Retardation effects in spectroscopic measurements of the Casimir-Polder interaction

J. C. Carvalho, P. Pedri, M. Ducloy, A. Laliotis
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引用次数: 6

Abstract

Spectroscopy is a unique experimental tool for measuring the fundamental Casimir-Polder interaction between excited state atoms, or other polarizable quantum objects, and a macroscopic surface. Spectroscopic measurements probe atoms at nanometric distances away from the surface where QED retardation is usually negligible and the atom-surface interaction is proportional to the inverse cube of the separation distance, otherwise known as the van der Waals regime. Here we focus on selective reflection, one of the main spectroscopic probes of Casimir-Polder interactions. We calculate for the first time selective reflection spectra using the full, distance dependent, Casimir-Polder energy shift and linewidth. We demonstrate that retardation can have significant effects, in particular for experiments with low-lying energy states. We also show that the effective probing depth of selective reflection spectroscopy depends on the transition linewidth. Our analysis allows us to calculate selective reflection spectra with composite surfaces, such as metasurfaces, dielectric stacks, or even bi-dimensional materials.
卡西米尔-波德相互作用光谱测量中的延迟效应
光谱学是一种独特的实验工具,用于测量激发态原子或其他可极化量子物体与宏观表面之间的基本卡西米尔-波德相互作用。光谱测量探测距离表面纳米距离的原子,在那里QED延迟通常可以忽略不计,原子-表面相互作用与分离距离的反立方成正比,否则称为范德华制度。这里我们关注的是选择性反射,这是卡西米尔-波德相互作用的主要光谱探针之一。我们首次使用全距离依赖、卡西米尔-波德能量位移和线宽计算了选择性反射光谱。我们证明了延迟可以有显著的影响,特别是在低能态的实验中。我们还表明,选择反射光谱的有效探测深度取决于过渡线宽度。我们的分析使我们能够计算复合表面的选择性反射光谱,如超表面,介电堆,甚至二维材料。
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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