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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 ASEP0504551
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleDecomposition 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, ORCID
    Source TitleJournal of Physical Chemistry C. - : American Chemical Society - ISSN 1932-7447
    Roč. 123, č. 16 (2019), s. 10639-10645
    Number of pages7 s.
    Languageeng - English
    CountryUS - United States
    KeywordsDISSOCIATIVE ELECTRON-ATTACHMENT ; TRANSITION-METAL CARBONYLS ; Fe(CO)5
    Subject RIVCF - Physical ; Theoretical Chemistry
    OECD categoryPhysical chemistry
    R&D ProjectsGJ16-10995Y 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 publishingLimited access
    Institutional supportUFCH-W - RVO:61388955
    UT WOS000466053600054
    EID SCOPUS85064381390
    DOI10.1021/acs.jpcc.9b00289
    AnnotationFocused 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.
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2020
    Electronic addresshttp://hdl.handle.net/11104/0296156
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