TY - JOUR
T1 - Simultaneous bright- and dark-field X-ray microscopy at X-ray free electron lasers
AU - Dresselhaus-Marais, Leora E.
AU - Kozioziemski, Bernard
AU - Holstad, Theodor S.
AU - Ræder, Trygve Magnus
AU - Seaberg, Matthew
AU - Nam, Daewoong
AU - Kim, Sungwon
AU - Breckling, Sean
AU - Choi, Sungwook
AU - Chollet, Matthieu
AU - Cook, Philip K.
AU - Folsom, Eric
AU - Galtier, Eric
AU - Gonzalez, Arnulfo
AU - Gorkhover, Tais
AU - Guillet, Serge
AU - Haldrup, Kristoffer
AU - Howard, Marylesa
AU - Katagiri, Kento
AU - Kim, Sungwon
AU - Kim, Sungwon
AU - Kim, Sungwon
AU - Kim, Hyunjung
AU - Knudsen, Erik Bergbäck
AU - Kuschel, Stephan
AU - Lee, Hae Ja
AU - Lin, Chuanlong
AU - McWilliams, R. Stewart
AU - Nagler, Bob
AU - Nielsen, Martin Meedom
AU - Ozaki, Norimasa
AU - Pal, Dayeeta
AU - Pablo Pedro, Ricardo
AU - Saunders, Alison M.
AU - Schoofs, Frank
AU - Sekine, Toshimori
AU - Simons, Hugh
AU - van Driel, Tim
AU - Wang, Bihan
AU - Yang, Wenge
AU - Yildirim, Can
AU - Poulsen, Henning Friis
AU - Eggert, Jon H.
N1 - Publisher Copyright:
© 2023, Springer Nature Limited.
PY - 2023
Y1 - 2023
N2 - The structures, strain fields, and defect distributions in solid materials underlie the mechanical and physical properties across numerous applications. Many modern microstructural microscopy tools characterize crystal grains, domains and defects required to map lattice distortions or deformation, but are limited to studies of the (near) surface. Generally speaking, such tools cannot probe the structural dynamics in a way that is representative of bulk behavior. Synchrotron X-ray diffraction based imaging has long mapped the deeply embedded structural elements, and with enhanced resolution, dark field X-ray microscopy (DFXM) can now map those features with the requisite nm-resolution. However, these techniques still suffer from the required integration times due to limitations from the source and optics. This work extends DFXM to X-ray free electron lasers, showing how the 10 12 photons per pulse available at these sources offer structural characterization down to 100 fs resolution (orders of magnitude faster than current synchrotron images). We introduce the XFEL DFXM setup with simultaneous bright field microscopy to probe density changes within the same volume. This work presents a comprehensive guide to the multi-modal ultrafast high-resolution X-ray microscope that we constructed and tested at two XFELs, and shows initial data demonstrating two timing strategies to study associated reversible or irreversible lattice dynamics.
AB - The structures, strain fields, and defect distributions in solid materials underlie the mechanical and physical properties across numerous applications. Many modern microstructural microscopy tools characterize crystal grains, domains and defects required to map lattice distortions or deformation, but are limited to studies of the (near) surface. Generally speaking, such tools cannot probe the structural dynamics in a way that is representative of bulk behavior. Synchrotron X-ray diffraction based imaging has long mapped the deeply embedded structural elements, and with enhanced resolution, dark field X-ray microscopy (DFXM) can now map those features with the requisite nm-resolution. However, these techniques still suffer from the required integration times due to limitations from the source and optics. This work extends DFXM to X-ray free electron lasers, showing how the 10 12 photons per pulse available at these sources offer structural characterization down to 100 fs resolution (orders of magnitude faster than current synchrotron images). We introduce the XFEL DFXM setup with simultaneous bright field microscopy to probe density changes within the same volume. This work presents a comprehensive guide to the multi-modal ultrafast high-resolution X-ray microscope that we constructed and tested at two XFELs, and shows initial data demonstrating two timing strategies to study associated reversible or irreversible lattice dynamics.
U2 - 10.1038/s41598-023-35526-5
DO - 10.1038/s41598-023-35526-5
M3 - Journal article
C2 - 37845245
AN - SCOPUS:85174303304
SN - 2045-2322
VL - 13
JO - Scientific Reports
JF - Scientific Reports
IS - 1
M1 - 17573
ER -