scholarly journals Luminescence Efficiency of Cadmium Tungstate (CdWO4) Single Crystal for Medical Imaging Applications

Crystals ◽  
2020 ◽  
Vol 10 (6) ◽  
pp. 429
Author(s):  
Christos Michail ◽  
Vaia Koukou ◽  
Niki Martini ◽  
George Saatsakis ◽  
Nektarios Kalyvas ◽  
...  
Keyword(s):  
Medical Imaging ◽  
Single Crystal ◽  
Optical Sensors ◽  
Light Output ◽  
High Energy ◽  
Published Data ◽  
X Rays ◽  
Cadmium Tungstate ◽  
X Ray ◽  
Luminescence Efficiency

Background: In this study, the light output of a cadmium tungstate (CdWO4) single crystal was measured under various X-ray radiographic energies. Methods: A CdWO4 single crystal (10 × 10 × 10 mm3) was exposed to X-rays in the 50–130 kVp range. Measurements were evaluated against published data for single crystals of equal dimensions (CaF2:Eu and Lu3Al5O12:Ce). Since the crystal was examined for application in medical imaging detectors, the emitted optical spectrum was classified with respect to the spectral compatibility of numerous commercial optical sensors. Results: The luminescence efficiency (LE) was found to constantly increase with X-ray energy and was higher than that of CaF2:Eu for energies above 90 kVp. However, the efficiency of the previously published Lu3Al5O12:Ce was found to be constantly higher than that of CdWO4. The light emitted from CdWO4 can be optimally detected by certain charge-coupled devices (CCDs), amorphous silicon photodiodes, and photocathodes. Conclusions: The high density (7.9 g/cm3) of CdWO4 and the luminescence signal of this material make it suitable for medical imaging (such as dual energy), high-energy physics or for applications of scintillators in harsh environments.

scholarly journals Absolute Luminescence Efficiency of Europium-Doped Calcium Fluoride (CaF2:Eu) Single Crystals under X-ray Excitation

Crystals ◽  
2019 ◽  
Vol 9 (5) ◽  
pp. 234 ◽  
Author(s):  
Christos Michail ◽  
Nektarios Kalyvas ◽  
Athanasios Bakas ◽  
Konstantinos Ninos ◽  
Ioannis Sianoudis ◽  
...  
Keyword(s):  
Medical Imaging ◽  
Single Crystal ◽  
Single Crystals ◽  
Optical Sensors ◽  
Calcium Fluoride ◽  
X Rays ◽  
Silicon Photomultipliers ◽  
X Ray ◽  
Luminescence Efficiency ◽  
Radiation Sensors

The absolute luminescence efficiency (AE) of a calcium fluoride (CaF2:Eu) single crystal doped with europium was studied using X-ray energies met in general radiography. A CaF2:Eu single crystal with dimensions of 10 × 10 × 10 mm3 was irradiated by X-rays. The emission light photon intensity of the CaF2:Eu sample was evaluated by measuring AE within the X-ray range from 50 to 130 kV. The results of this work were compared with data obtained under similar conditions for the commercially employed medical imaging modalities, Bi4Ge3O12 and Lu2SiO5:Ce single crystals. The compatibility of the light emitted by the CaF2:Eu crystal, with the sensitivity of optical sensors, was also examined. The AE of the 10 × 10 × 10 mm3 CaF2:Eu crystal peaked in the range from 70 to 90 kV (22.22 efficiency units; E.U). The light emitted from CaF2:Eu is compatible with photocathodes, charge coupled devices (CCD), and silicon photomultipliers, which are used as radiation sensors in medical imaging systems. Considering the AE results in the examined energies, as well as the spectral compatibility with various photodetectors, a CaF2:Eu single crystal could be considered for radiographic applications, including the detection of charged particles and soft gamma rays.

scholarly journals On the Optical Response of Tellurium Activated Zinc Selenide ZnSe:Te Single Crystal

Crystals ◽  
2020 ◽  
Vol 10 (11) ◽  
pp. 961
Author(s):  
Dionysios Linardatos ◽  
Anastasios Konstantinidis ◽  
Ioannis Valais ◽  
Konstantinos Ninos ◽  
Nektarios Kalyvas ◽  
...  
Keyword(s):  
Single Crystal ◽  
Energy Absorption ◽  
Quantum Efficiency ◽  
Zinc Selenide ◽  
Light Output ◽  
Absorption Efficiency ◽  
Detective Quantum Efficiency ◽  
X Ray ◽  
Luminescence Efficiency ◽  
Energy Absorption Efficiency

In this study, the light output of a zinc selenide activated with tellurium (ZnSe: Te) single crystal was measured for X-ray radiography applications. A cubic crystal (10 × 10 × 10 mm) was irradiated using X-rays with tube voltages from 50 to 130 kV. The resulting energy absorption efficiency, detective quantum efficiency, and absolute luminescence efficiency were compared to published data for equally sized GSO: Ce (gadolinium orthosilicate) and BGO (bismuth germanium oxide) crystals. The emitted light was examined to estimate the spectral compatibility with widely used optical sensors. Energy absorption efficiency and detective quantum efficiency of ZnSe: Te and BGO were found to be similar, within the X-ray energies in question. Light output of all three crystals showed a tendency to increase with increasing X-ray tube voltage, but ZnSe: Te stood at least 2 EU higher than the others. ZnSe: Te can be coupled effectively with certain complementary metal–oxide–semiconductors (CMOS), photocathodes, and charge-coupled-devices (CCD), as the effective luminescence efficiency results assert. These properties render the material suitable for various imaging applications, dual-energy arrays included.

The Basic Physical Principles of Ion, Electron, and X-Ray Detectors and Their Application to Microanalysis

1985 ◽  
Vol 43 ◽  
pp. 154-157
Author(s):  
A.J. Tousimis
Keyword(s):  
Ion Beam ◽  
Depth Resolution ◽  
Sample Surface ◽  
High Energy ◽  
X Rays ◽  
X Ray ◽  
Electrons And Ions ◽  
Spatial Depth ◽  
Minimum Surface Area ◽  
Physical Principles

An integral and of prime importance of any microtopography and microanalysis instrument system is its electron, x-ray and ion detector(s). The resolution and sensitivity of the electron microscope (TEM, SEM, STEM) and microanalyzers (SIMS and electron probe x-ray microanalyzers) are closely related to those of the sensing and recording devices incorporated with them.Table I lists characteristic sensitivities, minimum surface area and depth analyzed by various methods. Smaller ion, electron and x-ray beam diameters than those listed, are possible with currently available electromagnetic or electrostatic columns. Therefore, improvements in sensitivity and spatial/depth resolution of microanalysis will follow that of the detectors. In most of these methods, the sample surface is subjected to a stationary, line or raster scanning photon, electron or ion beam. The resultant radiation: photons (low energy) or high energy (x-rays), electrons and ions are detected and analyzed.

scholarly journals Lower resolution Laue neutron data yield correct nanocluster formulations

2014 ◽  
Vol 70 (a1) ◽  
pp. C187-C187
Author(s):  
Alison Edwards
Keyword(s):  
Neutron Diffraction ◽  
Single Crystal ◽  
Diffraction Pattern ◽  
Precise Determination ◽  
Data Sets ◽  
X Rays ◽  
Low Resolution ◽  
Neutron Data ◽  
X Ray ◽  
Product Formulation

"The renaissance in Laue studies - at neutron sources - provides us with access to single crystal neutron diffraction data for synthetic compounds without requiring synthesis of prohibitively large amounts of compound or improbably large crystals. Such neutron diffraction studies provide vital data where proof of the presence or absence of hydrogen in particular locations is required and which cannot validly be proved by X-ray studies. Since the commissioning of KOALA at OPAL in 2009[1] we have obtained numerous data sets which demonstrate the vital importance of measuring data even where the extent of the diffraction pattern is at relatively low resolution - especially when compared to that obtainable for the same compound with X-rays. In the Laue experiment performed with a fixed radius detector, data reduction is only feasible for crystals in the ""goldilocks"" zone – where the unit cell is relatively large for the detector, a correspondingly low resolution diffraction pattern in which adjacent spots are less affected by overlap will yield more data against which a structure can be refined than a pattern of higher resolution – one where neighbouring spots overlap rendering both unusable (in our current methodology). Analogous application of powder neutron diffraction in such determinations is also considered. Single crystal neutron diffraction studies of several important compounds (up to 5KDa see figure below)[2] in which precise determination of hydride content by neutron diffraction was pivotal to the final formulation will be presented. The neutron data sets typically possess 20% or fewer unique data at substantially "lower resolution" than the corresponding X-ray data sets. Careful refinement clearly reveals chemical detail which is typically unexplored in related X-ray diffraction studies reporting high profile chemistry despite the synthetic route being one which hydride ought to be considered/excluded in product formulation."

A multi-length-scale USAXS/SAXS facility: 10–50 keV small-angle X-ray scattering instrument

2013 ◽  
Vol 46 (5) ◽  
pp. 1508-1512 ◽  
Author(s):  
Byron Freelon ◽  
Kamlesh Suthar ◽  
Jan Ilavsky
Keyword(s):  
Small Angle ◽  
Soft Matter ◽  
High Energy ◽  
X Rays ◽  
X Ray ◽  
X Ray Scattering ◽  
Wide Range ◽  
And Performance ◽  
New Facility ◽  
Ray Scattering

Coupling small-angle X-ray scattering (SAXS) and ultra-small-angle X-ray scattering (USAXS) provides a powerful system of techniques for determining the structural organization of nanostructured materials that exhibit a wide range of characteristic length scales. A new facility that combines high-energy (HE) SAXS and USAXS has been developed at the Advanced Photon Source (APS). The application of X-rays across a range of energies, from 10 to 50 keV, offers opportunities to probe structural behavior at the nano- and microscale. An X-ray setup that can characterize both soft matter or hard matter and high-Zsamples in the solid or solution forms is described. Recent upgrades to the Sector 15ID beamline allow an extension of the X-ray energy range and improved beam intensity. The function and performance of the dedicated USAXS/HE-SAXS ChemMatCARS-APS facility is described.

A high-energy triple-axis X-ray diffractometer for the study of the structure of bulk crystals

2004 ◽  
Vol 37 (6) ◽  
pp. 901-910 ◽  
Author(s):  
C. Seitz ◽  
M. Weisser ◽  
M. Gomm ◽  
R. Hock ◽  
A. Magerl
Keyword(s):  
High Energy ◽  
X Rays ◽  
Bulk Crystals ◽  
X Ray Diffraction ◽  
X Ray ◽  
Peak Intensity ◽  
High Penetration ◽  
Massive Sample ◽  
Laue Geometry ◽  
The Ideal

A triple-axis diffractometer for high-energy X-ray diffraction is described. A 450 kV/4.5 kW stationary tungsten X-ray tube serves as the X-ray source. Normally, 220 reflections of thermally annealed Czochralski Si are employed for the monochromator and analyser. Their integrated reflectivity is about ten times higher than the ideal crystal value. With the same material as the sample, and working with the WKα line at 60 keV in symmetric Laue geometry for all axes, the full width at half-maximum (FWHM) values for the longitudinal and transversal resolution are 2.5 × 10−3and 1.1 × 10−4for ΔQ/Q, respectively, and the peak intensity for a non-dispersive setting is 3000 counts s−1. In particular, for a double-axis mode, an energy well above 100 keV from theBremsstrahlungspectrum can be used readily. High-energy X-rays are distinguished by a high penetration power and materials of several centimetre thickness can be analysed. The feasibility of performing experiments with massive sample environments is demonstrated.

A single crystal, linearly polarized Fe 2p X-ray absorption study of gillespite

1998 ◽  
Vol 62 (1) ◽  
pp. 65-75 ◽  
Author(s):  
P. F. Schofield ◽  
G. van der Laan ◽  
C. M. B. Henderson ◽  
G. Cressey
Keyword(s):  
Single Crystal ◽  
Ground State ◽  
Branching Ratio ◽  
Linear Dichroism ◽  
Electronic Charge ◽  
Magic Angle ◽  
X Rays ◽  
X Ray ◽  
Peak Structure ◽  
X Ray Absorption

AbstractThe Fe 2p X-ray absorption spectra of single crystal gillespite, BaFeSi4O10, show a strong linear dichroism, i.e. a large difference in the absorption when measured with the polarization of the X-rays either parallel or perpendicular to the plane of the FeO4 group. The isotropic spectrum, obtained from measurement at the ‘magic angle’, and the polarization dependent spectra have been compared to atomic multiplet calculations and show an excellent agreement with theory. Analysis of the branching ratio, the linear dichroism, and the detailed peak structure confirms that the 5A1 level is the ground state at room temperature and pressure. The 5B2 level is sufficiently low in energy that a distortion of the electronic charge density, induced by increased pressure, may result in a 5B2 ground state.

Sign in / Sign up

Export Citation Format

Share Document