Probing weak dipole-dipole interaction using phase-modulated non-linear spectroscopy

Phase-modulated non-linear spectroscopy with higher harmonic demodulation has recently been suggested to provide information on many-body excitations. In the present work we theoretically investigate the application of this method to infer the interaction strength between two particles that interact via weak dipole-dipole interaction. To this end we use full numerical solution of the Schr\"odinger equation with time-dependent pulses. For interpretation purpose we also derive analytical expressions in perturbation theory. We find one can detect dipole-dipole interaction via peak intensities (in contrast to line-shifts which typically are used in conventional spectroscopy). We provide a detailed study on the dependence of these intensities on the parameters of the laser pulse and the dipole-dipole interaction strength. Interestingly, we find that there is a phase between the first and second harmonic demodulated signal, whose value depends on the sign of the dipole-dipole interaction.Comment: 12 pages, 8 figures, Supporting information provided with the source file

Vibronic Lineshapes of PTCDA Oligomers in Helium Nanodroplets

Oligomers of the organic semiconductor PTCDA are studied by means of helium nanodroplet isolation (HENDI) spectroscopy. In contrast to the monomer absorption spectrum, which exhibits clearly separated, very sharp absorption lines, it is found that the oligomer spectrum consists of three main peaks having an apparent width orders of magnitude larger than the width of the monomer lines. Using a simple theoretical model for the oligomer, in which a Frenkel exciton couples to internal vibrational modes of the monomers, these experimental findings are nicely reproduced. The three peaks present in the oligomer spectrum can already be obtained taking only one effective vibrational mode of the PTCDA molecule into account. The inclusion of more vibrational modes leads to quasi continuous spectra, resembling the broad oligomer spectra

Coherent multidimensional spectroscopy in the gas phase

Recent work applying multidimentional coherent electronic spectroscopy at dilute samples in the gas phase is reviewed. The development of refined phase-cycling approaches with improved sensitivity has opened-up new opportunities to probe even dilute gas-phase samples. In this context, first results of 2-dimensional spectroscopy performed at doped helium droplets reveal the femtosecond dynamics upon electronic excitation of cold, weakly-bound molecules, and even the induced dynamics from the interaction with the helium environment. Such experiments, offering well-defined conditions at low temperatures, are potentially enabling the isolation of fundamental processes in the excitation and charge transfer dynamics of molecular structures which so far have been masked in complex bulk environments.Comment: Invited Review Articl

Wave packet dynamics in triplet states of Na2 attached to helium nanodroplets

The dynamics of vibrational wave packets excited in Na2 dimers in the triplet ground and excited states is investigated by means of helium nanodroplet isolation (HENDI) combined with femtosecond pump-probe spectroscopy. Different pathways in the employed resonant multi-photon ionization scheme are identified. Within the precision of the method, the wave packet dynamics appears to be unperturbed by the helium droplet environment

The excitation function for Li+HF-->LiF+H at collision energies below 80 meV

We have measured the dependence of the relative integral cross section of the reaction Li+HF-->LiF+H on the collision energy using crossed molecular beams. By varying the intersection angle of the beams from 37{\deg} to 90{\deg} we covered the energy range 25 meV < E_tr < 131 meV. We observe a monotonous rise of the cross section with decreasing energy over the entire energy range indicating that a possible translational energy threshold to the reaction is significantly smaller than 25 meV. The steep rise is quantitatively recovered by a Langevin-type excitation function based on a vanishing threshold and a mean interaction potential energy ~R^-2.5 where R is the distance between the reactants. To date all threshold energies deduced from ab-initio potentials and zero-point vibrational energies are at variance with our results, however, our findings support recent quantum scattering calculations that predict significant product formation at collision energies far below these theoretical thresholds.Comment: 8 pages, 7 figure

ELECTRONIC WAVE PACKET INTERFEROMETRY OF GAS PHASE SAMPLES: HIGH RESOLUTION SPECTRA AND COLLECTIVE EFFECTS

Time-resolved coherent spectroscopy has opened many new directions to study ultrafast dynamics in complex quantum systems. While most applications have been achieved in the condensed phase, we are focusing on dilute gas phase samples, in particular, on doped helium droplet beams. Isolation in such droplets at millikelvin temperatures provides unique opportunities to synthesize well-defined complexes, to prepare specific ro-vibronic states, and study their dynamics. To account for the small densities in our samples, we apply a phase modulation technique in order to reach enough sensitivity and a high spectral resolution in electronic wave packet interferometry experiments. The combination with mass-resolved ion detection enabled us e.g. to characterize vibrational structures of excimer molecules. By extending this technique we have observed collective resonances in samples of very low density (10$^8$,cm$^{-3}$). With a variant of this method, we are currently elaborating the implementation of nonlinear all-XUV spectroscopy