Stark quantum-beat spectroscopy: The electric dipole moment of NO (A2Σ+)

J. Gray, R. Farrow, J. L. Durant, L. Thorne
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引用次数: 0

Abstract

The γ-system (A2Σ+ X2Π) of nitric oxide (NO) is observed in many environments including combustion and atmospheric applications. Molecular properties of the A2Σ+ state are thus important in collision theories used to predict A-X radiative efficiencies. These theories often involve electric-multipole expansions,1,2 in which the permanent electric dipole moment of A2Σ+ (µA) is the leading term for long-range interactions. Moreover, µA is a basic property of the molecular charge distribution and has often been used to gauge the accuracy of ab initio quantum chemistry calculations.3-6 Here we describe measurements of Stark quantum beats in the fluorescence of NO from which we derive a precise value for µA in v'=0. This is the vibrational level most often excited in laser-based methods for detecting NO. Bergeman and Zare,7 using a radio frequency-optical double-resonance technique, provide the only other measurement of µA in a different vibrational level (v'=3). We thus also determine the change in µA with v', which provides a sensitive test of computed dipole moment functions.
Stark量子光谱:NO的电偶极矩(A2Σ+)
一氧化氮(NO)的γ-系统(A2Σ+ X2Π)在许多环境中被观察到,包括燃烧和大气应用。因此,A2Σ+态的分子性质在用于预测A-X辐射效率的碰撞理论中是重要的。这些理论通常涉及电-多极展开1,2,其中永久电偶极矩A2Σ+(µA)是远程相互作用的主要术语。此外,µA是分子电荷分布的基本性质,经常被用来衡量从头算量子化学计算的准确性。3-6在这里,我们描述了NO荧光中的Stark量子拍的测量结果,从中我们得出了v'=0时µa的精确值。这是在基于激光的检测NO的方法中最常激发的振动能级。Bergeman和Zare 7使用射频-光学双共振技术,提供了在不同振动水平(v'=3)下测量µa的唯一方法。因此,我们还确定了µA随v'的变化,这为计算偶极矩函数提供了灵敏的测试。
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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