Brett D. Depaola

Collimated blue and infrared beams generated by two-photon excitation in Rb vapor

Utilizing two-photon excitation in hot Rb vapor we demonstrate the generation of collimated optical fields at 420 and 1324 nm. Input laser beams at 780 and 776 nm enter a heated Rb vapor cell collinear and circularly polarized, driving Rb atoms to the 5D(5/2) state. Under phase-matching conditions coherence among the 5S(1/2)→5P(3/2)→5D(5/2)→6P(3/2) transitions produces a blue (420 nm) beam by four-wave mixing. We also observe a forward and backward propagating IR (1324 nm) beam, due to cascading decays through the 6S(1/2)→5(1/2) states. Power saturation of the generated beams is investigated by scaling the input powers to greater than 200 mW, resulting in a coherent blue beam of 9.1 mW power, almost an order of magnitude larger than previously achieved. We measure the dependences of both beams in relation to the Rb density, the frequency detuning between Rb ground-state hyperfine levels, and the input laser intensities.

Versatile cold atom target apparatus.

We report on a compact and transportable apparatus that consists of a cold atomic target at the center of a high resolution recoil ion momentum spectrometer. Cold rubidium atoms serve as a target which can be operated in three different modes: in continuous mode, consisting of a cold atom beam generated by a two-dimensional magneto-optical trap, in normal mode in which the atoms from the beam are trapped in a three-dimensional magneto-optical trap (3D MOT), and in high density mode in which the 3D MOT is operated in dark spontaneous optical trap configuration. The targets are characterized using photoionization.

Energy-dependent relative charge transfer cross sections of Cs++ Rb(5s, 5p)

Magneto optical trap recoil ion momentum spectroscopy is used to measure energy-dependent charge exchange cross sections in the Cs+ + Rb(5s, 5p) system over a range of projectile energies from 3.2 to 6.4 keV. The measurements are kinematically complete and yield cross sections that are differential in collision energy, scattering angle, and initial and final states.

Measurement of ionization in direct frequency comb spectroscopy

Direct frequency comb spectroscopy is currently one of the most precise techniques for studying the internal structure of atomic and molecular systems. In this technique, a train of ultrafast laser pulses excites states in the target system which then relax, emitting fluorescence. The measured fluorescence is then plotted as a function of the comb parameters. But according to recent theory, the ultrashort pulses from the comb laser can also significantly ionize the target. Here, we test this theory by measuring the ion signal from direct frequency comb spectroscopy. Furthermore, instead of actively controlling the frequency comb parameters, we allow them to drift passively, measuring them and the ion signal simultaneously. The experiments were found to be in satisfactory agreement with theory, and the passive comb approach was found to be functional, though not as convenient as the conventional actively locked comb.

Three-dimensional spatial imaging in multiphoton ionization rate measurements

An experiment is described in which an apparatus is used to demonstrate the feasibility of measuring multiphoton photoionization rates in the interaction of short pulsed lasers with atoms or molecules. With this methodology, the ionization rate is measured as a function of the spatial position in the beam-waist region of the laser through the direct three-dimensional spatial imaging of the ionization events. Thus, if the spatial dependence of the laser beam intensity were known, a series of experiments could yield the intensity dependence of multiphoton ionization without the assumptions or errors that are generally inherent in the integration over one or more dimensions in the laser focal volume.