Mass-ratio dependent strong-field dissociation of artificial helium hydride isotopologues

We study the effect of the nuclear-mass ratio in a diatomic molecular ion on the dissociation dynamics in strong infrared laser pulses. A molecular ion is a charged system, in which the dipole moment depends on the reference point and therefore on the position of the nuclear center of mass, so that the laser-induced dynamics is expected to depend on the mass asymmetry. Whereas usually both the reduced mass and the mass ratio are varied when different isotopologues are compared, we fix the reduced mass and artificially vary the mass ratio in a model system. This allows us to separate effects related to changes in the resonance frequency, which is determined by the reduced mass, from those that arise due to the mass asymmetry. Numerical solutions of the time-dependent Schrödinger equation are compared with classical trajectory simulations. We find that at a certain mass ratio, vibrational excitation is strongly suppressed, which decreases the dissociation probability by many orders of magnitude

A toolset of functionalized porphyrins with different linker strategies for application in bioconjugation

The reaction of amines with pentafluorophenyl-substituted A3B-porphyrins has been used to obtain different useful reactive groups for further functionalization and/or conjugation of these porphyrins to other substrates or materials. Porphyrins with alkenyl, alkynyl, amino, azido, epoxide, hydroxyl, and maleimido groups have thus been synthesized. For the first time such functionalized porphyrins have been conjugated to hyperbranched polyglycerol (hPG) as a biocompatible carrier system for photodynamic therapy (PDT) using the copper(I)-catalyzed 1,3-dipolar cycloaddition (CuAAC). The photocytotoxicity of selected porphyrins as well as of the porphyrin-hPG- conjugates has been assessed in cellular assays with human epidermoid carcinoma A-253 and squamous carcinoma CAL-27 cells. For several biomedical applications a release of the active drug and/or fluorescent dye is desired. Therefore, additionally, the synthesis of A3B-porphyrins with cleavable linker moieties is presented, namely disulfide, cleavable in a reductive environment, and acetal linkers whose cleavage is pH triggered

Outpacing movement — ultrafast volume coverage in neuropediatric magnetic resonance imaging

Background Conventional MRI sequences are often affected in neuropediatric imaging by unavoidable movements. Therefore, children younger than 6 years usually have to be examined under sedation/anesthesia. A new real-time MRI technique with automatic slice advancement allows for motion-robust T2-weighted volume coverage of the whole brain within a few seconds in adults. Objective To evaluate to which extent the new volume coverage method can be used to visualize cerebrospinal fluid and reduce the need for anesthesia in children. Materials and methods We assessed 30 children ages 6 years and younger with suspected or proven hydrocephalus, hygroma or macrocephalus using volume coverage sequences with 20 slices per second in three planes. If necessary, a parent was placed in the bore together with the child for calming and gentle immobilization. We compared visualization of cerebrospinal fluid spaces and course of the shunt catheter in volume coverage sequences vs. fast spin-echo sequences. Results The clinical issue could be sufficiently assessed in all children with use of volume coverage sequences, whereas conventional fast spin-echo sequences performed moderately to poorly. Visualization of the tip of a shunt failed in 16% of volume coverage scans and 27% of turbo spin-echo scans. A subsequent examination under anesthesia was never necessary. None of the examinations had to be stopped prematurely. Conclusion The motion-robust volume coverage sequences with T2-type contrast can be used to avoid sedation of children in the evaluation of cerebrospinal fluid spaces, even in the presence of vigorous motion. For other indications and contrasts, the technique must still be evaluated

Scalable quantum tomography in a photonic chip

© 2017 IEEE. We formulate a method of quantum tomography that scales linearly with the number of photons and involves only one optical transformation. We demonstrate it experimentally for two-photon entangled states using a special photonic chip

Non-Adiabatic Electronic and Vibrational Ring-Opening Dynamics resolved with Attosecond Core-Level Spectroscopy

Non-adiabatic dynamics and conical intersections play a central role in the chemistry of most polyatomic molecules, ranging from isomerization to heterocyclic ring opening and avoided photo-damage of DNA. Studying the underpinning correlated dynamics of electronic and nuclear wave packets is a major challenge in real-time and, many times involves optically dark transient states. We show that attosecond core-level spectroscopy reveals the pathway dynamics of neutral furan across its conical intersections and dark states. Our method measures electronic-nuclear correlations to detect the dephasing of electronic coherence due to nuclear motion and identifies the ring-opened isomer as the dominant product. These results demonstrate the efficacy of attosecond core level spectroscopy as a potent method to investigate the real-time dynamics of photochemical reaction pathways in complex molecular systems

Magnetic switching of nanoscale antidot lattices

We investigate the rich magnetic switching properties of nanoscale antidot lattices in the 200 nm regime. In-plane magnetized Fe, Co, and Permalloy (Py) as well as out-of-plane magnetized GdFe antidot films are prepared by a modified nanosphere lithography allowing for non-close packed voids in a magnetic film. We present a magnetometry protocol based on magneto-optical Kerr microscopy elucidating the switching modes using first-order reversal curves. The combination of various magnetometry and magnetic microscopy techniques as well as micromagnetic simulations delivers a thorough understanding of the switching modes. While part of the investigations has been published before, we summarize these results and add significant new insights in the magnetism of exchange-coupled antidot lattices.Web of Science775073

Molecular isomerization and fragmentation of polyatomic molecules controlled by inner-valence recollision-ionization

Control over various fragmentation reactions of a series of polyatomic molecules (acetylene, ethylene, 1,3-butadiene) by the optical waveform of intense few-cycle laser pulses is demonstrated experimentally. We show both experimentally and theoretically that the responsible mechanism is inelastic ionization from inner-valence molecular orbitals by recolliding electron wave packets

Oscillations in Quantum Entanglement During Rescattering

We study the time evolution of quantum entanglement between an electron and its parent ion during the rescattering due to a strong few-cycle laser pulse. Based on a simple one-dimensional model, we compute the Neumann entropy during the process for several values of the carrier-envelope phase. The local maxima of the oscillations in the Neumann entropy coincide with the zero crossings of the electric field of the laser pulse. We employ the Wigner function to qualitatively explain the quantum dynamics of rescattering in the phase space.Comment: 2 page

A high frequency builder software for arbitrary radio frequency signals

While the frequencies accessible by signal generators steadily rise, the synthesization of complex and arbitrary waveforms with high frequency components remains challenging, especially when restricted by an external reference clock. In this article, we present a comprehensive software package combined with state of the art hardware as a solution for the generation of highly sampled, arbitrary radio frequency waveforms. The software can be used to conduct both synchronous and heterodyne pump probe experiments due to a variety of different synchronization modules. While both kinds of modules allow for standard waveforms, such as sines, pulses, and bursts, as well as any arbitrary signal, the heterodyne modules additionally are not restricted by the reference clock frequency. Both the output and the synchronization module can be adapted to support additional measurement devices. Due to the modular software structure, individual classes can be exchanged while maintaining all functionalities. The software provides a user friendly graphical interface that allows us to compose, save, and load complex arbitrary waveforms within only a few steps. The frequency selectivity provided by the software hardware combination allows us to directly target specific excitation states of physical systems. Conducting a heterodyne scanning transmission x ray microscopy experiment, we are able to demonstrate the capabilities of the software when paired with a high sample rate arbitrary waveform generator. The heterodyne synchronization modules allow for unlimited flexibility leveraging arbitrary waveform generation to their full power. By solving the challenges of synthesizing highly complex electromagnetic waves, the software enables a large variety of experiments to be performed more convenientl