Publications by authors named "Johannes Will"

Silver nanowire (AgNW) networks have emerged as one of the most promising materials for flexible transparent conductive electrodes. These wires offer excellent electrical, optical, and mechanical properties and can be applied using low-cost printing techniques with the potential for upscaling. To elucidate the mechanical properties of nanowire networks for use in flexible electronics, it is essential to first characterize the behavior of individual wires adhered to the polymer surface under mechanical loading of the polymer.

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A comprehensive investigation of the impact of hydrogen (H) pretreatments on Ga-Pt supported catalytic active liquid metal solution (SCALMS) for propane dehydrogenation (PDH) is reported. Our approach bridges from model system investigations to real-world catalytic systems, which are tested in continuously operating PDH reactors. The microscopic and spectroscopic findings on model Ga-Pt systems suggest changes in the electronic structure and surface chemistry during SCALMS sample oxidation and H pretreatment, indicating potential modifications of the active sites involved in PDH.

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Antimony sulfide (SbS), a compound of earth-abundant elements with a highly anisotropic, quasi-layered crystal structure, has triggered growing interest as a solar absorber in photovoltaics and as a phase-change material in memory devices. However, challenges remain in achieving high-quality thin films with controlled nucleation and growth for optimal performance. Here, we investigate the phase transformation, crystal structure and properties, as well as the growth and degradation of atomic layer-deposited SbS thin films using TEM and correlative analysis.

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The stabilization of single-atom catalysts on semiconductor substrates is pivotal for advancing photocatalysis. TiO, a widely employed photocatalyst, typically stabilizes single atoms at oxygen vacancies-sites that are accessible but prone to agglomeration under illumination. Here, we demonstrate that cation vacancies in Ti-deficient TiO nanosheets provide highly stable anchoring sites for Pt single atoms, enabling persistent photocatalytic hydrogen evolution.

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We synthesize p-type TiO nanotubes that allow band-gap adjustment by quantum confinement. These tubes therefore enable reductive photocatalytic reactions that are not thermodynamically possible on classic titania photocatalysts. Here, we demonstrate the direct photocatalytic nitrate reduction to ammonia without any need of hole scavengers.

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Ti-deficient TiO nanosheets derived from lepidocrocite-type titanate delamination show a p-type conductivity with a band gap widened by the quantum confinement effect to 3.7 eV. This shift in the extended band positions─and thus in the electron transfer level─allows a direct photocatalytic nitrate reduction to ammonia without the use of any hole scavengers; this in contrast to classic TiO.

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Supported catalytically active liquid metal solutions (SCALMS) are materials composed of a liquid metal alloy deposited on a porous support. Due to the dynamic properties of the liquid metal alloy, these systems are suggested to form single atom sites, resulting in unique catalytic properties. Ga-Ni SCALMS were successfully applied to ethylene oligomerization, yielding catalysts that were stable up to 120 h time on stream.

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Article Synopsis
  • Interest in organic solar cells (OSCs) is increasing, with device performance linked to the nanomorphology of bulk heterojunctions (BHJs) developed during drying and post-treatment processes.
  • This study explores the impact of thermal annealing (TA) on the DRCN5T:PCBM blend using phase field simulations to understand how post-treatment affects BHJ morphology.
  • Simulation results reveal that the BHJ's morphological evolution during TA is primarily driven by the dissolution of smaller, unstable DRCN5T crystals and the anisotropic growth of larger crystals.
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Recently, the use of Pt in the form of single atoms (SA) has attracted considerable attention to promote the cathodic hydrogen production reaction from water in electrochemical or photocatalytic settings. First, produce suitable electrodes by Pt SA deposition on Direct current (DC)-sputter deposited titania (TiO) layers on graphene-these electrodes allow to characterization of the electrochemical properties of Pt single atoms and their investigation in high-resolution HAADF-STEM. For Pt SAs loaded on TiO, electrochemical H evolution shows only a very small overpotential.

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The widespread application of green hydrogen production technologies requires cost reduction of crucial elements. To achieve this, a viable pathway to reduce the iridium loading in proton exchange membrane water electrolysis (PEMWE) is explored. Herein, a scalable synthesis method based on a photodeposition process for a TiO@IrO core-shell catalyst with a reduced iridium content as low as 40 wt.

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  • The study examines how heavy water (DO) affects the formation and stability of CdS nanoparticles in comparison to normal water (HO), specifically through the lens of interactions with the ligand EDTA.
  • It uses advanced techniques like small angle X-ray scattering (SAXS) and scanning transmission electron microscopy to analyze changes in nanoparticle size and structure.
  • Findings show that the isotopic difference leads to significant changes in nanoparticle stability, suggesting that results from experiments in DO may not be applicable to those in normal water due to these isotopic effects.
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With recent advances in the field of single-atoms (SAs) used in photocatalysis, an unprecedented performance of atomically dispersed co-catalysts has been achieved. However, the stability and agglomeration of SA co-catalysts on the semiconductor surface may represent a critical issue in potential applications. Here, the photoinduced destabilization of Pt SAs on the benchmark photocatalyst, TiO , is described.

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Obesity is a pre-disposing condition for chronic obstructive pulmonary disease, asthma, and pulmonary arterial hypertension. Accumulating evidence suggests that metabolic influences during development can determine chronic lung diseases (CLD). We demonstrate that maternal obesity causes early metabolic disorder in the offspring.

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In situ TEM utilizing windowed gas cells is a promising technique for studying catalytic processes, wherein temperature is one of the most important parameters to be controlled. Current gas cells are only capable of temperature measurement on a global (mm) scale, although the local temperature at the spot of observation (µm to nm scale) may significantly differ. Thus, local temperature fluctuations caused by gas flow and heat dissipation dynamics remain undetected when solely relying on the global device feedback.

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Here, we evaluate three different noble metal co-catalysts (Pd, Pt, and Au) that are present as single atoms (SAs) on the classic benchmark photocatalyst, TiO. To trap the single atoms on the surface, we introduced controlled surface vacancies (Ti-O) on anatase TiO nanosheets by a thermal reduction treatment. After anchoring identical loadings of single atoms of Pd, Pt, and Au, we measure the photocatalytic H generation rate and compare it to the classic nanoparticle co-catalysts on the nanosheets.

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Article Synopsis
  • Semiconducting self-assembled monolayers (SAMs) are important for creating precise organic thin-film electronics by controlling the active layer's structure.
  • The study focuses on self-assembled monolayer field-effect transistors (SAMFETs) made from phosphonic acid oligomers of 3-hexylthiophene, showing that increasing the number of thiophene units enhances charge mobility in the devices.
  • Advanced techniques like X-ray reflectivity and X-ray photoelectron spectroscopy reveal that shorter oligomers align well with the substrate, whereas longer ones adopt a folded configuration, leading to a significant increase in mobility for the longer chains through molecular order adjustments.
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We theoretically propose and experimentally demonstrate the use of motional sidebands in a trapped ensemble of ^{87}Rb atoms to engineer tunable long-range XXZ spin models. We benchmark our simulator by probing a ferromagnetic to paramagnetic dynamical phase transition in the Lipkin-Meshkov-Glick model, a collective XXZ model plus additional transverse and longitudinal fields, via Rabi spectroscopy. We experimentally reconstruct the boundary between the dynamical phases, which is in good agreement with mean-field theoretical predictions.

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Light-induced halide segregation limits the bandgap tunability of mixed-halide perovskites for tandem photovoltaics. Here we report that light-induced halide segregation is strain-activated in MAPb(IBr) with Br concentration below approximately 50%, while it is intrinsic for Br concentration over approximately 50%. Free-standing single crystals of CHNHPb(IBr) (35%Br) do not show halide segregation until uniaxial pressure is applied.

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The mechanism behind the stability of organic nanoparticles prepared by liquid antisolvent (LAS) precipitation without a specific stabilizing agent is poorly understood. In this work, we propose that the organic solvent used in the LAS process rapidly forms a molecular stabilizing layer at the interface of the nanoparticles with the aqueous dispersion medium. To confirm this hypothesis, -octadecyltrichlorosilane (OTS)-functionalized silicon wafers in contact with water-solvent mixtures were used as a flat model system mimicking the solid-liquid interface of the organic nanoparticles.

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  • Researchers demonstrate precise control over the composition of perylene bisimide (PBI) monomers and aggregates on alumina nanoparticle surfaces.
  • Phosphonic acid functionalized PBI derivatives (PA-PBI) self-assemble into mixed monolayers with different ligands, creating core-shell nanoparticles (NPs) with tailored optical properties.
  • Advanced spectroscopy techniques and molecular dynamics simulations reveal how changes in shell composition affect PBI aggregation and optical behavior.
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Bronchopulmonary dysplasia (BPD) is a chronic lung disease of preterm infants, characterized by lung growth arrest and matrix remodeling. Various animal models provide mechanistic insights in the pathogenesis of BPD. Since there is increasing evidence that genetic susceptibility modifies the response to lung injury, we investigated strain-dependent effects in hyperoxia (HYX)-induced lung injury of newborn mice.

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  • Current-voltage hysteresis in organo-halide perovskite solar cells can be mitigated by engineering a thin methylammonium iodide-rich interface between the perovskite and metal oxide, improving cell performance.
  • Surface functionalization techniques enable control over the composition of this interface, transitioning it from lead (Pb) poor to Pb rich, while keeping the bulk properties of the perovskite films intact.
  • Advanced techniques like X-ray reflectivity and Kelvin probe force microscopy have provided insights into the structural changes at the interface and local potential variations, contributing to a new understanding of hysteresis in these solar cells.
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  • The research highlights the use of functional oligomers made from π-conjugated oligofluorenes to create amorphous monolayers that can selectively assemble.
  • These monolayers show strong lateral charge transport abilities in self-assembled monolayer field-effect transistors, even across long distances and amid mixed types of molecules.
  • The findings suggest that this oligomer approach could inspire innovative designs for new self-assembling semiconducting materials.
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Simple model organisms are instrumental for in vivo studies of developmental and cellular differentiation processes. Currently, the evolutionary distance to man of conventional invertebrate model systems and the complexity of genomes in vertebrates are critical challenges to modeling human normal and pathological conditions. The chordate Ciona intestinalis is an invertebrate chordate that emerged from a common ancestor with the vertebrates and may represent features at the interface between invertebrates and vertebrates.

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X-ray reflectivity measurements of increasingly more complex interfaces involving silicon (001) substrates reveal the existence of a thin low-density layer intruding between the single-crystalline silicon and the amorphous native SiO2 terminating it. The importance of accounting for this layer in modeling silicon/liquid interfaces and silicon-supported monolayers is demonstrated by comparing fits of the measured reflectivity curves by models including and excluding this layer. The inclusion of this layer, with 6-8 missing electrons per silicon unit cell area, consistent with one missing oxygen atom whose bonds remain hydrogen passivated, is found to be particularly important for an accurate and high-resolution determination of the surface normal density profile from reflectivities spanning extended momentum transfer ranges, now measurable at modern third-generation synchrotron sources.

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