Zhaoyang Wang, Ziyu Zhan, Anton N. Vetlugin, Jun-Yu Ou, Qiang Liu, Yijie Shen, Xing Fu
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引用次数: 0
Abstract
Quantum optics has advanced our understanding of the nature of light and enabled applications far beyond what is possible with classical light. The unique capabilities of quantum light have inspired the migration of some conceptual ideas to the realm of classical optics, focusing on replicating and exploiting non-trivial quantum states of discrete-variable systems. Here, we further develop this paradigm by building the analogy of quantum squeezed states using classical structured light. We have found that the mechanism of squeezing, responsible for beating the standard quantum limit in quantum optics, allows for overcoming the “standard spatial limit” in classical optics: the light beam can be “squeezed” along one of the transverse directions in real space (at the expense of its enlargement along the orthogonal direction), where its width becomes smaller than that of the corresponding fundamental Gaussian mode. We show that classical squeezing enables nearly sub-diffraction and superoscillatory light focusing, which is also accompanied by the nanoscale phase gradient of the size in the order of λ/100 (λ/1000), demonstrated in the experiment (simulations). Crucially, the squeezing mechanism allows for continuous tuning of both features by varying the squeezing parameter, thus providing distinctive flexibility for optical microscopy and metrology beyond the diffraction limit and suggesting further exploration of classical analogies of quantum effects.
期刊介绍:
ACS Medicinal Chemistry Letters is interested in receiving manuscripts that discuss various aspects of medicinal chemistry. The journal will publish studies that pertain to a broad range of subject matter, including compound design and optimization, biological evaluation, drug delivery, imaging agents, and pharmacology of both small and large bioactive molecules. Specific areas include but are not limited to:
Identification, synthesis, and optimization of lead biologically active molecules and drugs (small molecules and biologics)
Biological characterization of new molecular entities in the context of drug discovery
Computational, cheminformatics, and structural studies for the identification or SAR analysis of bioactive molecules, ligands and their targets, etc.
Novel and improved methodologies, including radiation biochemistry, with broad application to medicinal chemistry
Discovery technologies for biologically active molecules from both synthetic and natural (plant and other) sources
Pharmacokinetic/pharmacodynamic studies that address mechanisms underlying drug disposition and response
Pharmacogenetic and pharmacogenomic studies used to enhance drug design and the translation of medicinal chemistry into the clinic
Mechanistic drug metabolism and regulation of metabolic enzyme gene expression
Chemistry patents relevant to the medicinal chemistry field.