Metastable Evaporation of Molecules from Water Clusters.
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388955%3A_____%2F24%3A00598760" target="_blank" >RIV/61388955:_____/24:00598760 - isvavai.cz</a>
Výsledek na webu
<a href="https://hdl.handle.net/11104/0356355" target="_blank" >https://hdl.handle.net/11104/0356355</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1021/acs.jpca.4c04728" target="_blank" >10.1021/acs.jpca.4c04728</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Metastable Evaporation of Molecules from Water Clusters.
Popis výsledku v původním jazyce
We probe the stability of water clusters by means of their metastable decay probability extracted from two-dimensional reflectron time-of-flight mass spectra. Two different methods are used to ionize and potentially excite the clusters and trigger the evaporation: (i) attachment of electrons with near-zero energies, producing negatively charged (H2O)n- clusters, and (ii) electron impact ionization, producing protonated (H2O)nH+ clusters. The electron attachment is a soft ionization and therefore provides information about the size distribution of the neutral clusters in the beam due to a very limited amount of post-ionization loss of water molecules. A dependence of metastable fractions on the conditions of neutral clusters production prior to the electron attachment is reported. For the cations, the higher energy electron impact ionization leads to a more extensive metastable loss of water molecules. The results are discussed in the light of neutral cluster excitation energy distributions and, for negative clusters, also in terms of binding energies. The experiments demonstrate clearly the role of the excess electron vs the excess proton in the two different charge states of the clusters around sizes N = 50-55, for which binding energies of the anions are derived from the data.
Název v anglickém jazyce
Metastable Evaporation of Molecules from Water Clusters.
Popis výsledku anglicky
We probe the stability of water clusters by means of their metastable decay probability extracted from two-dimensional reflectron time-of-flight mass spectra. Two different methods are used to ionize and potentially excite the clusters and trigger the evaporation: (i) attachment of electrons with near-zero energies, producing negatively charged (H2O)n- clusters, and (ii) electron impact ionization, producing protonated (H2O)nH+ clusters. The electron attachment is a soft ionization and therefore provides information about the size distribution of the neutral clusters in the beam due to a very limited amount of post-ionization loss of water molecules. A dependence of metastable fractions on the conditions of neutral clusters production prior to the electron attachment is reported. For the cations, the higher energy electron impact ionization leads to a more extensive metastable loss of water molecules. The results are discussed in the light of neutral cluster excitation energy distributions and, for negative clusters, also in terms of binding energies. The experiments demonstrate clearly the role of the excess electron vs the excess proton in the two different charge states of the clusters around sizes N = 50-55, for which binding energies of the anions are derived from the data.
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
2024
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 A
ISSN
1089-5639
e-ISSN
1520-5215
Svazek periodika
128
Číslo periodika v rámci svazku
40
Stát vydavatele periodika
US - Spojené státy americké
Počet stran výsledku
11
Strana od-do
8679-8689
Kód UT WoS článku
001324845500001
EID výsledku v databázi Scopus
2-s2.0-85205437941