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EGAS41 - Swansea University

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41 st EGAS PL 7 Gdańsk 2009<br />

Chemistry at ultracold temperatures:<br />

Observation of the smallest droplet of acid<br />

Martina Havenith<br />

Physical Chemistry II, NC 7/72, Ruhr <strong>University</strong> Bochum, 44780 Bochum, Germany<br />

E-mail: martina.havenith@rub.de<br />

Acid dissociation and subsequent solvation of its charged fragments, including the hydrated<br />

proton, is one of the most fundamental chemical processes. In contrast to ambient<br />

bulk water environments, understanding mechanisms that allow for ionization in small<br />

networks at ultracold conditions are relevant from atmospheric to interstellar chemistry,<br />

but remain largely unexplored.<br />

In Bochum we have set up a He-nanodroplet apparatus in combination with a homebuilt<br />

cw-Optical Parametric Oscillator IR (OPO) with full frequency coverage in the<br />

range from 2600 to 3400 cm −1 , high output power (up to 2.7 W), and high resolution<br />

(0.0001 cm −1 ) [1]. Briefly (35), helium droplets with an average size of 8500 He were<br />

formed in a supersonic expansion of precooled (16 K) gaseous helium through a 5 µm<br />

diameter nozzle. These droplets provide a gentle matrix for step-by-step aggregation of<br />

molecular clusters, via a controllable pickup process governed by Poisson’s statistics [2],<br />

allowing for IR high-resolution spectroscopy.<br />

We report the first experimental observation of a microscopic aqueous droplet of acid<br />

reported at ultracold (0.37 K) temperatures. Furthermore we will discuss specific reaction<br />

mechanism at ultracold temperatures [3]. Here, we report full dissociation of a single HCl<br />

molecule with exactly four water molecules in superfluid helium nanodroplets as a result<br />

of molecular aggregation at 0.37 K.<br />

References<br />

[1] K. von Haeften, A. Metzelthin, S. Rudolph, V. Staemmler, M. Havenith, Phys. Rev.<br />

Lett. 95, 215301 (2005)<br />

[2] J.P. Toennies, A.F. Vilesov, Angew. Chem. Int. Ed. 43, 2622 (2004)<br />

[3] A. Gutberlet, G. Schwaab, Ö. Birer, M. Masia, A. Kaczmarek, H. Forbert, M. Havenith,<br />

D. Marx, Science, in press<br />

44

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