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Delocalized electronic behavior observed in transition metal oxide clusters under strong-field excitation

机译:在强场激发下在过渡金属氧化物簇中观察到的离域电子行为

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摘要

Heterogeneously composed clusters are exposed to intensity resolved, 100 fs laser pulses to reveal the energy requirements for the production of the high charge states of both metal and nonmetal ions. The ionization and fragmentation of group V transition metal oxide clusters are here examined with laser intensities ranging nearly four orders in magnitude (~3 10 ~(11) Wcm ~2 to ~2 10 ~(15) Wcm ~2) at 624 nm. The ionization potentials of the metal atoms are measured using both multiphoton ionization and tunneling ionization models. We demonstrate that the intensity selective scanning method can be utilized to measure the low ionization potentials of transition metals (~7 eV). The high charge states demonstrate an enhancement in ionization that is three orders of magnitude lower in laser intensity than predicted for the atomic counterparts. Finally, the response from the various metals and the oxygen is compared to elucidate the mechanism of enhanced ionization that is observed. Specifically, the sequence of ion appearances demonstrates delocalized electron behavior over the entire cluster.
机译:非均质组成的簇暴露于强度为100 fs的激光脉冲下,揭示出产生金属和非金属离子的高电荷态所需的能量。 V族过渡金属氧化物簇的电离和破碎在624 nm处用接近四个数量级(〜3 10〜(11)Wcm〜2至〜2 10〜(15)Wcm〜2)的激光强度进行检查。使用多光子电离和隧穿电离模型都可以测量金属原子的电离电势。我们证明了强度选择性扫描方法可用于测量过渡金属的低电离势(〜7 eV)。高电荷态显示出电离的增强,其激光强度比原子对应物的预测低三个数量级。最后,比较各种金属和氧气的响应,以阐明观察到的增强电离的机理。具体来说,离子出现的顺序表明了整个簇上电子的离域行为。

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