scale of the detail approaches the probe size. X-ray ptychography, a coherent-scattering-based imaging scheme that effectively removes the probe from the image data, returns accurate spectra from regions smaller than the probe size. We show through simulation how the long tails on the PSF of an x-ray optic can cause spectral distortion near a boundary between two spectrally distinct regions. The resulting apparent point spectra can appear mixed, with the species on one side of the boundary seeming to be present on the other even at a distance from the boundary equal to several times the spatial resolution. We further demonstrate the effect experimentally and show that ptychographic microscopy can return the expected spectra from a model system, whereas conventional microscopy does not.

Using X-ray microscopy and spectromicroscopy, vascular smooth muscle cells (VSMCs) were imaged, prepared without using additional embedding material or staining, but by applying simple, noncryo fixation techniques. The cells were imaged with a compact source transmission X-ray microscope and a scanning transmission X-ray microscope (STXM). With the STXM, spectromicroscopy was performed at the C K-edge and the Ca LIII,II-edges. VSMCs were chosen because of their high amount of actin stress fibers, so that the actin cytoskeleton should be visible. Other parts of the cell, such as the nucleus and organelles, were also identified from the micrographs. Both in the spectra and the images, the effects of the different preparation procedures were observable. Furthermore, Ca hotspots were detected and their density is determined.