| Literature DB >> 35418587 |
Frieder Koch1,2, Adam Kubec1,3, Mikhail Lyubomirskiy4, Felix Wittwer5,6,7, Maik Kahnt8, Ken Vidar Falch5, Jan Garrevoet5, Martin Seyrich5,6, Christian David1, Christian G Schroer5,6,9.
Abstract
Imaging large areas of a sample non-destructively and with high resolution is of great interest for both science and industry. For scanning coherent X-ray diffraction microscopy, i. e., ptychography, the achievable scan area at a given spatial resolution is limited by the coherent photon flux of modern X-ray sources. Multibeam X-ray ptychography can improve the scanning speed by scanning the sample with several parallel mutually incoherent beams, e. g., generated by illuminating multiple focusing optics in parallel by a partially coherent beam. The main difficulty with this scheme is the robust separation of the superimposed signals from the different beams, especially when the beams and the illuminated sample areas are quite similar. We overcome this difficulty by encoding each of the probing beams with its own X-ray phase plate. This helps the algorithm to robustly reconstruct the multibeam data. We compare the coded multibeam scans to uncoded multibeam and single beam scans, demonstrating the enhanced performance on a microchip sample with regular and repeating structures.Entities:
Year: 2022 PMID: 35418587 PMCID: PMC9008058 DOI: 10.1038/s41598-022-09466-5
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.379
Figure 1(a) Experimental setup with the lens array (A), the pinhole array (B), the sample (C) and the detector (D). (b) Lens combination generating two uncoded probes. (c) Lens combination generating two coded probes. (d) Lens combination generating three coded probes. (e) All nine probes, reconstructed in the sample plane at 7 keV.
Figure 2Reconstructed images of a Siemens star test sample and corresponding probes. Red and purple arrows show reconstruction defects. Blue/green dashed rectangles show which probe scanned which region of the sample: (a) uncoded probe case with the probes shown in (p1) and (p2), (a1) is the magnified center of the test pattern; (b) coded probe case, with the probes shown in (cp1) and (cp2), (b1) is the magnified center of the test pattern. The vertical scale bars represent 3 μm, the horizontal scale bars represent 4 μm. The gray scale indicates the sample phase shift in radians. Phases of the probes are color-coded.
Figure 3Cropped intermediate reconstruction results of the Siemens star after 200 iterations using (a) similar probes and (b) coded probes. The scale bars have a length of 1.5 μm. The grayscale indicates phase shift in radians. (c) Comparison of the evolution of the normalized error during the reconstruction of the scan of the Siemens star test sample with uncoded beams and coded beams. The sharp downward steps every 50 iterations are a result of the position correction being performed at these iterations.
Figure 4Evaluation of the resolution using line profiles. (a) Measurement with a single probe, (b) measurement with two coded probes, (c) corresponding profiles. The full width at half maximum value for the single beam profile is 64 nm and for the two beam profile 68 nm. The scale bars represent 3 nm.
Figure 5Reconstruction results from the microchip sample: (a) full view of the scanned area. The horizontal scale bar represents 8 μm. (b) enlarged view of the area marked by the green square. (c) enlarged view of the area marked by the red square. The vertical scale bars represent 3 μm. The grayscale indicates the phase shift in radians.
Figure 6Resolution estimates of the images recorded of the microchip: (a) Fourier ring correlation of the reconstruction of two identical and consecutive scans, estimating a resolution of 95 nm. (b) edge feature on the phase image chosen for a line profile (orange line). The scale bar (red) has a length of 2 μm. (c) the extracted profile across the edge feature (orange) and the fit of an error function (blue) giving a resolution estimate of 114 nm.