| Literature DB >> 26798816 |
R A Kirian, S Awel, N Eckerskorn1, H Fleckenstein2, M Wiedorn, L Adriano3, S Bajt3, M Barthelmess2, R Bean4, K R Beyerlein2, L M G Chavas2, M Domaracky, M Heymann2, D A Horke2, J Knoska, M Metz, A Morgan2, D Oberthuer2, N Roth2, T Sato2, P L Xavier, O Yefanov2, A V Rode1, J Küpper, H N Chapman.
Abstract
A major challenge in high-resolution x-ray free-electron laser-based coherent diffractive imaging is the development of aerosol injectors that can efficiently deliver particles to the peak intensity of the focused X-ray beam. Here, we consider the use of a simple convergent-orifice nozzle for producing tightly focused beams of particles. Through optical imaging we show that 0.5 μm particles can be focused to a full-width at half maximum diameter of 4.2 μm, and we demonstrate the use of such a nozzle for injecting viruses into a micro-focused soft-X-ray FEL beam.Entities:
Year: 2015 PMID: 26798816 PMCID: PMC4711644 DOI: 10.1063/1.4922648
Source DB: PubMed Journal: Struct Dyn ISSN: 2329-7778 Impact factor: 2.920
FIG. 1.(a) Schematic of the aerosol injector assembly and convergent nozzle. Liquid drops are formed in a nebulization chamber via a gas-dynamic virtual nozzle, which then pass through a transport tube before reaching the convergent nozzle depicted in (b). Particle trajectories closely follow the gas streamlines within the convergent nozzle, which is at near-atmospheric pressure. Upon exiting the nozzle, the pressure suddenly drops, and the ejected high-speed particles follow nearly straight-line trajectories, though they may accelerate slightly upon exiting. All particles cross over the nozzle's axis of symmetry at a common focal point that varies only slightly with the initial position of the particles at the exit orifice. The slightly curved trajectories of particles exiting the nozzle are exaggerated for illustrative purposes.
FIG. 2.(a) The cross section of a ceramic injector tip obtained through x-ray tomography, which shows the 30° convergent cone and exit orifice of 100-μm diameter. (b) Image of the ceramic injector tip. (c) Image showing the nozzle mounted to the transport tube in vacuum. The end of a 400-μm-diameter fiber optic used for illuminating particles is shown to the left of the injector tip.
FIG. 3.(a) A sum of 500 exposures of 100-ns duration laser illumination, revealing streaks from 500-nm diameter particles. (b) Particle positions determined from streak intensity centroids from 43 000 images, each with 5 laser pulses.
FIG. 4.(a) and (b) Histograms formed from particle positions for 500 and 200 nm latex sphere, respectively. As described in the main text, the units of here correspond to conditions in which particles are introduced into the injector at a rate of 1 MHz. (c) and (d) Gaussian fits to the focal regions (gray boxes drawn in (a) and (b)) of the density histograms.
FIG. 5.(a) A scanning electron microscope image of granulovirus particles. (b) A single-shot diffraction pattern from an isolated granulovirus, isolated from the much greater number of aggregated particle clusters. (c) A plot of the average total diffracted x-ray photon counts as a function of injector position. Error bars indicate the standard deviation in each measurement.