Dipole moments induced in three interacting molecules

Fluids composed of infrared inactive molecules, such as homonuclear diatomics, absorb infrared radiation by virtue of dipole moments induced by molecular interactions. The induced dipoles of two colliding molecules and their associated absorption spectra are generally well known, both from theory and experiment. More recently, empirical models of the most significant dipole components of three interacting molecules have been obtained which permit semi-quantitative predictions of the intensities of the various spectroscopic observations of the ternary spectra, e.g., third virial coefficients of collision-induced absorption spectra, triple transitions, and intercollisional dips. Both the pairwise-additive and the irreducible dipole components are considered. These ternary components should affect the spectra and optical properties also of liquids. It is suggested that the accounting for these effects gives novel information on the structure of liquids through a better understanding of the triple distribution function.     

Selecting molecules embedded in nanodroplets (clusters) of superfluid helium

A method of selecting molecules embedded in nanodroplets (clusters) of superfluid helium is proposed, which is based on the selective vibrational excitation of embedded molecules by intense IR laser radiation. This action leads to a significant decrease in size of the excited clusters, after which these clusters are separated with respect to size via scattering of the cluster beam on a crossing atomic beam. The method is described in detail and the possibility of selecting SF₆ molecules in liquid helium nanodroplets using the excitation by CO₂ laser radiation and the angular separation via scattering on a xenon atomic beam is demonstrated. The results show that, by using this technique, it is possible to separate molecules with respect to isotope (element) composition. Advantages and drawbacks of the method are analyzed.     

Changing the fragmentation pattern of molecules in helium nanodroplets by co-embedding with water

Individual amino acid molecules embedded in helium nanodroplets fragment extensively when the beam is ionized by electron bombardment. However, we find that when glycine and tryptophan are picked up right after, or right before, a small amount of water, the mass spectra become significantly altered. For glycine, the detected ions consist almost entirely of intact protonated amino acids, with or without a few water molecules attached. In other words, the presence of water exerts a striking “buffering” effect on the ionization-induced fragmentation. For tryptophan the effect is weaker but also present. In both cases, the hydroxyl group lost upon ionization overwhelmingly comes from the water partner (in strong contrast to the situation observed when amino acids are picked up by neat water clusters). A complementary experiment involving DCl molecules co-embedded with water shows that in this case Cl and/or DCl invariably leave the droplet upon ionization. The observed patterns may be steered by the analytes' dipole moments or by solvation effects.     

Dragging of polarizable nanodroplets by distantly solvated ions

We show by molecular dynamics simulations that ions intercalated in carbon and boron-nitride nanotubes can be solvated at distance in polarizable nanodroplets adsorbed on their surfaces. When the ions are driven in the nanotubes by electric fields, the adsorbed droplets are dragged together with them. We illustrate this phenomenon by dragging assemblies of 20-10,000 water molecules by individual Na+ and Cl- ions. This ion-facilitated dragging could be applied in molecular delivery, separation, and desalination.     

Photoelectron spectroscopy of doped helium nanodroplets

The photoionization dynamics of aniline doped helium droplets has been investigated by photoelectron spectroscopy. The photoelectron spectra resemble closely that of gas phase aniline, except for a droplet-size-dependent shift. This shift is caused by lowering of the ionization threshold upon solvation and can be readily estimated. The individual peaks in the photoelectron spectrum are broadened towards lower kinetic energy which is attributed to the relaxation of the photoelectrons as they pass through the helium droplet.     

Bridging the gap between small clusters and nanodroplets: spectroscopic study and computer simulation of carbon dioxide solvated with helium atoms

High resolution infrared spectra of He(N)-CO2 clusters with N up to 17 have been studied in the region of the CO2 nu(3) fundamental band. The B rotational constant initially drops as expected for a normal molecule, reaching a minimum for N=5. Its subsequent rise for N=6 to 11 can be interpreted as the transition from a normal (though floppy) molecule to a quantum solvation regime. For N>13, the B value becomes approximately constant with a value about 17% larger than that measured in much larger helium nanodroplets. Quantum Monte Carlo calculations of pure rotational spectra are in excellent agreement with the measured B in this size range and complement the experimental study with detailed structural information. For a larger cluster size (N=30-50) the simulations show a clear sign of convergence towards the nanodroplet B value.     

Formation of cold bialkali dimers on helium nanodroplets

Cold alkali diatomic molecules (LiCs, NaCs) in the lowest vibrational state of the electronic triplet ground state are formed on superfluid helium nanodroplets. Using photoionization detection the excitation spectra of the transitions are recorded. The splitting of the vibrational structure in the LiCs spectrum, not observed in the NaCs spectrum, is interpreted in terms of molecular fine structure. The spectra are well reproduced by a model based on quantum chemistry potential curves including spin-orbit coupling, in combination with an asymmetric line shape function to account for cluster-induced broadening. Our refined potential curves provide important input data for the photoassociation of ultracold dipolar alkali molecules from atomic quantum gases.Received: 1 July 2004, Published online: 26 October 2004PACS: 36.40.Mr Spectroscopy and geometrical structure of clusters - 34.50.Gb Electronic excitation and ionization of molecules; intermediate molecular states (including lifetimes, state mixing, etc.) - 33.20.-t Molecular spectra     

Dopant-induced ignition of helium nanodroplets in intense few-cycle laser pulses

We demonstrate ultrafast resonant energy absorption of rare-gas doped He nanodroplets from intense few-cycle (~10 fs) laser pulses. We find that less than 10 dopant atoms "ignite" the droplet to generate a nonspherical electronic nanoplasma resulting ultimately in complete ionization and disintegration of all atoms, although the pristine He droplet is transparent for the laser intensities applied. Our calculations at those intensities reveal that the minimal pulse length required for ignition is about 9 fs.     

Infrared laser spectroscopy of diacetylene and cyclopropane in helium nanodroplets

High resolution infrared laser spectroscopy has been used to obtain rotationally resolved vibrational spectra of diactyelene and cyclopropane in helium nanodroplets. In part, this work was motivated by the need for a large database of rotational constants for molecules solvated in liquid helium. Data of this type provides benchmarks with which to test the theoretical methods that are currently being developed for calculating the effect of the helium on the rotational dynamics of these solvated molecules. In general, the correlated motion of the helium and the molecule results in an effective moment of inertia that is considerably larger than that of the gas phase molecule.     

Evaporative cooling of helium nanodroplets with angular momentum conservation

Evaporative cooling of helium nanodroplets is studied with a statistical rate model that includes, for the first time, angular momentum conservation. While the final temperature of the droplets is almost identical to that previously predicted and later observed, the distribution of total droplet energy and angular momentum states is vastly more excited than a canonical distribution at the same temperature. It is found that the final angular momentum of the droplets is highly correlated with the initial direction, and that a significant fraction of the alignment of the total angular momentum should be transferred to the rotational angular momentum of an embedded molecule.     

Stability of two-component alkali clusters formed on helium nanodroplets

The stability of two-component clusters consisting of light (Na or K) and heavy (Rb or Cs) alkali atoms formed on helium nanodroplets is studied by femtosecond laser ionization in combination with mass spectrometry. Characteristic stability patterns reflecting electron shell-closures are observed in dependence of the total number of atoms contained in the mixed clusters. Faster decay of the stability of mixed clusters compared to the pure light ones as a function of size indicates a destabilizing effect of heavy alkali atoms on light alkali clusters, presumably due to second order spin-orbit interaction.     

Heteronuclear and homonuclear high-spin alkali trimers on helium nanodroplets

The electronic excitation spectra of all possible homo- and heteronuclear high-spin (quartet) trimers of K and Rb (KxRb(3-x), x=0...3) assembled on the surface of superfluid helium droplets, are measured in the spectral range from 10,600 to 17,400 cm(-1). A regular series of corresponding bands is observed, reflecting the similar electronic structure of all these trimers. For the assignment and separation of overlapping bands, we determine x directly, with mass-selected beam depletion, and indirectly with a V-type double-resonance scheme. The assignment is confirmed by high-level ab initio calculations of the electronic structure of the bare trimers. The level structure is rationalized in terms of harmonic-oscillator states of the three valence electrons in a quantum-dot-like confining potential. We predict that three should be a magic number for high-spin alkali clusters.     

Quantum interference spectroscopy of rubidium-helium exciplexes formed on helium nanodroplets

Femtosecond multiphoton pump-probe photoionization is applied to helium nanodroplets doped with rubidium (Rb). The yield of Rb+ ions features pronounced quantum interference (QI) fringes demonstrating the coherence of a superposition of electronic states on a time scale of tens of picoseconds. Furthermore, we observe QI in the yield of formed RbHe exciplex molecules. The quantum interferogram allows us to determine the vibrational structure of these unstable molecules. From a sliced Fourier analysis one cannot only extract the population dynamics of vibrational states but also follow their energetic evolution during the RbHe formation.     

Laser kinetic spectroscopy of solvated dye molecules

Journal of Russian Laser Research -     

Resonant charging of Xe clusters in helium nanodroplets under intense laser fields

We theoretically investigate the impact of multiple plasmon resonances on the charging of Xe clusters embedded in He nanodroplets under intense pump-probe laser excitation (τ = 25 fs, I ₀ = 2.5 × 10¹⁴   W/cm², λ = 800 nm). Our molecular dynamics simulations on Xe₃₀₉He_10 000 and comparison to results for free Xe₃₀₉ give clear evidence for selective resonance heating in the He shell and the Xe cluster, but no corresponding double hump feature in the final Xe charge spectra is found. Though the presence of the He shell substantially increases the maximum charge states, the pump-probe dynamics of the Xe spectra from the embedded system is similar to that of the free species. In strong contrast to that, the predicted electron spectra do show well-separated and pronounced features from highly efficient plasmon assisted electron acceleration for both resonances in the embedded clusters. A detailed analysis of the underlying ionization and recombination dynamics is presented and explains the apparent disaccord between the resonance features in the ion and electron spectra.     

Magnetic dichroism of potassium atoms on the surface of helium nanodroplets

The population ratio of Zeeman sublevels of atoms on the surface of superfluid helium droplets (T=0.37 K) has been measured. Laser induced fluorescence spectra of K atoms are measured in the presence of a moderately strong magnetic field (2.9 kG). The relative difference between the two states of circular polarization of the exciting laser is used to determine the electron spin polarization of the ensemble. Equal fluorescence levels indicate that the two spin sublevels of the ground-state K atom are equipopulated, within 1%. Thermalization to 0.37 K would give a population ratio of 0.35. We deduce that the rate of spin relaxation induced by the droplet must be <520/s. For the K2 triplet dimer we find instead full thermalization of the spin.