Hydrated Formic Acid Clusters and their Interaction with Electrons
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388955%3A_____%2F24%3A00584315" target="_blank" >RIV/61388955:_____/24:00584315 - isvavai.cz</a>
Výsledek na webu
<a href="https://hdl.handle.net/11104/0352245" target="_blank" >https://hdl.handle.net/11104/0352245</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1002/cphc.202400071" target="_blank" >10.1002/cphc.202400071</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Hydrated Formic Acid Clusters and their Interaction with Electrons
Popis výsledku v původním jazyce
We investigate ion formation in hydrated formic acid (FA) clusters upon collision with electrons of variable energy, focusing on electron ionization at 70 eV (EI) and low-energy (1.5–15 eV) electron attachment (EA). To uncover details about the composition of neutral clusters, we aim to elucidate the ion formation processes in FAM ⋅ WN clusters initiated by interaction with electrons and determine the extent of cluster fragmentation. EI predominantly produces protonated [FAm+H]+ ions, and in FA-rich clusters, the stable ring structures surrounding H3O+ ions are formed. In contrast, EA leads to a competition between the formation of intact [FAm ⋅ Wn]− and dissociated [FAm ⋅ Wn−H]− fragment ions, influenced by the cluster size, level of hydration, and electron energy. Our findings reveal a predisposition of low-energy EA towards forming [FAm ⋅ Wn]−, while higher electron energies tend to favor the formation of [FAm ⋅ Wn−H]− due to intracluster ion-molecule reactions. The comparison of positive and negative ion spectra suggests that the mass spectra of FA-rich clusters may indicate their actual size and composition. On the other hand, the more weakly bound water evaporation from the clusters depends strongly on the ionization. Thus, for the hydrated clusters, the neutral cluster size can hardly be estimated from the mass spectra.
Název v anglickém jazyce
Hydrated Formic Acid Clusters and their Interaction with Electrons
Popis výsledku anglicky
We investigate ion formation in hydrated formic acid (FA) clusters upon collision with electrons of variable energy, focusing on electron ionization at 70 eV (EI) and low-energy (1.5–15 eV) electron attachment (EA). To uncover details about the composition of neutral clusters, we aim to elucidate the ion formation processes in FAM ⋅ WN clusters initiated by interaction with electrons and determine the extent of cluster fragmentation. EI predominantly produces protonated [FAm+H]+ ions, and in FA-rich clusters, the stable ring structures surrounding H3O+ ions are formed. In contrast, EA leads to a competition between the formation of intact [FAm ⋅ Wn]− and dissociated [FAm ⋅ Wn−H]− fragment ions, influenced by the cluster size, level of hydration, and electron energy. Our findings reveal a predisposition of low-energy EA towards forming [FAm ⋅ Wn]−, while higher electron energies tend to favor the formation of [FAm ⋅ Wn−H]− due to intracluster ion-molecule reactions. The comparison of positive and negative ion spectra suggests that the mass spectra of FA-rich clusters may indicate their actual size and composition. On the other hand, the more weakly bound water evaporation from the clusters depends strongly on the ionization. Thus, for the hydrated clusters, the neutral cluster size can hardly be estimated from the mass spectra.
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
<a href="/cs/project/GA24-11390S" target="_blank" >GA24-11390S: Nanoklastry atmosférických aerosolů v experimentech s molekulovými paprsky a počítačových simulacích</a><br>
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2024
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
ChemPhysChem
ISSN
1439-4235
e-ISSN
1439-7641
Svazek periodika
25
Číslo periodika v rámci svazku
10
Stát vydavatele periodika
US - Spojené státy americké
Počet stran výsledku
8
Strana od-do
e202400071
Kód UT WoS článku
001180593300001
EID výsledku v databázi Scopus
2-s2.0-85186848821