Enabling Coarse X-ray Fluorescence Imaging Scans with Enlarged Synchrotron Beam by Means of Mosaic Crystal Defocusing Optics.
Jonas BaumannChristian KörnigTheresa StauferChristopher SchlesigerOliver SchmutzlerFlorian GrünerWolfgang MalzerBirgit KanngießerPublished in: International journal of molecular sciences (2022)
Trace elements, functionalized nanoparticles and labeled entities can be localized with sub-mm spatial resolution by X-ray fluorescence imaging (XFI). Here, small animals are raster scanned with a pencil-like synchrotron beam of high energy and low divergence and the X-ray fluorescence is recorded with an energy-dispersive detector. The ability to first perform coarse scans to identify regions of interest, followed by a close-up with a sub-mm X-ray beam is desirable, because overall measurement time and X-ray dose absorbed by the (biological) specimen can thus be minimized. However, the size of X-ray beams at synchrotron beamlines is usually strongly dependent on the actual beamline setup and can only be adapted within specific pre-defined limits. Especially, large synchrotron beams are non-trivial to generate. Here, we present the concept of graphite-based, convex reflection optics for the one-dimensional enlargement of a 1 mm wide synchrotron beam by a factor of 5 to 10 within a 1 m distance. Four different optics are tested and characterized and their reflection properties compared to ray tracing simulations. The general shape and size of the measured reflection profiles agree with expectations. Enhancements with respect to homogeneity and efficiency can be expected with improved optics manufacturing. A mouse phantom is used for a proof-of-principle XFI experiment demonstrating the applicability of coarse and fine scans with the suggested optics design.
Keyphrases
- dual energy
- fluorescence imaging
- electron microscopy
- computed tomography
- high resolution
- molecular dynamics
- image quality
- monte carlo
- photodynamic therapy
- air pollution
- single molecule
- magnetic resonance
- ionic liquid
- mass spectrometry
- magnetic resonance imaging
- positron emission tomography
- liquid chromatography
- tandem mass spectrometry