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Physical Review Letters

Heteronuclear and Homonuclear High-Spin Alkali Trimers on Helium Nanodroplets

Johann Nagl, Gerald Auböck, Andreas W. Hauser, Olivier Allard, Carlo Callegari, Wolfgang Ernst

Published Feb 13, 2008• 53 citations
Publisher

Abstract

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.

DOI
10.1103/physrevlett.100.063001

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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.
Nanometer-sized helium droplets, each containing about 10(4) helium atoms, were used as an inert substrate on which to form previously unobserved, spin-3/2 (quartet state) alkali trimers. Dispersed fluorescence measurements reveal that, upon electronic excitation, the quartet trimers undergo intersystem crossing to the doublet manifold, followed by dissociation of the doublet trimer into an atom and a covalently bound singlet dimer. As shown by this work, aggregates of spin-polarized alkali metals represent ideal species for the optical study of fundamental chemical dynamics processes including nonadiabatic spin conversion, change of bonding nature, and unimolecular dissociation.
We analyze three-body nonadditive interactions and characterize critical points on potential energy surfaces of the lowest A2B{A}_{2}BA2​B (A,B=Li,Na,K,Rb,CsA,B=\mathrm{Li},\mathrm{Na},\mathrm{K},\mathrm{Rb},\mathrm{Cs}A,B=Li,Na,K,Rb,Cs) quartet states using high-level ab initio calculations. Our calculations indicate that near equilibrium geometries, large nonadditive effects are stabilizing the systems. We also show that trimer formation reactions are always energetically allowed even for low-lying rovibrational states of heteronuclear triplet-$\ensuremath{\Sigma}$ dimers.
Superfluid helium nanodroplets provide a versatile substrate to cool atoms and molecules, and to assemble weakly bound complexes. Absence of spin-relaxation mechanisms makes He nanodroplets ideal to isolate open-shell atoms and create a spin-polarized system. Here, we show the first coherent manipulation of such a system by resonant excitation of a magnetic-dipole transition. Observation of approximately 50 Rabi oscillations demonstrates coherent population transfer with minimal dephasing. Ours is also the first application of ESR spectroscopy to doped He nanodroplets. This unique environment results in extremely sharp lines and hyperfine-resolved spectra: those of single 39K and 85Rb dopant atoms presented here denote an increase of the Fermi contact interaction, which we can follow as a function of droplet size, reflecting the distortion of the valence-electron wave function due to the surrounding He.
We measured laser-induced-fluorescence (LIF) and beam-depletion (BD) spectra of rubidium atoms (5S-5P transition) on the surface of superfluid helium nanodroplets (M-He_{N} with M=Rb). It is known that when M is a lighter alkali atom electronic excitation always leads to detachment of the excited atom (M;{*}). The dissociation energy, few tens cm;{-1}, comes either as photon excess energy or from the barrierless formation of a M;{*}-He exciplex. We observe that this picture does not hold when M=Rb and the photon excess energy is small: we are able to excite atoms without detaching them from the droplet, thanks to a barrier preventing formation of the exciplex. This system is ideally suited for optical spin pumping in a He nanodroplet, whose achievement we explicitly demonstrate in a pump-probe magnetic circular dichroism experiment.
The study of small clusters is intended to fill the knowledge gap between single atoms and bulk material. He nanodroplets are an ideal matrix for preparing and investigating clusters in a superfluid environment. Alkali-metal atoms are only bound very weakly to their surface by van der Waals forces. Due to the formation process, high-spin states of alkali-metal clusters on He nanodroplets are favorably observed, which is in contrast to the abundance in other preparation processes. Until now, the prevailing opinion was that stable clusters of the heavy alkali-metal atoms, rubidium (Rb) and cesium (Cs) on He nanodroplets, are limited to 5 and 3 atoms, respectively (Schulz et al., Phys. Rev. Lett. 2004, 92, 13401). Here, we present stable complexes of Rb(n)⁺ and Cs(n)⁺ consisting of up to n = 30 atoms, with the detection of large alkali-metal clusters being strongly enhanced by one-photon ionization. Our results also suggest that we monitored both high-spin and low-spin state clusters created on nanodroplets. The van der Waals bound high-spin alkali-metal clusters should show strong magnetic behavior, while low-spin states are predicted to exhibit metallic characteristics. Alkali-metal clusters prepared in these two configurations appear to be ideal candidates for investigating nanosized particles with ferromagnetic or metallic properties.