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EGAS41 - Swansea University

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41 st EGAS PL 2 Gdańsk 2009<br />

Quantitative experiments on electron-molecule collisions<br />

Michael Allan<br />

Department of Chemistry, <strong>University</strong> of Fribourg, chemin du Musée 9, 1700 Fribourg,<br />

Switzerland<br />

E-mail: michael.allan@unifr.ch,<br />

The talk will start with a brief overview of areas of application of electron induced chemistry<br />

and point out which demands and challenges do these applications place on the<br />

fundamental research of electron-molecule collisions. A few examples of how these challenges<br />

have been met will be presented:<br />

Combined theoretical and experimental effort has recently improved our understanding<br />

and capacity to deliver cross sections for electronic excitation of atoms [1], important for<br />

lightning and plasma propulsion.<br />

The emerging Focused Electron Beam Induced Processing (FEBIP) technology inspired<br />

the research of electron collisions by directing our attention to new types of compounds<br />

– the metalorganic compounds used as precursors there [2]. An example of such<br />

a precursor is Pt(PF 3 ) 4 [3] and electron scattering results on this compound will be presented.<br />

Chemical change in polyatomic molecules is very important in the applied systems,<br />

but quantitative calculations are nearly always limited to diatomic molecules and absolute<br />

measurements are still quite rare. An important recent progress towards improving this<br />

situation is the ab-initio calculation [4] and absolute measurement [5] of the DEA cross<br />

section for the prototype polyatomic molecule acetylene and its di-deutero isotopomer.<br />

The assignment of the resonant bands and our understanding of the dissociative electron<br />

attachment mechanism for polyatomic molecules at higher energies – the domain of<br />

Feshbach resonances, with two excited electrons – is still very limited. Light has recently<br />

been shed into this problem, primarily from experiment, by studying the trends in a large<br />

number of compounds [6]. A number of rules and selectivities have been identified and in<br />

certain cases qualitatively rationalized by calculations of the potential surfaces of the parent<br />

Rydberg states of the Feshbach resonances. These processes still present an unsolved<br />

challenge for the theory.<br />

An important conclusion is that electron scattering in the past has often been motivated<br />

by the desire to discover new resonances and cross sections were often measured<br />

only in relative units, for only one process, and over limited energy and angular ranges to<br />

permit the observation of a given resonance. The primary challenge posed by the applications<br />

is the need to measure (and calculate) cross sections in absolute units, over wide<br />

energy and angular ranges, and for all the accessible processes.<br />

References<br />

[1] M. Allan, K. Franz, H. Hotop, O. Zatsarinny, K. Bartschat, J. Phys. B: At. Mol. Opt.<br />

Phys. 42, 044009 (2009)<br />

[2] I. Utke, P. Hoffmann, J. Melngailis, J. Vac. Sci. Technol. B 26, 1197 (2008)<br />

[3] M.H. Ervin et al., J. Vac. Sci. Technol. B 25, 2250 (2007)<br />

[4] S.T. Chourou, A.E. Orel, Phys. Rev. A 77, 042709 (2008)<br />

[5] O. May, J. Fedor, B.C. Ibanescu, M. Allan, Phys. Rev. A, 77, 040701(R) (2008)<br />

[6] B.C. Ibanescu, M. Allan, Phys. Chem. Chem. Phys. (2009) DOI:10.1039/B904945B<br />

39

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