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首页> 外文期刊>Physical Review, A. Atomic, molecular, and optical physics >Nonlinear optical spectroscopy of single, few, and many molecules: Nonequilibrium Green's function QED approach
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Nonlinear optical spectroscopy of single, few, and many molecules: Nonequilibrium Green's function QED approach

机译:单分子,少分子和多分子的非线性光学光谱:非平衡格林函数QED方法

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摘要

Nonlinear optical signals from an assembly of N noninteracting particles consist of an incoherent and a coherent component, whose magnitudes scale similar to N and similar to N(N-1), respectively. A unified microscopic description of both types of signals is developed using a quantum electrodynamical (QED) treatment of the optical fields. Closed nonequilibrium Green's function expressions are derived that incorporate both stimulated and spontaneous processes. General (n+1)-wave mixing experiments are discussed as an example of spontaneously generated signals. When performed on a single particle, such signals cannot be expressed in terms of the nth order polarization, as predicted by the semiclassical theory. Stimulated processes are shown to be purely incoherent in nature. Within the QED framework, heterodyne-detected wave mixing signals are simply viewed as incoherent stimulated emission, whereas homodyne signals are generated by coherent spontaneous emission.
机译:来自N个非相互作用粒子集合的非线性光学信号由非相干分量和相干分量组成,其大小分别类似于N和N(N-1)。使用光场的量子电动力学(QED)处理,可以开发出两种信号的统一微观描述。闭合非平衡格林函数表达式导出了受激过程和自发过程。讨论一般(n + 1)波混合实验作为自发生成信号的示例。当在单个粒子上执行时,如半经典理论所预测的,此类信号无法用n阶极化表示。事实证明,受刺激的过程纯粹是不连贯的。在QED框架内,将外差检测到的混波信号简单地视为非相干受激发射,而零差信号则由相干自发产生。

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