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Register a new userSlow Molecules Produced by Photodissociation
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A simple method to control molecular translation with a chemical reaction is demonstrated. Slow NO molecules have been produced by partially canceling the molecular beam velocity of NO$_2$ with the recoil velocity of the NO photofragment. The NO$_2$ molecules were photodissociated using a UV laser pulse polarized parallel to the molecular beam. The spatial profiles of NO molecules showed two peaks corresponding to decelerated and accelerated molecules, in agreement with theoretical prediction. A significant portion of the decelerated NO molecules stayed around the initial dissociation positions even several hundred nanoseconds after their production.
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We derive total (atomic + molecular) hydrogen densities in giant molecular clouds (GMCs) in the nearby spiral galaxy M33 using a method that views the atomic hydrogen near regions of recent star formation as the product of photodissociation. Far-UV photons emanating from a nearby OB association produce a layer of atomic hydrogen on the surfaces of nearby GMCs. Our approach provides an estimate of the total hydrogen density in these GMCs from observations of the excess far-UV emission that reaches the GMC from the OB association, and the excess 21-cm radio HI emission produced after these far-UV photons convert H2 into HI on the GMC surface. The method provides an alternative approach to the use of CO emission as a tracer of H2 in GMCs, and is especially sensitive to a range of density well below the critical density for CO(1-0) emission. We describe our PDR method in more detail and apply it using GALEX far-UV and VLA 21-cm radio data to obtain volume densities in a selection of GMCs in the nearby spiral galaxy M33. We have also examined the sensitivity of the method to the linear resolution of the observations used; the results obtained at 20 pc are similar to those for the larger set of data at 80 pc resolution. The cloud densities we derive range from 1 to 500 cm-3, with no clear dependence on galactocentric radius; these results are generally similar to those obtained earlier in M81, M83, and M101 using the same method.
We employ the velocity map imaging technique to measure kinetic energy and angular distributions of state selected CH3 (v2=0,1,2,3) and Br (2P3/2,2P1/2) photofragments produced by methyl bromide photolysis at 215.9 nm. These results show unambiguously that the Br and Br* forming channels result in different vibrational excitation of the umbrella mode of the methyl fragment. Low energy structured features appear on the images which arise from CH3Br+ photodissociation near 330 nm. The excess energy of the probe laser photon is channeled into CH3+ vibrational excitation, most probably in the nu_4 degenerate bend
We report on the production of cold, state-selected H$_2^+$ molecular ions in a linear RF trap. The ions are produced by (3+1) resonance-enhanced multi-photon ionisation (REMPI) of H$_2$, and sympathetically cooled by laser-cooled Be$^+$ ions. After demonstrating and characterizing the REMPI process, we use photodissociation by a deep UV laser at 213~nm to verify the high vibrational purity of the produced H$_2^+$ ion samples. Moreover, the large difference between the photodissociation efficiencies of ions created in the $v=0$ and $v=1$ levels provides a way to detect a $v=0 to 1$ transition. These results pave the way towards high-resolution vibrational spectroscopy of H$_2^+$ for fundamental metrology applications.
Chemical reactions at ultracold temperatures are expected to be dominated by quantum mechanical effects. Although progress towards ultracold chemistry has been made through atomic photoassociation, Feshbach resonances and bimolecular collisions, these approaches have been limited by imperfect quantum state selectivity. In particular, attaining complete control of the ground or excited continuum quantum states has remained a challenge. Here we achieve this control using photodissociation, an approach that encodes a wealth of information in the angular distribution of outgoing fragments. By photodissociating ultracold 88Sr2 molecules with full control of the low-energy continuum, we access the quantum regime of ultracold chemistry, observing resonant and nonresonant barrier tunneling, matter-wave interference of reaction products and forbidden reaction pathways. Our results illustrate the failure of the traditional quasiclassical model of photodissociation and instead are accurately described by a quantum mechanical model. The experimental ability to produce well-defined quantum continuum states at low energies will enable high-precision studies of long-range molecular potentials for which accurate quantum chemistry models are unavailable, and may serve as a source of entangled states and coherent matter waves for a wide range of experiments in quantum optics.
We study interaction of generic asymmetric molecules with a pair of strong time-delayed short laser pulses with crossed linear polarizations. We show that such an excitation not only provides unidirectional rotation of the most polarizable molecular axis, but also induces a directed torque along this axis, which results in the transient orientation of the molecules. The asymmetric molecules are chiral in nature and different molecular enantiomers experience the orienting action in opposite directions causing out-of-phase oscillation of their dipole moments. The resulting microwave radiation was recently suggested to be used for analysis/discrimination of chiral molecular mixtures. We reveal the mechanism behind this laser induced orientation effect, show that it is classical in nature, and envision further applications of light with skewed polarization.
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