| Literature DB >> 33177558 |
Yudong Yao1, Yi Jiang1, Jeffrey A Klug1, Michael Wojcik1, Evan R Maxey1, Nicholas S Sirica2, Christian Roehrig1, Zhonghou Cai1, Stefan Vogt1, Barry Lai1, Junjing Deng3.
Abstract
X-ray ptychography is a rapidly developing coherent diffraction imaging technique that provides nanoscale resolution on extended field-of-view. However, the requirement of coherence and the scanning mechanism limit the throughput of ptychographic imaging. In this paper, we propose X-ray ptychography using multiple illuminations instead of single illumination in conventional ptychography. Multiple locations of the sample are simultaneously imaged by spatially separated X-ray beams, therefore, the obtained field-of-view in one scan can be enlarged by a factor equal to the number of illuminations. We have demonstrated this technique experimentally using two X-ray beams focused by a house-made Fresnel zone plate array. Two areas of the object and corresponding double illuminations were successfully reconstructed from diffraction patterns acquired in one scan, with image quality similar with those obtained by conventional single-beam ptychography in sequence. Multi-beam ptychography approach increases the imaging speed, providing an efficient way for high-resolution imaging of large extended specimens.Entities:
Year: 2020 PMID: 33177558 PMCID: PMC7658249 DOI: 10.1038/s41598-020-76412-8
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.996
Figure 1Schematic of multi-beam ptychography. Multiple illuminations are generated by a set of focusing optics comprised of Fresnel zone plates (FZP), central stops (CS) and order sorting apertures (OSA). The inset images are and visible light micrographs of the house-made FZP array with 150 m diameter and 70 nm outmost zone width.
Figure 2Double-beam ptychography with two illuminations focused by two zone plates with a separation of 1 mm. Measured diffraction patterns with (a) double beams and (b) each single beam (beam 1 and 2). (c) and (d) are reconstructed phase images of double-beam ptychography showing the two sample regions that were simultaneously scanned. Two single-beam ptychographic scans were taken in sequence by blocking one of the two beams at a time, their reconstructed results are shown in (e) with beam 1 and in (f) with beam 2, respectively.
Figure 3Power spectrum of the reconstructed region marked by the green box in Fig. 2f for double-beam and single-beam ptychography. (a) Vertical power spectrum density; (b) horizontal power spectrum density.
Figure 4“Self-portrait” of the FZP array with double-beam ptychography. (a) STXM image of two zone plates with double-beam illumination. (b) and (c) Ptychographic reconstruction of two datasets extracted from two regions, marked by black boxes in (a), having different zone widths.
Figure 5Reconstructions for double-beam ptychography with a beam separation of . Reconstructed phase images of two sample regions for (a) and (b) double-beam; (d) and (e) two single beams illuminating the same region, sequentially. Insets in (b) and (e) show a zoomed region denoted by the red box in (b). Reconstructed probes for (c) double-beam and (f) two single beams; a complex color scale is used with the brightness corresponding to amplitude and the hue indicating relative phase-shift. (g) Line-cut profile for the selected region marked by the green line in the inset of (b).