ABSTRACT
The electronic structures of ThCl and ThCl+ have been examined using laser induced fluorescence and two-photon ionization techniques. Rotationally resolved spectra, combined with the predictions from relativistic electronic structure calculations, show that the ground state of the neutral molecule is Th+(7s26d)Cl-, X2Δ3/2. Dispersed fluorescence spectra for ThCl revealed the ground state vibrational levels v = 0-10 and low energy electronic states that also originate from the atomic ion 7s26d configuration. Pulsed field ionization-zero kinetic energy photoelectron spectroscopy established an ionization energy (IE) for ThCl of 51 344(5) cm-1, and the ThCl+ vibrational term energies of the v = 1-3 levels. The zero-point level of the first electronically excited state was found at 949(2) cm-1. Comparisons with high-level theoretical results indicate that the ground and excited states are Th2+(7s6d)Cl- X3Δ1 and Th2+(7s2)Cl- Σ+1, respectively. Relativistic coupled cluster composite thermochemistry calculations yielded an IE within 1.2 kcal/mol of experiment and a bond dissociation energy (118.3 kcal/mol) in perfect agreement with previous experiments.
ABSTRACT
We present a novel compact design for a multichannel atomic oven which generates collimated beams of refractory atoms for fieldable laser spectroscopy. Using this resistively heated crucible, we demonstrate spectroscopy of an erbium sample at 1300 °C with improved isotopic resolution with respect to a single-channel design. In addition, our oven has a high thermal efficiency. By minimizing the surface area of the crucible, we achieve 2000 °C at 140 W of applied electrical power. As a result, the design does not require any active cooling and is compact enough to allow for its incorporation into fieldable instruments.
ABSTRACT
The BaO(+) cation is of interest from the perspectives of electronic structure and the potential for cooling to ultra-cold temperatures. Spectroscopic data for the ion have been obtained using a two-color photoionization technique. The ionization energy for BaO was found to be 6.8123(3) eV. The ground state of BaO(+) was identified as X(2)Σ(+), and both vibrational and rotational constants were determined. Vibrationally resolved spectra were recorded for A(2)Π, the first electronically excited state. These data yielded the term energy, vibrational frequency, and the spin-orbit interaction constant. Relativistic electronic structure calculations were carried out using multi-reference configuration interaction (MRCI), coupled cluster and density functional theory methods. Transition moments for the pure vibrational and A(2)Π-X(2)Σ(+) transitions were predicted using the MRCI method.
ABSTRACT
Gas-phase ThS has been produced via the reaction of laser ablated Th with H2S. Rotationally resolved electronic spectra were recorded by laser-induced fluorescence (LIF) over the range 17500-24000 cm(-1). Resonance-enhanced multiphoton ionization was used in conjunction with a time-of-flight mass spectrometer to confirm the assignments of nine LIF bands to ThS. Using excitation of a ThS band centered at 22118 cm(-1), a dispersed fluorescence spectrum revealed a vibrational progression of the X(1)Σ(+) ground electronic state and the term energies of two low-lying excited states ((3)Δ1 and (3)Δ2). Two-color photoionization spectroscopy was used to study ThS(+). An accurate ionization energy for ThS was obtained (54425(3) cm(-1)); ThS(+) vibronic term energies up to v = 7 in the X(2)Σ(+) ground state and v = 3 in the (2)Δ3/2 first excited state were recorded. High-level electronic structure calculations, with inclusion of the spin-orbit interactions yielded predictions that were in good agreement with the experimental data for ThS and ThS(+). The spectroscopic properties of ThS/ThS(+) are compared with those of the valence isoelectronic pairs ThO/ThO(+), HfO/HfO(+), and HfS/HfS(+).
