Rydberg Molecules Bound by Strong Light Fields

Simon Hollerith, Valentin Walther, Kritsana Srakaew, David Wei, Daniel Adler, Suchita Agrawal, Pascal Weckesser, Immanuel Bloch, Johannes Zeiher
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Abstract

The coupling of an isolated quantum state to a continuum is typically associated with decoherence and decreased lifetime. For coupling rates larger than the bandwidth of the associated continuum, decoherence can be mitigated, and new stable eigenstates emerge. Here, we laser-couple diatomic molecules of highly excited Rydberg atoms, so-called Rydberg macrodimers, to a continuum of free motional states. Enabled by their small vibrational eigenfrequencies, we achieve the regime of strong continuum couplings and observe the appearance of new resonances. We explain the observed spectroscopic features as molecular states emerging in the presence of the light field using a Fano model. For atoms arranged on a lattice, we predict the strong continuum coupling to even stabilize triatomic molecules and find the first signatures of these by observing three-atom loss correlations using quantum gas microscopy. Our results present a mechanism to control decoherence and bind polyatomic molecules using strong light-matter interactions.

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被强光场束缚的里德伯分子
孤立量子态与连续体的耦合通常与退相干和寿命缩短有关。当耦合率大于相关连续体的带宽时,退相干现象会得到缓解,并出现新的稳定特征态。在这里,我们用激光将高度激发的雷德贝格原子的硅原子分子(即所谓的雷德贝格大分子)耦合到自由运动态的连续体中。在它们的小振动特征频率的帮助下,我们实现了强连续态耦合,并观察到新共振的出现。我们利用法诺模型将观测到的光谱特征解释为在光场存在下出现的分子状态。对于排列在晶格上的原子,我们预测强连续相耦合甚至能稳定三原子分子,并通过量子气体显微镜观测三原子损耗相关性,首次发现了这些分子的特征。我们的研究结果提出了一种利用强光-物质相互作用控制退相干和结合多原子分子的机制。
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