324 results match your criteria: "Research Center Optimas[Affiliation]"

In this contribution, the divergent modular synthesis of photoredox-active dyads, triads and a tetrad descending from one ligand precursor is presented by combining "chemistry-on-the-ligand", stepwise complexation and "chemistry-on-the-complex" with minimal synthetic efforts. In the final step, Pd-mediated borylation and subsequent Suzuki-Miyaura cross-coupling was employed to introduce the different (multi)donor moieties at the preassembled P-A dyad subunit. The (spectro-)electrochemical data revealed preserved redox properties of the subunits and minimal driving force for oxidative quenching by the naphthalene diimide-based (NDI) acceptor and, thus, high-energy charge separated (CS) states.

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The facilitation of Rydberg excitations in a gas of atoms provides an ideal model system to study epidemic evolution on (dynamic) networks and self-organization of complex systems to the critical point of a nonequilibrium phase transition. Using Monte Carlo simulations and a machine learning algorithm we show that the universality class of this phase transition can be tuned but is robust against decay inherent to the self-organization process. The classes include directed percolation (DP), the most common class in short-range spreading models, and mean-field (MF) behavior, but also different types of anomalous directed percolation (ADP), characterized by rare long-range excitation processes.

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The microscopic pair structure of superfluids has profound consequences on their properties. Delocalized pairs are predicted to be less affected by static disorder than localized pairs. Ultracold gases allow tuning the pair size via interactions, where for resonant interaction superfluids show largest critical velocity, i.

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Zinc and copper effect mechanical cell adhesion properties of the amyloid precursor protein.

Biol Chem

December 2024

Department of Human Biology and Human Genetics, RPTU Kaiserslautern-Landau, Erwin-Schrödinger-Str. 13, D-67663 Kaiserslautern, Germany.

The amyloid precursor protein (APP) can be modulated by the binding of copper and zinc ions. Both ions bind with low nanomolar affinities to both subdomains (E1 and E2) in the extracellular domain of APP. However, the impact of ion binding on structural and mechanical trans-dimerization properties is yet unclear.

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Embedding quantum dots into porous matrices is a very beneficial approach for generating hybrid nanostructures with unique properties. In this contribution we explore strategies to dope nanoporous SiO thin films made by atomic layer deposition and selective wet chemical etching with precise control over pore size with CdSe quantum dots. Two distinct strategies were employed for quantum dot deposition: in situ growth of CdSe nanocrystals within the porous matrix via successive ionic layer adsorption reaction, and infiltration of pre-synthesized quantum dots.

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The generation of laser pulses with controlled optical waveforms, and their measurement, lie at the heart of both time-domain and frequency-domain precision metrology. Here, we obtain mid-infrared waves via intra-pulse difference-frequency generation (IPDFG) driven by 16-femtosecond near-infrared pulses, and characterise the jitter of sub-cycle fractions of these waves relative to the gate pulses using electro-optic sampling (EOS). We demonstrate sub-attosecond temporal jitter at individual zero-crossings and sub-0.

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Nonlinear Effects on Charge Fractionalization in Critical Chains.

Phys Rev Lett

August 2024

Physics Department and Research Center OPTIMAS, University of Kaiserslautern-Landau, 67663 Kaiserslautern, Germany.

We investigate the generic transport in a one-dimensional strongly correlated fermionic chain beyond linear response. Starting from a Gaussian wave packet with positive momentum on top of the ground state, we find that the numerical time evolution splits the signal into at least three distinct fractional charges moving with different velocities. A fractional left-moving charge is expected from conventional Luttinger liquid theory, but for the prediction of the two separate right-moving packets the nonlinearity of the dispersion must also be taken into account.

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Field-resolved infrared spectroscopy (FRS) of impulsively excited molecular vibrations can surpass the sensitivity of conventional time-integrating spectroscopies, owing to a temporal separation of the molecular signal from the noisy excitation. However, the resonant response carrying the molecular signal of interest depends on both the amplitude and phase of the excitation, which can vary over time and across different instruments. To date, this has compromised the accuracy with which FRS measurements could be compared, which is a crucial factor for practical applications.

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We present CdSe@CdS nanorods coated with a redox-active polydopamine (PDA) layer functionalized with cobaloxime-derived photocatalysts for efficient solar-driven hydrogen evolution in aqueous environments. The PDA-coating provides reactive groups for the functionalization of the nanorods with different molecular catalysts, facilitates charge separation and transfer of electrons from the excited photosensitizer to the catalyst, and reduces photo-oxidation of the photosensitizer. X-ray photoelectron spectroscopy (XPS) confirms the successful functionalization of the nanorods with cobalt-based catalysts, whereas the catalyst loading per nanorod is quantified by total reflection X-ray fluorescence spectrometry (TXRF).

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Spin-wave dynamics in perpendicularly magnetized antidot multilayers.

J Phys Condens Matter

July 2024

Department of Condensed Matter and Materials Physics, S. N. Bose National Centre for Basic Sciences, Block JD, Sector III, Salt Lake, Kolkata 700106, India.

Using all-optical time-resolved magneto-optical Kerr effect measurements we demonstrate an efficient modulation of the spin-wave (SW) dynamics via the bias magnetic field orientation around nanoscale diamond shaped antidots that are arranged on a square lattice within a [Co(0.75 nm)/Pd(0.9 nm)]multilayer with perpendicular magnetic anisotropy (PMA).

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We propose a mechanism for engineering chiral interactions in Rydberg atoms via a directional antiblockade condition, where an atom can change its state only if an atom to its right (or left) is excited. The scalability of our scheme enables us to explore the many-body dynamics of kinetically constrained models with unidirectional character. We observe nonergodic behavior via either scars, confinement, or localization, upon simply tuning the strength of two driving fields acting on the atoms.

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Small anionic nickel clusters with ethanol are investigated with a combination of mass-selective infrared photodissociation spectroscopy in a molecular beam and density functional theory simulations at the BLYP/6-311g(d,p) and TPSSh/def2-TZVPP level. In this context, the O-H stretching vibration of the ethanol is analyzed to obtain information about the structural motif, the geometry of the metal core, and the spin state of the clusters. For the [Ni2(EtOH)]- and [Ni3(EtOH)]- clusters, we assign quartet states of motifs with a hydrogen bond from the ethanol to the linear nickel core.

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Scanning force microscopy (SFM) is one of the most widely used techniques in biomaterials research. In addition to imaging the materials of interest, SFM enables the mapping of mechanical properties and biological responses with sub-nanometer resolution and piconewton sensitivity. This review aims to give an overview of using the scanning force microscope (SFM) for investigations on dental materials.

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One of the key challenges for spintronic and quantum technologies is to achieve active control of the spin angular momentum of electrons in nanoscale materials on ultrafast, femtosecond timescales. While conventional ferromagnetic materials and materials supporting spin texture suffer both from conceptional limitations in miniaturization and inefficiency of optical and electronic manipulation, non-magnetic centrosymmetric layered materials with hidden spin polarization may offer an alternative pathway to manipulate the spin degree of freedom by external stimuli. Here we demonstrate an approach for generating transient spin polarization on a femtosecond timescale in the otherwise spin-unpolarized band structure of the centrosymmetric 2H-stacked group VI transition metal dichalcogenide WSe.

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Article Synopsis
  • The study investigates the plastic properties of a high-entropy alloy (HfNbTaTiZr) using simulated nanoindentation tests, comparing it to a standard Ta crystal.
  • Key findings reveal that the high-entropy alloys exhibit less dislocation relaxation and minimal dislocation emission compared to the Ta crystal, indicating unique dislocation behavior.
  • The presence of short-range order in the alloy increases its stiffness and hardness, leads to a larger plastic zone and higher dislocation density, and eliminates twinning plasticity, contrasting with the behavior of the elemental Ta under stress.
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We present an all-optical method to measure and compensate for residual magnetic fields present in a cloud of ultracold atoms trapped in an optical dipole trap. Our approach leverages the increased loss from the trapped atomic sample through electromagnetically induced absorption. Modulating the excitation laser provides coherent sidebands, resulting in a Λ-type pump-probe scheme.

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Polymer-semiconductor hybrid materials or composites have been investigated with respect to their microstructure, optical, photoconductive, and ferroelectric properties. For this purpose, either CdSe quantum dots or (Cd:Zn)S microparticles were dispersed in poly(vinylidenefluoride-trifluoroethylene) solution and hot pressed to films. In both material systems, the electrical conductivity and the polarization behavior could be controlled by the intensity of the optical excitation.

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A Photoswitchable Metallocycle Based on Azobenzene: Synthesis, Characterization, and Ultrafast Dynamics.

Chemistry

May 2024

Fachbereich Chemie, RPTU Kaiserslautern-Landau, Erwin-Schrödinger-Straße 52-54, 67663, Kaiserslautern, Germany.

The novel photoswitchable ligand 3,3'-Azobenz(metPA) (1) is used to prepare a [Cu(1)](BF) metallocycle (2), whose photoisomerization was characterized using static and time-resolved spectroscopic methods. Optical studies demonstrate the highly quantitative and reproducible photoinduced cyclic E/Z switching without decay of the complex. Accordingly and best to our knowledge, [Cu(1)](BF) constitutes the first reversibly photoswitchable (3d)-metallocycle based on azobenzene.

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Parasitic mixing in photomixers as continuous wave terahertz sources.

Sci Rep

March 2024

Department of Materials Characterization and Testing, Fraunhofer Institute for Industrial Mathematics ITWM, 67663, Kaiserslautern, Germany.

We present observations of parasitic frequency components in the emission spectrum of typical photomixer sources for continuous wave (CW) terahertz generation. Broadband tunable photomixer systems are often used in combination with direct power detectors, e.g.

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Excitons are realizations of a correlated many-particle wave function, specifically consisting of electrons and holes in an entangled state. Excitons occur widely in semiconductors and are dominant excitations in semiconducting organic and low-dimensional quantum materials. To efficiently harness the strong optical response and high tuneability of excitons in optoelectronics and in energy-transformation processes, access to the full wavefunction of the entangled state is critical, but has so far not been feasible.

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Near continuous phase transitions, universal power-law scaling, characterized by critical exponents, emerges. This behavior reflects the singular responses of physical systems to continuous control parameters like temperature or external fields. Universal scaling extends to non-equilibrium dynamics in isolated quantum systems after a quench, where time takes the role of the control parameter.

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Self-Assembly of the Chiral Donor-Acceptor Molecule DCzDCN on Cu(100).

ACS Appl Mater Interfaces

February 2024

Department of Physics and Research Center OPTIMAS, RPTU Kaiserslautern-Landau, Erwin-Schroedinger-Str. 56, 67663 Kaiserslautern, Germany.

Donor-acceptor (D-A) structured molecules are essential components of organic electronics. The respective molecular structures of these molecules and their synthesis are primarily determined by the intended area of application. Typically, D-A molecules promote charge separation and transport in organic photovoltaics or organic field-effect transistors.

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Persistent magnetic coherence in magnets.

Nat Mater

May 2024

Department of Applied Physics, University of Tokyo, Tokyo, Japan.

When excited, the magnetization in a magnet precesses around the field in an anticlockwise manner on a timescale governed by viscous magnetization damping, after which any information carried by the initial actuation seems to be lost. This damping appears to be a fundamental bottleneck for the use of magnets in information processing. However, here we demonstrate the recall of the magnetization-precession phase after times that exceed the damping timescale by two orders of magnitude using dedicated two-colour microwave pump-probe experiments for a YFeO microstructured film.

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Coherent Off-Axis Terahertz Tomography with a Multi-Channel Array and f-theta Optics.

Sensors (Basel)

January 2024

Fraunhofer Insititute for Industrial Mathematics ITWM, 67663 Kaiserslautern, Germany.

Terahertz tomography is a promising method among non-destructive inspection techniques to detect faults and defects in dielectric samples. Recently, image quality was improved significantly through the incorporation of information and off-axis data. However, this improvement has come at the cost of increased measurement time.

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