We demonstrate the feasibility of soft X-ray absorption spectroscopy in the water window using a table-top laser-based approach with organic molecules and inorganic salts in aqueous solution. A high-order harmonic source delivers femtosecond pulses of short wavelength radiation in the photon energy range from 220 to 450 eV. We report static soft X-ray absorption measurements in transmission on the solvated compounds O=C(NH 2 ) 2 , CaCl 2 , and NaNO 3 using flatjet technology. We monitor the absorption of the molecular samples between the carbon (∼280 eV) and nitrogen (∼400 eV) K-edges and compare our results with previous measurements performed at the BESSYII facility. We discuss the roles of pulse stability and photon flux in the outcome of our experiments. Our work paves the way toward table-top femtosecond, solution-phase soft X-ray absorption spectroscopy in the water window.

In this work, we experimentally study the angle-dependent single ionization of carbon dioxide (CO2) by linearly and circularly polarized pulses. The angle dependence of the ionization probability by linearly polarized pulses extracted from time-domain measurements on an impulsively-excited rotational wave-packet is compared with data obtained from a direct angle-scan measurement. The results from the measurement with linear and circular polarization are consistent with the adiabatic ionization approximation. We extend the time-domain method to extract the dependence of the asymptotic momentum distribution of fragment ions on the orientation of the molecular axis, and apply it to investigate dissociative double ionization of CO2. We show that such measurements can directly test the validity of the axial recoil approximation.

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Wavelength-resolved fluorescence spectra of jet-cooled LaH were obtained from D1, E1, and 0(+)((3)Σ(-)) states by exciting isolated rotational levels. The observation of a(3)Δ(1) and a(3)Δ(2) states at 1259.5(5) and 1646(1) cm(-1), respectively, established the missing energy link between the singlet and triplet manifolds. The low-energy b(3)Π(0,1) and B(1)Δ(2) states predicted earlier from ab initio studies were also observed for the first time. Vibrational constants ω(e) = 1418(2) cm(-1), ω(e)x(e) = 15.6(7) cm(-1) for the ground and ΔG(1∕2) = 1326.1(7) and 1312(1) cm(-1), respectively, for the a(3)Δ(1) and b(3)Π(1) states were also determined. Vibrational frequencies were found to be in excellent agreement with earlier ab initio values. However, ab initio term energies and spin-orbit separation of (3)Δ(2)-(3)Δ(1) and (3)Π(1)-(3)Π(0) were found to be in poor agreement with the present observations. Also, the (3)Π state that was predicted to be inverted is observed to be regular.