通过超冷三体重组形成范德瓦耳斯分子的自旋层次结构

Jing-Lun Li, Paul S. Julienne, Johannes Hecker Denschlag, José P. D'Incao
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引用次数: 0

摘要

我们通过玻色碱原子的超冷三体重组,从理论上研究了弱结合原子范德华分子的产物态分布。我们发现了零磁场下自旋倾向规则的两级层次结构。主要倾向规则指出,几乎所有分子产物都保留反应物原子对的总超细自旋,而不保留总自旋的分子产物则受到高度抑制。对于主要分子产物,存在保留反应物原子对某些自旋成分(如原子超细自旋或总电子自旋或核自旋)的次要倾向。第二倾向因物种而异,主要取决于有效电子交换和超细相互作用之间的相互作用。产物态分布的自旋敏感性有可能为控制超冷三体对撞中的态对态反应速率开辟新的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Spin hierarchy in van der Waals molecule formation via ultracold three-body recombination
We theoretically investigate the product-state distribution of weakly bound diatomic van der Waals molecules via ultracold three-body recombination of bosonic alkali atoms. We find a two-level hierarchy of spin propensity rules at zero magnetic field. The primary propensity rule states that nearly all molecular products conserve the total hyperfine spin of reactant atomic pairs, while molecular products not conserving the total spin are highly suppressed. For the dominant molecular products, there is a secondary propensity to conserve certain spin components of the reactant pair such as the atomic hyperfine spins, or the total electronic or nuclear spins. The second propensity varies across species and depends fundamentally on the interplay between effective electronic exchange and hyperfine interactions. The spin sensitivity of product-state distribution can potentially open up new avenues for controlling state-to-state reaction rates in ultracold three-body recombination.
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