单镜面附近激发态极化原子的自发辐射简

利用格林函数和费米黄金定律,我们计算了单镜面附近的激发态极化原子的自发辐射率.结果表明:原子的自发辐射与原子的极化偶极距取向有关,并且随着原子与镜面间距的增大,辐射率呈现正弦形式的振荡.当偶极距取向与镜面方向平行时,自发辐射的正弦式振荡最为激烈.但是随着极化方向与镜面方向夹角的增大,自发辐射的振荡越来越弱.当偶极距取向与镜面垂直时,振荡几乎消失.利用光子的闭合轨道理论,我们可以发现激发态原子偶极距取向影响辐射光子数的多少,从而可以改变原子的自发辐射率.     

原子在两个平行镜面间两层电介质板中的自发辐射率

利用光子的闭合轨道理论,我们研究了原子在两个平行镜面间两层电介质板（折射率分别为n1,n2）中的自发辐射率. 自发辐射率呈现出多周期的振荡结构。自发辐射率的傅立叶变换中的每一个峰和光子从原子出发到返回原子的一条闭合轨道相对应。结果表明自发辐射率和两层电介质的宽度和折射率有关。和只有一层电介质的辐射率比较,当两层电介质的折射率n1 和 n2 差别很小时, 两层电介质之间分界面的反射效应可以忽略;但是当二者的差别很大时,发射效应变得非常重要且自发辐射率中的振荡减弱。本文的结果为原子在不同电介质间的自发辐射率的研究提供了新的理解。     

原子与热库相互作用系统中的三体纠缠特性

利用Ket-Bra纠缠态方法,求解了原子与热库相互作用系统中的密度矩阵主方程,得到了密度矩阵的演化表达式.考虑三个二能级原子独立与热库相互作用的情况,利用负本征值度量三体纠缠,研究了系统中原子间的三体纠缠特性.采用数值计算方法,讨论了热库平均光子数和原子自发辐射率对原子间三体纠缠特性的影响.研究结果表明:随原子自发辐射率和热库平均光子数的增大,原子间的三体纠缠衰减加快.     

介质腔中自发辐射原子的寿命分布

在本文中,我们研究了半无限大介质板夹层对空腔中激发态原子的自发辐射率的影响,并利用寿命分布函数来描述原子衰变动力学的性质,在对称和非对称的结构中,分别计算了以原子在板中的相对位置为自变量的原子自发辐射率的函数,计算结果表明,原子的自发辐射率与介质腔的宽度以及外层半无限大介质板的折射率有关,介质腔可以增强或抑制激发态原子的激发,当介质腔的宽度足够大时,原子的寿命分布呈现指数衰减的形势,这些理论结果和实验值相符合的非常好.     

光子闭合轨道理论对单镜面附近原子自发辐射率的解释

利用腔量子电动力学计算了原子在全反射镜面附近的自发辐射率。结果表明,所得的震荡谱和原子到镜面的距离有关。通过傅立叶变换,得到与这些振荡谱相对应的频率谱。为了解释这种现象,我们首次将闭合轨道理论用于研究辐射原子在单镜面附近的自发辐射率,给出了对原子自发辐射现象新的理论解释。     

原子相干性对 V型三能级原子自发辐射的影响

本文分别就两种模型,即三能级原子与单模场和双模场的V型相互作用,研究了原子相干性对原子自发辐射的影响.发现在单模情况,原子相干性导致原子自发辐射的消除;而在双模情况,两个跃迁通道的自发辐射是相互独立的,原子相干性不导致原子自发辐射的消除.     

有限厚度拓扑绝缘体平板附近原子的自发辐射特性

对有限厚度拓扑绝缘体(TI)平板附近及其腔内二能级原子的自发辐射特性进行了研究。利用并矢格林函数表示偶极子平行和垂直于材料边界时的自发辐射率表达式,通过多次反射理论计算了平板的反射矩阵,对影响自发辐射率的各种因素进行了数值计算与分析。研究结果表明,忽略耗散时,平行偶极子的自发辐射率被抑制,而垂直偶极子的被增强;当板或腔存在耗散时,TI可以有效抑制原子的自发辐射率,使其附近原子在任何偶极方向的衰减均受到抑制。     

单镜面附近激发态极化原子的自发辐射

利用格林函数和费米黄金定律,我们计算了单镜面附近的激发态极化原子的自发辐射率。结果表明：原子的自发辐射与原子的极化偶极距取向有关,并且随着原子与镜面间距的增大,辐射率呈现正弦形式的振荡。当偶极距取向与镜面方向平行时,自发辐射的正弦式振荡最为激烈。但是随着极化方向与镜面方向夹角的增大,自发辐射的振荡越来越弱。当偶极距取向与镜面垂直时,振荡几乎消失。利用光子的闭合轨道理论,我们可以发现激发态原子偶极距取向影响辐射光子数的多少,从而可以改变原子的自发辐射率。     

基于频域有限差分法的二维自发辐射特性研究

原子自发辐射效率的提高对单光子源等光电子设备的研究和制造具有重要的意义.本文推导了自发辐射率和局域态密度的格林函数表示形式,通过频域有限差分法求解格林函数,得到自发辐射率的数值特性.分析了在不同金属材料、结构以及辐射波长下的自发辐射率,探讨了其内在的物理机理,结果表明:特定波长下介质的表面等离激元效应会增强自发辐射,不同材料和结构对辐射效率的提高有不同的影响.该研究结果可为新型纳米器件及光电子设备的制造以及优化提供重要的参考.     

激光场缀饰的原子的自发辐射特性——谱的瞬时行为,Aulter-Townes双重线的选择性激发

本文从理论上研究了共振激光场缀饰的原子自发辐射谱随时间的演化.讨论了系统的初态“制备”及其对原子激发过程和自发辐射过程的影响,比较了全量子理论与半经典理论对激光场与原子共振相互作用的研究,当驱动场处于相干态时,它们之间可以建立等价关系,对自发辐射谱的时间特性及其观测和有关的一些物理概念进行了讨论.     

Formation of three-body entanglement via a vacuum optical cavity induction in Tavis-Cummings model

After briefly introducing Akhtarshenas, concurrence vector and subvector for describing many-body entanglement, we investigate the entanglement formation for a system which contains three bodies, i.e. two identical atoms and a single- model cavity field, in the Tavis-Cummings model by calculating the concurrences. The results show that the coupling strength between two atoms, the decay cavity and the atomic spontaneous emission can change the entanglement of formation according to different modes： these factors destroy periodicity and symmetry of all concurrences, and that the coupling strength of two atoms does not change the peak value of concurrence （C）, but the strength of decay cavity and the atomic spontaneous emission decline in the peak value of concurrence （C） and the latter is more serious than the former under the same strengths. The concurrence vector and subvector are a useful measure of entanglement for a pure state of the many-body system, in that it can give novel pictures about the entanglements for the entire system and between its inner bodies.     

损耗调制CO_2激光脉冲的噪声特性

由于自发辐射噪声的涨落,ＣＯ２激光器的脉冲峰值强度与时间延迟密切相关。理论和实验研究发现,对于典型的Ｂ类ＣＯ２激光器,在损耗调制情况下,当脉冲峰值出现在最低腔损耗ｔ０之前时,初始自发辐射噪声越大,相对于阈值点的第一个渡跃时间ｔＦＰ越小,对应的峰值强度越小;当脉冲峰值出现在最低腔损耗ｔ０之后时,初始自发辐射噪声越大,相对于阈值点的第一个渡跃时间ｔＦＰ越小,对应的峰值强度则越大。     

损耗调制CO2激光脉冲的噪声特性

由于自发辐射噪声的涨落,CO2激光器的脉冲峰值强度与时间延迟密切相关。理论和实验研究发现,对于典型的B类CO2激光器．在损耗调制情况下,当脉冲峰值出现在最低腔损耗to之前时,初始自发辐射噪声越大,相对于阈值点的第一个渡跃时间tFP越小,对应的峰值强度越小;当脉冲峰值出现在最低腔损耗to之后时,初始自发辐射噪声越大,相对于阈值点的第一个渡跃时间tFP越小,对应的峰值强度则越大。     

Coherence-controlled stationary entanglement between two atoms embedded in a bad cavity injected with squeezed vacuum

We investigate the entanglement between two atoms in an overdamped cavity injected with squeezed vacuum when these two atoms are initially prepared in coherent states. It is shown that the stationary entanglement exhibits a strong dependence on the initial state of the two atoms when the spontaneous emission rate of each atom is equal to the collective spontaneous emission rate, corresponding to the case where the two atoms are close together. It is found that the stationary entanglement of two atoms increases with decreasing effective atomic cooperativity parameter. The squeezed vacuum can enhance the entanglement of two atoms when the atoms are initially in coherent states. Valuably, this provides us with a feasible way to manipulate and control the entanglement, by changing the relative phases and the amplitudes of the polarized atoms and by varying the effective atomic cooperativity parameter of the system, even though the cavity is a bad one. When the spontaneous emission rate of each atom is not equal to the collective spontaneous emission rate, the steady-state entanglement of two atoms always maintains the same value, as the amplitudes of the polarized atoms varies. Moreover, the larger the degree of two-photon correlation, the stronger the steady-state entanglement between the atoms.     

Manifestation of the van der Waals surface interaction in the spontaneous emission of atoms into an optical nanofiber

We study the spontaneous emission of atoms near an optical nanofiber and analyze the coupling efficiency of the spontaneous emission into a nanofiber. We also investigate the influence of the van der Waals interaction of atoms with the surface of the optical nanofiber on the spectrum of coupled light. Using, as an example, ⁸⁵Rb atoms we show that the van der Waals interaction may considerably extend the red wing of the spontaneous emission line and, accordingly, produce a well-defined asymmetry of the spontaneous emission spectrum coupled into an optical nanofiber.     

Hydrogen passivation effect on the yellow-green emission band and bound exciton in n - ZnO

Photoluminescence (PL) measurements performed on as-grown, hydrogenated, and annealed n-type ZnO bulk samples investigated the origins of their yellow (2.10 eV) and green (2.43 eV) emission bands. After hydrogenation, the defect-related peak at 2.10 eV was no longer present in the room temperature PL spectrum, the peak intensity at 2.43 eV was unchanged, and the intensity of the emission peak at 3.27 eV increased significantly. These results indicate that yellow band emission is due to oxygen vacancies, as the emission peak at 2.10 eV disappears when hydrogen atoms passivate these vacancies. The emission peak at 2.43 eV originates from complexes between oxygen vacancies and other crystal defects. We discuss the shallow donor impurities arising due to these hydrogen atoms in the ZnO bulk sample.     

Spontaneous emission of two interacting atoms near an interface

The spontaneous emission rate of two interacting excited atoms near a dielectric interface is studied using the photon closed-orbit theory and the dipole image method. The total emission rate of one atom during the emission process is calculated as a function of the distance between the atom and the interface. The results suggest that the spontaneous emission rate depends not only on the atomic-interface distances, but also on the orientation of the two atomic dipoles and the initial distance between the two atoms. The oscillation in the spontaneous emission rate is caused by the interference between the outgoing electromagnetic wave emitted from one atom and other waves arriving at this atom after traveling along various classical orbits. Each peak in the Fourier transformed spontaneous emission rate corresponds with one action of photon classical orbit.     

Amplified spontaneous emission and its application for population of resonant states of the Xe and Kr atoms

To extend the capabilities of the existing spectroscopic methods of investigation and diagnostics of gaseous media, we consider a macroscopic effect of an increase in the rate of spontaneous emission, which results in the transition of a considerable part of excited molecules to lower-lying optically accessible states with light pulse emission along the direction of propagation of the exciting laser radiation. As an application of the effect of amplified spontaneous emission, we propose the population with its help of optically inaccessible electronic states of atoms and molecules.