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Decomposition of Iron Pentacarbonyl Induced by Singly and Multiply Charged Ions and Implications for Focused Ion Beam-Induced Deposition
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SYSNO ASEP 0504551 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Článek ve WOS Title Decomposition of Iron Pentacarbonyl Induced by Singly and Multiply Charged Ions and Implications for Focused Ion Beam-Induced Deposition Author(s) Indrajith, S. (FR)
Rousseau, P. (FR)
Huber, B. A. (FR)
Nicolafrancesco, C. (FR)
Domaracka, A. (FR)
Grygoryeva, Kateřina (UFCH-W)
Nag, Pamir (UFCH-W) ORCID, RID, SAI
Sedmidubská, Barbora (UFCH-W)
Fedor, Juraj (UFCH-W) ORCID
Kočišek, Jaroslav (UFCH-W) RID, ORCIDSource Title Journal of Physical Chemistry C. - : American Chemical Society - ISSN 1932-7447
Roč. 123, č. 16 (2019), s. 10639-10645Number of pages 7 s. Language eng - English Country US - United States Keywords DISSOCIATIVE ELECTRON-ATTACHMENT ; TRANSITION-METAL CARBONYLS ; Fe(CO)5 Subject RIV CF - Physical ; Theoretical Chemistry OECD category Physical chemistry R&D Projects GJ16-10995Y GA ČR - Czech Science Foundation (CSF) EF16_026/0008382 GA MŠMT - Ministry of Education, Youth and Sports (MEYS) 7AMB17FR047 GA MŠMT - Ministry of Education, Youth and Sports (MEYS) Method of publishing Limited access Institutional support UFCH-W - RVO:61388955 UT WOS 000466053600054 EID SCOPUS 85064381390 DOI 10.1021/acs.jpcc.9b00289 Annotation Focused ion beams are becoming important tools in nanofabrication. The underlying physical processes in the substrate were already explored for several projectile ions. However, studies of ion interaction with precursor molecules for beam-assisted deposition are almost nonexistent. Here, we explore the interaction of various projectile ions with iron pentacarbonyl. We report fragmentation patterns of isolated gas-phase iron pentacarbonyl after interaction with 4 He + at a collision energy of 16 keV, 4 He 2+ at 16 keV, 20 Ne + at 6 keV, 20 Ne 4+ at 40 keV, 40 Ar + at 3 keV, 40 Ar 3+ at 21 keV, 84 Kr 3+ at 12 keV, and 84 Kr 17+ at 255 keV. These projectiles cover interaction regimes ranging from collisions dominated by nuclear stopping through collisions dominated by electronic stopping to soft resonant electron-capture interactions. We report a surprising efficiency of Ne + in the Fe(CO) 5 decomposition. The interaction with multiply charged ions results in a higher content of parent ions and slow metastable fragmentation due to the electron-capture process. The release of CO groups during the decomposition process seems to take off a significant amount of energy. The fragmentation mechanism may be described as Fe being trapped within a CO cluster. Workplace J. Heyrovsky Institute of Physical Chemistry Contact Michaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196 Year of Publishing 2020 Electronic address http://hdl.handle.net/11104/0296156
Number of the records: 1