| Literature DB >> 31074429 |
Adrian P Mancuso1, Andrew Aquila1, Lewis Batchelor1, Richard J Bean1, Johan Bielecki1, Gannon Borchers1, Katerina Doerner1, Klaus Giewekemeyer1, Rita Graceffa1, Oliver D Kelsey1, Yoonhee Kim1, Henry J Kirkwood1, Alexis Legrand1, Romain Letrun1, Bradley Manning1, Luis Lopez Morillo1, Marc Messerschmidt1, Grant Mills1, Steffen Raabe1, Nadja Reimers1, Adam Round1, Tokushi Sato1, Joachim Schulz1, Cedric Signe Takem1, Marcin Sikorski1, Stephan Stern1, Prasad Thute1, Patrik Vagovič1, Britta Weinhausen1, Thomas Tschentscher1.
Abstract
The European X-ray Free-Electron Laser (FEL) became the first operational high-repetition-rate hard X-ray FEL with first lasing in May 2017. Biological structure determination has already benefitted from the unique properties and capabilities of X-ray FELs, predominantly through the development and application of serial crystallography. The possibility of now performing such experiments at data rates more than an order of magnitude greater than previous X-ray FELs enables not only a higher rate of discovery but also new classes of experiments previously not feasible at lower data rates. One example is time-resolved experiments requiring a higher number of time steps for interpretation, or structure determination from samples with low hit rates in conventional X-ray FEL serial crystallography. Following first lasing at the European XFEL, initial commissioning and operation occurred at two scientific instruments, one of which is the Single Particles, Clusters and Biomolecules and Serial Femtosecond Crystallography (SPB/SFX) instrument. This instrument provides a photon energy range, focal spot sizes and diagnostic tools necessary for structure determination of biological specimens. The instrumentation explicitly addresses serial crystallography and the developing single particle imaging method as well as other forward-scattering and diffraction techniques. This paper describes the major science cases of SPB/SFX and its initial instrumentation - in particular its optical systems, available sample delivery methods, 2D detectors, supporting optical laser systems and key diagnostic components. The present capabilities of the instrument will be reviewed and a brief outlook of its future capabilities is also described. open access.Entities:
Keywords: XFEL; instrumentation; serial crystallography
Year: 2019 PMID: 31074429 PMCID: PMC6510195 DOI: 10.1107/S1600577519003308
Source DB: PubMed Journal: J Synchrotron Radiat ISSN: 0909-0495 Impact factor: 2.616
Summary of basic parameters of the the SPB/SFX instrument
| Parameter | Value/range | Units |
|---|---|---|
| Photon energy | 3–16 | keV |
| Pulse energy (maximum) | ∼1–5 | mJ |
| Photons per pulse (maximum) | ∼1–8 | 1012 photons |
| Focal spot size | ∼100s, 1 | nm, µm |
| Repetition rate | 10 × 1350 (maximum at highest pulse energy) | s−1 |
| 10 × 2700 (maximum at lower pulse energies) | ||
| Pulse duration (range) | A few 100 | fs |
| Detector pixel size (AGIPD) | 200 × 200 | µm |
| Upstream detector | AGIPD, four independent quadrants (4 × 512 × 512 pixels) | NA |
| Downstream detectors (to be installed in future) | AGIPD and Jungfrau, both 4 megapixel | NA |
| Single-photon sensitivity | Yes | NA |
| Detector dynamic range at 12 keV | >104 | photons |
| Detector frame rate AGIPD (burst) | 4.5 | MHz |
| Sample–detector distances | 0.12 to ∼6 | m |
| Sample delivery options | Liquid jet, aerosol jet, fixed targets | NA |
| Miscellanea | Pump–probe laser | NA |
Figure 1Iconographic layout of components of the SPB/SFX instrument. Approximate distances of components in the SASE1 XTD9 tunnel, SPB/SFX optics hutch and SPB/SFX experiment hutch are given relative to the common focal plane of the upstream interaction region. X-ray beam direction is indicated by the grey arrows.
Figure 2Overview of SASE1 hutches. X-ray beam direction is left to right, top to bottom. SPB/SFX X-ray radiation hutches are depicted in dark blue with SPB/SFX laser hutches, laboratory, control rooms and service rooms depicted in light blue. The vertical column in grey is the so-called ‘sample elevator’ used to transport material from the upstairs biological laboratory to the preparation laboratory adjacent to the SPB/SFX experiment hutch. A 2D overhead engineering view of the instrumentation is placed into the hutch model for context.
Figure 3CAD-model of the JJ X-ray transfocator unit (left) and photograph of the lens cassettes inside the chamber installed in the XTD9 tunnel (right).
Figure 4Arrangement of the beryllium lenses in the tranfocator unit, where green colour indicates in which position within the lens cassette the lens is placed. The arrangement is such that differing numbers of lenses can be placed into the beam by moving arms in or out, allowing for the focusing of different photon energies to the same plane in the interaction region.
Figure 5Representation of the horizontal optical layout of the SPB/SFX instrument. The incident beam from XTD9 is shown in red, with the 1 µm-scale system in green and the 100 nm-scale system in blue. The 0 m mark in the longitudinal distance denotes the common focal plane of the two systems. Figure adapted from Bean et al. (2016 ▸).
Figure 6Representation of the vertical optical layout of the SPB/SFX instrument. The incident beam from XTD9 is shown in red, with the 1 µm-scale system in green and the 100 nm-scale system in blue. The 0 m mark in the longitudinal distance denotes the common focal plane of the two systems. Figure adapted from Bean et al. (2016 ▸).
Figure 7Overview of a beam diagnostic device at the SPB/SFX instrument. (a) UHV-compatible mounting block for four scintillators (S) and optical mirrors (M). (b) Overview of a Type I diagnostic device with a standard DN63CF cube as its basic building block (B). The three-point mount (M) for camera (C) and optics (O) can be removed without breaking the vacuum inside the cube for maintenance and baking. The scintillators are inserted into the beam via a motorized translation (T). An optical filter (F) is used to block transmission of the blue light from the reference laser which causes fluorescence emission from the scintillator just like the X-ray beam and thus can be visualized in the same way. (c) Illustrative example output from a Type I diagnostic device: diffraction from an instrument slit system closed to a gap of a few tens of micrometres in the horizontal and vertical direction, as imaged in a plane more than 22 m downstream at a photon energy of 9.3 keV. Only a very small fraction from the much larger incident beam was selected here. The image is a background-corrected average of 647 single-FEL-pulse images.
Figure 8Schematic of the core components in the instrument beam stop (IBS). While a large fraction of the beam is attenuated by B4C blocks (a) arranged in a V-shaped layout, the initial material to attenuate the X-ray beam is a diamond disc at an incidence angle of about 2°. A camera setup is used to monitor the fluorescence signal caused by the X-ray beam incident on the diamond.
Figure 9Schematic of an aerosol injector. The droplets are formed inside the aerosolization chamber from the Rayleigh instability in a thin liquid jet originating from a flow focusing nozzle. The gas necessary for the flow focusing is further used both to create an atmosphere where the droplets are able to evaporate and to provide the stream-lines inside the aerodynamic lens used to focus the particles into a narrow beam. Between the aerosolization chamber and the lens stack, a nozzle-skimmer stage is inserted to limit the gas load inside the lens stack. Adapted from Hantke et al. (2018 ▸).
Figure 10Example serial crystallography data taken using the AGIPD 1Mpx during early user experiments at SPB/SFX. Note the well defined Bragg peaks that span a large fraction of the detector’s dynamic range. This figure was originally published in (a) Grünbein et al. (2018a ▸) and (b) Wiedorn et al. (2018 ▸) and is licenced under a Creative Commons Attribution 4.0 International Licence.
Figure 11(a) Mechanical design of the AGIPD 1Mpx detector inside its vacuum tank. The detector consists of four movable quadrants, which are predominantly moved in an iris fashion to adjust the central hole size. Each quadrant in turn consists of four AGIPD FEMs. (b) CAD-model of the AGIPD in its most upstream position (sample-to-detector distance ∼120 mm). The compressed bellows can also be seen between the sample chamber and the AGIPD vacuum chamber. The sample chamber is deliberately shown empty so one can see the AGIPD sensors (in green) that detect the X-ray photons.
Description of basic laser parameters
The 800 nm source is tunable from 750 to 850 nm (longer than 15 fs).
| Wavelength λ | 800 nm | 1030 nm |
| Pulse duration (FWHM) | 15–300 fs (nearly Fourier-transform-limited) | <1 ps or 400 ps (chirped) |
Laser set points
| Set point | Repetition rate (MHz) | E1030 nm (mJ) | E800 nm (mJ) |
|---|---|---|---|
| 1 | 4.5 | 1 | 0.05 |
| 2 | 1.13 | 4 | 0.3 |
| 3 | 0.188 | 21 | 1.5 |
| 4 | 0.1 | 40 | 2.5 |
Figure 12Laser optics layout in the SPB/SFX instrument laser hutch (ILH) for the upstream interaction region (IRU). The optics table size is 1500 mm × 3000 mm (h × w) (left area) and 3600 mm × 1500 mm (h × w) (right area). Beam from the SASE1 common pump laser installed in the central laser hutch (CLH) enters from the left. The optical path to IRU exits top left, and transport of the common pump laser to the optical table for the downstream interaction region (IRD) is shown at the top.