首页> 外文期刊>The Journal of Chemical Physics >Adiabatic and vertical ionization energies of 1,4-diazabicyclo[2,2,2]-octar measured by zero electron kinetic energy spectroscopy and Rydberg extrapolation
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Adiabatic and vertical ionization energies of 1,4-diazabicyclo[2,2,2]-octar measured by zero electron kinetic energy spectroscopy and Rydberg extrapolation

机译:零电子动能谱和里德伯格外推法测量的1,4-二氮杂双环[2,2,2]-八重体的绝热和垂直电离能

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We have used a combination of high-n Rydberg spectroscopy and zero electron kinetic energy (ZEKE) spectroscopy to measure the adiabatic and vertical ionization energies of 1 ,4-diazabicyclo[2,2,2]-octane to high precision. A comparison of the two methods revealed that where extended and unperturbed Rydberg series can be observed, the precision with which the ionization energy of a molecule can be measured is up to six times better via Rydberg extrapolation than with high resolution ZEKE spectroscopy. The difference in precision derives, not from any inherent shortcoming in the resolution achievable with ZEKE spectroscopy, but from errors that arise in evaluating the field ionization redshift. Accurate vertical ionization energies of 59 049.0 ± 0.1 and 58 889.9 ± 0.1 cm’ were obtained for ionization to the 24~’ and 25±1 vibrational levels in the ion. A value for the adiabatic ionization energy of 58033.3 ± 0.3 cm1 has been measured by ZEKE spectroscopy for the first time. The precision with which we have been able to account for the field ionization redshift has been improved by calibrating the ZEKE spectrum against the v25 Rydberg spectrum. The ZEKE spectra presented here were recorded using a double inverted pulse sequence with field strengths as low as 140 mV cm’. The result was exceptionally well-resolved spectra revealing the rotational contour of each ZEKE band. For the 24±1 and 25+1 bands the spectra revealed a strong central Q branch, with weaker P and R branches, consistent with a propensity for angular momentum transfer to the Rydberg electron rather than within the core. In contrast to what is commonly observed in ZEKE spectroscopy, where rotational autoionization often results in branches associated with negative AJ appearing with enhanced intensity, the R branch appears with significantly enhanced intensity compared to the very weak P branch. ? 2000 American Institute of Physics.
机译:我们已使用高n里德伯格光谱和零电子动能(ZEKE)光谱的组合来高精度测量1,4-二氮杂双环[2,2,2]辛烷的绝热和垂直电离能。两种方法的比较表明,在可以观察到扩展的和不受干扰的Rydberg级数的情况下,通过Rydberg外推法可以测量分子电离能的精度比高分辨率ZEKE光谱法高六倍。精度的差异并非源于ZEKE光谱仪在分辨率上的任何固有缺陷,而是源于评估场电离红移所产生的误差。对于离子中的24〜'和25±1的振动水平,获得了准确的垂直电离能59 049.0±0.1和58 889.9±0.1 cm'。绝热电离能的值首次通过ZEKE光谱仪测量为58033.3±0.3 cm1。通过相对于v25 Rydberg光谱校准ZEKE光谱,可以提高解决电场电离红移的精度。此处显示的ZEKE光谱是使用双反向脉冲序列记录的,场强低至140 mV cm'。结果是非常清晰的光谱,揭示了每个ZEKE波段的旋转轮廓。对于24±1和25 + 1谱带,光谱显示出强的中心Q分支,较弱的P和R分支,这与将角动量转移到Rydberg电子而不是在核内的倾向一致。与在ZEKE光谱中通常观察到的相反,在旋转光谱中,旋转自电离通常会导致与负AJ相关的分支出现强度增强,而与非常弱的P分支相比,R分支强度明显增强。 ? 2000美国物理研究所。

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