Energy-Transfer Dye Laser in SolGel Silica

Coumarin 460 transfers radiative energy to disodium fluorescein when solgel silica is doped with the dyes, producing disodium fluorescein lasing in superradiant mode at a 3.3% peak efficiency under low-energy transverse pumping by a 1.5-mJ N(2) laser, with disodium fluorescein being present at a concentration below its lasing threshold value.     

Sol-gel silica laser tunable in the blue

Doped and undoped silica slabs were fabricated through the use of the sol-gel technique. Extended UV transmission was observed for HCl-catalyzed sol-gel silica. Under transverse pumping with a XeCl laser, narrow-linewidth (<0.9-nm) laser oscillation from silica slabs doped with coumarin 460 (C460) was achieved in a grating-resonator cavity configured in the grazing-indicence geometry. Tuning of the C460-doped silica laser extended from 468 to 494 nm. The conversion efficiency of the narrow-linewidth blue laser was 5.5%.     

Inside Front Cover: An Ultraviolet Organic Thin‐Film Solid‐State Laser for Biomarker Applications (Adv. Mater. 1/2005)

Thin‐film organic solid‐state lasers operating in the ultraviolet wavelength region are fabricated using a novel spiro‐linked material as active organic layer in an optically pumped distributed feedback (DFB) structure in work reported by Riedl and co‐workers on p. 31. The laser wavelength is tunable between 377.7 nm and 395 nm, the shortest laser wavelength reported so far for thin‐film organic solid‐state lasers. The lasers' suitability for spectroscopic applications was tested by use as an excitation source for solutions containing the common fluorescent dyes Coumarin 6, Coumarin 152, and Rhodamine 6G.     

有机改性光功能固态凝胶基质材料的制备与性能研究

用溶胶一凝胶（Sel－Gel）方法成功地制备了RhodamineB激光染料掺杂的有机无机复合硅钛凝胶玻璃,在二极管泵浦Nd：YAG激光器倍频光（532nm）作用下,得到了连续可调的激光输出．用IR、TG／DTA、光谱等手段分析了凝胶基质材料的热学、力学及光学等性能,实验发现,有机改性凝胶玻璃成胶以及机械加工、热学、力学及光学等性能均较好,是一种适于各类激光染料及非线性染料掺杂的理想固态基质材料．     

Multimode laser emission from dye doped polymer optical fiber

Multimode laser emission is observed in a polymer optical fiber doped with a mixture of Rhodamine 6G (Rh 6G) and Rhodamine B (Rh B) dyes. Tuning of laser emission is achieved by using the mixture of dyes due to the energy transfer occurring from donor molecule (Rh 6G) to acceptor molecule (Rh B). The dye doped poly(methyl methacrylate)-based polymer optical fiber is pumped axially at one end of the fiber using a 532 nm pulsed laser beam from a Nd:YAG laser and the fluorescence emission is collected from the other end. At low pump energy levels, fluorescence emission is observed. When the energy is increased beyond a threshold value, laser emission occurs with a multimode structure. The optical feedback for the gain medium is provided by the cylindrical surface of the optical fiber, which acts as a cavity. This fact is confirmed by the mode spacing dependence on the diameter of the fiber.     

Red-green-blue laser emissions from dye-doped poly(vinyl alcohol) films

A microscope slide acting as a passive waveguide was coated by three separate poly(vinyl alcohol) films that were doped with Coumarin 460, Disodium Fluorescein, and Rhodamine 640 perchlorate. On collinear pumping by a nitrogen laser, these dyes furnished primary red-green-blue laser emissions that were collected and waveguided by the microscope slide but exited from both ends. Frosting the waveguide exit introduced light scattering at the glass-air interface and spatially overlaid the red-green-blue laser emissions that emerged as a uniform white-light beam.     

Utilization of the Yellow Component of a Copper-Vapor Laser for Extending the Tuning Range of a Rhodamine 6G Dye Laser by Use of an Additional Dye in a Novel Coupled Resonator Scheme

We demonstrate the use of both 510.6- and 578.2-nm components and the extension of the tuning range of a Rhodamine 6G dye laser in a novel coupled resonator scheme. Rhodamine 6G is pumped by 510.6-nm light in one resonator and Sulforhodamine B is pumped by 578.2 nm in the other. The spectral tuning range of 564-609 nm of the Rhodamine 6G laser is extended up to 640 nm. A two-mirror arrangement ensures continuous tuning across the spectral ranges of the two dyes by rotation of a single plane mirror.     

Studies on the effect of organic additives on the monolithicity and optical properties of the rhodamine 6G doped silica xerogels

Rhodamine 6G (R6G) laser dye doped silica xerogels were prepared by sol–gel processing using tetraethylorthosilicate [TEOS, Si(OC₂H₅)₄] precursor, citric acid (CTA) catalyst and ethanolic R6G in the presence of various organic additives such as formamide (FA), N′methylformamide (N′MF), dimethylformamide (DMF), acetamide (AA), glycerol (GLY), oxalicacid (OXA), ethyleneglycol (EG) and diethyleneglycol (DEG). The organic additive/TEOS molar ratio was varied from 0.001 to 0.1 by keeping the TEOS/EtOH/H₂O/CTA/R6G molar ratio constant at 1:5:7:1.2×10⁻³:9.2×10⁻⁶. It was found from the spectral studies of the additive modified R6G doped silica xerogels that the absorption maxima at 530 nm and emission maxima at 565 nm were increased with the addition of organic additive and with the increase of the additive/TEOS molar ratio. The transparency of the R6G doped silica xerogels was increased with the increase of additive/TEOS molar ratio from 0.001 to 0.1 with OXA, DEG and EG and in the case of DMF, N′MF, FA, AA and GLY, the transparency of the samples increased up to 0.014 of additive/TEOS molar ratio and then decreased for >0.014 of additive/TEOS molar ratio. Monolithic samples were obtained with all the organic additives. The percentage volume shrinkage of the samples was less EG and DEG and more with OXA additives.     

Photoluminescence of Rhodamine 6G-doped amorphous TiO2 thin films grown by sol–gel

Rhodamine 6G (Rh6G)-doped amorphous titanium thin films were prepared by the sol–gel technique. The films were grown at room temperature (RT) and supported on silica-glass substrates, which were previously chemically activated. Photoluminescence (PL) spectra were registered at RT by using as photo excitation the 325 nm He–Cd line. The PL versus the photon energy emission curves peak at around 3.2 eV, which open the possible application of this material for solid-state UV laser devices manufacturing.     

Catalytic properties of silica/silver nanocomposites

The catalytic properties of silver nanoparticles supported on silica and the relation between catalytic activity of silver particles and the support (silica) size are investigated in the present article. The silver nanoparticles with 4 nm diameters were synthesized and were attached to silica spheres with sizes of 40, 78, 105 nm, respectively. The reduction of Rhodamine 6G (R6G) by NaBH4 was designed by using the SiO2/Ag core-shell nanocomposites as catalysts. The experimental results demonstrated that the catalytic activity of silica/silver nanoparticles depends on not only the concentration of catalysts (silver) but also the support silica size. Silver particles supported on small SiO2 spheres (approximately 40 nm) show high catalytic activity. Moreover, by making a comparison between the UV-vis spectra of the catalyst before and after the catalytic reaction, we found that the position of surface plasma resonance (SPR) peak of Ag nanoparticles changes little. The above results suggested that the size and morphology of silver particles were probably kept unchanged after the reduction of R6G and also implied that the catalytic activity of silver particles was hardly lost during the catalytic reaction.     

Biological laser action

The narrowing of the spectral linewidth and the increasing of the peak intensity characteristic of laser action were observed in emission spectra of dye-infused biological tissues. The tissue was infused with a solution of Rhodamine 640 perchlorate in ethanol and then excited with frequency-doubled Q-switched Nd:YAG laser pulses. The dependence of emission linewidth on the excitation radiant exposure and dye concentration was investigated. Laser action was also observed in biologically compatible fluorescein sodium dye dissolved in phosphate-buffered saline mixed with scattering polystyrene spheres. The sharp spectral peaks of laser action in tissues may find applications in the detection of superficial disease.     

Long-pulse narrow-linewidth dispersive solid-state dye-laser oscillator

We report on narrow-linewidth long-pulse laser emission from a dispersive solid-state dye-laser oscillator. Output energy was ~0.4 mJ/pulse at laser linewidths of 650 MHz and pulse lengths of 105 ns FWHM. The solid-state gain medium utilized was Rhodamine 6G dye-doped 2-hydroxyethyl methacrylate:methyl methacrylate.     

Comparison of laser performance of dye molecules in sol-gel, polycom, ormosil, and poly(methyl methacrylate) host media

Laser performance is described for Rhodamine 590, Pyrromethene 567, Perylene red, and Perylene orange in inorganic porous sol-gel glass, poly(methyl methacrylate)(PMMA), a composite of porous sol-gel glass with PMMA and organically modified silicate ormosil glass. Lasers were excited with a flash-lamp-pumped dye laser in the long-pulse-length regime (3 μs, 506 nm, 300 mJ) and a second-harmonic Nd:YAG laser in the short-pulse-length regime (6 or 15 ns, 532 nm, 60 mJ). The feasibility of long-pulse-length operation is demonstrated, detailed characteristics of short-pulse operation are described, and laser damage measurements are given. The nonpolar perylene dyes had better performance in partially organic hosts, and the ionic rhodamine and pyrromethene dyes performed best in the inorganic sol-gel glass host.     

Ultrabright Fluorescent Mesoporous Silica Nanoparticles

The first successful approach to synthesizing ultrabright fluorescent mesoporous silica nanoparticles is reported. Fluorescent dye is physically entrapped inside nanochannels of a silica matrix created during templated sol–gel self‐assembly. The problem of dye leakage from open channels is solved by incorporation of hydrophobic groups in the silica matrix. This makes the approach compatible with virtually any dye that can withstand the synthesis. The method is demonstrated using the dye Rhodamine 6G. The obtained 40‐nm silica particles are about 30 times brighter than 30‐nm coated water‐soluble quantum dots. The particles are substantially more photostable than the encapsulated organic dye itself.     

Distributed feedback leaky laser emission from dye doped gel-glass dispersed liquid crystal thin film patterned by soft lithography

Gel-glass dispersed liquid crystal (GDLC) thin films doped with organic laser dye Rhodamine 6G (R6G) were prepared via a sol-gel procedure of tetraethyl orthosilicate (TEOS) and ethyl triethoxisilane (ETES). As characterized by scanning electronic microscope (SEM), surface-relief structures were successfully patterned on lower refractive index GDLC thin films by soft lithographic technology, which support distributed feedback (DFB) laser emission based on leaky mode propagation. The performance of the DFB laser emission was investigated and the spectral narrowing of the emitted radiation and the fine structure pattern were found to be controlled by the doping concentration of liquid crystal (LC) 4-cyano-4′-pentylbiphenyl (5CB). We also showed the synchronous excitation of a DFB lasing with random lasing mediated by light scattering inside the same GDLC leaky waveguide.     

Effective random laser action in Rhodamine 6G solution with Al nanoparticles

We have studied the random laser action in Rhodamine 6G (Rh6G) ethylene glycol solution with Al nanoparticles. The experiment results are obtained by pumping with a nanosecond (7 ns) laser pulse, which demonstrated the existence of effective random laser emission. It is found that the threshold of the random laser depends on the concentration of the Rh6G and the concentration of Al nanoparticles. The concentration and diameter of Al nanoparticles have effects on the optical path; a higher concentration or a larger diameter results in a shorter optical path length. Also multimode survival and mode competition have been observed at a relatively high concentration (0.08 M) of Rh6G, where the concentration of Al nanoparticles is 0.0015 M.     

Fluorescence studies of Rhodamine 6G functionalized silicon oxide nanostructures

Selective anchoring of optically active molecules on nanostructured surfaces is a promising step towards the creation of nanoscale devices with new functionalities. Recently we have demonstrated the electrostatic attachment of charged fluorescent molecules on silicon oxide nanostructures prepared by atomic force microscopy (AFM) nanolithography via local anodic oxidation (LAO) of dodecyl-terminated silicon. In this paper we report on our findings from a more detailed optical investigation of the bound dye Rhodamine 6G. High sensitivity optical wide field microscopy as well as confocal laser microscopy have been used to characterize the Rhodamine fluorescence emission. A highly interesting question concerns the interaction between an emitter close to a silicon surface because mechanisms such as energy transfer and fluorescence quenching will occur which are still not fully understood. Since the oxide thickness can be varied during preparation continuously from 1 to ～ 5 nm, it is possible to investigate the fluorescence of the bound dye in close proximity to the underlying silicon. Using confocal laser microscopy we were also able to obtain optical spectra from the bound molecules. Together with the results from an analysis of their photochemical bleaching behaviour, we conjecture that some of the Rhodamine 6G molecules on the structure are interacting with the oxide, causing a spectral shift and differences in their photochemical properties.     

Random laser action from a natural flexible biomembrane-based device

Abstract

Incoherent random lasing action in flexible eggshell membranes infiltrated with rhodamine 6G laser dyes is demonstrated. Laser radiation is achieved by exciting samples with 1-ns pulses at 526 nm. A threshold of 58 μJ/pulse is measured for the samples. The minimum threshold decreases to 35 μJ/pulse after the sample is coated with gold nanoparticles using a magnetron sputtering technique. The peaks of emission spectra are observed to redshift from 576 to 596 nm as dye concentration rises from 0.03 to 0.6 wt%. A linewidth of approximately 5 nm is obtained for most samples. This study is expected to offer a new way to induce lasing emission using biological microfibrils, and enriches basic knowledge of biophotonics.     

On-column surface-enhanced Raman spectroscopy detection in capillary electrophoresis using running buffers containing silver colloidal solutions

Direct on-column surface-enhanced Raman spectroscopy (SERS) detection is demonstrated in capillary electrophoresis (CE). Distinctive SERS spectra of two test compounds, riboflavin and Rhodamine 6G, are obtained in 100 microm i.d. fused-silica capillaries under CE conditions using running buffers that contain silver colloidal solutions. Detection is performed using an unmodified commercial Raman spectrometer in a confocal microscope mode of operation. The effects of laser power, wavelength, spectra acquisition time, silver colloidal concentration, and applied voltage (i.e., flow rate) on the quality of SERS spectra are evaluated. Using laser powers of 17 mW (at the sample) at 515 nm and employing 1 s spectral acquisition times, spectra with bands exhibiting signal-to-noise ratios greater than 10 could be obtained for 1.0 x 10(-6) M riboflavin and very low nanomolar concentrations of Rhodamine 6G. This was accomplished without optimization of silver colloidal solution compositions and by using a low-throughput spectrometer. Incorporation of the colloidal solutions into running buffers is shown to have little effect on the separation of the test compounds as monitored using a laser-induced fluorescence instrumental scheme. However, SERS spectra degrade if the capillary is not rinsed between experiments. Riboflavin and Rhodamine 6G spectra are obtained on-the-fly for actual CE separations. In the case of the latter solute, the injected quantity was approximately 90 amol.     

一种有机掺杂体系的光致发光及薄膜电致发光研究

将具有薄膜电致发光（ＴＦＥＬ）性能的有机络合染料８－羟基喹啉铝（Ａｌｑ３）掺以染料罗丹明６Ｇ（Ｒ６Ｇ），用真空热蒸发的方法获得了峰值波长５７５ｎｍ的黄色直流电致发光（ＥＬ）。通过对不同掺杂浓度的粉末，溶液，薄膜样品及电致发光器件的光谱及寿命测量和对比，证实了能量传递的存在并初步探讨了可能的途径。同时发现掺杂器件ＥＬ谱的形状随驱动电压升高发生明显的改变，基质（Ａｌｑ３）的发射（相对于掺杂剂Ｒ６Ｇ的发射）明显增强，对这一现象产生的原因作了分析，并由此讨论了有机掺杂ＴＦＥＬ中复合，发射区域等问题。