Positive ionization and electron attachment of hexafluoropropylene oxide in different cluster environments
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388955%3A_____%2F19%3A00495943" target="_blank" >RIV/61388955:_____/19:00495943 - isvavai.cz</a>
Výsledek na webu
<a href="http://hdl.handle.net/11104/0288792" target="_blank" >http://hdl.handle.net/11104/0288792</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.ijms.2018.10.018" target="_blank" >10.1016/j.ijms.2018.10.018</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Positive ionization and electron attachment of hexafluoropropylene oxide in different cluster environments
Popis výsledku v původním jazyce
The hexafluoropropylene oxide, C3F6O (HFPO), is commonly used in technological processes involving low-temperature plasmas. In relevance to such processes, we investigate the electron ionization and attachment to HFPO molecules in various cluster environments. Either pure (HFPO)N clusters or the clusters deposited on larger argon nanoparticles (HFPO)N·ArM are generated in molecular beams in vacuum. The cluster beam is intercepted with a beam of either slow (0–15 eV) or faster (70 eV) electrons, yielding negative or positive ions, respectively, and their mass spectra are recorded. Qualitatively, the spectra of free and Ar-deposited clusters are similar, exhibiting the same ion fragments. The cluster environment suppresses the fragmentation after ionization for both positively and negatively charged clusters, namely, the parent ions (HFPO)n+/− are present in the spectra. The fragmentation is more suppressed in the Ar-deposited clusters. In both the positive ionization and attachment, new fragmentation channels or ion-molecule reactions in the clusters lead to production of new fragments not observed in the gas phase. Mechanisms of these reactions and ionization processes are discussed.
Název v anglickém jazyce
Positive ionization and electron attachment of hexafluoropropylene oxide in different cluster environments
Popis výsledku anglicky
The hexafluoropropylene oxide, C3F6O (HFPO), is commonly used in technological processes involving low-temperature plasmas. In relevance to such processes, we investigate the electron ionization and attachment to HFPO molecules in various cluster environments. Either pure (HFPO)N clusters or the clusters deposited on larger argon nanoparticles (HFPO)N·ArM are generated in molecular beams in vacuum. The cluster beam is intercepted with a beam of either slow (0–15 eV) or faster (70 eV) electrons, yielding negative or positive ions, respectively, and their mass spectra are recorded. Qualitatively, the spectra of free and Ar-deposited clusters are similar, exhibiting the same ion fragments. The cluster environment suppresses the fragmentation after ionization for both positively and negatively charged clusters, namely, the parent ions (HFPO)n+/− are present in the spectra. The fragmentation is more suppressed in the Ar-deposited clusters. In both the positive ionization and attachment, new fragmentation channels or ion-molecule reactions in the clusters lead to production of new fragments not observed in the gas phase. Mechanisms of these reactions and ionization processes are discussed.
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
Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.
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
International Journal of Mass Spectrometry
ISSN
1387-3806
e-ISSN
—
Svazek periodika
435
Číslo periodika v rámci svazku
JAN 2019
Stát vydavatele periodika
NL - Nizozemsko
Počet stran výsledku
6
Strana od-do
145-150
Kód UT WoS článku
000453773300019
EID výsledku v databázi Scopus
2-s2.0-85055551911