Erica Sutcliffe, Nathanael P. Kazmierczak, Ryan G. Hadt
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引用次数: 0
摘要
顺磁分子的可调谐性和空间精度使其对量子传感具有吸引力。然而,基于微波的常规探测方法的时间和空间分辨率较低,而与室温解决方案兼容的光学方法仍然难以实现。在这里,我们利用泵浦探针偏振光谱学来初始化和跟踪分子中的电子自旋相干性。K 2 IrCl 6 水溶液设计用于将自旋与光有效耦合,可在室温和微摩尔浓度下检测几皮秒的自由感应衰减。研究发现,粘度会强烈改变退相干寿命。这种方法将实验时间分辨率提高了 5 个数量级,从而有可能观察到分子电子自旋相干性,而传统技术只能在 25 K 以下显示相干性。
Ultrafast all-optical coherence of molecular electron spins in room-temperature water solution
The tunability and spatial precision of paramagnetic molecules makes them attractive for quantum sensing. However, usual microwave-based detection methods have poor temporal and spatial resolution, and optical methods compatible with room-temperature solutions have remained elusive. In this study, we utilized pump-probe polarization spectroscopy to initialize and track electron spin coherence in a molecule. Designed to efficiently couple spins to light, aqueous potassium hexachloroiridate(IV) enabled detection of few-picosecond free-induction decay at room temperature and micromolar concentrations. Viscosity was found to strongly vary decoherence lifetimes. This approach has improved the experimental time resolution by up to five orders of magnitude, making it possible to observe molecular electron spin coherence in a system that only exhibits coherence below 25 kelvin with traditional techniques.
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