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Walther, Dominik; Viehweg, Johannes; Haueisen, Jens; Mäder, Patrick
A systematic comparison of deep learning methods for EEG time series analysis. - In: Frontiers in neuroinformatics, ISSN 1662-5196, Bd. 17 (2023), 1067095, S. 01-17

Analyzing time series data like EEG or MEG is challenging due to noisy, high-dimensional, and patient-specific signals. Deep learning methods have been demonstrated to be superior in analyzing time series data compared to shallow learning methods which utilize handcrafted and often subjective features. Especially, recurrent deep neural networks (RNN) are considered suitable to analyze such continuous data. However, previous studies show that they are computationally expensive and difficult to train. In contrast, feed-forward networks (FFN) have previously mostly been considered in combination with hand-crafted and problem-specific feature extractions, such as short time Fourier and discrete wavelet transform. A sought-after are easily applicable methods that efficiently analyze raw data to remove the need for problem-specific adaptations. In this work, we systematically compare RNN and FFN topologies as well as advanced architectural concepts on multiple datasets with the same data preprocessing pipeline. We examine the behavior of those approaches to provide an update and guideline for researchers who deal with automated analysis of EEG time series data. To ensure that the results are meaningful, it is important to compare the presented approaches while keeping the same experimental setup, which to our knowledge was never done before. This paper is a first step toward a fairer comparison of different methodologies with EEG time series data. Our results indicate that a recurrent LSTM architecture with attention performs best on less complex tasks, while the temporal convolutional network (TCN) outperforms all the recurrent architectures on the most complex dataset yielding a 8.61% accuracy improvement. In general, we found the attention mechanism to substantially improve classification results of RNNs. Toward a light-weight and online learning-ready approach, we found extreme learning machines (ELM) to yield comparable results for the less complex tasks.



https://doi.org/10.3389/fninf.2023.1067095
Pöthig, Pascal; Grätzel, Michael; Bergmann, Jean Pierre
Influence of different surface conditions on mechanical properties during ultrasonic welding of aluminum wire strands and copper terminals. - In: Welding in the world, ISSN 1878-6669, Bd. 67 (2023), 6, S. 1427-1436

Ultrasonic metal welding (USMW) has become considerable attention in terms of its suitable applications compared to conventional fusion welding techniques. The main advantage of USMW results from the comparatively low process times and joining temperatures below the melting point. Thus, USMW is particularly used for the joining of dissimilar material combinations, e.g., aluminum and copper (Al/Cu), in battery cell production or wiring harness applications. However, process fluctuations in USMW of Al/Cu joints can occur due to varying surface conditions of the joining materials. Therefore, this study investigated different surface conditions of copper terminals and their effects on mechanical properties. At first, three different surface conditions were generated, respectively: surface cleaning (sulfuric acid and ethanol), structuring process by laser, and structuring process by milling. These modifications are compared with the terminals in the initial state (contaminated). The characterization of the terminal surfaces was carried out with 3-D laser scanning microscopy as well as light microscopy. The mechanical conditions were examined with shear tensile tests. The tensile tests showed a significant influence of the surface condition on the resulting failure loads compared to the initial state. The highest failure loads could be achieved with the structured terminals (+ 48%), whereas contaminated terminals and terminals with notches exhibited comparatively poor failure loads (- 28%). This can be explained by varying interface formations between the terminal and the wire, which was detected by metallography and SEM analysis. Furthermore, it was figured out that the interface between aluminum and copper exhibits a firm and formed closure bond and hence increased failure loads for laser-structured terminals. Additional investigations by SEM revealed no detectable occurrence of intermetallic phases.



https://doi.org/10.1007/s40194-023-01490-x
Maheu, Clément; Zare Pour, Mohammad Amin; Damestoy, Iban; Ostheimer, David; Mellin, Maximilian; Moritz, Dominik Christian; Paszuk, Agnieszka; Jaegermann, Wolfram; Mayer, Thomas; Hannappel, Thomas; Hofmann, Jan Philipp
Tapered cross section photoelectron spectroscopy provides insights into the buried interfaces of III-V semiconductor devices. - In: Advanced materials interfaces, ISSN 2196-7350, Bd. 10 (2023), 3, 2201648, S. 1-9

Interfaces are key elements that define electronic properties of the final device. Inevitably, most of the active interfaces of III-V semiconductor devices are buried and it is therefore not straightforward to characterize them. The Tapered Cross Section Photoelectron Spectroscopy (TCS-PES) approach is promising to address such a challenge. That the TCS-PES can be used to study the relevant heterojunction in epitaxial III-V architectures prepared by metalorganic chemical vapor deposition is demonstrated here. A MULTIPREP polishing system that enables controlling the angle between the sample holder and the polishing plate has been employed to improve the reproducibility of the polishing procedure. With this procedure, that preparing the TCS of III-V semiconductor devices with tapering angles lower than 0.02˚ is possible is demonstrated. The PES provides then information about the buried interfaces of Ge|GaInP and GaAs|GaInP layer stacks. Both, chemical and electronic properties have been measured by PES. It evidences that the preparation of the TCSs under an uncontrolled atmosphere modifies the pristine properties of the critical buried heterointerfaces. Surface states and reaction layers are created on the TCS surface, which restrict unambiguous conclusions on buried interface energetics.



https://doi.org/10.1002/admi.202201648
Hu, Yongxu; Zheng, Lei; Li, Jie; Huang, Yinan; Wang, Zhongwu; Lu, Xueying; Yu, Li; Wang, Shuguang; Sun, Yajing; Ding, Shuaishuai; Ji, Deyang; Lei, Yong; Chen, Xiaosong; Li, Liqiang; Hu, Wenping
Organic phase-change memory transistor based on an organic semiconductor with reversible molecular conformation transition. - In: Advanced science, ISSN 2198-3844, Bd. 10 (2023), 4, 2205694, S. 1-8

Phase-change semiconductor is one of the best candidates for designing nonvolatile memory, but it has never been realized in organic semiconductors until now. Here, a phase-changeable and high-mobility organic semiconductor (3,6-DATT) is first synthesized. Benefiting from the introduction of electrostatic hydrogen bond (S&hahog;&hahog;&hahog;H), the molecular conformation of 3,6-DATT crystals can be reversibly modulated by the electric field and ultraviolet irradiation. Through experimental and theoretical verification, the tiny difference in molecular conformation leads to crystalline polymorphisms and dramatically distinct charge transport properties, based on which a high-performance organic phase-change memory transistor (OPCMT) is constructed. The OPCMT exhibits a quick programming/erasing rate (about 3 s), long retention time (more than 2 h), and large memory window (i.e., large threshold voltage shift over 30 V). This work presents a new molecule design concept for organic semiconductors with reversible molecular conformation transition and opens a novel avenue for memory devices and other functional applications.



https://doi.org/10.1002/advs.202205694
Hamatschek, Christopher; Augsburg, Klaus; Schobel, David; Gramstat, Sebastian; Stich, Anton; Gulden, Florian; Hesse, David
Comparative study on the friction behaviour and the particle formation process between a laser cladded brake disc and a conventional grey cast iron disc. - In: Metals, ISSN 2075-4701, Bd. 13 (2023), 2, 300, S. 1-19

Brake-wear particle emissions are the result of the components of a friction brake being in tribological contact, and they are classified as non-exhaust emissions. Since most of the emitted particles belong to the size classes of particulate matter (≤10 μm) and differ significantly in terms of their physico-chemical properties from automotive exhaust emissions, this source is of particular relevance to human health and, therefore, the focus of scientific studies. Previous studies have shown that coated brake discs offer significant wear and emission reduction potential. Nevertheless, no studies are available that describe the specific particle formation process, the contact conditions, the structure of the friction layer and the differences compared to conventional grey cast iron discs. The aim of this study is to describe those differences. For this purpose, the tribological behaviour, the structure of the friction layer and the associated particle dynamics within the friction contact between a laser cladding coated disc and a conventional grey cast iron disc are compared. The required investigations are carried out both ex situ (stationary) and in situ (dynamic). Parallel to the tribological investigations, the particle emission behaviour is determined on an inertia dynamometer using a constant volume sampling system (CVS) and equipment for particle number and particle size distribution measurement. The results show that, for two different brake pads, the laser cladding brake disc has lower wear and less particulate emissions than the grey cast iron brake disc. The wear behaviour of the coating varies significantly for the two brake pads. By contrast, the grey cast iron brake disc shows a significantly lower influence.



https://doi.org/10.3390/met13020300
Radivoievych, Aleksandar; Kolp, Benjamin; Grebinyk, Sergii; Prylutska, Svitlana; Ritter, Uwe; Zolk, Oliver; Glökler, Jörn Felix; Frohme, Marcus; Grebinyk, Anna
Silent death by sound: C60 fullerene sonodynamic treatment of cancer cells. - In: International journal of molecular sciences, ISSN 1422-0067, Bd. 24 (2023), 2, 1020, S. 1-17

The acoustic pressure waves of ultrasound (US) not only penetrate biological tissues deeper than light, but they also generate light emission, termed sonoluminescence. This promoted the idea of its use as an alternative energy source for photosensitizer excitation. Pristine C60 fullerene (C60), an excellent photosensitizer, was explored in the frame of cancer sonodynamic therapy (SDT). For that purpose, we analyzed C60 effects on human cervix carcinoma HeLa cells in combination with a low-intensity US treatment. The time-dependent accumulation of C60 in HeLa cells reached its maximum at 24 h (800 ± 66 ng/106 cells). Half of extranuclear C60 is localized within mitochondria. The efficiency of the C60 nanostructure’s sonoexcitation with 1 MHz US was tested with cell-based assays. A significant proapoptotic sonotoxic effect of C60 was found for HeLa cells. C60′s ability to induce apoptosis of carcinoma cells after sonoexcitation with US provides a promising novel approach for cancer treatment.



https://doi.org/10.3390/ijms24021020
Herrmann, Andreas; Zekri, Mohamed; Maâlej, Ramzi; Rüssel, Christian
The effect of glass structure on the luminescence spectra of Sm3+-doped aluminosilicate glasses. - In: Materials, ISSN 1996-1944, Bd. 16 (2023), 2, 564, S. 1-12

Peralkaline Sm3+-doped aluminosilicate glasses with different network modifier ions (Mg2+, Ca2+, Sr2+, Ba2+, Zn2+) were investigated to clarify the effect of glass composition and glass structure on the optical properties of the doped Sm3+ ions. For this purpose, the Sm3+ luminescence emission spectra were correlated with the molecular structure of the glasses derived by molecular dynamics (MD) simulations. The different network modifier ions have a clear and systematic effect on the peak area ratio of the Sm3+ emission peaks which correlates with the average rare earth site symmetry in the glasses. The highest site symmetry is found for the calcium aluminosilicate glass. Glasses with network modifier ions of lower and higher ionic radii show a notably lower average site symmetry. The symmetry could be correlated to the rare earth coordination number with oxygen atoms derived by MD simulations. A coordination number of 6 seems to offer the highest average site symmetry. Higher rare earth coordination probabilities with non-bridging oxygen result in an increased splitting of the emission peaks and a notable broadening of the peaks. The zinc containing glass seems to play a special role. The Zn2+ ions notably modify the glass structure and especially the rare earth coordination in comparison to the other network modifier ions in the other investigated glasses. The knowledge on how glass structure affects the optical properties of doped rare earth ions can be used to tailor the rare earth absorption and emission spectra for specific applications.



https://doi.org/10.3390/ma16020564
Saeidi, Hamidreza; Mozaffari, Morteza; Ilbey, Serhat; Dutz, Silvio; Zahn, Diana; Azimi, Gholamhassan; Bock, Michael
Effect of europium substitution on the structural, magnetic and relaxivity properties of Mn-Zn ferrite nanoparticles: a dual-mode MRI contrast-agent candidate. - In: Nanomaterials, ISSN 2079-4991, Bd. 13 (2023), 2, 331, S. 1-19

Magnetic nanoparticles (MNPs) have been widely applied as magnetic resonance imaging (MRI) contrast agents. MNPs offer significant contrast improvements in MRI through their tunable relaxivities, but to apply them as clinical contrast agents effectively, they should exhibit a high saturation magnetization, good colloidal stability and sufficient biocompatibility. In this work, we present a detailed description of the synthesis and the characterizations of europium-substituted Mn-Zn ferrite (Mn0.6Zn0.4EuxFe2−xO4, x = 0.00, 0.02, 0.04, 0.06, 0.08, 0.10, and 0.15, herein named MZF for x = 0.00 and EuMZF for others). MNPs were synthesized by the coprecipitation method and subsequent hydrothermal treatment, coated with citric acid (CA) or pluronic F127 (PF-127) and finally characterized by X-ray Diffraction (XRD), Inductively Coupled Plasma (ICP), Vibrating Sample Magnetometry (VSM), Fourier-Transform Infrared (FTIR), Dynamic Light Scattering (DLS) and MRI Relaxometry at 3T methods. The XRD studies revealed that all main diffraction peaks are matched with the spinel structure very well, so they are nearly single phase. Furthermore, XRD study showed that, although there are no significant changes in lattice constants, crystallite sizes are affected by europium substitution significantly. Room-temperature magnetometry showed that, in addition to coercivity, both saturation and remnant magnetizations decrease with increasing europium substitution and coating with pluronic F127. FTIR study confirmed the presence of citric acid and poloxamer (pluronic F127) coatings on the surface of the nanoparticles. Relaxometry measurements illustrated that, although the europium-free sample is an excellent negative contrast agent with a high r2 relaxivity, it does not show a positive contrast enhancement as the concentration of nanoparticles increases. By increasing the europium to x = 0.15, r1 relaxivity increased significantly. On the contrary, europium substitution decreased r2 relaxivity due to a reduction in saturation magnetization. The ratio of r2/r1 decreased from 152 for the europium-free sample to 11.2 for x = 0.15, which indicates that Mn0.6Zn0.4Eu0.15Fe1.85O4 is a suitable candidate for dual-mode MRI contrast agent potentially. The samples with citric acid coating had higher r1 and lower r2 relaxivities than those of pluronic F127-coated samples.



https://doi.org/10.3390/nano13020331
Zhao, Junping; Wang, Yahui; Qian, Yudan; Jin, Huile; Tang, Xinyue; Huang, Zaimei; Lou, Jiayi; Zhang, Qingcheng; Lei, Yong; Wang, Shun
Hierarchical design of cross-linked NiCo2S4 nanowires bridged NiCo-hydrocarbonate polyhedrons for high-performance asymmetric supercapacitor. - In: Advanced functional materials, ISSN 1616-3028, Bd. 33 (2023), 4, 2210238, S. 1-14

Engineering core-shell materials with rationally designed architectures and components is an effective strategy to fulfill the high-performance requirements of supercapacitors. Herein, hierarchical candied-haws-like NiCo2S4NiCo(HCO3)2 core-shell heterostructure (NiCo2S4@HCs) is designed with NiCo(HCO3)2 polyhedrons being tightly strung by cross-linked NiCo2S4 nanowires. This rational design not only creates more electroactive sites but also suppresses the volume expansion during the charge-discharge processes. Meanwhile, density functional theory calculations ascertain that the formation of NiCo2S4@HCs heterostructure simultaneously facilitates OH− adsorption/desorption and accelerates electron transfer within the electrode, boosting fast and efficient redox reactions. Ex situ X-ray diffraction and Raman measurements reveal that gradual phase transformations from NiCo(HCO3)2 to NiCo(OH)2CO3 and then to highly-active NiCoOOH take place during the cycles. Therefore, NiCo2S4@HCs demonstrates an ultrahigh capacitance of 3178.2 F g−1 at 1 A g−1 and a remarkable rate capability of 2179.3 F g−1 at 30 A g−1. In addition, the asymmetric supercapacitor NiCo2S4@HCs//AC exhibits a high energy density of 69.6 W h kg−1 at the power density of 847 W kg−1 and excellent cycling stability with 90.2% retained capacitance after 10 000 cycles. Therefore, this novel structural design has effectively manipulated the interface charge states and guaranteed the structural integrity of electrode materials to achieve superior electrochemical performances.



https://doi.org/10.1002/adfm.202210238
Tan, Xinu; Liu, Yushun; Li, Feitao; Qiu, Risheng; Liu, Qing
Formation of nanocrystalline γ-ZrH in Zr-Nb alloy: crystal structure and twinning. - In: Micron, ISSN 1878-4291, Bd. 167 (2023), 103414

In the present work, the lattice parameter and the twins of γ-ZrH hydride in Zr-2.5Nb-1Si were characterized using high resolution electron microscopy. The lattice parameters of γ-ZrH (P42/mmc, Zr2H2 unit cell) is determined to be a= 0.336nm, c=0.508nm. Twinning γ-ZrH hydride ({011}<0̅11> type) is for the first time reported in zirconium alloys, whose orientation relationship with α-Zr is [100]γ-twins // [1̅210]α and (011)γ-twins // (0002)α. The formation process of γ-ZrH twins is also discussed based on a ‘grow-in’ mechanism during the transformation from α-Zr to γ-ZrH hydride.



https://doi.org/10.1016/j.micron.2023.103414