We have used picosecond THz pulses to induce transient field-free orientation of OCS molecules. Coherent optical Raman excitation prepares the molecules in rotational superposition states prior to THz irradiation, substantially enhancing the degree of orientation. The time-dependent alignment and orientation are characterized via Coulomb explosion in an intense probe laser. The degree of OCS orientation is an order of magnitude larger than previously observed following THz irradiation and is achieved with a significantly smaller THz field.The field-free orientation level is comparable to that generated using pulsed, two-color laser fields but is obtained with negligible target ionization.
We have measured and calculated doubly differential cross sections for ionization of atomic hydrogen using 75-keV proton impact for fixed projectile energy losses as a function of scattering angle. This collision system represents a pure three-body system and thus offers an accurate test of the theoretical description of the few-body dynamics without any complications presented by electron correlation in many-electron targets. Comparison between experiment and several theoretical models reveals that the projectile-target nucleus interaction is best described by the operator of a second-order term of the transition amplitude. Higher-order contributions in the projectile-electron interaction, on the other hand, are more appropriately accounted for in the final-state wave function.
We have measured differential cross sections for single and dissociative capture for 25 and 75 keV protons colliding with H 2 and He. Significant differences were found depending on whether the projectile beam was coherent or incoherent. For 75 keV p + H 2 these differences can be mostly associated with molecular two-center interference and possibly some contributions from path interference. For 25 keV (both targets) they are mostly due to path interference between different impact parameters leading to the same scattering angles and, for the H 2 target, possibly some contributions from molecular two-center interference.
In this article we describe the design, construction and implementation of our ion-atom hybrid system incorporating a high resolution time of flight mass spectrometer (TOFMS). Potassium atoms ( 39 K) in a Magneto Optical Trap (MOT) and laser cooled calcium ions ( 40 Ca + ) in a linear Paul trap are spatially overlapped and the combined trap is integrated with a TOFMS for radial extraction and detection of reaction products. We also present some experimental results showing interactions between 39 K + and 39 K, 40 Ca + and 39 K + as well as 40 Ca + and 39 K pairs. Finally, we discuss prospects for cooling CaH + molecular ions in the hybrid ion-atom system.
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