Electron storage ring BESSY as a source of calculable spectral photon flux in the x‐ray region

1992 ◽  
Vol 63 (1) ◽  
pp. 1539-1542 ◽  
Author(s):  
D. Arnold ◽  
G. Ulm
Author(s):  
A. Zholents ◽  
J. Byrd ◽  
S. Chattopadhyay ◽  
H. Chong ◽  
T.E. Glover ◽  
...  
Keyword(s):  

1985 ◽  
Vol 138 (3) ◽  
pp. 279-284 ◽  
Author(s):  
G. Schmahl ◽  
B. Niemann ◽  
D. Rudolph ◽  
P. Guttmann ◽  
V. Sarafis

1981 ◽  
Vol 59 (11) ◽  
pp. 1811-1816
Author(s):  
J. B. A. Mitchell ◽  
J. Wm. McGowan ◽  
G. M. Bancroft

The 10 GeV CHEER electron storage ring will produce more than 1 MW of synchrotron radiation per turn with photon energies extending from the far infrared to the hard X-ray region. The critical energy of the synchrotron radiation spectrum will be 22 keV.Applications of hard X-rays to materials analysis are described and a discussion of some of the problems which will be encountered in implementing a synchrotron radiation facility at CHEER is presented.


2002 ◽  
Vol 30 (9) ◽  
pp. 531-537 ◽  
Author(s):  
Takahiro INOUE ◽  
Shuji MIYAMOTO ◽  
Sho AMANO ◽  
Takayasu MOCHIZUKI ◽  
Mitsuyasu YATSUZUKA

IUCrJ ◽  
2021 ◽  
Vol 8 (1) ◽  
pp. 124-130
Author(s):  
Wonhyuk Jo ◽  
Fabian Westermeier ◽  
Rustam Rysov ◽  
Olaf Leupold ◽  
Florian Schulz ◽  
...  

X-ray photon correlation spectroscopy (XPCS) is a routine technique to study slow dynamics in complex systems at storage-ring sources. Achieving nanosecond time resolution with the conventional XPCS technique is, however, still an experimentally challenging task requiring fast detectors and sufficient photon flux. Here, the result of a nanosecond XPCS study of fast colloidal dynamics is shown by employing an adaptive gain integrating pixel detector (AGIPD) operated at frame rates of the intrinsic pulse structure of the storage ring. Correlation functions from single-pulse speckle patterns with the shortest correlation time of 192 ns have been calculated. These studies provide an important step towards routine fast XPCS studies at storage rings.


2020 ◽  
Vol 27 (6) ◽  
pp. 1662-1673
Author(s):  
Valentina Bonino ◽  
Daniele Torsello ◽  
Carmelo Prestipino ◽  
Lorenzo Mino ◽  
Marco Truccato

X-ray synchrotron sources, possessing high power density, nanometric spot size and short pulse duration, are extending their application frontiers up to the exploration of direct matter modification. In this field, the use of atomistic and continuum models is now becoming fundamental in the simulation of the photoinduced excitation states and eventually in the phase transition triggered by intense X-rays. In this work, the X-ray heating phenomenon is studied by coupling the Monte Carlo method (MC) with the Fourier heat equation, to first calculate the distribution of the energy absorbed by the systems and finally to predict the heating distribution and evolution. The results of the proposed model are also compared with those obtained removing the explicit definition of the energy distribution, as calculated by the MC. A good approximation of experimental thermal measurements produced irradiating a millimetric glass bead is found for both of the proposed models. A further step towards more complex systems is carried out, including in the models the different time patterns of the source, as determined by the filling modes of the synchrotron storage ring. The two models are applied in three prediction cases, in which the heating produced in Bi2Sr2CaCu2O8+δ microcrystals by means of nanopatterning experiments with intense hard X-ray nanobeams is calculated. It is demonstrated that the temperature evolution is strictly connected to the filling mode of the storage ring. By coupling the MC with the heat equation, X-ray pulses that are 48 ps long, possessing an instantaneous photon flux of ∼44 × 1013 photons s−1, were found to be able to induce a maximum temperature increase of 42 K, after a time of 350 ps. Inversely, by ignoring the energy redistribution calculated with the MC, peaks temperatures up to hundreds of degrees higher were found. These results highlight the importance of the energy redistribution operated by primary and secondary electrons in the theoretical simulation of the X-ray heating effects.


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