Imaging of spatial many-body wave functions via linear momentum measurements.

The equivalence of a complete characterization of linear momenta of fragments from a many-body fragmentation process and the spatial wave function of the many-body system is discussed. Our experiment on three-body dissociation of state selected H3 and D3 molecules into ground-state hydrogen atoms strongly suggests the existence of such a close relationship as it is also predicted by theory in the form of the imaging theorem. We conclude that prudent imaging of many-body fragmentation provides a laboratory view of the squared many-body wave function at a spatial scale of molecular dimensions at which fragments exit into the realm of independent free particles.

Entanglement dynamics of a strongly driven trapped atom.

We study the entanglement between the internal electronic and the external vibrational degrees of freedom of a trapped atom which is driven by two lasers into electromagnetically induced transparency. It is shown that basic features of the intricate entanglement dynamics can be traced to Landau-Zener splittings (avoided crossings) in the spectrum of the atom-laser field Hamiltonian. We further construct an effective Hamiltonian that describes the behavior of entanglement under dissipation induced by spontaneous emission processes. The proposed approach is applicable to a broad range of scenarios for the control of entanglement between electronic and translational degrees of freedom of trapped atoms through suitable laser fields.

Chemical sensing and imaging with pulsed terahertz radiation.

Over the past decade, terahertz spectroscopy has evolved into a versatile tool for chemically selective sensing and imaging applications. In particular, the potential to coherently generate and detect short, and hence, broadband terahertz pulses led to the development of efficient and compact spectrometers for this interesting part of the electromagnetic spectrum, where common packaging materials are transparent and many chemical compounds show characteristic absorptions. Although early proof-of-principle demonstrations have shown the great potential of terahertz spectroscopy for sensing and imaging, the technology still often lacks the required sensitivity and suffers from its intrinsically poor spatial resolution. In this review we discuss the current potential of terahertz pulse spectroscopy and highlight recent technological advances geared towards both enhancing spectral sensitivity and increasing spatial resolution.

Stark field control of nonadiabatic dynamics in triatomic hydrogen.

We show experimentally that an external electric field can be used to control the amplitudes of nonadiabatic paths taken by a dissociating molecule. In the example presented here, this control is achieved by Stark-field mixing in H(3) Rydberg states with different decay paths. The final state continuum is in each path formed by three-particle wave packets of slow neutral hydrogen atoms in their electronic ground state. Their momentum vector correlations show signs of interference, since the molecule can access the identical continuum via two distinctly different paths, involving different nonadiabatic coupling mechanisms. As an added feature a preferred alignment of the fragmentation plane in the laboratory frame emerges, corresponding to a selective dissociation of molecules oriented along the field direction.

Lattice modes mediate radiative coupling in metamaterial arrays.

We show that a resonant response with very high quality factors can be achieved in periodic metamaterials by radiatively coupling their structural elements. The coupling is mediated by lattice modes and can be efficiently controlled by tuning the lattice periodicity. Using a recently developed terahertz (THz) near-field imaging technique and conventional far-field spectroscopy together with numerical simulations we pinpoint the underlying mechanisms. In the strong coupling regimes we identify avoided crossings between the plasmonic eigenmodes and the diffractive lattice modes.

Terahertz near-field imaging of electric and magnetic resonances of a planar metamaterial.

Experimental investigations of the microscopic electric and in particular the magnetic near-fields in metamaterials remain highly challenging and current studies rely mostly on numerical simulations. Here we report a terahertz near-field imaging approach which provides spatially resolved measurements of the amplitude, phase and polarization of the electric field from which we extract the microscopic magnetic near-field signatures in a planar metamaterial constructed of split-ring resonators (SRRs). In addition to studying the fundamental resonances of an individual double SRR unit we further investigate the interaction with neighboring elements.

Interactions and dynamics in ionic liquids.

Precise dielectric spectra have been determined at 25 degrees C over the exceptionally broad frequency range of 0.1

Picosecond dynamics and microheterogenity of water+dioxane mixtures.

Dielectric spectra from 200 MHz up to 3 THz were determined to study the fast dynamics of dilute water+1,4-dioxane. epsilon(nu) could be fitted by a collision induced oscillator at high frequencies plus two Debye relaxations in the microwave region. Isotope substitution was used to assign water and dioxane modes. The presence of the cooperative hydrogen-bond network relaxation down to a water mole fraction of 0.005 suggests a microheterogeneous structure of the mixtures even at low water content. The collision mode of dioxane at approximately 2 THz grows upon water addition, revealing the presence of H2O molecules in dioxane-rich domains.

Terahertz time-domain spectroscopy and imaging of artificial RNA.

We use terahertz time-domain spectroscopy (THz-TDS) to measure the far-infrared dielectric function of two artificial RNA single strands, composed of polyadenylic acid (poly-A) and polycytidylic acid (poly-C). We find a significant difference in the absorption between the two types of RNA strands, and we show that we can use this difference to record images of spot arrays of the RNA strands. Under controlled conditions it is possible to use the THz image to distinguish between the two RNA strands. We discuss the requirements to sample preparation imposed by the lack of sharp spectral features in the absorption spectra.

Experimental study of photodetachment in a strong laser field of circular polarization.

Negative fluorine ions are exposed to a circularly polarized infrared laser pulse with a peak intensity on the order of 2.6 x 10(13) W/cm(2). A fundamental difference, as compared to the case of linearly polarized field, is found in the absence of any structure in the photoelectron spectrum that can be associated with the quantum interference effect. This observation is in accord with our recent predictions [S. Beiser, Phys. Rev. A 70, 011402 (2004)10.1103/Phys. Rev. A.70. 011402]. The experiment reveals that the length gauge is appropriate for the description of the field interaction in the frame of the strong field approximation.

Maps of nonadiabatic coupling in triatomic hydrogen.

We show in an experiment that dissociation of state-selected neutral H3* molecules into three ground-state hydrogen atoms reveals highly structured maps of correlation in the motion of the three atoms. These maps provide a direct view of the internal molecular couplings which initiate dissociation.

Production of energetic electrons in the process of photodetachment of F-.

An imaging technique is used to record an energy and angle resolved spectrum of electrons produced by photodetachment of F- in a strong infrared laser pulse. The spectrum involves contributions from more than 23 excess photon detachment channels. Its higher energy part extends beyond the classical cutoff value, and it appears as a pronounced plateau localized within a small angle along the laser polarization axis. A Keldysh-like theory is able to qualitatively reproduce the spectrum without taking into account the rescattering mechanism. The role of the parity of the initial bound state is discussed.