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Erscheinungsjahr
- 2021 (299) (entfernen)
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- Zeitschriftenartikel (299) (entfernen)
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- Additive manufacturing (14)
- MALDI-TOF MS (12)
- Quantum yield (12)
- Polylactide (11)
- Mechanical properties (10)
- Corrosion (9)
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- 6 Materialchemie (121)
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- 1 Analytische Chemie; Referenzmaterialien (29)
- 6.1 Oberflächen- und Dünnschichtanalyse (29)
- 9.3 Schweißtechnische Fertigungsverfahren (26)
- 6.6 Physik und chemische Analytik der Polymere (24)
- 7 Bauwerkssicherheit (24)
Paper des Monats
- ja (2)
Das Widerstandspunktschweißen ist ein etabliertes Fügeverfahren in der Automobilindustrie. Es wird vor allem bei der Herstellung sicherheitsrelevanter Bauteile, zum Beispiel der Karosserie, eingesetzt. Daher ist eine kontinuierliche Prozessüberwachung unerlässlich, um die hohen Qualitätsanforderungen zu erfüllen. Künstliche neuronale Netzalgorithmen können zur Auswertung der Prozessparameter und -signale eingesetzt werden, um die individuelle Schweißpunktqualität zu gewährleisten. Die Vorhersagegenauigkeit solcher Algorithmen hängt von dem zur Verfügung gestellten Trainingsdatensatz ab. In diesem Beitrag wird untersucht, inwieweit die Vorhersagegüte eines künstlichen neuronalen Netzes durch Auswertung einer Prozessgröße, dem dynamischen Widerstand, verbessert werden kann.
Crouzier, L. ; Feltin, N. ; Delvallée, A. ; Pellegrino, Francesco ; Maurino, V. ; Cios, Grzegorz ; Tokarski, T. ; Salzmann, Christoph ; Deumer, J. ; Gollwitzer, C. ; Hodoroaba, Vasile-Dan
In this paper, the accurate determination of the size and size distribution of bipyramidal anatase nanoparticles (NPs) after deposition as single particles on a silicon substrate by correlative Scanning Electron Microscopy (SEM) with Atomic Force Microscopy (AFM) analysis is described as a new measurement procedure for metrological purposes. The knowledge of the exact orientation of the NPs is a crucial step in extracting the real 3D dimensions of the particles. Two approaches are proposed to determine the geometrical orientation of individual nano‐bipyramides: (i) AFM profiling along the long bipyramid axis and (ii) stage tilting followed by SEM imaging. Furthermore, a recently developed method, Transmission Kikuchi Diffraction (TKD), which needs preparation of the crystalline NPs on electron‐transparent substrates such as TEM grids, has been tested with respect to its capability of identifying the geometrical orientation of the individual NPs. With the NPs prepared homogeneously on a TEM grid, the transmission mode in a SEM, i.e., STEM‐in‐SEM (or T‐SEM), can be also applied to extract accurate projection dimensions of the nanoparticles from the same sample area as that analysed by SEM, TKD and possibly AFM. Finally, Small Angle X‐ray Scattering (SAXS) can be used as an ensemble technique able to measure the NPs in liquid suspension and, with ab‐initio knowledge of the NP shape from the descriptive imaging techniques, to provide traceable NP size distribution and particle concentration.
Kunc, F. ; Nirmalananthan-Budau, Nithiya ; Rühle, Bastian ; Sung, Y. ; Johnston, L.J. ; Resch-Genger, Ute
Risk assessment of nanomaterials requires not only standardized toxicity studies but also validated methods for nanomaterial surface characterization with known uncertainties. In this context, a first bilateral interlaboratory comparison on Surface group quantification of nanomaterials is presented that assesses different reporter-free and labeling methods for the quantification of the total and accessible number of amine functionalities on commercially available silica nanoparticles that are widely used in the life sciences. The overall goal of this comparison is the identification of optimum methods as well as achievable measurement uncertainties and the comparability of the results across laboratories. We also examined the robustness and ease of implementation of the applied analytical methods and discussed method-inherent limitations. In summary, this comparison presents a first step toward the eventually required standardization of methods for surface group quantification.
Stawski, Tomasz ; Smales, Glen Jacob ; Scoppola, E. ; Jha, D. ; Morales, L. F. G. ; Moya, A. ; Wirth, R. ; Pauw, Brian Richard ; Emmerling, Franziska ; Van Driessche, A. E. S.
In recent years, we have come to appreciate the astounding intricacies associated with the formation of minerals from ions in aqueous solutions. In this context, a number of studies have revealed that the nucleation of calcium sulfate systems occurs nonclassically, involving the aggregation and reorganization of nanosized prenucleation species. In recent work, we have shown that this particle-mediated nucleation pathway is actually imprinted in the resultant micrometer-sized CaSO4 crystals. This property of CaSO4 minerals provides us with the unique opportunity to search for evidence of nonclassical nucleation pathways in geological environments.
In particular, we focused on large anhydrite Crystals extracted from the Naica Mine in Mexico. We were able to shed light on this mineral's growth history by mapping defects at different length scales. Based on this, we argue that the nanoscale misalignment of the structural subunits, observed in the initial calcium sulfate crystal seeds, propagates through different length scales both in morphological, as well as in strictly crystallographic aspects, eventually causing the formation of large mesostructured single crystals of anhydrite. Hence, the nonclassical nucleation mechanism introduces a “seed of imperfection,” which leads to a macroscopic “single” crystal whose fragments do not fit together at different length scales in a self-similar manner. Consequently, anisotropic voids of various sizes are formed with very welldefined walls/edges. However, at the same time, the material retains in part its single crystal nature.
Laser-induced periodic surface structures (LIPSS) are a simple and robust route for the nanostructuring of solids that can create various surface functionalities featuring applications in optics, medicine, tribology, energy technologies, etc. While the current laser technologies already allow surface processing rates at the level of m2/min, industrial applications of LIPSS are sometimes hampered by the complex interplay between the nanoscale surface topography and the specific surface chemistry, as well as by limitations in controlling the processing of LIPSS and in the long-term stability of the created surface functions. This Perspective article aims to identify some open questions about LIPSS, discusses the pending technological limitations, and sketches the current state of theoretical modelling. Hereby, we intend to stimulate further research and developments in the field of LIPSS for overcoming these limitations and for supporting the transfer of the LIPSS technology into industry.
Scaling of phonon frequencies and electron binding energies with interatomic distances in InxGa1−xN
(2021)
Katsikini, M. ; Filintoglou, K. ; Pinakidou, F. ; Pilatsikas, N. ; Arvanitidis, J. ; Christofilos, D. ; Paloura, E.C. ; Ves, S. ; Reinholz, Uwe ; Papadomanolaki, E. ; Lliopoulos, E.
In-K-edge x-ray absorption fine structure (EXAFS), x-ray photoelectron, and Raman spectroscopy results are combined for a comprehensive study of InxGa1−xN layers with energy gaps extending over nearly the whole visible spectrum. The In–N and In–(In,Ga) distances determind by EXAFS are used for the derivation of the In–N bond ionicity as well as for the phonon frequency dependence of the LO and B21 modes, assessed by Raman, and the N 1s, In 3d5/2, Ga 3s, and Ga 2p1/2 electron binding energies on those distances. Phonon confinement due to perturbation of the periodic potential caused by the alloying is also quantified.
Ellipsometry-based approach for the characterization of mesoporous thin films for H2 technologies
(2021)
Porous thin layer materials are gaining importance in different fields of technology and pose a challenge to the accurate determination of materials properties important for their function. In this work, we demonstrate a hybrid measurement technique using ellipsometry together with other independent methods for validation. Ellipsometry provides information about the porosity of different mesoporous films (PtRuNP/OMC = 45%; IrOx = 46%) as well as about the pore size (pore radius of ca. 5 nm for PtRuNP/OMC). In addition, the electronic structure of a material, such as intraband transitions of a mesoporous IrOx film, can be identified, which can be used to better understand the mechanisms of chemical processes. In addition, we show that ellipsometry can be used as a scalable imaging and visualization method for quality assurance in production. These require accurate and traceable measurements, with reference materials playing an important role that include porosity and other related properties. We show that our novel analytical methods are useful for improving analytical work in this entire field.
In Part I of this paper, we have described a modification brought to the model of Lu (X.-G. Lu et al., Comput. Coupling Phase Diagr. Thermochem. 29 (2005) 49–55) in order to avoid extrapolation problems at high pressure and temperature. We now extend this approach to the study of a binary system: Os–Pt. For this, a complete description (equation of state) of Os at high pressure/high temperature is provided including the liquid phase. The thermodynamic assessment of the system Os–Pt has been carried out at ambient pressure by the Calphad method. All this study has been supported by first principles, special quasi-random structure (including under high pressure) and phonon calculations. Finally, using the high pressure description of metastable structures (hcp Pt and fcc Os), we have been able to obtain by extrapolation a complete description of Os–Pt system up to 500 GPa. Recent experimental data for Os–Pt system obtained up to 50 GPa at various temperatures up to 2300 °C may us allow to validate our modeling approach.