1,342 results match your criteria: "and Center for Nanoscience[Affiliation]"

Spatiotemporal Spectroscopy of Fast Excited-State Diffusion in 2D Covalent Organic Framework Thin Films.

J Am Chem Soc

January 2025

Department of Chemistry and Center for NanoScience (CeNS), University of Munich (LMU), Butenandtstraße 5-13, Munich 81377, Germany.

Covalent organic frameworks (COFs), crystalline and porous conjugated structures, are of great interest for sustainable energy applications. Organic building blocks in COFs with suitable electronic properties can feature strong optical absorption, whereas the extended crystalline network can establish a band structure enabling long-range coherent transport. This peculiar combination of both molecular and solid-state materials properties makes COFs an interesting platform to study and ultimately utilize photoexcited charge carrier diffusion.

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Biomolecular structures are typically determined using frozen or crystalline samples. Measurement of intramolecular distances in solution can provide additional insights into conformational heterogeneity and dynamics of biological macromolecules and their complexes. The established molecular ruler techniques used for this (NMR, FRET, and EPR) are, however, limited in their dynamic range and require model assumptions to determine absolute distance or distance distributions.

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Aptamer melting biosensors for thousands of signaling and regenerating cycles.

Biosens Bioelectron

March 2025

School of Food Science and Engineering, National R&D Center for Goat Dairy Products Processing Technology, Shaanxi University of Science and Technology, Xi'an, 710021, China. Electronic address:

Due to their recognition abilities and inherent regenerability, aptamers have great potential in biosensing applications. However, effective signal transduction and regeneration strategies are still required. Herein, we develop a melting-based aptamer sensing strategy capable of homogeneous signaling with over 1000 regenerating cycles without significant deterioration of performance.

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Photons, Excitons, and Electrons in Covalent Organic Frameworks.

J Am Chem Soc

November 2024

Department of Chemistry and Center for NanoScience, University of Munich (LMU), Butenandtstr. 5-13, 81377 Munich, Germany.

Covalent organic frameworks (COFs) are created by the condensation of molecular building blocks and nodes to form two-dimensional (2D) or three-dimensional (3D) crystalline frameworks. The diversity of molecular building blocks with different properties and functionalities and the large number of possible framework topologies open a vast space of possible well-defined porous architectures. Besides more classical applications of porous materials such as molecular absorption, separation, and catalytic conversions, interest in the optoelectronic properties of COFs has recently increased considerably.

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The intricate interplay between DNA and proteins is key for biological functions such as DNA replication, transcription and repair. Dynamic nanoscale observations of DNA structural features are necessary for understanding these interactions. Here we introduce graphene energy transfer with vertical nucleic acids (GETvNA), a method to investigate DNA-protein interactions that exploits the vertical orientation adopted by double-stranded DNA on graphene.

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Biosensors play key roles in medical research and diagnostics. However, the development of biosensors for new biomolecular targets of interest often involves tedious optimization steps to ensure a high signal response at the analyte concentration of interest. Here we show a modular nanosensor platform that facilitates these steps by offering ways to decouple and independently tune the signal output as well as the response window.

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Article Synopsis
  • The study focuses on predicting the optical properties of large arrays of luminescent nanowires, which is crucial for developing integrated photonic devices, but it's complicated by varying geometries and individual differences of the nanowires.!* -
  • Researchers conducted high-throughput spectroscopy on 16,800 InGaAs quantum heterostructures to evaluate luminescence efficiency and emission energy trends, finding that larger pre-patterned diameters improve uniformity.!* -
  • Anomalies in emission energy linked to rotational twinning in the InGaAs area were noted, leading to significant shifts in energy due to quantum confinement effects, helping optimize the relationship between geometry and optical properties in quantum nanowires.!*
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Article Synopsis
  • The study investigates the energy transfer properties of 2D titanium carbide MXene materials and explores their use in single-molecule biosensing for the first time.
  • DNA origami structures are employed to precisely position single dye molecules on the MXene surface, allowing for controlled experiments on energy transfer efficiency.
  • Findings demonstrate that MXenes can serve as effective nanorulers for measuring distances at the molecular level, showcasing their potential for biosensing applications that require high sensitivity to small distance changes.
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Dimensionality reduction in bulk-boundary reaction-diffusion systems.

Phys Rev E

September 2024

Arnold Sommerfeld Center for Theoretical Physics and Center for NanoScience, Department of Physics, Ludwig-Maximilians-Universität München, Theresienstraße 37, D-80333 München, Germany.

Intracellular protein patterns regulate many vital cellular functions, such as the processing of spatiotemporal information or the control of shape deformations. To do so, pattern-forming systems can be sensitive to the cell geometry by means of coupling the protein dynamics on the cell membrane to dynamics in the cytosol. Recent studies demonstrated that modeling the cytosolic dynamics in terms of an averaged protein pool disregards possibly crucial aspects of the pattern formation, most importantly concentration gradients normal to the membrane.

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Antisolvent controls the shape and size of anisotropic lead halide perovskite nanocrystals.

Nat Commun

October 2024

Soft Condensed Matter Group and Center for NanoScience, Faculty of Physics, Ludwig-Maximilians-Universität München, Geschwister-Scholl-Platz 1, Munich, Germany.

Colloidal lead halide perovskite nanocrystals have potential for lighting applications due to their optical properties. Precise control of the nanocrystal dimensions and composition is a prerequisite for establishing practical applications. However, the rapid nature of their synthesis precludes a detailed understanding of the synthetic pathways, thereby limiting the optimisation.

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Advanced breast cancer, as well as ineffective treatments leading to surviving cancer cells, can result in the dissemination of these malignant cells from the primary tumor to distant organs. Recent research has shown that microRNA 200c (miR-200c) can hamper certain steps of the invasion-metastasis cascade. However, it is still unclear whether miR-200c expression alone is sufficient to prevent breast cancer cells from metastasis formation.

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Understanding and controlling the photoexcited quasiparticle (QP) dynamics in monolayer (ML) transition metal dichalcogenides (TMDs) lays the foundation for exploring the strongly interacting, nonequilibrium two-dimensional (2D) QP and polaritonic states in these quantum materials and for harnessing the properties emerging from these states for optoelectronic applications. In this study, scanning tunneling microscopy/spectroscopy (STM/scanning tunneling spectroscopy) with light illumination at the tunneling junction is performed to investigate the QP dynamics in ML MoS on an Au(111) substrate with nanoscale corrugations. The corrugations on the surface of the substrate induce nanoscale local strain in the overlaying ML MoS single crystal, which result in energetically favorable spatial regions where photoexcited QPs, including excitons, trions, and electron-hole plasmas, accumulate.

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Giant Valley Zeeman Splitting in Vanadium-Doped WSe Monolayers.

Small

December 2024

Departamento de Física, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, 30123-970, Brazil.

2D dilute magnetic semiconductors (DMS) based on transition metal dichalcogenides (TMD) offer an innovative pathway for advancing spintronic technologies, including the potential to exploit phenomena such as the valley Zeeman effect. However, the impact of magnetic ordering on the valley degeneracy breaking and on the enhancement of the optical transitions g-factors of these materials remains an open question. Here, a giant effective g-factors ranging between ≈-27 and -69 for the bound exciton at 4 K in vanadium-doped WSe monolayers, obtained through magneto-photoluminescence (PL) experiments is reported.

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Evolution of the conformational dynamics of the molecular chaperone Hsp90.

Nat Commun

October 2024

Center for Protein Assemblies, Department Bioscience, School of Natural Sciences, Technical University Munich, Garching, Germany.

Hsp90 is a molecular chaperone of central importance for protein homeostasis in the cytosol of eukaryotic cells, with key functional and structural traits conserved from yeast to man. During evolution, Hsp90 has gained additional functional importance, leading to an increased number of interacting co-chaperones and client proteins. Here, we show that the overall conformational transitions coupled to the ATPase cycle of Hsp90 are conserved from yeast to humans, but cycle timing as well as the dynamics are significantly altered.

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The possibility to combine organic semiconducting materials with inorganic halide perovskites opens exciting pathways toward tuning optoelectronic properties. Exploring stable and nontoxic, double perovskites as a host for electroactive organic cations to form two-dimensional (2D) hybrid materials is an emerging opportunity to create both functional and lead-free materials for optoelectronic applications. By introducing naphthalene and pyrene moieties into Ag-Bi-I and Cu-Bi-I double perovskite lattices, intrinsic electronic challenges of double perovskites are addressed and the electronic anisotropy of 2D perovskites can be modulated.

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Field theory of enzyme-substrate systems with restricted long-range interactions.

Phys Rev E

August 2024

Arnold Sommerfeld Center for Theoretical Physics and Center for NanoScience, Department of Physics, Ludwig-Maximilians-Universität München, D-80333 Munich, Germany and Max Planck Institute for the Physics of Complex Systems, D-01138 Dresden, Germany.

Enzyme-substrate kinetics form the basis of many biomolecular processes. The interplay between substrate binding and substrate geometry can give rise to long-range interactions between enzyme binding events. Here we study a general model of enzyme-substrate kinetics with restricted long-range interactions described by an exponent -γ.

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During mitosis in eukaryotic cells, mechanical forces generated by the mitotic spindle pull the sister chromatids into the nascent daughter cells. How do mitotic chromosomes achieve the necessary mechanical stiffness and stability to maintain their integrity under these forces? Here we use optical tweezers to show that ions involved in physiological chromosome condensation are crucial for chromosomal stability, stiffness and viscous dissipation. We combine these experiments with high-salt histone depletion and theory to show that chromosomal elasticity originates from the chromatin fibre behaving as a flexible polymer, whereas energy dissipation can be explained by modelling chromatin loops as an entangled polymer solution.

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We present a way to encode more information in fluorescence imaging by splitting the original point spread function (PSF), which offers broadband operation and compatibility with other PSF engineering modalities and existing analysis tools. We demonstrate the approach using the 'Circulator', an add-on that encodes the fluorophore emission band into the PSF, enabling simultaneous multicolor super-resolution and single-molecule microscopy using essentially the full field of view.

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scEpiAge: an age predictor highlighting single-cell ageing heterogeneity in mouse blood.

Nat Commun

August 2024

Laboratory of Nutrition and Metabolic Epigenetics, Department of Health Sciences and Technology, ETH Zurich, Zurich, Switzerland.

Ageing is the accumulation of changes and decline of function of organisms over time. The concept and biomarkers of biological age have been established, notably DNA methylation-based clocks. The emergence of single-cell DNA methylation profiling methods opens the possibility of studying the biological age of individual cells.

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Interpenetrated Donor-Acceptor Heterojunctions in 2D Conjugated Dibenzo[,]chrysene-Based Kagome Covalent Organic Frameworks.

ACS Appl Mater Interfaces

September 2024

Department of Chemistry and Center for NanoScience (CeNS), University of Munich (LMU), Butenandtstraße 5-13, 81377 Munich, Germany.

Dibenzo[,]chrysene can be viewed as a constrained propeller-shaped tetraphenylethylene with reduced curvature and has been utilized to construct dual-pore kagome covalent organic frameworks (COFs) with tightly packed two-dimensional (2D) layers owing to its rigid and more planar structural characteristics. Here, we introduce 2D COFs based on the node 4,4',4″,4‴-(dibenzo[,]chrysene-2,7,10,15-tetraphenyl)tetraamine (DBCTPTA) featuring extended conjugation compared to the dibenzo[,]chrysene-3,6,11,14-tetraamine (DBCTA) node. We establish two exceptionally crystalline imine-linked 2D COFs with a hexagonal dual-pore kagome structure based on the DBCTPTA core.

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Spontaneous Photonic Jammed Packing of Core-Shell Colloids in Conductive Aqueous Inks for Non-Iridescent Structural Coloration.

ACS Appl Mater Interfaces

October 2024

Department of Materials and Optoelectronic Science and Center for Nanoscience and Nanotechnology, National Sun Yat-Sen University, Kaohsiung 80424, Taiwan.

Integrating structural colors and conductivity into aqueous inks has the potential to revolutionize wearable electronics, providing flexibility, sustainability, and artistic appeal to electronic components. This study aims to introduce bioinspired color engineering to conductive aqueous inks. Our self-assembly approach involves mixing poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) with sulfonic acid-modified polystyrene (sPS) colloids to generate non-iridescent structural colors in the inks.

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Article Synopsis
  • Eukaryotic cells can change shape and move through tight spaces, but how this relates to their nuclei is still not well understood.
  • This study focuses on mesenchymal cancer cell nuclei as they travel through narrow hydrogel channels, revealing that migration speed and frequency peak when channel widths are similar to the nuclear diameter.
  • The researchers discovered that as nuclei migrate through these channels, they deform and change shape, with both pulling and pushing forces from the cytoskeleton playing a role in their movement under confinement.
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Significantly reducing the iridium content in oxygen evolution reaction (OER) catalysts while maintaining high electrocatalytic activity and stability is a key priority in the development of large-scale proton exchange membrane (PEM) electrolyzers. In practical catalysts, this is usually achieved by depositing thin layers of iridium oxide on a dimensionally stable metal oxide support material that reduces the volumetric packing density of iridium in the electrode assembly. By comparing two support materials with different structure types, it is shown that the chemical nature of the metal oxide support can have a strong influence on the crystallization of the iridium oxide phase and the direction of crystal growth.

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Nanoscale Mechanical Manipulation of Ultrathin SiN Membranes Enabling Infrared Near-Field Microscopy of Liquid-Immersed samples.

Small

November 2024

Chair in Hybrid Nanosystems and Center for NanoScience, Nano-Institute Munich, Faculty of Physics, Ludwig-Maximilians-University, Königinstr. 10, 80539, München, Germany.

Scattering scanning near-field optical microscopy (s-SNOM) is a powerful technique for mid-infrared spectroscopy at nanometer length scales. By investigating objects in aqueous environments through ultrathin membranes, s-SNOM has recently been extended toward label-free nanoscopy of the dynamics of living cells and nanoparticles, assessing both the optical and the mechanical interactions between the tip, the membrane and the liquid suspension underneath. Here, the study reports that the tapping AFM tip induces a reversible nanometric deformation of the membrane manifested as either an indentation or protrusion.

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Contrasting Ultra-Low Frequency Raman and Infrared Modes in Emerging Metal Halides for Photovoltaics.

ACS Energy Lett

August 2024

Department of Physics, Clarendon Laboratory, University of Oxford, Parks Road, Oxford OX1 3PU, United Kingdom.

Article Synopsis
  • Lattice dynamics play a crucial role in the performance of photovoltaic materials by influencing factors like disorder, cooling, recombination, and charge transport.
  • The study focuses on soft metal-halide perovskites, which show unique low-frequency Raman spectra, the cause of which has been widely debated.
  • Using advanced spectroscopic techniques, the researchers propose that the central Raman peak arises from a combination of broadening of low-energy phonon modes and Bose-Einstein statistics, enhancing our understanding of how light interacts with these materials in solar energy applications.
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