The X-ray diffraction is a technique used for the non-destructive determination of the structure of the materials, generally inorganic, and solid state. Such a technique is based on the properties of the atoms to spread out electromagnetic radiation. Assuming that the spread from each element is independent from that of the other, it is possible to formulate a theory of diffraction for three-dimensional crystal lattices. 


The equipment

The four-circle X-ray diffractometer is a commercial PanalyticalX'pert based on copper cathode technology and designed to allow the analysis of a wide range of materials, from micrometer powders to thin films and/or nano-engineered heterostructures, through the use of appropriate modules that optimize the experimental configuration. In particular, the use of a Ge 4-bounce double monochromator allows the selection of only one wavelength Ka1 (0.15405 nm) of the copper source, so as to enable the structural analysis of thin films and/or hetero-epitaxial structures with very high resolution, while for the analysis of materials with a low power diffraction (e.g. powders) the use of a simple collimator greatly increases the number of incident photons, although with a worse energy resolution of the source. At these two limit configurations, an intermediate configuration will be added (scheduled on Sep.2015) by the use of a hybrid module composed of single monochromator and converging mirror which allows a reasonable energy resolution of the source (i.e. a single wavelength Ka1) and a considerable increase of the incidents photons compared with the configuration with the Ge-monochromator (i.e. a factor 50-60 in number of photons). The positioning of the samples can be achieved and remotely controlled in all the three dimensions, so as to allow also the structural mapping of two-dimensional objects (e.g. large wafers). 

The equipment within the NFFA-Framework

Structural information such as the epitaxy relation between thin films and template crystals, or the dimensionality of the powders' grains, and other characteristics of the material, are critical to understanding the processes of synthesis of materials and their optimization. The access to XRD workstation (located at the CNR-IOM building) will be granted within the NFFA-project's activities, either to structurally characterize the thin films and the heterostructures grown by PLD/MBE clusters, as well as samples provided by users. 


X-ray source Philips high intensity ceramic sealed tube (3kW)
Wavelength Cu Ka (1.5405 Å)
Incident beam optics interchangeable fixed slits and one Soller slit.
Diffracted beam optics fixed slit plus programmable receiving slit, graphite analyzer
Detectors sealed proportional counter
Sample stage texture cradle with sample translation
Software Philips X’PERT suite: Data Collector, Graphics & Identify, Texture
Goniometer Minimum step size 0.0001˚
Open Eulerian Cradle Chi rotation: +/- 92˚
Phi rotation: 2 x 360˚
x,y translation: 100 x 100 mm
z translation: minimum step size 1 µm

The map of techniques

at MM building at Q2 building at Elettra experimental hall at CNR-IOM cloud at Fermi-T-Rex laboratory Surface & Nano Science Lab, STM/STS PLD XPS & ambient pressure XAS ARPES & Spin ARPES MOKE & Masked deposition system XPS MBE Oxides SPRINT laboratory SEM XRD PVD data repository open data data analysis
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Scientists in charge