In this work, we demonstrate measurements of photodestruction rates of translationally cold, charged biomolecules. The long-term stable storage of the molecular ions in an ion trap at ultra-high vacuum conditions allows measurement of small rates and verification that rates are linear in photodestruction laser intensity. Measurements were performed on singly protonated molecules of the organic compound glycyrrhetinic acid (C30H46O4), dissociated by a continuous-wave UV laser (266 nm) using different intensities. The molecules were sympathetically cooled by simultaneously trapped laser-cooled barium ions to translational temperatures of below 150 mK. Destruction rates of less than 0.05 s^-1 and a cross section of (1.1 +/- 0.1) * 10^-17 cm^2 have been determined. An extension to tunable UV laser sources would permit high-resolution dissociation spectroscopic studies on a wide variety of cold complex molecules.
Photoelectron imaging techniques are used to experimentally investigate photodetachment of negative ions in a strong laser-field as well as the orbital alignment dynamics in the residual neutral.\n\nStrong-field photodetachment in a linearly polarized pulsed laser with 100 fs pulse length is used to create a wave packet in the neutral atoms of carbon, germanium and silicon. The negative ions of these three atomic species are isoelectronic with a half-filled
p-shell. The photodetachment rate is highly dependent on the magnetic quantum number $m_\\ell$ with the orbital with $m_\\ell = 0$ having a detachment rate of an order of magnitude larger than orbitals with $m_\\ell$ non-zero, with the polarization axis acting as a quantization axis. The residual neutral is thus left in an aligned state after photodetachment. The aligned state constitutes of a coherent superposition of fine-structure states and the population in the different orbitals will accordingly display a time-dependent spatial oscillation. The created wave packet is subsequently probed through photoionization by a second strong-field laser pulse.\n\nSecondly, a tomographic method is implemented to observe the three-dimensional distribution of photoelectrons produced in strong-field photodetachment processes. The method makes no assumptions of the existence of any symmetry axes in the photoelectron distribution and is thus applicable to any laser polarization ellipticity. Traditional imaging methods are dependent on the photoelectron distribution to be cylindrically symmetric by using either linearly or circularly polarized light, a requirement which can be lifted by using a tomographic technique. The method is applied to multiphoton detachment of the negative ion of silver.\n\nFinally, strong-field photodetachment of homonuclear diatomic negative ions is performed. The possibility of the additional electron being ejected from either of the two atomic centers can significantly alter the photoelectron distribution compared to an atomic negative ion with the same detachment energy. Experiments are performed on C
2−, Si
2− and Ag
2− and compared to theoretical models.