Two-dimensional (2D) materials exhibit the potential to transform semiconductor technology. Their rich compositional and stacking varieties allow tailoring materials' properties toward device applications. Monolayer to multilayer gallium sulfide (GaS) with its ultraviolet band gap, which can be tuned by varying the layer number, holds promise for solar-blind photodiodes and light-emitting diodes as applications.
View Article and Find Full Text PDFObjectives: To develop and share a deep learning method that can accurately identify optimal inversion time (TI) from multi-vendor, multi-institutional and multi-field strength inversion scout (TI scout) sequences for late gadolinium enhancement cardiac MRI.
Materials And Methods: Retrospective multicentre study conducted on 1136 1.5-T and 3-T cardiac MRI examinations from four centres and three scanner vendors.
Defects play a critical role for the functionality and performance of materials, but the understanding of the related effects is often lacking, because the typically low concentrations of defects make them difficult to study. A prominent case is the topological defects in two-dimensional materials such as graphene. The performance of graphene-based (opto-)electronic devices depends critically on the properties of the graphene/metal interfaces at the contacting electrodes.
View Article and Find Full Text PDFBackground: Anticoagulation for subsegmental pulmonary embolism (SSPE) is controversial.
Aim: To assess the impact of clinical context on anticoagulation and outcomes of SSPE.
Methods: We electronically searched computed tomography pulmonary angiogram reports to identify SSPE.
Objectives: To develop an image-based automatic deep learning method to classify cardiac MR images by sequence type and imaging plane for improved clinical post-processing efficiency.
Methods: Multivendor cardiac MRI studies were retrospectively collected from 4 centres and 3 vendors. A two-head convolutional neural network ('CardiSort') was trained to classify 35 sequences by imaging sequence (n = 17) and plane (n = 10).
Metal complexes at surfaces and interfaces play an important role in many areas of modern technology, including catalysis, sensors, and organic electronics. An important aspect of these interfaces is the possible exchange of the metal center, because this reaction can drastically alter the properties of the metal complex and thus of the interface. Here, we demonstrate that such metal exchange reactions are indeed possible and can proceed already at moderate temperatures even in the absence of solvents.
View Article and Find Full Text PDFAlthough the exact knowledge of the binding energy of organic adsorbates on solid surfaces is of vital importance for the realization of molecular nanostructures and the theoretical modelling of molecule-substrate interactions, an experimental determination is by no means trivial. Temperature-programmed desorption (TPD) is a widely used technique that can provide such information, but a quantitative analysis requires detailed knowledge of the pre-exponential factor of desorption and is therefore rarely performed on a quantitative level for larger molecules that often exhibit notable mutual intermolecular interactions. Here, we provide a thorough anlysis of TPD data of monolayers of pentacene and perfluoropentacene adsorbed on Au(111) that serve as a model system for polycyclic aromatic hydrocarbons adsorbed on noble metal surfaces.
View Article and Find Full Text PDFHybrid systems of two-dimensional (2D) materials such as transition metal dichalcogenides (TMDCs) and organic semiconductors (OSCs) have become subject of great interest for future device architectures. Although OSC-TMDC hybrid systems have been used in first device demonstrations, the precise preparation of ultra-thin OSC films on TMDCs has not been addressed. Due to the weak van der Waals interaction between TMDCs and OSCs, this requires precise knowledge of the thermodynamics at hand.
View Article and Find Full Text PDFThe quest for planar sp-hybridized carbon allotropes other than graphene, such as graphenylene and biphenylene networks, has stimulated substantial research efforts because of the materials' predicted mechanical, electronic, and transport properties. However, their syntheses remain challenging given the lack of reliable protocols for generating nonhexagonal rings during the in-plane tiling of carbon atoms. We report the bottom-up growth of an ultraflat biphenylene network with periodically arranged four-, six-, and eight-membered rings of sp-hybridized carbon atoms through an on-surface interpolymer dehydrofluorination (HF-zipping) reaction.
View Article and Find Full Text PDFA solvent-free dilithium porphyrin was synthesized by direct reaction of free-base meso-tetraphenylporphyrin with elemental lithium in ultra-high vacuum. The reaction product dilithium tetraphenylporphyrin was studied by temperature-programmed desorption mass spectrometry (TPD-MS) and hard X-ray photoelectron spectroscopy (HAXPES). The solid-state reaction is thermodynamically favored, according to density functional theory (DFT) calculations.
View Article and Find Full Text PDFThe binary lead fluoride Pb F was synthesized by the reaction of anhydrous HF with Pb O or by the reaction of BrF with PbF . The compound was characterized by single-crystal and powder X-ray diffraction, IR, Raman, and solid-state MAS F NMR spectroscopy, as well as thermogravimetric analysis, XP and near-edge X-ray absorption fine structure (NEXAFS) spectroscopy. Solid-state quantum-chemical calculations are provided for the vibrational analyses and band assignments.
View Article and Find Full Text PDFInterfaces between organic semiconductors and metallic layers are ubiquitous in organic (opto-) electronic devices and can significantly influence their functionality. Here, we studied in situ prepared metal-organic interfaces, which were obtained by vapor deposition of metals (Co, Fe) onto organic semiconductor films (2H-tetraphenylporphyrin), with hard x-ray photoelectron spectroscopy. In these systems, the interphase zones, which are formed by diffusion and reaction of the metal in the organic material, can be clearly distinguished spectroscopically from the unreacted organic bulk, since they comprise the corresponding metalloporphyrins, CoTPP and FeTPP.
View Article and Find Full Text PDFA Li4Ti5O12 (LTO) film was coated as buffer layer onto a LiNi0.5Mn1.5O4 (LNMO) high-voltage cathode, and after cycling of the cathode in a battery electrolyte, the LTO film was investigated by means of synchrotron radiation based hard X-ray photoelectron spectroscopy (HAXPES).
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