Strong-field quantum control in the extreme ultraviolet domain using pulse shaping.

Tailored light-matter interactions in the strong coupling regime enable the manipulation and control of quantum systems with up to unit efficiency, with applications ranging from quantum information to photochemistry. Although strong light-matter interactions are readily induced at the valence electron level using long-wavelength radiation, comparable phenomena have been only recently observed with short wavelengths, accessing highly excited multi-electron and inner-shell electron states. However, the quantum control of strong-field processes at short wavelengths has not been possible, so far, because of the lack of pulse-shaping technologies in the extreme ultraviolet (XUV) and X-ray domain.

Method of kinetic energy reconstruction from time-of-flight mass spectra.

We present a method for the reconstruction of ion kinetic energy distributions from ion time-of-flight mass spectra through ion trajectory simulations. In particular, this method is applicable to complicated spectrometer geometries with largely anisotropic ion collection efficiencies. A calibration procedure using a single ion mass peak allows the accurate determination of parameters related to the spectrometer calibration, experimental alignment, and instrument response function, which improves the agreement between simulations and experiment.

Vibrational Quenching of Optically Pumped Carbon Dimer Anions.

Careful control of quantum states is a gateway to research in many areas of science such as quantum information, quantum-controlled chemistry, and astrophysical processes. Precise optical control of molecular ions remains a challenge due to the scarcity of suitable level schemes, and direct laser cooling has not yet been achieved for either positive or negative molecular ions. Using a cryogenic wire trap, we show how the internal quantum states of C_{2}^{-} anions can be manipulated using optical pumping and inelastic quenching collisions with H_{2} gas.

Symmetry Dependence of the Continuum Coupling in the Chemi-ionization of Li(2S) by He(2S, 2P).

In the literature, the chemi-ionization of Li in the 2S ground level by He in a metastable state is typically described as an electron transfer process in which an electron from the 2s orbital of Li is transferred to the 1s orbital of He while an electron from the 2s orbital of He is ejected. Therefore, one would not assume that the orbital of the valence electron of He strongly influences the coupling strength of the collision complex to the ionization continuum. However, we observe that the chemi-ionization rate is decreased when He is laser-excited from the metastable 2S level to the 2P level (with = 0, 1, 2).

Two-dimensional electronic spectroscopy of an ultracold gas.

Femtosecond coherent multidimensional spectroscopy is demonstrated for an ultracold gas.  A setup for phase modulation spectroscopy is used to probe the 3S-2P transition in an 800K-cold sample of Li atoms confined in a magneto-optical trap. The observation of a double quantum coherence response, a signature of interparticle interactions, paves the way for detailed investigations of few- and many-body effects in ultracold gases using this technique.

Extreme Ultraviolet Wave Packet Interferometry of the Autoionizing HeNe Dimer.

Femtosecond extreme ultraviolet wave packet interferometry (XUV-WPI) was applied to study resonant interatomic Coulombic decay (ICD) in the HeNe dimer. The high demands on phase stability and sensitivity for vibronic XUV-WPI of molecular-beam targets are met using an XUV phase-cycling scheme. The detected quantum interferences exhibit vibronic dephasing and rephasing signatures along with an ultrafast decoherence assigned to the ICD process.

Spin-state-controlled chemi-ionization reactions between metastable helium atoms and ground-state lithium atoms.

We demonstrate the control of He(2S)-Li(2S) chemi-ionization reactions by all-optical electron-spin-state preparation of both atomic species prior to the collision process. Our results demonstrate that chemi-ionization is strongly suppressed (enhanced) for non-spin-conserving (spin-conserving) collisions at thermal energies. These findings are in good agreement with a model based on spin angular momentum coupling of the prepared atomic states to the quasi-molecular states.

Development and characterization of high-repetition-rate sources for supersonic beams of fluorine radicals.

We present and compare two high-pressure, high-repetition-rate electric-discharge sources for the generation of supersonic beams of fluorine radicals. The sources are based on dielectric-barrier-discharge (DBD) and plate-discharge units attached to a pulsed solenoid valve. The corrosion-resistant discharge sources were operated with fluorine gas seeded in helium up to backing pressures as high as 30 bars.

Dynamics of Photoexcited Cs Atoms Attached to Helium Nanodroplets.

We present an experimental study of the dynamics following the photoexcitation and subsequent photoionization of single Cs atoms on the surface of helium nanodroplets. The dynamics of excited Cs atom desorption and readsorption as well as CsHe exciplex formation are measured by using femtosecond pump-probe velocity map imaging spectroscopy and ion time-of-flight spectrometry. The time scales for the desorption of excited Cs atoms off helium nanodroplets as well as the time scales for CsHe exciplex formation are experimentally determined for the 6p states of Cs.

Preparation of individual magnetic sub-levels of He(2S) in a supersonic beam using laser optical pumping and magnetic hexapole focusing.

We compare two different experimental techniques for the magnetic-sub-level preparation of metastable He in the 2S level in a supersonic beam, namely, magnetic hexapole focusing and optical pumping by laser radiation. At a beam velocity of v = 830 m/s, we deduce from a comparison with a particle trajectory simulation that up to 99% of the metastable atoms are in the M = +1 sub-level after magnetic hexapole focusing. Using laser optical pumping via the 2P-2S transition, we achieve a maximum efficiency of 94% ± 3% for the population of the M = +1 sub-level.

Unravelling the full relaxation dynamics of superexcited helium nanodroplets.

The relaxation dynamics of superexcited superfluid He nanodroplets is thoroughly investigated by means of extreme-ultraviolet (XUV) femtosecond electron and ion spectroscopy complemented by time-dependent density functional theory (TDDFT). Three main paths leading to the emission of electrons and ions are identified: droplet autoionization, pump-probe photoionization, and autoionization induced by re-excitation of droplets relaxing into levels below the droplet ionization threshold. The most abundant product ions are He2+, generated by droplet autoionization and by photoionization of droplet-bound excited He atoms.

Single-Source, Collinear Merged-Beam Experiment for the Study of Reactive Neutral-Neutral Collisions.

We present two methods for studying reactive collisions between two atomic or molecular species: a collinear merged-beam method in which two gas pulses from a single supersonic beam source are coalesced and an intrabeam-scattering technique in which a single gas pulse is used. Both approaches, which rely on the laser cooling and deceleration of a laser-coolable species inside a Zeeman slower, can be used for a wide range of scattering studies. Possible experimental implementations of the proposed methods are outlined for autoionizing collisions between helium atoms in the metastable 2S state and a second, atomic or molecular species.

Production of rotationally cold methyl radicals in pulsed supersonic beams.

We present a comparison of two technically distinct methods for the generation of rotationally cold, pulsed supersonic beams of methyl radicals (CH): a plate discharge source operating in the glow regime and a dielectric barrier discharge source. The results imply that the efficiency of both sources is comparable and that molecular beams with similar translational and rotational temperatures are formed. Methane (CH) proved to be the most suitable radical precursor species.

Getting a grip on the transverse motion in a Zeeman decelerator.

Zeeman deceleration is an experimental technique in which inhomogeneous, time-dependent magnetic fields generated inside an array of solenoid coils are used to manipulate the velocity of a supersonic beam. A 12-stage Zeeman decelerator has been built and characterized using hydrogen atoms as a test system. The instrument has several original features including the possibility to replace each deceleration coil individually.

Reaction of hydroxyl radicals with C4H5N (pyrrole): temperature and pressure dependent rate coefficients.

Absolute (pulsed laser photolysis, 4-639 Torr N(2) or air, 240-357 K) and relative rate methods (50 and 760 Torr air, 296 K) were used to measure rate coefficients k(1) for the title reaction, OH + C(4)H(5)N → products (R1). Although the pressure and temperature dependent rate coefficient is adequately represented by a falloff parametrization, calculations of the potential energy surface indicate a complex reaction system with multiple reaction paths (addition only) in the falloff regime. At 298 K and 760 Torr (1 Torr = 1.