Self-organized arrays of submicrometer particle of organic dye and its near-field optical study

Organic dye particles of micrometer and submicrometer diameters were prepared by a wetting/dewetting procedure on a hydrophilic glass surface and a self-organized one- or two-dimensional registration was observed. To analyze the molecular assembly in these particles the near-field-excited near-field fluorescence from single particles were detected, while the majority of particles with diameters around 2 μm or less did not show fluorescence. Far-field fluorescence, in contrast, was observed for every particle, and the intensity depended on the excitation polarization when a polarized evanescent field was used for excitation, indicating that the molecules’ transition moment within dye particles orient parallel to the substrate surface. These two observations suggest that the near-field at the tip of the probe was polarized parallel to the probe axis. Another observation, that neighboring particles show similar molecular orientations, suggests that the dewetting process contributed to the alignment of the molecular directions in adjacent particles, which further proves that the dye particles were formed by a self-organizing mechanism.     

Magneto-optic Fluorescence Behavior of Anthracene and Its Derivatives in a Diluted Magnetic Fluid Solution.

Variations in the fluorescence in the intensities of anthracene derivatives under a magnetic field were investigated in the presence of a dilute magnetic fluid. When excitation was carried out with light that was polarized parallel to the magnetic field, the intensity of the fluorescence that was polarized paralell to the magnetic field decreased by about 10%. Although the fluorescence intensities of most of the anthracene derivatives showed a similar decrease in magnitude, that of 9,10-dimethylanthracene showed a large decrease. On the other hand, fluorescence increased when excitation and fluorescence were perpendicular to the magnetic field. The obtained phenomena can be explaned by the formation of anisotropic assembly of magnetic fluid particles in the solution.     

近场显微干涉成像中的探测角度和偏振问题研究

用偶极子耦合系统来模拟近场干涉测量中的探针样品关系,并利用各电场分量之间的组合方程组精确计算出其可能探测到的强度和相位像。结果显示,近场干涉所测量到的近场像的分辨力和探测器的方位及参考光的偏振方向之间有较强的依赖关系,随着探测器位置不同或者参考光偏振方向的变化,同一样品在同一照明条件下所得到的图像也会发生明显的改变。在倏逝波照明的情况下,近场像的精确度随着探测器相对于样品视角的增大而改善,且在不同偏振方向的近场像中,只有偏振方向垂直于样品表面的像能真实反映样品的细节分布,且同时具有足够的强度分布。     

Polarisationseffekte des Fluoreszenzlichtes von Anthrazenkristallen und Plastikszintillator in Abhängigkeit von Deuteronenenergie und Temperatur

Investigations of the optical isotropic plastic scintillator showed that the fluorescence light is more polarized perpendicular than parallel to the particle impact direction. Furtheron the fluorescence light polarization of anthracene crystals proved to be dependent on particle impact direction. Both the degree of fluorescence light polarization of plastic scintillator and the dependence of fluorescence light polarization of anthracene crystals could be explained by the mechanism of energy travelling from direct excited to light emitting molecules.     

扫描近场光学显微镜的光耦合偶极子模型

为了研究扫描近场光学显微镜中探针和粗糙样品表面的耦合相互作用,提出了一种光耦合偶极子模型.在该模型中,探针和样品突起都由光极化偶极子表示,在准静态电磁场近似的情况下样品表面的诱导极化效应由影像偶极子表示,应用偶极子辐射理论可以得到系统的自洽场方程.此模型提供了一种直观分析扫描近场光学显微镜中探针和样品相互作用机理的方法.在此基础上,进一步讨论了金属样品的近场成像特点和其特有的局域光学共振现象.数值结果表明：不同于一般的介质样品,金属样品的近场图像与入射光频率直接相关,改变入射光的频率,获得的样品近场图像的形状和对比度都会发生变化.特别是当入射光频率处于样品极化共振范围内时,金属纳米粒子的极化率会出现光极化共振,这样就可以获得样品粒子的最大有效尺寸,为提高系统的分辨率提供了一条重要途径.     

Controlled rotation and orientation of rubrene particles and Escherichia coli using optical tweezers

Optical trapping and rotating of suspended micro-sized rubrene particles were performed using optical tweezers with circularly polarized light. The experimental results show that the rotation speed of the rubrene particles is proportional to the laser power, and the orientation of the rubrene particles can be controlled by the optical tweezers with linearly polarized light. Interestingly, by combining with the rubrene particle, the Escherichia coli (E. coli) can be rotated and oriented by optical tweezers. However, the rotating and orientating are mainly determined by the characteristics of rubrene particles. Our experiment provides a simple and convenient way to orient biological particles even if they are not sensitive to the polarization of the laser beam. Moreover, the rubrene can emit strong fluorescence when excited by the laser at the wavelength of 532 nm, and which can be potential applied to manipulate other particles with the fluorescence characteristics.     

The Influence of Defects on the Propagation Light within Polymeric Optical Waveguides Studied by Polarized Near-Field Scanning Optical Microscopy

We have developed a polarization-preserving near-field scanning optical microscopy (NSOM) optical fiber probe and with it observed the influence of defects and weak stresses on a propagation light within polymeric optical waveguides. To characterize the influence, we intentionally printed an indentation in the vicinity of the waveguide and then evaluated the resulting influence using polarized guide-collection-mode NSOM images taken around the indentation. When transverse magnetic polarized light enters a waveguide, the light intensity becomes greater on the near side of the indentation than on the far side, as measured by a linearly polarized component perpendicular to the direction of light propagation. The most probable cause of this phenomenon is microdefects generated by the printing of the indentation. The polarized NSOM technique is useful in searching for small defects or stresses within integrated photonic devices.     

Application of Fluorescence with Polarized Light to Evaluate the Orientation of Dyes Adsorbed in Layered Materials

A new method of fluorescence polarization is applied to evaluate the angle of the preferential orientation of Rhodamine 6G (R6G) dye adsorbed in supported thin films of Laponite (Lap) clay. The method is based in the determination of the fluorescence dichroic ratio, obtained from the recorded fluorescence spectra with the detection polarizer horizontally and vertically oriented, as a function of the twisted angle of the film around its vertical axis, keeping the excitation polarizer in a fixed direction. The validity of the method is checked by comparing the experimental results obtained with both vertically and horizontally polarized excitations to that previously provided by absorption spectroscopy with linearly polarized light. A preferential orientation angle with respect to the normal to the clay layer of 62° is derived for R6G monomers adsorbed in Lap films.     

Influence of interaction of chromophores, linked by the unconjugated chain, on the luminescence properties of biscyanine dyes

Deactivation of electronically excited state of chemically bound dimers – biscyanines with two chromophores linked by unconjugated chains and corresponding monomer dye was investigated. It was found that the quantum yield of dimer fluorescence is lower than that of a monomer dye. The amount of quantum yield of fluorescence decreases with the increase of chromophores interaction degree (the decrease of the isolating polymethylene bridge length). It is shown on the basis of the external heavy-atom effect studies that the decrease of biscyanines fluorescence ability is connected with the enhancment of singlet–triplet intersystem crossing (S₁T₁). It has been established that the probability of the triplet states population in biscyanines with chromophores in parallel arrangement is considerably higher than that in similar compounds with an angular arrangement of chromophores. The delayed fluorescence was observed in the case of dyes with parallel arrangment of chromophores.     

Spatial photoselection of single molecules on the surface of spherical microcavities

We show that ultrasensitive microdroplet-stream fluorescence techniques combined with surfactant forms of Rhodamine dyes can be used to probe single molecules on the surfaces of spherical microcavities. Individual octadecyl Rhodamine B molecules, shown previously by ensemble measurements to be localized and oriented at the surfaces of liquid microspheres, were spatially photoselected primarily along great circles lying perpendicular or parallel to the detection axis by use of polarized laser excitation. A polarization dependence is observed in the distribution of single-molecule fluorescence amplitudes that can be interpreted qualitatively in terms of position-dependent fluorescence-collection efficiencies.     

Controllable and switchable chiral near-fields in symmetric graphene metasurfaces

A strong chiral near-field plays significant roles in the detection, separation and sensing of chiral molecules. In this paper, a simple and symmetric metasurface is proposed to generate strong chiral near-fields with both circularly polarized light and linearly polarized light illuminations in the mid-infrared region. Owing to the near-field interaction between plasmonic resonant modes of two nanosheets excited by circularly polarized light, there is a strong single-handed chiral near-field in the gap between the two graphene nanosheets and the maximum enhancement of the optical chirality could reach two orders of magnitude. As expected, the intensity and the response wavelength of the chiral near-fields could be controlled by the Fermi level and geometrical parameters of the graphene nanosheets, as well as the permittivity of the substrate. Meanwhile, based on the interaction between the incident field and scattered field, the one-handed chiral near-field in the gap also could be generated by the linearly polarized light excitation. For the two cases, the handedness of the chiral near-field could be switched by the polarized direction of the incident light. These results have potential opportunities for applications in molecular detection and sensing.     

Back focal plane imaging of Tamm plasmons and their coupled emission

The unique optical properties of Tamm plasmons (TPs) – such as flexible wavevector matching conditions including inplane wavevector within the light line, and existing both S‐ and P‐polarized TPs − facilitate them for direct optical excitation. The Tamm plasmon‐coupled emission (TPCE) from a combined photonic–plasmonic structure sustaining both surface plasmons (SPs) and TPs is described in this paper. The sensitivity of TPCE to the emission wavelength and polarization is examined with back focal plane imaging and verified with the numerical calculations. The results reveal that the excited probe can couple with both TPs and SPs, resulting in surface plasmon‐coupled emission (SPCE) and TPCE, respectively. The TPCE angle is strongly dependent on the wavelength allowing for spectral resolution using different observation angles. These Tamm structures provide a new tool to control the optical emission from dye molecules and have many potential applications in fluorescence‐based sensing and imaging.     

Method of improving optical poling efficiency in polymer films

The alignment of dye molecules in optically poled polymer films is modeled. We point out that when writing beams (fundamental and second harmonic) are linearly polarized with their polarization directions parallel, the majority of the dye molecules in a poled film are axially oriented perpendicular to the writing-beam polarization, whereas the minority are polar oriented parallel to the writing-beam polarization. Only the latter, however, contribute to the second-order nonlinearity of the film. This model is verified by experiments. Based on the model, a new method of improving optical poling efficiency is put forward.     

Investigation of the Doughnut Effect in Cy3-Labeled Protein Microarrays using Scanning Near-Field Optical Microscope

We demonstrate the fluorescence mapping of protein microarrays by the technique of scanning near-field optical microscopy (SNOM) and confocal microscopy. Micron sized spots (300 μm) of human Immunoglobulin G (hIgG) protein with and without a Cy3 dye labeling have been fabricated on glass substrates by an immobilization method which makes use of calixcrown derivatives termed Prolinker. We have also tried to probe into the well-known “doughnut effect” observed in fluorescence images of proteins using the SNOM technique. The topographic and fluorescence SNOM images revealed that the number of proteins at the boundary of the spot were more than at the center in the case of the microarray spot which showed brighter luminescence at the edge than at the center in the confocal image.     

数值分析在不同偏振时复杂样品的近场强度分布

采用三维时域有限差分法(FDTD),模拟计算了光子扫描隧道显微镜(PSTM)系统中的介质和银质金属样品在不同偏振模式光源下的近场强度分布。使用介质小样品检验探针性能,在探针不同位置计算得到了相似的近场强度分布图,说明编写的程序是可信的。给出了等高扫描时p偏振和s偏振条件下,“PSTM”字样介质样品和银质金属样品上方5nm处的近场强度分布图,结果显示:对介质样品,p偏振波能较好的反映样品的形貌,这是由入射电场的方向决定的;银质金属有表面增强作用,对不同偏振波均能在某种程度上反映样品的形貌,仍有待近一步的研究。     

用偏振荧光光谱表征乙醇-水团簇分子的取向行为

采用波长为236nm紫外光激励乙醇水溶液获得荧光光谱并对其偏振特性进行了研究.实验中分别改变入射光的偏振度，在300—400nm波段内进行荧光光谱、水平和垂直偏振荧光光谱检测.实验结果表明，当采用线偏振光照射乙醇水溶液时，其发射的荧光具有一定的偏振性，并计算了其偏振度.经理论分析得到了描述荧光偏振态的四个斯托克斯矢量，进而对该荧光的偏振状态进行了描述，通过对乙醇-水溶液的米勒矩阵的计算，对溶液中分子的取向特性进行了分析.本结果能对乙醇-水团簇分子的结构提供理论参考. 关键词： 荧光光谱 偏振光谱 斯托克斯矢量 米勒矩阵     

Dependence of femtosecond time-resolved magneto-optical Kerr rotation on the direction of polarization of the probe beam

We demonstrate that the femtosecond time-resolved magneto-optical Kerr rotation oscillates with the direction of polarization of the probe beam when a sample of Al0.25Ga0.75As/GaAs multi-quantum wells is excited by a circularly polarized pump and detected by a linearly polarized probe at wavelengths from 800 to 830 nm. Analytical expressions are derived to explain the mechanism, which is in good agreement with the numerical computation and the experimental data. The results suggest that the Kerr signal can ...     

Modification of single molecule fluorescence by a scanning probe

We examine the optical near-field interaction between different types of scanning tips and single oriented fluorescent molecules. We demonstrate the influence of a tip on the excitation intensity as well as on the integrated fluorescence signal, the excited state lifetime, and the angular emission of single molecules. By using a standard model describing the radiation of an oscillating dipole close to a nanosphere or a flat interface, we interpret our observations and describe some central criteria for obtaining fluorescence enhancement or quenching. PACS 33.80.-b; 07.79.Fc; 78.90.+t     

Enhanced backward-directed multiphoton-excited fluorescence from dielectric microcavities

We demonstrate theoretically and experimentally that one-, two-, and three-photon excited fluorescence from dye molecules in spherical microcavities has an asymmetrical angular distribution and is enhanced in the backward direction. The enhancement ratios (of intensities at 180 degrees and 90 degrees ) are 9, 5, and 1.8 for three-, two-, and one-photon excitation, respectively. Even larger ratios are expected for microspheres with an index of refraction larger than that used in the experiments. Because of the reciprocity principle and concentration of the incident wave inside particles, the backward enhancement is expected to occur even with nonspherical particles.     

飞秒荧光亏蚀光谱技术研究液相体系取向弛豫

溶液中分子的快速弛豫过程直接反映了溶液中溶质和周围溶剂分子间的相互作用[1- 3 ] .在液相体系中分子取向通常是随机分布的 .当溶质分子被线偏振光激发至激发态时 ,其分子取向将由原来各向同性的球形分布瞬间变成各向异性的椭球分布 .由于溶质分子周围大量溶剂分子的存在 ,通过二者之间相互作用 ,激发态溶质分子在一定方向上的取向优势将很快弛豫掉 .这种溶液中的取向弛豫过程通常是几个到几百皮秒[1- 3 ] .飞秒分辨荧光亏蚀光谱原理和实验方法见文献[4 - 7] .当溶液中的溶质分子被线偏振飞秒激光脉冲激发至电子激发态时 ,经过一定的延迟…