Multiple ionisation and fragmentation of molecules

B. Siegmann, U. Werner, H. Lutz
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引用次数: 8

Abstract

The multiple ionisation and dissociation of molecules, e.g. H2, N2, H2O, CH4 and C60, by fast ions was studied using a position- and time-sensitive multi-particle detector. The data obtained allow a clear separation of various reaction channels. Of special interest are the ‘Coulomb explosion’ processes like N2 → Nq+ +Nn+ or H2O → H+ + H+ +On+. For these reactions the coincident measurement of the momenta of correlated fragment ion yields a kinematically complete image of the molecular break-up process, and the fragmentation energy as well as angular correlations can be derived for each individual event. In the case of H2 as target molecule the CE model describes the fragmentation energy rather well, whereas in the case of more complex molecules, e.g. N2, CO and CH4, the simple CE model is insufficient to explain the measured energy and angular spectra. Better agreement was achieved with ab initio MCSCF calculations which take into account several molecular states of the fragmenting highly charged molecular ion.
分子的多次电离和分裂
利用位置和时间敏感的多粒子探测器研究了快速离子对H2、N2、H2O、CH4和C60等分子的多重电离和解离。所获得的数据可以清楚地区分各种反应通道。特别有趣的是“库仑爆炸”过程,如N2→Nq+ +Nn+或H2O→H+ + H+ +On+。对于这些反应,相关碎片离子动量的同步测量产生分子破裂过程的运动学完整图像,并且可以推导出每个单独事件的碎片能量和角相关性。以H2为目标分子时,CE模型较好地描述了裂解能,而对于更复杂的分子,如N2、CO和CH4,简单的CE模型不足以解释测量的能量和角谱。从头算MCSCF计算得到了更好的一致性,该计算考虑了破碎的高电荷分子离子的几种分子状态。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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