Ivo Zizak

A customizable software for fast reduction and analysis of large X‐ray scattering data sets: applications of the new DPDAK package to small‐angle X‐ray scattering and grazing‐incidence small‐angle X‐ray scattering

DPDAK is a software for simple and fast on- and offline reduction and analysis of X-ray scattering data. It is an open-source software with a plug-in structure allowing tailored extensions.

Effect of iron-carbide formation on the number of active sites in Fe–N–C catalysts for the oxygen reduction reaction in acidic media

In this work Fe–N–C catalysts were prepared by the oxalate-supported pyrolysis of FeTMPPCl or H2TMPP either in the presence or absence of sulfur. The well-known enhancing effect of sulfur-addition on the oxygen reduction activity was confirmed for these porphyrin precursors. The pyrolysis process was monitored in situ by high-temperature X-ray diffraction under synchrotron radiation (HT-XRD) and thermogravimetry coupled with mass-spectroscopy (TG-MS). It was found that the beneficial effect of sulfur could be attributed to the prevention of iron-carbide formation during the heat-treatment process. In the case of pyrolysis of the sulfur-free precursors an excessive iron-carbide formation leads to disintegration of FeN4-centers, hence limiting the number of ORR active sites on the final catalyst. Physical characterization of the catalysts by bulk elemental analysis, X-ray diffraction (XRD), Raman and 57Fe Mosbauer spectroscopy confirmed the outcome from HT-XRD and TG-MS. It could be shown that the avoidance of carbide formation during pyrolysis represents a promising way to enhance the density of ORR active sites on those catalysts. This can be done either by sulfur-addition or the performance of an intermediate acid leaching. As iron carbide is often found as a by-product in the preparation of Fe–N–C catalysts this work gives some general strategies for enhancing the density of active sites enabling higher current densities.

Investigation of bone and cartilage by synchrotron scanning-SAXS and -WAXD with micrometer spatial resolution

Biological materials such as bone or wood are hierarchically structured to optimize mechanical and other properties. Several methods and experimental techniques are usually needed to study these materials on different length scales. We developed a device for small angle X-ray scattering (SAXS) and wide-angle X-ray diffraction (WAXD), optimized for position resolved investigations of bone sections using synchrotron radiation. Thin samples can be scanned with 20 µm steps, acquiring two-dimensional SAXS or WAXD patterns at every point. The system was tested by performing one-dimensional scans across bone cartilage interfaces, revealing information about size, shape and orientation of nanometer sized mineral particles as well as about crystal type and texture of these particles.

On the Influence of Sulphur on the Pyrolysis Process of FeTMPP-Cl-based Electro- Catalysts with Respect to Oxygen Reduction Reaction (ORR) in Acidic Media

Pyrolysis of chloroiron-tetramethoxyphenyl-porphyrin (FeTMPP-Cl) in the presence of iron oxalate (± sulphur) leads to the formation of higly porous and active catalysts for the oxygen reduction reaction (ORR). In order to clarify the influence of sulphur the pyrolysis process is analyzed by thermogravimetry (TG) and by high-temperature X-ray diffraction (HT-XRD). In the absence of sulphur iron carbide (FexC) is formed which catalyses the proceeding graphitisation of the pyrolysis products. As a result catalytic active centres are decomposed by this reaction. This can be avoided by the addition of sulphur because iron monosulphide (FeS; troilite) is formed instead of FexC. Furthermore, FeS can easily be removed in a successive etching step so that nearly all inactive by-products can be removed. The results are in accordance with the higher electrochemical performance of the sulphur containing catalysts.

In Situ Observation of Gating Phenomena in the Flexible Porous Coordination Polymer Zn2(BPnDC)2(bpy) (SNU-9) in a Combined Diffraction and Gas Adsorption Experiment

The intrinsic structural dynamic during the adsorption of CO2 at 195 K and N2 at 77 K on flexible porous coordination polymer Zn2(BPnDC)2(bpy) (SNU-9) was studied in situ by powder XRD. The crystal structures of as made and solvent free (activated) phases were determined by single crystal X-ray diffraction. During the structural transformation caused by activation, the rearrangement of Zn-O bonds occurs that leads to changes in coordination environment of Zn atoms. Such changes lead to the contraction of the unit cell and to decreasing unit cell volume of nearly 28% in comparison to the pristine as made structure. The solvent accessible volume of the unit cell decreases from 40.8% to 12.8%. The adsorption of CO2 and N2 on SNU-9 proceeds in a different way: the formation of intermediate phase during the CO2 adsorption could be postulated, while the transformation from narrow pore form to the open structure occurs in quasi-one-step in the case of N2 adsorption (the intermediate phase is formed only in very narrow pressure region). The transformation of the structure is guest dependent and the differences in the structures of CO2@SNU-9 at 195 K and N2@SNU-9 at 77 K were proven by Pawley and Rietveld refinements of powder XRD patterns. The structure of N2@SNU-9 is identical to this of as synthesized phase, while the structure of CO2@SNU-9 differs slightly.

Combining scanning probe microscopy and x-ray spectroscopy

A new versatile tool, combining Shear Force Microscopy and X-Ray Spectroscopy was designed and constructed to obtain simultaneously surface topography and chemical mapping. Using a sharp optical fiber as microscope probe, it is possible to collect locally the visible luminescence of the sample. Results of tests on ZnO and on ZnWO4 thin layers are in perfect agreement with that obtained with other conventional techniques. Twin images obtained by simultaneous acquisition in near field of surface topography and of local visible light emitted by the sample under X-Ray irradiation in synchrotron environment are shown. Replacing the optical fibre by an X-ray capillary, it is possible to collect local X-ray fluorescence of the sample. Preliminary results on Co-Ti sample analysis are presented.

High temperature stability of Cr-carbides in an experimental Co–Re-based alloy

Abstract The stability of the microstructure at high temperatures was studied in an experimental Co–Re-based alloy. The experimental alloy is mainly strengthened by Cr-carbides, particularly by those in the form of thin lamellar plates. Electron microscopic investigation on samples exposed for up to 1 000 h to temperatures of 1 000 and 1 200 °C showed that Cr23C6 type carbides present in the alloy in different morphologies are unstable at these temperatures. It was also observed that the alloy hardness dropped after exposing the samples to elevated temperatures and much of this loss occurred within the first 100 h. In-situ diffraction measurements with synchrotron radiation showed that carbide dissolution started as early as 3 h of holding at 1 000 °C. Moreover, in-situ small angle neutron scattering results indicated that the carbides at the grain boundaries and the blocky carbides dissolve first and then the thin lamellar carbides. Further, the enrichment of Cr in the Co-matrix phase, which took place due to the dissolution of Cr-carbides, stabilized a Cr–Re-rich σ phase. Although the dissolution of lamellar carbides results in a significant loss of strength, the formation of σ phase with extremely high hardness partly compensated the for loss. The σ phase is stable even at 1 200 °C.

Adhesion measurement of a buried Cr interlayer on polyimide

A fundamental knowledge and understanding of the adhesion behaviour of metal–polymer systems is important as interface failure leads to a complete breakdown of flexible devices. A combination of in situ atomic force microscopy for studying topological changes and in situ synchrotron based stress measurements both during film tensile testing were used to estimate the adhesion energy of a thin bilayer film. The film systems consisted of 50–200 nm Cu with a 10 nm Cr adhesion layer on 50 μm thick polyimide. If the Cu film thickness is decreased to 50 nm the Cr interlayer starts dominating the system behaviour. An apparent transition from plastic to predominantly brittle deformation behaviour of the Cu can be observed. Then, compressive stresses in the transverse direction are high enough to cause delamination and buckling of the Cr interlayer from the substrate. This opens a new route to induce buckling of a brittle interlayer between a ductile film and a compliant substrate which is used to determine the interfacial adhesion energy.

Nanostructural changes in crystallizable controlling units determine the temperature-memory of polymers

Temperature-memory polymers remember the temperature, where they were deformed recently, enabled by broad thermal transitions. In this study, we explored a series of crosslinked poly[ethylene-co-(vinyl acetate)] networks (cPEVAs) comprising crystallizable polyethylene (PE) controlling units exhibiting a pronounced temperature-memory effect (TME) between 16 and 99 °C related to a broad melting transition (∼100 °C). The nanostructural changes in such cPEVAs during programming and activation of the TME were analyzed via in situ X-ray scattering and specific annealing experiments. Different contributions to the mechanism of memorizing high or low deformation temperatures (Tdeform) were observed in cPEVA, which can be associated to the average PE crystal sizes. At high deformation temperatures (>50 °C), newly formed PE crystals, which are established during cooling when fixing the temporary shape, dominated the TME mechanism. In contrast, at low Tdeform (<50 °C), corresponding to a cold drawing scenario, the deformation led preferably to a disruption of existing large crystals into smaller ones, which then fix the temporary shape upon cooling. The observed mechanism of memorizing a deformation temperature might enable the prediction of the TME behavior and the knowledge based design of other TMPs with crystallizable controlling units.

Surface acoustic wave propagation in graphene film

Surface acoustic wave (SAW) propagation in a graphene film on the surface of piezoelectric crystals was studied at the BESSY II synchrotron radiation source. Talbot effect enabled the visualization of the SAW propagation on the crystal surface with the graphene film in a real time mode, and high-resolution x-ray diffraction permitted the determination of the SAW amplitude in the graphene/piezoelectric crystal system. The influence of the SAW on the electrical properties of the graphene film was examined. It was shown that the changing of the SAW amplitude enables controlling the magnitude and direction of current in graphene film on the surface of piezoelectric crystals.