Decomposition of Iron Pentacarbonyl Induced by Singly and Multiply Charged Ions and Implications for Focused Ion Beam-Induced Deposition
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68407700%3A21340%2F19%3A00349560" target="_blank" >RIV/68407700:21340/19:00349560 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/61388955:_____/19:00504551
Výsledek na webu
<a href="https://doi.org/10.1021/acs.jpcc.9b00289" target="_blank" >https://doi.org/10.1021/acs.jpcc.9b00289</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1021/acs.jpcc.9b00289" target="_blank" >10.1021/acs.jpcc.9b00289</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Decomposition of Iron Pentacarbonyl Induced by Singly and Multiply Charged Ions and Implications for Focused Ion Beam-Induced Deposition
Popis výsledku v původním jazyce
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 He-4(+) at a collision energy of 16 keV, He-4(2+) at 16 keV, Ne-20(+) at 6 keV, Ne-20(4+) at 40 keV, Ar-40(+) at 3 keV, Ar-40(3+) at 21 keV, Kr-84(3+) at 12 keV, and Kr-84(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.
Název v anglickém jazyce
Decomposition of Iron Pentacarbonyl Induced by Singly and Multiply Charged Ions and Implications for Focused Ion Beam-Induced Deposition
Popis výsledku anglicky
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 He-4(+) at a collision energy of 16 keV, He-4(2+) at 16 keV, Ne-20(+) at 6 keV, Ne-20(4+) at 40 keV, Ar-40(+) at 3 keV, Ar-40(3+) at 21 keV, Kr-84(3+) at 12 keV, and Kr-84(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.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10403 - Physical chemistry
Návaznosti výsledku
Projekt
—
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2019
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Journal of Physical Chemistry C
ISSN
1932-7447
e-ISSN
1932-7455
Svazek periodika
123
Číslo periodika v rámci svazku
16
Stát vydavatele periodika
US - Spojené státy americké
Počet stran výsledku
7
Strana od-do
10639-10645
Kód UT WoS článku
000466053600054
EID výsledku v databázi Scopus
2-s2.0-85064381390