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Photoionisation processes of oxygen and acetylene in the vacuum ultraviolet region

机译:真空紫外区中氧气和乙炔的光电离过程

摘要

Photoionisation mass measurements on oxygen and acetylene molecules have been made in the wavelength region from 1100 to 400 A by using synchrotron radiation as a light source. Photoionisation spectra in oxygen are obtained for the molecular ion O2+ and for the fragment ion O+, and in acetylene are obtained for the molecular ion C2H2+ and for fragment ions C2H+, C2+, CH2+ and CH+. To assign the spectral structures of C2H2+, ab initio calculations have been performed for excitation from the second (3δg) and third (2δu) outer molecular orbitals. In the molecular ion spectra of these molecules, several broad structures are observed besides sharp structures due to autoionisation from rydberg states. The broad fetures are discussed in support of theoretical calculations. New Rydberg series (npπu←3δg) converging to the second ionisation threshold were found in the spectra of the molecular ion C2H2+. In the fragment ion spectra, appearance potentials of frabment ions are obtained from onsets of the spectra. Various decay channels after photoionisation are also decided in terms of the onsets.
机译:通过使用同步加速器辐射作为光源,已经在1100至400 A的波长范围内对氧和乙炔分子进行了光电离质量测量。在氧气中获得了分子离子O2 +和碎片离子O +的光电离光谱,在乙炔中获得了分子离子C2H2 +和碎片离子C2H +,C2 +,CH2 +和CH +的光电离光谱。若要分配C2H2 +的光谱结构,从头开始计算了从第二(3μg)和第三(2μu)外分子轨道的激发。在这些分子的分子离子光谱中,除了由于锐德堡态自电离而产生的尖锐结构外,还观察到了几种宽泛的结构。讨论了广泛的功能以支持理论计算。在分子离子C2H2 +的光谱中发现收敛到第二个电离阈值的新Rydberg系列(npÏuâ†3μg)。在碎片离子光谱中,碎片离子的出现电势是从光谱开始时获得的。光电离后的各种衰变通道也取决于开始时间。

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