Experimental determination of the spin-rotation coupling in Na-Xe molecules

M. Hou, B. Feng, Jian Zhang, Y. She, Zhong-Lu Mi, TienJie Chen
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Abstract

A theory for calculating the spin–rotation coupling coefficient in alkali-metal–noble-gas van der Waals molecules was recently presented.1 It assumes the spin–rotation interaction in alkali-metal–noble-gas molecules to be mainly due to the spin–orbit interaction of the alkali-metal valence electron within the core of the noble gas, and predicts that the spin–rotation constant γ should depend on the spin–orbit interaction in the noble gas and be almost independent of the spin–orbit interaction of the alkali-metal atom. Experimentally, only a few of the possible pairs of the different alkali-metal atoms with different noble-gas atoms have been investigated. By measuring the sodium spin relaxation rate as a function of the helium buffer-gas pressure and the width of the sodium magnetic slowing-down curve, we report in this paper our experimentally determined value of the spin–rotation interaction constant in Na–Xe molecules γ = (1.1 ± 0.3)MHz. The measured value is nearly the same as was measured in K–Xe, Rb–Xe, and Cs–Xe.1 This result shows a reasonable agreement with the theoretical prediction.
Na-Xe分子中自旋-旋耦合的实验测定
最近提出了一种计算碱金属-稀有气体-范德华分子自旋-旋耦合系数的理论假设碱金属-稀有气体分子中的自旋-旋转相互作用主要是由于稀有气体核心内碱金属价电子的自旋-轨道相互作用,并预测自旋-旋转常数γ应取决于稀有气体中的自旋-轨道相互作用,而几乎与碱金属原子的自旋-轨道相互作用无关。在实验上,只研究了几种不同碱金属原子与不同稀有气体原子可能形成的对。通过测量钠自旋弛豫速率与氦缓冲气体压力和钠磁慢化曲线宽度的关系,我们实验确定了Na-Xe分子的自旋-旋转相互作用常数γ =(1.1±0.3)MHz。测量值与K-Xe、Rb-Xe、cs - xe的测量值基本一致计算结果与理论预测基本一致。
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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