Dr. Jörg Grenzer
x-ray laboratory
Phone: +49 351 260 3389, +49 351 260 2406
Fax: +49 351 260 13389, +49 351 260 3438

Andrea Scholz
Phone: +49 351 260 3153, +49 351 260 3534
Fax: +49 351 260 13153, +49 351 260 3438

X-ray Laboratory

The X-ray laboratory at the HZDR (Institute of Ion Beam Physics and Materials Research) operates 5 different laboratory diffractometers.

are optimized to cover a wide range of tasks in materials research. All units operate with Cu radiation (Kα: 0.154 nm / 8.042 keV).



Θ-Θ Powder-diffractometer



diffraction on powders and polycrystalline materials

Bragg-Brentano-geometry using a graphite secondary monochromator and a scintillator

Θ-2Θ 4-Cirle diffractometer



reflectivity and diffuse scattering, diffarction, orientational and texture investigations

parallel beam optics (Göbelspiegel), scintillator,

optional a secondary monochromator

Θ-Θ 4-circle diffractometer



thin film analytics, diffraction, reflectivity, orientational and texture investigations, reciprocal space maps

parallel beam optics (Göbelspiegel), hybride monochromator,


point like beam (300µm), proportional counter, area detector

Θ-2Θ diffractometer



reflectivity and diffuse scattering, diffarction

point like beam (300µm), position sensitive detector

(beam diameter can be reduced down to 50µm)


4+2-circle HR- diffractometer


GE (Seifert)

reflectivity, diffraction, high resolution diffraction, reciprocal space maps, orientational and texture investigations, grazing incidence garzing exit diffraction

point like beam (~1mm),

horizontal or vertical geometry,


variable ource and detector optics

sample envoiriments

DHS 900

Anton Paar

temperature dependend measurements

high temperature chamber (up to 900°C) vacuum (1 mbar) or inert/forming gas





high temperature chamber (up to 1000°C) vacuum (<10-5 mbar) or inert/forming gas

Topics of Research

The development of new high-performance materials, new materials for micro- and nano-technology requires a constantly evolving analytics, in particular to clarify the relationship between the atomic microstructure and the practice-relevant macroscopic material properties. The aim is by means of material science to achieve a targeted design of materials with specific properties. Structural studies are the key to establish a connection between the functional and structural properties which generate this function. This knowledge makes it possible to design new materials with precisely defined characteristics. Thin nanostructured layers can, for example, affect surface and interfacial properties such that the material properties of conventional materials can be adjusted to match a particular task. The function of the nanostructures is not only determined by their internal structure, but in large part by their morphology and surface characteristics.

Crystallisation and phase analysis

The atomic structure, particularly the formation of (nano-) crystallites, which evolves during a deposition process, during modification with ion beams or in connection with subsequent annealing steps, decisively influence the material properties. For materials undergoing only structural changes at a thin surface layer, the method of the grazing (or glancing) incidence diffraction is used. By varying the angle of incidence, the sensitivity in terms of a thin surface layer can be greatly improved.
These studies relate to various topics such as light metal materials, materials for biomedical applications, metallic layers, semiconductor nanoclusters, metal-ceramic interfaces, transparent oxides, etc. In addition to the phase formation as a function of the different technological steps also the development of the crystallite size, the change of the lattice constants as well as their statistical distribution function can be studied. As appropriate for thin films and possible texture effects are investigated. The objective is, for example, to observe or to keep track of orientation relationships between substrate and a deposited layer.

X-ray reflectometry

With X-ray reflectometry one gains information to the layer thicknesses, the surface and interface roughness and the density of the materials. The method is applied, for example, to study the ion beam mixing in Co/Cu multilayers, the change of the density in SiC after implantation or to assess the quality of BN layers from an IBAD process. The quality of the semiconductor substrate surfaces or of hetero-structure interfaces can be as wellas investigated.

High Resolution Diffractometry

The triple-axis diffractometer is primarily used to study smallest lattice strains, e.g., after ion implantation into Si, ZrO, or in III-V semiconductor heterostructures and their relaxation after some treatment.

Powder Diffraction

This method is the default method for phase identification mainly of polycrystalline materials. The investigation of crystalline and semi-crystalline powder-like materials goes in many cases back to topics of the Institute of Resource Ecology (uranyl complexes, geological samples, ...).


Dr. Jörg Grenzer
x-ray laboratory
Phone: +49 351 260 3389, +49 351 260 2406
Fax: +49 351 260 13389, +49 351 260 3438

Andrea Scholz
Phone: +49 351 260 3153, +49 351 260 3534
Fax: +49 351 260 13153, +49 351 260 3438