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Angular and energy distribution of fragment ions in dissociative double photoionization of acetylene molecules at 39 eV

机译:在39 eV下乙炔分子的解离双光电离中碎片离子的角度和能量分布

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摘要

The two-body dissociation reactions of the dication, C _2H22+, produced by 39.0 eV double photoionization of acetylene molecules, have been studied by coupling photoelectron-photoion-photoion coincidence and ion imaging techniques. The results provide the kinetic energy and angular distributions of product ions. The analysis of the results indicates that the dissociation leading to C _2H ~2H ~2 products occurs through a metastable dication with a lifetime of 108 ± 22 ns, and a kinetic energy release (KER) distribution exhibiting a maximum at ~4.3 eV with a full width at half maximum (FWHM) of about 60. The reaction leading to CH 2++C+ occurs in a time shorter than the typical rotational period of the acetylene molecules (of the order of 10 -12 s). The KER distribution of product ions for this reaction, exhibits a maximum at ~4.5 eV with a FWHM of about 28. The symmetric dissociation, leading to CH ~2 CH ~2, exhibits a KER distribution with a maximum at ~5.2 eV with a FWHM of 44. For the first two reactions the angular distributions of ion products also indicate that the double photoionization of acetylene occurs when the neutral molecule is mainly oriented perpendicularly to the light polarization vector.
机译:通过耦合光电子-光子-光子重合和离子成像技术,研究了由39.0 eV乙炔分子的双光子化产生的双金属离子C _2H22 +的两体解离反应。结果提供了产物离子的动能和角分布。结果分析表明,通过亚稳的指示,发生C _2H〜2H〜2产物的离解,其寿命为108±22 ns,动能释放(KER)分布在〜4.3 eV时最大,而半峰全宽(FWHM)约为60。导致CH 2 ++ C +的反应发生的时间比乙炔分子的典型旋转周期(约10 -12 s)短。对于该反应,产物离子的KER分布在〜4.5 eV处最大,FWHM约为28。对称解离导致CH〜2 CH〜2,在〜5.2 eV处具有最大KER分布。 FWHM为44。对于前两个反应,离子产物的角度分布还表明,当中性分子主要垂直于光偏振矢量取向时,乙炔会发生双光电离。

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