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Solid State Communications

Resonance interaction between a neutral molecule and a metal surface

Constantine Mavroyannis

Published Aug 1, 1977• 9 citations
Publisher
DOI
10.1016/0038-1098(77)91009-2

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The interface of neutral Rydberg atoms in the gas phase with a solid surface is of interest in many fields of modern research. This interface poses a particular challenge for any application in which Rydberg atoms are close to a substrate but also opens up the possibility of studying properties of the surface material itself through the atomic response. In this review the focus is on the process of electron tunneling from the excited state into the substrate that occurs when a Rydberg atom is located in front of a surface at a range of a few hundred nm and is demonstrated with a metallic surface. It is shown how variations in this ionisation mechanism can provide a powerful tool to probe image-charge effects, measure small superficial electric stray or patch fields and how charge transfer from the Rydberg atom can be in resonance with energetically discrete surface states.

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Synopsis Doped He droplets constitute an important environment as ultracold homogeneous matrices for spectroscopic studies. Alkali metal dopants have a series of interesting properties due to their unusual bonding behavior. Neutral atoms attached to the surface of the droplet, forming eventually cold molecules via collisions, while charged dopants form solvation shells, related with the low mobility of the ions in experiments. So, investigations on the underlying intermolecular, markedly orientational ionic, forces, and on the miscoscopic structures of alkali-cation-He complexes is essential.
We investigate the energetics of the atom exchange reaction in the SrF + alkali-metal atom and CaF + alkali-metal atom systems. Such reactions are possible only for collisions of SrF and CaF with the lithium atoms, while they are energetically forbidden for other alkali-metal atoms. Specifically, we focus on SrF interacting with Li, Rb, and Sr atoms and use ab initio methods to demonstrate that the SrF + Li and SrF + Sr reactions are barrierless. We present potential energy surfaces for the interaction of the SrF molecule with the Li, Rb, and Sr atoms in their energetically lowest-lying electronic spin states. The obtained potential energy surfaces are deep and exhibit profound interaction anisotropies. We predict that the collisions of SrF molecules in the rotational or Zeeman excited states most likely have a strong inelastic character. We discuss the prospects for the sympathetic cooling of SrF and CaF molecules using ultracold alkali-metal atoms.
The interface of neutral Rydberg atoms in the gas phase with a solid surface is of interest in many fields of modern research. This interface poses a particular challenge for any application in which Rydberg atoms are close to a substrate but also opens up the possibility of studying properties of the surface material itself through the atomic response. In this review the focus is on the process of electron tunneling from the excited state into the substrate that occurs when a Rydberg atom is located in front of a surface at a range of a few hundred nm and is demonstrated with a metallic surface. It is shown how variations in this ionisation mechanism can provide a powerful tool to probe image-charge effects, measure small superficial electric stray or patch fields and how charge transfer from the Rydberg atom can be in resonance with energetically discrete surface states.