Excited states of Pt(PF₃)₄ andb their role in focused electron beam nanofabrication
- Zlatar, Matija Department of Chemistry, Institute of Chemistry, Technology and Metallurgy (IChTM), University of Belgrade, Serbia
- Allan, Michael Department of Chemistry, University of Fribourg, Switzerland
- Fedor, Juraj J. Heyrovský Institute of Physical Chemistry v.v.i., The Czech Academy of Sciences, Prague, Czech Republic
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19.05.2016
Published in:
- The Journal of Physical Chemistry C. - 2016, vol. 120, no. 19, p. 10667–10674
English
Electron induced chemistry of metal-containing precursor molecules is central in focused electron beam induced deposition (FEBID). While some elementary processes leading to precursor decomposition were quantitatively characterized, data for neutral dissociation is missing. We provide this data for the model precursor Pt(PF3)4 by using the available cross sections for electronic excitation and characterizing fragmentation of the excited states theoretically by TDDFT. The potential energy curves for a number of states visible in the experimental electron energy loss spectra are dissociative, either directly or via conical intersections, indicating that the quantum yield for dissociation is close to 100%. Taking into account typical electron energy distribution at the FEBID spot reveals that the importance of neutral dissociation exceeds that of dissociative electron attachment, which has been so far considered to be the dominant decomposition process. We thus established neutral dissociation as an important, albeit often neglected, channel for FEBID using Pt(PF3)4. The calculations revealed a number of other phenomena that can play a role in electron induced chemistry of this compound, e.g., a considerable increase of bond dissociation energy with sequential removal of multiple ligands.
- Faculty
- Faculté des sciences et de médecine
- Department
- Département de Chimie
- Language
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- English
- Classification
- Chemistry
- License
- License undefined
- Identifiers
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- RERO DOC 261097
- DOI 10.1021/acs.jpcc.6b02660
- Persistent URL
- https://folia.unifr.ch/unifr/documents/305094
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