

research papers

Thermal behavior of single-crystal scintillators for high-speed X-ray imaging
aAdvanced Photon Source, Argonne National Laboratory, 9700 South Cass Avenue, Argonne,
IL 60439, USA
*Correspondence e-mail: [email protected]
Indirect detection of X-rays using single-crystal scintillators is a common approach for high-resolution X-ray imaging. With the high X-ray
available from synchrotron sources and recent advances in high-speed visible-light cameras, these measurements are increasingly used to obtain time-resolved images of dynamic phenomena. The X-ray on the scintillator must, in many cases, be limited to avoid thermal damage and failure of the scintillator, which in turn limits the obtainable light levels from the scintillator. In this study, a transient one-dimensional numerical simulation of the temperature and stresses within three common scintillator crystals (YAG, LuAG and LSO) used for high-speed X-ray imaging is presented. Various conditions of thermal loading and convective cooling are also presented.Keywords: scintillators; X-ray imaging; thermal behaviour.
1. Introduction
A common method for high-resolution X-ray imaging at synchrotrons is indirect imaging
with single-crystal scintillators (Bonse & Busch, 1996; Koch et al., 1998
). The X-ray beam illuminates the scintillator, which is in turn imaged with visible-light
microscopy. This method can provide resolutions below 1 µm, which is better than existing
detectors which detect X-rays directly or use phosphor powders (Martin & Koch, 2006
). Scintillators are also highly resistant to radiation damage, and this method takes
advantage of easily available visible-light microscopy hardware.
A particularly compelling application of X-ray imaging is to study dynamic phenomena,
including applications as diverse as the fluid dynamics of fuel injection and sprays
(Moon et al., 2014; Halls et al., 2017
), mechanical motions inside devices (Baimpas et al., 2013
), the flow of blood in blood vessels (Jamison et al., 2012
), shock-wave propagation (Olbinado et al., 2017
) and the dynamics of metallic foam formation (Rack et al., 2009
). To study highly dynamic phenomena, where fast framing rates and short exposure
times are essential, a high visible light output from the scintillator is essential,
necessitating an intense X-ray beam. White beam, either from a bending magnet or an
undulator, is typically used to provide the high X-ray needed for such experiments. However, only a small fraction of the X-ray energy absorbed
by the scintillator is emitted as visible light, resulting in significant heating
of the scintillator. As this heating occurs in a thin crystal of modest dimensions,
significant increases in temperature can be expected.
Heating of the scintillator material can have detrimental effects. Anecdotally, it
is known that excessive X-ray illumination can lead to cracking of the scintillators,
which are typically single crystals and hence quite brittle. Moreover, scintillator
light output is dependent on temperature (Yanagida et al., 2013). As such, if significant temperature gradients exist in scintillators, the resulting
image will not faithfully reflect the distribution of in the sample, distorting the resulting images. There appears to be little, if any,
work in the literature quantifying the heating experienced by scintillators in high-intensity
X-ray beams, nor analysis of the resulting stresses in the scintillators.
In the current work, one-dimensional transient thermal simulations are conducted on three commonly used single-crystal scintillator materials: YAG, LuAG and LSO. Simulations have been performed for both filtered and unfiltered white-beam illumination for a range of scintillator thicknesses and convective heat-transfer coefficients. In addition, the thermal stresses caused by the heating of the scintillator have been calculated and compared with the ultimate stress of the scintillator materials.
2. Methods
To simulate the temperatures and stresses in scintillator crystals during illumination
from a synchrotron X-ray beam, transient axisymmetric one-dimensional numerical simulations
have been undertaken. As such, temperature is a function of radial position r and time t. For these simulations, a finite volume approach has been taken. A schematic of the
simulation setup is given in Fig. 1. The heat transfer and temperature distributions are assumed to be axisymmetric.
The temperature of the outer boundary of the scintillator (r = R) is fixed, as might be expected for a scintillator mounted onto a highly conductive
metal holder. Each element of the discretized domain experiences radial heat conduction,
convective heat transfer from both free faces to the surroundings and radiative heat
transfer from both free faces. An explicit numerical method was used to step through
time, using a predictor–corrector approach to improve accuracy. Pertinent parameters
of the simulation are given in Table 1
; although these values are representative of imaging experiments at the 7-BM beamline
of the Advanced Photon Source (APS), the dimensions are similar to those used at other
synchrotron beamlines.
|
![]() |
Figure 1 Simulation setup |
The simulations were initiated with the scintillator at the same temperature as the
surroundings (300 K). A region in the center of the scintillator was then subjected
to a heat generation qgen due to absorption of the X-ray beam. To provide relevant parameters for illumination,
the heat loading per unit illuminated area was calculated in XOP (Sánchez del Rio & Dejus, 2011) for absorption of the beam from an APS bending magnet at a position 35 m from the
source through an aperture 1 mm × 1 mm in size. Two illumination conditions were simulated
for each scintillator material and thickness combination. One is a relatively unfiltered
bending-magnet white beam (filtered only with 750 µm of beryllium from the beamline
windows). This corresponds to illumination used for high-speed imaging. The second
condition used illumination additionally filtered with a 250 µm-thick copper filter.
This is a typical configuration used for hard X-ray tomography of dense samples at
the APS 7-BM beamline.
Several validation steps were undertaken to ensure the accuracy of the numerical scheme. The results of a simulation without convection or radiation matched the temperature distribution calculated from an analytical solution to the heat-conduction equations. For a scintillator with an initial temperature higher than the surroundings, the rate of cooling with radiative and conductive heat transfer but no conduction matched analytical calculations. Tests of convergence in terms of spatial and temporal discretization were also performed and the simulations were found to be well converged with the discretization used. It should be noted that the time step was limited by the stability of the explicit scheme used, not the accuracy of the solution.
Three scintillator materials were simulated in this work. The first is YAG, which
has been widely used in X-ray imaging applications for many years. YAG is hard, stable
and has a relatively short et al., 2016), which is essential for high-speed imaging, though it has a relatively low effective
Z, limiting its ability to absorb high-energy X-rays. The second material is LuAG,
which shares many properties with YAG, but with a higher effective Z. The for LuAG is relatively long, which limits its use for high-speed applications (Rutherford
et al., 2016
). The final material is LSO. Both LSO and LYSO are fast, high-Z scintillators with high light output, making them attractive for high-speed imaging
applications. While LYSO arguably sees more use for imaging applications, far more
of the physical property data required for these simulations were available in the
literature for LSO than LYSO, which is chemically similar to LYSO. All of these materials
are doped with cerium for use as scintillators; this doping was ignored for this work,
given the paucity of quantitative data on the cerium loading of the different crystals
and the potential for variations between scintillator suppliers.
Several assumptions have been made in this analysis. This analysis has ignored the
energy emitted by the scintillator as light. This tends to be a relatively small fraction
of the total energy input from the X-ray beam, and the literature regarding absolute
light output of scintillators tends to be somewhat inconsistent. This analysis also
ignores temperature and stress variations through the thickness of the scintillator.
While this should be a good assumption for thin scintillators, it may break down for
thicker scintillators, particularly under unfiltered white-beam illumination. Fig.
2 shows the energy deposition versus depth in the scintillator for YAG with both unfiltered
and filtered illumination based on XOP simulations. The surface illuminated by the
beam experiences the greatest degree of heating. The heating rapidly diminishes for
unfiltered illumination but diminishes much more slowly for filtered illumination.
![]() |
Figure 2 Energy deposition versus depth in the scintillator for YAG under both unfiltered and filtered WB illumination. |
The properties of the scintillators are also assumed to be constant with temperature, which will not be correct for scintillators experiencing large heating effects. The scintillators are also assumed to be isotropic materials. This is not true for LSO in particular, but greatly eases the analysis, as it allows the problem to be treated as a 1D transient heat transfer problem, rather than 2D. It should also be noted that the fixed temperature at the rim of the scintillator may not hold in practice under intense illumination, depending on the
of the holder and the quality of the thermal contact between the scintillator and holder.Once the temperature distribution of the scintillator as a function of time has been
found, an analysis of the thermal stresses of the scintillator can also be performed.
Again, the scintillator properties are assumed to be both isotropic and constant with
temperature. It is further assumed that the scintillator undergoes plane stress and
does not buckle (i.e. the scintillator remains flat). For an axisymmetric sample undergoing thermal stress,
the radial displacement u of the material as a function of r is given by (Bickford, 1998)
In this equation, α is the linear coefficient, ν is Poisson's ratio, T is the temperature difference between the scintillator at radius r and the surroundings and C is a constant that can be solved by assuming zero radial stress at the edge of the scintillator. The term uT is used to collect all terms explicitly dependent on the scintillator temperature distribution. This can be solved for the radial and circumferential stresses (σr and σθ, respectively), using E as the elastic modulus of the scintillator as
Several material properties are needed for the scintillators to complete the thermal
simulation. These include . It should be noted that for the most part these properties are for undoped parent
scintillator materials (finding relevant properties in the literature on the doped
crystals was quite challenging). The values for some of the mechanical properties
have been assumed based on similar crystals due to the challenges of finding reliable
mechanical property data for certain crystals. Poisson's ratio for all crystals is
assumed to be 0.25, which matches the values found in the literature for YAG (Monteseguro
et al., 2015
). Given the potential variability in mechanical properties depending on crystal growth
and processing between suppliers, the aforementioned assumptions seem unlikely to
materially add to the error in this analysis.
|
|
|
|
|
|
3. Results
Plots of the radial temperature distribution versus time with unfiltered white-beam
illumination for the three scintillator materials are given in Fig. 3 for a scintillator thickness of 100 µm and an illuminated region 0.5 mm in radius.
For these data, no convective cooling was permitted; these data represent the behavior
of scintillators in a vacuum chamber. Several trends are evident. At short times,
heating occurs only in the center of the scintillator, corresponding to the region
illuminated by the X-ray beam. As time progresses, heat conduction causes warming
of the surrounding regions as well. A majority of the heating occurs within the first
second of illumination; after 5–10 s of illumination, the temperature distribution
can largely be considered steady-state. The sharpest temperature gradients are found
near the edge of the illuminated region (r = 0.5 mm). Overall, the temperature gradients are modest, indicating that thermal
conduction effectively smooths the temperature gradients. It thus seems likely that
the neglect of thermal gradients through the scintillator thickness is well justified.
![]() |
Figure 3 Radial distribution of scintillator temperature versus time for unfiltered white-beam illumination, 0.5 mm illuminated radius, 100 µm scintillator thickness for (a) YAG, (b) LuAG and (c) LSO. |
All scintillators show significant degrees of heating. YAG undergoes the least heating, with significantly greater heating for LuAG. The temperature rise of the LSO crystal is, by comparison, quite remarkable. These trends, which were seen throughout the simulations, were a consequence of two factors. First, LuAG and LSO have significantly greater X-ray absorption than YAG and, as such, absorb significantly more X-ray
Second, the thermal diffusivity of YAG is somewhat higher than LuAG, which is in turn far higher than that of LSO. Lower values of thermal diffusivity inhibit the conduction of heat away from the illuminated region and into the scintillator holder, leading to higher temperatures throughout the scintillator. The combination of these two factors leads to the dramatically higher temperatures for LSO compared with YAG and LuAG. It should be noted that these degrees of temperature rise call into question the assumption of constant mechanical and thermal properties used for this analysis.Fig. 4 shows the temperature at the center of the scintillators as a function of time under
white-beam illumination for various scintillator thicknesses. As shown in Fig. 3
, the YAG scintillator demonstrates the lowest temperatures, followed by LuAG, with
LSO demonstrating the highest temperatures. For all thicknesses, the vast majority
of the heating is complete within 5 s of the onset of illumination. The time period
of the thermal transient is weakly dependent on thickness, with thicker scintillators
reaching thermal equilibrium more slowly.
![]() |
Figure 4 Centerline scintillator temperature versus time for various scintillator thicknesses. Unfiltered white-beam illumination, 0.5 mm illuminated radius for (a) YAG, (b) LuAG and (c) LSO. |
The thickness also clearly has a significant impact on the scintillator temperature.
Except for LSO, the thinnest scintillators show the highest temperatures. This is
tied directly to the absorption of the beam by the scintillator. As Fig. 2 demonstrates, the illuminated surface of the scintillator experiences the greatest
X-ray especially for unfiltered white beam. As scintillator thickness increases, attenuation
of the beam causes the amount of heat deposition to increase more slowly than the
thickness, while the cross-sectional area available for conduction increases linearly
with thickness. Thus, the added thermal loading for thicker scintillators is more
than compensated for by the greater cross-sectional area available for heat conduction,
leading to lower overall temperatures than for thinner scintillators.
The temperature history of the scintillators is quite different when the illumination
is filtered. Fig. 5 shows the centerline time history for the scintillators, like in Fig. 4
, but with filtered white-beam illumination. The temperatures of the different thicknesses
are much lower than for unfiltered beam, which is expected due to the lower heat load.
The temperatures for the different thicknesses are all much closer to each other than
in Fig. 4
. This is again logical; as shown in Fig. 2
, the total heat loading will increase nearly linearly with additional thickness,
nearly balancing the effect of greater cross sectional area for conduction. The thinner
scintillators still show a slightly faster approach to thermal equilibrium than thicker
scintillators. The highest temperatures are no longer seen in the thinnest scintillators,
which is probably the result of radiative losses at the surface of the scintillator,
which play a greater role for the thinner scintillators. Despite the filtering, however,
the LSO scintillator still shows a significant temperature rise due to illumination
by the X-ray beam.
![]() |
Figure 5 Centerline scintillator temperature versus time for various scintillator thicknesses. Filtered white-beam illumination, 0.5 mm illuminated radius for (a) YAG, (b) LuAG and (c) LSO. |
One of the major concerns with the heating of scintillators is fracture of the scintillators
due to thermal stresses. Fig. 6 shows the thermal stress as a function of r for the three scintillators with and without filtering of the illumination 10 s after
the start of illumination (i.e. virtually steady-state). The stress distribution is compressive near the center of
the scintillator, with tensile stresses near the edge. This is logical, since the
center of the scintillator expands due to heating much more than the edges. The highest
stress magnitudes are consistently found in the center of the scintillator. The trends
in the stress magnitude follow the trends in temperature: the highest stresses are
found for LSO, the next highest for LuAG and the lowest stresses for YAG.
![]() |
Figure 6 Steady-state radial and circumferential thermal stress for 100 µm-thick scintillators under (a) unfiltered and (b) filtered white-beam illumination. No convective heat transfer, 0.5 mm illuminated radius. |
These results help to explain the anecdotal finding that LSO is more easily damaged
by intense illumination than LuAG or YAG. The stress magnitude is much greater in
LSO than the other crystals. As shown in Table 7, the ultimate strength of LSO is also much lower than YAG. As such, LSO will fracture
at a much lower level of illumination than the other crystals. Even with filtered
illumination, the compressive stresses at the center of the LSO crystal are a significant
fraction of the crystal's ultimate strength. Furthermore, the anisotropic material
properties of LSO may add additional stress to the crystal beyond what is shown in
this analysis, which assumes isotropic material properties.
As might be expected, illumination over a larger area leads to higher temperatures
and stresses. Fig. 7 shows the centerline temperature history for YAG and LSO; the behavior for LuAG is
intermediate between these two examples. The steady-state stress for all three scintillators
with illumination over a region 2 mm in diameter can be seen in Fig. 8
, compared with the 1 mm illumination diameter in Fig. 6
. The temperature rise of the scintillator is much higher than for the 1 mm illumination
diameter. The stress fields also become much larger in magnitude. For unfiltered beam,
the peak stress magnitude is now a large fraction of the ultimate stress of LuAG.
For filtered beam, the peak stress of the LSO crystal is approximately half of the
ultimate stress of the crystal. Given the potential errors due to the assumptions
underpinning this analysis (isotropic material properties, fixed outer rim temperature),
failure of LSO under constant filtered beam illumination is a distinct possibility.
![]() |
Figure 7 Centerline scintillator temperature versus time for various scintillator thicknesses. Unfiltered white-beam illumination, 1.0 mm illuminated radius for (a) YAG and (b) LSO. |
![]() |
Figure 8 Steady-state radial and circumferential thermal stress for 100 µm-thick scintillators under (a) unfiltered and (b) filtered white-beam illumination. No convective heat transfer, 1.0 mm illuminated radius. |
The previous results have all assumed no convective cooling of the scintillators,
such as would be found in vacuum operation. In normal use, scintillators are used
in air or another gas environment, raising the possibility of either natural or forced
convective cooling of the scintillator. Figs. 9(a)–9(c) show the time history of the radial temperature distribution with various convective
heat-transfer coefficients for a YAG scintillator, and can be compared with Fig. 3
(a), which shows the same case with no convective heat transfer; the trends are similar
for other scintillators. The addition of h = 100 W m−2 K−1 convective heat transfer slightly decreases the ultimate temperature of the scintillator.
The effects become more significant at 300 W m−2 K−1. Convective heat transfer has three major effects. First, the peak temperature in
the scintillator is reduced. Second, the temperature of the unilluminated region of
the crystal becomes much closer to the ambient temperature. Third, the time evolution
of the temperature distribution becomes much more rapid. The heating of the crystal
at short timescales (<0.1 s) is barely affected by the convective cooling. However,
the heating process largely ends by 0.5 s after the start of illumination.
![]() |
Figure 9 Centerline scintillator temperature versus time for various convective heat transfer coefficients. Unfiltered white-beam illumination, 0.5 mm illuminated radius, YAG scintillator, 100 µm thickness for h (W m−2 K−1) = (a) 100, (b) 300 and (c) 1000. |
Fig. 10 shows the time history of the centerline temperature for various YAG scintillator
thicknesses for h = 300 W m−2 K−1 convective heat-transfer coefficient. When compared with Fig. 4
(a), the temperatures are all lower; this effect is quite dramatic for the thinner scintillators.
Convection occurs only on the surfaces of the scintillator, and as such is quite effective
at cooling thin scintillators, while having a more minor effect for thicker scintillators.
This reduction in heating significantly reduces the stresses within the crystals,
especially for thin crystals, as shown in Fig. 11
.
![]() |
Figure 10 Centerline scintillator temperature versus time for various scintillator thicknesses. Unfiltered white-beam illumination, 0.5 mm illuminated radius, YAG scintillator and h = 300 W m−2 K−1. |
![]() |
Figure 11 Circumferential stress for various scintillator thicknesses. Unfiltered white-beam illumination, 0.5 mm illuminated radius, YAG scintillator for (a) h = 0 W m−2 K−1 and (b) h = 300 W m−2 K−1. |
4. Discussion
While the previous results show clearly that thermal loading due to intense synchrotron beams can lead to the mechanical failure of scintillators, a further issue is changes in the scintillator light output as a result of temperature changes. For example, if a fast shutter is used to control the illumination of the scintillator, heating of the scintillator can cause temporal drifts in the scintillator light output. If one attempts to image dynamic phenomena, such temporal drifts in light conversion efficiency of the scintillator will make quantitative absorption measurements of dynamic systems difficult.
Relatively little published data exist regarding the sensitivity of scintillator light
output to temperature effects. Existing literature data suggest that YAG shows a decrease
in light output for a given illumination as temperature increases above room temperature,
though LuAG:Pr shows an increase in light output at moderately elevated temperatures,
which may also occur for LuAG:Ce (Yanagida et al., 2013). Given the temperature gradients in the scintillators, this should appear as non-uniform
light output. An example to demonstrate such effects is shown in Fig. 12
, taken from a series of liquid spray images. White beam from an APS bending magnet
at the 7-BM beamline was filtered with 750 µm beryllium (from beamline windows), then
illuminated a 100 µm-thick, 12 mm-diameter LuAG:Ce scintillator located 36 m from
the X-ray source. A Photron SA-4 high-speed camera recorded images of the scintillator
for a time period of 3 s after the beamline shutter was opened. As the scintillator
was illuminated, the light output in the center of the scintillator first increased
slightly, then decreased markedly, as would be expected from the previous results.
In this case, the scintillator is clearly undergoing a great deal of heating in the
center of the illuminated area. After further filtering this beam with 500 µm of silicon,
the beam was allowed to illuminate the scintillator for a longer period of time; the
crystal mechanically failed after approximately 10 s of illumination.
![]() |
Figure 12 Images of scintillator output when exposed to an intense X-ray beam. LuAG scintillator, 100 µm thickness, 12 mm diameter, located 36 m from the X-ray source. Illumination from unfiltered APS bending-magnet white beam (beam size 3.15 mm × 3.15 mm). Images were recorded after the start of illumination of (a) 0.1 s, (b) 1.0 s, (c) 1.5 s, (d) 2.0 s and (e) 3.0 s. |
Several strategies exist to mitigate changes in light output caused by heating, though they have drawbacks. Fast shuttering of the X-ray beam can limit thermal effects by limiting the total energy deposited in the scintillator, and has been applied quite successfully at some beamlines, though this limits the time duration over which imaging can be performed. Thicker scintillators suffer less heating and lower thermal stresses, but limit the resolution possible with an imaging system. The use of more thermally stable scintillators can allow for greater illumination of the scintillator without thermal damage. Filtering of the incident beam is also helpful, but changes the signal level and spectrum (for polychromatic beams).
Convective cooling provides an alternative method to combat beam-induced heating.
While ineffective for short pulses of X-rays, it can significantly reduce scintillator
temperatures for longer exposure imaging, especially for thin scintillators. The convective
heat-transfer coefficients simulated in this work are high, but can be reasonably
achieved with the impingement of a gas jet on the scintillators (Yan & Saniei, 1997). Moreover, recent work (Zhou et al., 2018
) suggests that purging around scintillators can prevent soiling of the scintillators. By directing this
gas flow appropriately, it could be used for both maintaining scintillator cleanliness
and providing active cooling.
It is clear from the above results that heating effects are especially severe for thin scintillators unless steps are taken to reduce thermal loading. This is unfortunate, since thin scintillators are preferred for high-resolution imaging due to the limited depth of field of high-magnification microscopes. Thin scintillators cannot absorb as much of a high-energy X-ray beam as thick scintillators, so a potential avenue to achieve adequate light output for time-resolved measurements at high spatial resolution is to use a more intense X-ray beam. These simulations show that such approaches must be taken with great care to avoid thermal damage to the scintillator.
5. Conclusions
Finite-volume simulations of the thermal response of three common X-ray scintillator materials to both filtered and unfiltered white-beam illumination have been performed. The simulations included the influence of thermal conduction, convection and radiation. Across all simulations, YAG experienced the lowest degree of heating, followed by LuAG, with LSO experiencing by far the highest degree of heating; this is directly tied to the absorption and heat transfer properties of the scintillator materials. For unfiltered beam, thinner scintillators experienced the greatest degree of heating, while this effect is greatly reduced with filtering of the incident beam. The degree of heating is such that stress levels exceeding the ultimate stress of the scintillator materials can be induced. The introduction of convective cooling can reduce the heating seen in the scintillators, especially for thin scintillators, though high levels of convection are needed to achieve such cooling.
Acknowledgements
The author would like to thank Katarzyna Matusik from the Argonne X-ray Science Division for discussions of this work and assistance in obtaining the images in Fig. 12.
Funding information
The measurements in this work were conducted at the 7-BM beamline of the Advanced Photon Source and were supported by the US Department of Energy (DOE), Office of Science, Office of Basic Energy Sciences (Contract No. DE-AC02-06CH11357).
References
Aggarwal, R. L., Ripin, D. J., Ochoa, J. R. & Fan, T. Y. (2005). J. Appl. Phys., 98, 103514. CrossRef Google Scholar
Baimpas, N., Drakopoulos, M., Connolley, T., Song, X., Pandazaras, C. & Korsunsky,
A. M. (2013). J. Synchrotron Rad. 20, 316–323. Web of Science CrossRef CAS IUCr Journals Google Scholar
Bickford, W. (1998). Advanced Mechanics of Materials. Menlo Park, CA: Longman. Google Scholar
Bonse, U. & Busch, F. (1996). Prog. Biophys. Mol. Biol., 65, 133–169. CrossRef Google Scholar
Cong, H., Zhang, H., Wang, J., Yu, W., Fan, J., Cheng, X., Sun, S., Zhang, J., Lu,
Q., Jiang, C. & Boughton, R. I. (2009). J. Appl. Cryst. 42, 284–294. CrossRef IUCr Journals Google Scholar
Fu, Y., Li, J., Wang, C., Xie, T., Li, W., Wu, L. & Pan, Y. (2016). J. Alloy. Compd, 664, 595–601. CrossRef Google Scholar
Halls, B. R., Radke, C. D., Reuter, B. J., Kastengren, A. L., Gord, J. R. & Meyer,
T. R. (2017). Opt. Express, 25, 1605. CrossRef Google Scholar
Jamison, R. A., Siu, K. K. W., Dubsky, S., Armitage, J. A. & Fouras, A. (2012). J. Synchrotron Rad. 19, 1050–1055. Web of Science CrossRef CAS IUCr Journals Google Scholar
Koch, A., Raven, C., Spanne, P. & Snigirev, A. (1998). J. Opt. Soc. Am. A, 15, 1940. Web of Science CrossRef Google Scholar
Kuwano, Y., Sudo, K., Ishizawa, N. & Yamada, T. (2004). J. Cryst. Growth, 260, 159–165. CrossRef Google Scholar
Marion, J. (1985). Appl. Phys. Lett. 47, 694–696. CrossRef Google Scholar
Martin, T. & Koch, A. (2006). J. Synchrotron Rad. 13, 180–194. Web of Science CrossRef CAS IUCr Journals Google Scholar
Monteseguro, V., Rodriguez-Hernandez, P. & Munoz, A. (2015). J. Appl. Phys. 118, 245902. CrossRef Google Scholar
Moon, S., Gao, Y., Wang, J., Fezzaa, K. & Tsujimura, T. (2014). Fuel, 133, 299–309. CrossRef CAS Google Scholar
Olbinado, M. P., Just, X., Gelet, J-.L., Lhuissier, P., Scheel, M., Vagovic, P., Sato,
T., Graceffa, R., Schulz, J., Mancuso, A., Morse, J. & Rack, A. (2017). Opt. Express, 25, 13857–13871. CrossRef Google Scholar
Rack, A., García-Moreno, F., Baumbach, T. & Banhart, J. (2009). J. Synchrotron Rad. 16, 432–434. Web of Science CrossRef CAS IUCr Journals Google Scholar
Rutherford, M. E., Chapman, D. J., White, T. G., Drakopoulos, M., Rack, A. & Eakins,
D. E. (2016). J. Synchrotron Rad. 23, 685–693. Web of Science CrossRef CAS IUCr Journals Google Scholar
Sánchez del Río, M. & Dejus, R. J. (2011). Proc. SPIE, 8141, 814115. Google Scholar
Scalise, L., Rinaldi, D., Davi, F. & Paone, N. (2011). Nucl. Instrum. Methods Phys. Res. B, 654, 122–126. CrossRef Google Scholar
Yanagida, T., Fijimoto, Y., Kurosawa, S., Kamada, K., Takahashi, H., Fukazawa, Y.,
Nikl, M. & Chani, V. (2013). Jpn. J. App. Phys. 52, 076401. CrossRef Google Scholar
Yan, X. & Saniei, N. (1997). Intl J. Heat Fluid Flow, 18, 591–599. CrossRef Google Scholar
Zhou, T., Wang, H., Connolley, T., Scott, S., Baker, N. & Sawhney, K. (2018). J. Synchrotron Rad. 25, 801–807. Web of Science CrossRef CAS IUCr Journals Google Scholar
This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
