I. A. Vartanyants
National Research Nuclear University MEPhI
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Featured researches published by I. A. Vartanyants.
Nature | 2006
Mark August Pfeifer; Garth J. Williams; I. A. Vartanyants; Ross Harder; Ian K. Robinson
Coherent X-ray diffraction imaging is a rapidly advancing form of microscopy: diffraction patterns, measured using the latest third-generation synchrotron radiation sources, can be inverted to obtain full three-dimensional images of the interior density within nanocrystals. Diffraction from an ideal crystal lattice results in an identical copy of this continuous diffraction pattern at every Bragg peak. This symmetry is broken by the presence of strain fields, which arise from the epitaxial contact forces that are inevitable whenever nanocrystals are prepared on a substrate. When strain is present, the diffraction copies at different Bragg peaks are no longer identical and contain additional information, appearing as broken local inversion symmetry about each Bragg point. Here we show that one such pattern can nevertheless be inverted to obtain a ‘complex’ crystal density, whose phase encodes a projection of the lattice deformation. A lead nanocrystal was crystallized in ultrahigh vacuum from a droplet on a silica substrate and equilibrated close to its melting point. A three-dimensional image of the density, obtained by inversion of the coherent X-ray diffraction, shows the expected facetted morphology, but in addition reveals a real-space phase that is consistent with the three-dimensional evolution of a deformation field arising from interfacial contact forces. Quantitative three-dimensional imaging of lattice strain on the nanometre scale will have profound consequences for our fundamental understanding of grain interactions and defects in crystalline materials. Our method of measuring and inverting diffraction patterns from nanocrystals represents a vital step towards the ultimate goal of atomic resolution single-molecule imaging that is a prominent justification for development of X-ray free-electron lasers.
Applied Physics Letters | 2010
Andreas Schropp; Pit Boye; J. M. Feldkamp; Robert Hoppe; Jens Patommel; Dirk Samberg; Sandra Stephan; K. Giewekemeyer; R. N. Wilke; Tim Salditt; J. Gulden; Adrian P. Mancuso; I. A. Vartanyants; E. Weckert; Sebastian Schöder; Manfred Burghammer; C. G. Schroer
We have carried out a ptychographic scanning coherent diffraction imaging experiment on a test object in order to characterize the hard x-ray nanobeam in a scanning x-ray microscope. In addition to a high resolution image of the test object, a detailed quantitative picture of the complex wave field in the nanofocus is obtained with high spatial resolution and dynamic range. Both are the result of high statistics due to the large number of diffraction patterns. The method yields a complete description of the focus, is robust against inaccuracies in sample positioning, and requires no particular shape or prior knowledge of the test object.
New Journal of Physics | 2010
Adrian P. Mancuso; Th. Gorniak; Florian Staier; O. Yefanov; Ruth Barth; Christof Christophis; Bernd Reime; J. Gulden; A. Singer; Michala E. Pettit; Th. Nisius; Th. Wilhein; C. Gutt; G. Grübel; N. Guerassimova; Rolf Treusch; J. Feldhaus; S. Eisebitt; E. Weckert; Michael Grunze; Axel Rosenhahn; I. A. Vartanyants
Coherent x-ray imaging represents a new window to imaging non- crystalline, biological specimens at unprecedented resolutions. The advent of free-electron lasers (FEL) allows extremely high flux densities to be delivered to a specimen resulting in stronger scattered signal from these samples to be measured. In the best case scenario, the diffraction pattern is measured before the sample is destroyed by these intense pulses, as the processes involved in radiation damage may be substantially slower than the pulse duration. In this case, the scattered signal can be interpreted and reconstructed to yield a faithful image of the sample at a resolution beyond the conventional radiation damage limit. We employ coherent x-ray diffraction imaging (CXDI) using the free-electron
Review of Scientific Instruments | 2012
W. F. Schlotter; J. J. Turner; Michael Rowen; P. A. Heimann; Michael Holmes; O. Krupin; M. Messerschmidt; Stefan Moeller; J. Krzywinski; Regina Soufli; Mónica Fernández-Perea; N. Kelez; Sooheyong Lee; Ryan Coffee; G. Hays; M. Beye; N. Gerken; F. Sorgenfrei; Stefan P. Hau-Riege; L. Juha; J. Chalupsky; V. Hajkova; Adrian P. Mancuso; A. Singer; O. Yefanov; I. A. Vartanyants; Guido Cadenazzi; Brian Abbey; Keith A. Nugent; H. Sinn
The soft x-ray materials science instrument is the second operational beamline at the linac coherent light source x-ray free electron laser. The instrument operates with a photon energy range of 480-2000 eV and features a grating monochromator as well as bendable refocusing mirrors. A broad range of experimental stations may be installed to study diverse scientific topics such as: ultrafast chemistry, surface science, highly correlated electron systems, matter under extreme conditions, and laboratory astrophysics. Preliminary commissioning results are presented including the first soft x-ray single-shot energy spectrum from a free electron laser.
Physical Review B | 2010
M. Altarelli; R. P. Kurta; I. A. Vartanyants
In a recent article (P.Wochner et al., PNAS (2009)) x-ray scattering intensity correlations around a ring, in the speckle diffraction pattern of a colloidal glass, were shown to display a remarkable ~ cos(n
Structural Dynamics | 2015
Andy Aquila; A. Barty; Christoph Bostedt; Sébastien Boutet; G. A. Carini; Daniel P. DePonte; P. S. Drell; Sebastian Doniach; K. H. Downing; T. Earnest; Hans Elmlund; Veit Elser; M. Gühr; Janos Hajdu; Jerome Hastings; Stefan P. Hau-Riege; Zhirong Huang; E. E. Lattman; Filipe R. N. C. Maia; Stefano Marchesini; A. Ourmazd; C. Pellegrini; Robin Santra; Ilme Schlichting; Christian G. Schroer; John C. Spence; I. A. Vartanyants; Soichi Wakatsuki; William I. Weis; Garth J. Williams
\phi
Optics Express | 2012
A. Singer; F. Sorgenfrei; Adrian P. Mancuso; N. Gerasimova; Oleksandr Yefanov; J. Gulden; Thomas Gorniak; Tobias Senkbeil; A. Sakdinawat; Yongmin Liu; David T. Attwood; S. Dziarzhytski; D. D. Mai; Rolf Treusch; E. Weckert; Tim Salditt; Axel Rosenhahn; W. Wurth; I. A. Vartanyants
) dependence on the angular coordinate
Physical Review E | 2012
U. Lorenz; N M Kabachnik; E. Weckert; I. A. Vartanyants
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Optics Express | 2011
Thomas Gorniak; R. Heine; Adrian P. Mancuso; Florian Staier; Christof Christophis; Michala E. Pettitt; A. Sakdinawat; Rolf Treusch; N. Guerassimova; J. Feldhaus; C. Gutt; G. Grübel; S. Eisebitt; André Beyer; Armin Gölzhäuser; E. Weckert; Michael Grunze; I. A. Vartanyants; Axel Rosenhahn
around the ring, with integer index n depending on the magnitude of the scattering wavevector. With an analytical derivation that preserves full generality in the Fraunhofer diffraction limit, we clarify the relationship of this result to previous x-ray studies of bond-orientation order, and provide a sound basis to the statement that the angular intensity correlations deliver information on local bond arrangements in a disordered (or partially ordered) system. We present a detailed analysis of the angular cross-correlation function and show its applicability for studies of wide range of structural properties of disordered systems, from local structure to spatial correlations between distant structural elements.
Scientific Data | 2016
Anna Munke; Jakob Andreasson; Andrew Aquila; Salah Awel; Kartik Ayyer; Anton Barty; Richard Bean; Peter Berntsen; Johan Bielecki; Sébastien Boutet; Maximilian Bucher; Henry N. Chapman; Benedikt J. Daurer; Hasan Demirci; Veit Elser; Petra Fromme; Janos Hajdu; Max F. Hantke; Akifumi Higashiura; Brenda G. Hogue; Ahmad Hosseinizadeh; Yoonhee Kim; Richard A. Kirian; Hemanth K. N. Reddy; Ti Yen Lan; Daniel S. D. Larsson; Haiguang Liu; N. Duane Loh; Filipe R. N. C. Maia; Adrian P. Mancuso
Intense femtosecond x-ray pulses from free-electron laser sources allow the imaging of individual particles in a single shot. Early experiments at the Linac Coherent Light Source (LCLS) have led to rapid progress in the field and, so far, coherent diffractive images have been recorded from biological specimens, aerosols, and quantum systems with a few-tens-of-nanometers resolution. In March 2014, LCLS held a workshop to discuss the scientific and technical challenges for reaching the ultimate goal of atomic resolution with single-shot coherent diffractive imaging. This paper summarizes the workshop findings and presents the roadmap toward reaching atomic resolution, 3D imaging at free-electron laser sources.