首页> 外文期刊>The Journal of Chemical Physics >Revealing isomerism in sodium-water clusters: Photoionization spectra of Na(H2O)(n) (n=2-90)
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Revealing isomerism in sodium-water clusters: Photoionization spectra of Na(H2O)(n) (n=2-90)

机译:揭示钠 - 水簇中的异构性:Na(H2O)(n)的光离子光谱(n = 2-90)

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Soft ionization of sodium tagged polar clusters is increasingly used as a powerful technique for sizing and characterization of small aerosols with possible application, e.g., in atmospheric chemistry or combustion science. Understanding the structure and photoionization of the sodium doped clusters is critical for such applications. In this work, we report on measurements of photoionization spectra for sodium doped water clusters containing 2-90 water molecules. While most of the previous studies focused on the ionization threshold of the Na(H2O)(n) clusters, we provide for the first time full photoionization spectra, including the high-energy region, which are used as reference for a comparison with theory. As reported in previous work, we have seen an initial drop of the appearance ionization energy with cluster size to values of about 3.2 eV for n < 5. In the size range from n = 5 to n = 15, broad ion yield curves emerge; for larger clusters, a constant range between signal appearance (similar to 2.8 eV) and signal saturation (similar to 4.1 eV) has been observed. The measurements are interpreted with ab initio calculations and ab initio molecular dynamics simulations for selected cluster sizes (n <= 15). The simulations revealed theory shortfalls when aiming at quantitative agreement but allowed us identifying structural motifs consistent with the observed ionization energy distributions. We found a decrease in the ionization energy with increasing coordination of the Na atom and increasing delocalization of the Na 3s electron cloud. The appearance ionization energy is determined by isomers with fully solvated sodium and a highly delocalized electron cloud, while both fully and incompletely solvated isomers with localized electron clouds can contribute to the high energy part of the photoionization spectrum. Simulations at elevated temperatures show an increased abundance of isomers with low ionization energies, an entropic effect enabling size selective infrar
机译:钠标记极性簇的软电离越来越多地用作具有可能应用的小气溶胶的尺寸和表征的强大技术,例如,在大气化学或燃烧科学中。了解钠掺杂簇的结构和光相对于这些应用至关重要。在这项工作中,我们报告了含有2-90个水分子的掺杂水簇的光离心光谱的测量。虽然最先前的大多数研究专注于Na(H2O)(n)簇的电离阈值,但我们提供了第一次完全光相消光谱,包括高能区域,其用作与理论相比的参考。如先前的工作所述,我们已经看到了簇尺寸的外观电离能量的初始滴,对于N <5.在尺寸范围内从n = 5到n = 15,宽离子产量曲线出现;对于较大的簇,已经观察到信号外观(类似于2.8eV)和信号饱和度(类似于4.1eV)之间的恒定范围。测量以AB Initio计算和AB Initio分子动力学模拟进行了解释,用于选定的簇大小(n <= 15)。仿真旨在瞄准定量协议时的理论短缺,但允许我们识别与观察到的电离能量分布一致的结构基序。我们发现电离能量减少,随着Na原子的协调和增加Na 3S电子云的临床化的增加。外观电离能由异构体与具有完全溶解的钠和高度分层的电子云的异构体测定,同时全部和不完全溶胀的异构体具有局部电子云的高能量部分可以有助于光相消光谱的高能部分。升高温度的模拟显示出具有低电离能量的异构体增加,熵效应使得尺寸选择性红外

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