Polarization effects in attosecond photoelectron spectroscopy

We study the influence of polarization effects in streaking by combined atto- and femtosecond pulses. The polarization-induced terms alter the streaking spectrum. The normal streaking spectrum, which maps to the vector potential of the femtosecond pulse, is modified by a contribution following the field instead. We show that polarization effects may lead to an apparent temporal shift, that needs to be properly accounted for in the analysis. The effect may be isolated and studied by angle-resolved photoelectron spectroscopy from oriented polar molecules. We also show that polarization effects will lead to an apparent temporal shift of 50 as between photoelectrons from a 2p and 1s state in atomic hydrogen.Comment: 4 pages, 3 figure

Magnetometry with entangled atomic samples

We present a theory for the estimation of a scalar or a vector magnetic field by its influence on an ensemble of trapped spin polarized atoms. The atoms interact off-resonantly with a continuous laser field, and the measurement of the polarization rotation of the probe light, induced by the dispersive atom-light coupling, leads to spin-squeezing of the atomic sample which enables an estimate of the magnetic field which is more precise than that expected from standard counting statistics. For polarized light and polarized atoms, a description of the non-classical components of the collective spin angular momentum for the atoms and the collective Stokes vectors of the light-field in terms of effective gaussian position and momentum variables is practically exact. The gaussian formalism describes the dynamics of the system very effectively and accounts explicitly for the back-action on the atoms due to measurement and for the estimate of the magnetic field. Multi-component magnetic fields are estimated by the measurement of suitably chosen atomic observables and precision and efficiency is gained by dividing the atomic gas in two or more samples which are entangled by the dispersive atom-light interaction.Comment: 8 pages, 11 figure

Geometric phases in open tripod systems

We first consider stimulated Raman adibatic passages (STIRAP) in a closed four-level tripod system. In this case, the adiabatic eigenstates of the system acquire real geometric phases. When the system is open and subject to decoherence they acquire complex geometric phases that we determine by a Monte Carlo wave function approach. We calculate the geometric phases and the state evolution in the closed as well as in the open system cases and describe the deviation between these in terms of the phases acquired. When the system is closed, the adiabatic evolution implements a Hadamard gate. The open system implements an imperfect gate and hence has a fidelity below unity. We express this fidelity in terms of the acquired geometric phases.Comment: 10 pages 7 figure

Electrostatic attraction of nanoobjects - a versatile strategy towards mesostructured transition metal compounds

This highlight summarizes current challenges of mesostructuring and focuses on the scope and the potential of the ELAN – (electrostatic attraction of nanoobjects) strategy in mesostructuring of transition metal compounds. It discusses the limitations of this concept and highlights prominent examples. ELAN exploits the Coulomb attraction between inorganic precursors and polymeric templates in order to prevent macrophase separation. Essential requirements for ELAN are tailor-made, mesoscopic polyelectrolytic templates and charged molecular oligo-ions or stable colloids carrying a surface charge. The ELAN-strategy is highly reliable and opens the way to crystalline, mesoporous transition metal compounds with predefined polymorphism. It also provides the possibility to adjust wall chemistry and reactivity as well as the flexibility to synthesise different mesostructures (spheres, non-woven arrays or hexagonally ordered phases)

Orientation-dependent ionization yields from strong-field ionization of fixed-in-space linear and asymmetric top molecules

The yield of strong-field ionization, by a linearly polarized probe pulse, is studied experimentally and theoretically, as a function of the relative orientation between the laser field and the molecule. Experimentally, carbonyl sulfide, benzonitrile and naphthalene molecules are aligned in one or three dimensions before being singly ionized by a 30 fs laser pulse centered at 800 nm. Theoretically, we address the behaviour of these three molecules. We consider the degree of alignment and orientation and model the angular dependence of the total ionization yield by molecular tunneling theory accounting for the Stark shift of the energy level of the ionizing orbital. For naphthalene and benzonitrile the orientational dependence of the ionization yield agrees well with the calculated results, in particular the observation that ionization is maximized when the probe laser is polarized along the most polarizable axis. For OCS the observation of maximum ionization yield when the probe is perpendicular to the internuclear axis contrasts the theoretical results.Comment: 14 pages, 4 figure

Strong-field ionization of atoms and molecules: The two-term saddle point method

We derive an analytical formula for the ionization rate of neutral atoms and molecules in a strong monochromatic field. Our model is based on the strong-field approximation with transition amplitudes calculated by an extended saddle point method. We show that the present two-term saddle point method reproduces even complicated structures in angular resolved photo electron spectra

Control and femtosecond time-resolved imaging of torsion in a chiral molecule

We study how the combination of long and short laser pulses, can be used to induce torsion in an axially chiral biphenyl derivative (3,5-difluoro-3',5'-dibromo-4'-cyanobiphenyl). A long, with respect to the molecular rotational periods, elliptically polarized laser pulse produces 3D alignment of the molecules, and a linearly polarized short pulse initiates torsion about the stereogenic axis. The torsional motion is monitored in real-time by measuring the dihedral angle using femtosecond time-resolved Coulomb explosion imaging. Within the first 4 picoseconds, torsion occurs with a period of 1.25 picoseconds and an amplitude of 3 degrees in excellent agreement with theoretical calculations. At larger times the quantum states of the molecules describing the torsional motion dephase and an almost isotropic distribution of the dihedral angle is measured. We demonstrate an original application of covariance analysis of two-dimensional ion images to reveal strong correlations between specific ejected ionic fragments from Coulomb explosion. This technique strengthens our interpretation of the experimental data.Comment: 11 pages, 9 figure

Mesostructured ZnO/Au nanoparticle composites with enhanced photocatalytic activity

Ease of catalyst separation from reaction mixtures represents a significant advantage in heterogeneous photocatalytic wastewater treatment. However, the activity of the catalyst strongly depends on its surface-to-volume ratio. Here, we present an approach based on cylindrical polybutadiene-block-poly(2-vinylpyridine) polymer brushes as template, which can be simultaneously loaded with zinc oxide (ZnO) and gold (Au) nanoparticles. Pyrolytic template removal of the polymer yields in mesostructured ZnO/Au composites, showing higher efficiencies in the photocatalytic degradation of ciprofloxacin and levofloxacin (generic antibiotics present in clinical wastewater) as compared to neat mesostructured ZnO. Upscaling of the presented catalyst is straightforward promising high technical relevance

SosA inhibits cell division in Staphylococcus aureus in response to DNA damage.

Inhibition of cell division is critical for viability under DNA-damaging conditions. DNA damage induces the SOS response that in bacteria inhibits cell division while repairs are being made. In coccoids, such as the human pathogen, Staphylococcus aureus, this process remains poorly studied. Here, we identify SosA as the staphylococcal SOS-induced cell division inhibitor. Overproduction of SosA inhibits cell division, while sosA inactivation sensitizes cells to genotoxic stress. SosA is a small, predicted membrane protein with an extracellular C-terminal domain in which point mutation of residues that are conserved in staphylococci and major truncations abolished the inhibitory activity. In contrast, a minor truncation led to SosA accumulation and a strong cell division inhibitory activity, phenotypically similar to expression of wild-type SosA in a CtpA membrane protease mutant. This suggests that the extracellular C-terminus of SosA is required both for cell division inhibition and for turnover of the protein. Microscopy analysis revealed that SosA halts cell division and synchronizes the cell population at a point where division proteins such as FtsZ and EzrA are localized at midcell, and the septum formation is initiated but unable to progress to closure. Thus, our findings show that SosA is central in cell division regulation in staphylococci