120 results match your criteria: "Institute for Materials Science and Max Bergmann Center of Biomaterials[Affiliation]"

The rapid development of two-dimensional (2D) transition-metal dichalcogenides has been possible owing to their special structures and remarkable properties. In particular, palladium diselenide (PdSe) with a novel pentagonal structure and unique physical characteristics have recently attracted extensive research interest. Consequently, tremendous research progress has been achieved regarding the physics, chemistry, and electronics of PdSe.

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Two-dimensional covalent organic frameworks (2D COFs) have attracted attention as versatile active materials in many applications. Recent advances have demonstrated the synthesis of monolayer 2D COF via an air-water interface. However, the interfacial 2D polymerization mechanism has been elusive.

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Accurate knowledge of transport properties of Li-insertion materials in application-relevant temperature ranges is of crucial importance for the targeted optimization of Li-ion batteries (LIBs). Galvanostatic intermittent titration technique (GITT) is a widely applied method to determine Li-ion diffusion coefficients of electrode materials. The well-known calculation formulas based on Weppner's and Huggins' approach, imply a square-root time dependence of the potential during a GITT pulse.

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The morphology of small-molecule organic semiconducting materials can vary from single crystals via polycrystalline films with varying grain sizes to amorphous structures, depending on the process conditions. This structural variety affects the electronic properties and, thus, the performance of organic electronic devices. A nucleation-equilibration approach is investigated, whose focus is on the construction of morphologies with controlled variations in the average grain size.

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Two-dimensional Covalent Organic Frameworks (2D COFs) have attracted a lot of interest because of their potential for a broad range of applications. Different combinations of their molecular building blocks can lead to new materials with different physical and chemical properties. In this study, the elasticity of different single-layer tetrabenzoporphyrin (H2-TBPor) and phthalocyanine (H2-Pc) based 2D COFs is numerically investigated using a density-functional based tight-binding approach.

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The shape of objects has a strong influence on their dynamics. Here, we present comparative studies of two different motile objects, spherical Ag/AgCl Janus particles and polystyrene Janus nanorods, that move due to an ionic self-diffusiophoretic propulsion mechanism when exposed to blue light. In this paper, we propose a method to fabricate Janus rodlike particles with high aspect ratios and hemispherical tip shapes.

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The investigation of molecular interactions between silica phases and organic components is crucial for elucidating the main steps involved in the biosilica mineralization process. In this respect, the structural characterization of the organic/inorganic interface is particularly useful for a deeper understanding of the dominant mechanisms of biomineralization. In this work, we have investigated the interaction of selectively C- and N-labeled atoms of organic long-chain polyamines (LCPAs) with Si-labeled atoms of a silica layer at the molecular level.

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The physical origin of the so-called chirality-induced spin selectivity (CISS) effect has puzzled experimental and theoretical researchers over the past few years. Early experiments were interpreted in terms of unconventional spin-orbit interactions mediated by the helical geometry. However, more recent experimental studies have clearly revealed that electronic exchange interactions also play a key role in the magnetic response of chiral molecules in singlet states.

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In vitro characterization of osteoblast cells on polyelectrolyte multilayers containing detonation nanodiamonds.

Biomed Mater

August 2020

Institute for Materials Science and Max Bergmann Center of Biomaterials, Technische Universität Dresden, Dresden, Germany. Bio- and Nanotechnology, Fraunhofer Institute for Ceramic Technologies and Systems IKTS Material Diagnostics, Dresden, Germany. Both authors contributed equally to this manuscript.

Nanoparticle-enhanced coatings of bone implants are a promising method to facilitate sustainable wound healing, leading to an increase in patient well-being. This article describes the in vitro characterization of osteoblast cells interacting with polyelectrolyte multilayers, which contain detonation nanodiamonds (NDs), as a novel class of carbon-based coating material, which presents a unique combination of photoluminescence and drug-binding properties. The cationic polyelectrolyte, namely polydiallyldimethylammonium chloride (PDDA), has been used to immobilize NDs on silica glass.

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The chirality-induced spin selectivity effect has been confirmed experimentally for a large class of organic molecules. Adequately modeling the effect remains a challenging task, with both phenomenological models and first-principles simulations yielding inconclusive results. Building upon a previously presented model by K.

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Tunable Photodetectors via In Situ Thermal Conversion of TiS to TiO.

Nanomaterials (Basel)

April 2020

Materials Science Factory, Instituto de Ciencia de Materiales de Madrid (ICMM-CSIC), E-28049 Madrid, Spain.

In two-dimensional materials research, oxidation is usually considered as a common source for the degradation of electronic and optoelectronic devices or even device failure. However, in some cases a controlled oxidation can open the possibility to widely tune the band structure of 2D materials. In particular, we demonstrate the controlled oxidation of titanium trisulfide (TiS), a layered semicon-ductor that has attracted much attention recently thanks to its quasi-1D electronic and optoelectron-ic properties and its direct bandgap of 1.

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In the majority of photocatalytic applications, the photocatalyst is dispersed as a suspension of nanoparticles. The suspension provides a higher surface for the photocatalytic reaction in respect to immobilized photocatalysts. However, this implies that recovery of the particles by filtration or centrifugation is needed to collect and regenerate the photocatalyst.

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We demonstrate the functionalization of silicon nanowire based field effect transistors (SiNW FETs) FETs with stimuli-responsive polymer brushes of poly(N-isopropylacrylamide) (PNIPAAM) and poly(acrylic acid) (PAA). Surface functionalization was confirmed by atomic force microscopy, contact angle measurements, and verified electrically using a silicon nanowire based field effect transistor sensor device. For thermo-responsive PNIPAAM, the physicochemical properties (i.

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proMAD: semiquantitative densitometric measurement of protein microarrays.

BMC Bioinformatics

February 2020

Institute of Health and Biomedical Innovation, Queensland University of Technology, Kelvin Grove, Queensland, 4059, Australia.

Background: Protein microarrays are a versatile and widely used tool for analyzing complex protein mixtures. Membrane arrays utilize antibodies which are captured on a membrane to specifically immobilize several proteins of interest at once. Using detection antibodies, the bound protein-antibody-complex is converted into visual signals, which can be quantified using densitometry.

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Spin-Polarized Electron Transmission in DNA-Like Systems.

Biomolecules

December 2019

GISC, Departamento de Física de Materiales, Universidad Complutense, E-28040 Madrid, Spain.

The helical distribution of the electronic density in chiral molecules, such as DNA and bacteriorhodopsin, has been suggested to induce a spin-orbit coupling interaction that may lead to the so-called chirality-induced spin selectivity (CISS) effect. Key ingredients for the theoretical modelling are, in this context, the helically shaped potential of the molecule and, concomitantly, a Rashba-like spin-orbit coupling due to the appearance of a magnetic field in the electron reference frame. Symmetries of these models clearly play a crucial role in explaining the observed effect, but a thorough analysis has been largely ignored in the literature.

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A zinc selective oxytocin based biosensor.

J Mater Chem B

January 2020

Institute of Chemistry and The Center for Nanoscience and Nanotechnology, The Hebrew University of Jerusalem, Jerusalem 91904, Israel.

Oxytocin is a peptide hormone with high affinity to both Zn and Cu ions compared to other metal ions. This affinity makes oxytocin an attractive recognition layer for monitoring the levels of these essential ions in biofluids. Native oxytocin cannot differentiate between Cu and Zn ions and hence it is not useful for sensing Zn in the presence of Cu.

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Engineering conducting polymer thin films with morphological homogeneity and long-range molecular ordering is intriguing to achieve high-performance organic electronics. Polyaniline (PANI) has attracted considerable interest due to its appealing electrical conductivity and diverse chemistry. However, the synthesis of large-area PANI thin film and the control of its crystallinity and thickness remain challenging because of the complex intermolecular interactions of aniline oligomers.

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Bacterial surface layer proteins (S-layer) possess unique binding properties for metal ions. By combining the binding capability of S-layer proteins with the optical properties of gold nanoparticles (AuNP), namely plasmonic resonance, a colorimetric detection system for metal and metalloid ions in water was developed. Eight S-layer proteins from different bacteria species were used for the functionalization of AuNP.

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Two iron porphyrin complexes with either mesityl (FeTMP) or thiophene (FeT3ThP) peripheral substituents were attached to basal pyrolytic graphite and Ag electrodes via different immobilization methods. By combining cyclic voltammetry and in-operando surface-enhanced Raman spectroscopy along with MD simulations and DFT calculations, their respective surface attachment, redox chemistry and activity toward electrocatalytic oxygen reduction was investigated. For both porphyrin complexes, it could be shown that catalytic activity is restricted to the first (few) molecular layer(s), although electrodes covered with thiophene-substituted complexes showed a better capability to consume the oxygen at a given overpotential even in thicker films.

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Beyond the State of the Art: Novel Approaches for Thermal and Electrical Transport in Nanoscale Devices.

Entropy (Basel)

August 2019

Nano-Bio Spectroscopy Group and European Theoretical Spectroscopy Facility (ETSF), Universidad del Pais Vasco CFM CSIC-UPV/EHU-MPC and DIPC, Av. Tolosa 72, 20018 San Sebastian, Spain.

Almost any interaction between two physical entities can be described through the transfer of either charge, spin, momentum, or energy. Therefore, any theory able to describe these transport phenomena can shed light on a variety of physical, chemical, and biological effects, enriching our understanding of complex, yet fundamental, natural processes, e.g.

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Peptides are very common recognition entities that are usually attached to surfaces using multistep processes. These processes require modification of the native peptides and of the substrates. Using functional groups in native peptides for their assembly on surfaces without affecting their biological activity can facilitate the preparation of biosensors.

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A crucial goal for increasing thermal energy harvesting will be to progress towards atomistic design strategies for smart nanodevices and nanomaterials. This requires the combination of computationally efficient atomistic methodologies with quantum transport based approaches. Here, we review our recent work on this problem, by presenting selected applications of the PHONON tool to the description of phonon transport in nanostructured materials.

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Exploring the write-in process in molecular quantum cellular automata: a combined modelingand first-principle approach.

J Phys Condens Matter

October 2019

Institute for Materials Science and Max Bergmann Center of Biomaterials, Dresden University of Technology, 01062 Dresden, Germany. Max Planck Institute for the Physics of Complex Systems, 01187 Dresden, Germany.

The molecular quantum cellular automata paradigm (m-QCA) offers a promising alternative framework to current CMOS implementations. A crucial aspect for implementing this technology concerns the construction of a device which effectively controls intramolecular charge-transfer processes. Tentative experimental implementations have been developed in which a voltage drop is created generating the forces that drive a molecule into a logic state.

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Emerging pollutants are an essential class of recalcitrant contaminants that are not eliminated from water after conventional treatment. Here, a photocatalytic microporous membrane based on polyvinylidene difluoride-co-trifluoroethylene (PVDF-TrFE) with immobilised TiO nanoparticles, prepared by solvent casting, was tested against representative emerging pollutants. The structure and composition of these polymeric membranes were characterized by scanning electron microscopy, energy dispersive X-ray spectroscopy, Fourier-transform infrared spectroscopy, porosimetry, and contact angle goniometry.

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We explore an n-type doping strategy of semiconducting single-walled carbon nanotubes (sc-SWCNTs) by a covalent functionalization in ammonia plasma and elucidate the effect of air exposure on thermoelectric properties of the sc-SWCNTs before and after doping. Without doping, the sc-SWCNT films have a Seebeck coefficient of 125 μV/K and a power factor (PF) of 95 μW/m K in ambient conditions. Heating of such films in air up to 100 °C and above is not changing their thermoelectric properties noticeably; however, the films can be converted to an n-type material simply by gas desorption at low pressure and room temperature, showing an outstanding negative Seebeck coefficient of -133 μV/K and a PF of 55 μW/m K.

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