Probing Methanol Cluster Growth by Vacuum Ultraviolet Ionization

被引:17
作者
Bandyopadhyay, Biswajit [1 ]
Kostko, Oleg [1 ]
Fang, Yigang [1 ]
Ahmed, Musahid [1 ]
机构
[1] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Div Chem Sci, Berkeley, CA 94720 USA
关键词
VUV PHOTOIONIZATION; HYDRATED PROTONS; MIXED CLUSTERS; HYDROGEN-ION; WATER; SOLVATION; SPECTROSCOPY; SIMULATION; MOLECULES; DYNAMICS;
D O I
10.1021/acs.jpca.5b00912
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The ability to probe the formation and growth of clusters is key to answering fundamental questions in solvation and nucleation phenomena. Here, we present a mass spectrometric study of methanol cluster dynamics to investigate these two major processes. The clusters are produced in a molecular beam and ionized by vacuum ultraviolet (VUV) radiation at intermediate distances between the nozzle and the skimmer sampling different regimes of the supersonic expansion. The resulting cluster distribution is studied by time-of-flight mass spectrometry. Experimental conditions are optimized to produce intermediate size protonated methanol and methanol-water clusters and mass spectra and photoionization onsets and obtained. These results demonstrate that intensity distributions vary significantly at various nozzle to ionization distances. Ion-molecule reactions closer to the nozzle tend to dominate leading to the formation of protonated species. The protonated trimer is found to be the most abundant ion at shorter distances because of a closed solvation shell, a larger photoionization cross section compared to the dimer, and an enhanced neutral tetramer precursor. On the other hand, the protonated dimer becomes the most abundant ion at farther distances because of low neutral density and an enhanced charged protonated monomer-neutral methanol interaction. Thomson's liquid drop model is used to qualitatively explain the observed distributions.
引用
收藏
页码:4083 / 4092
页数:10
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