An optofluidic prism tuned by two laminar flows

This paper presents a tunable optofluidic prism based on the configuration of two laminar flow streams with different refractive indices in a triangular chamber. The chambers with 70° and 90° apex angles are designed based on simulation results, which provide the optimum working range and avoid recirculating flows in the chambers. In addition, a hydrodynamic model has been developed to predict the tuning of the prisms by the variation in the flow rates. Prisms with different refractive indices are realized using benzyl alcohol and deionized (DI) water as the inner liquids, respectively. The mixture of ethylene glycol and DI water with an effective refractive index matched to that of the microchannel is used as the outer liquid. The apex angle of the prism is tuned from 75° to 135° by adjusting the ratio of the two flow rates. Subsequently, the deviation angle of the output light beam is tuned from -13.5° to 22°. One of the new features of this optofluidic prism is its capability to transform from a symmetric to an asymmetric prism with the assistance of a third flow. Two optical behaviours have been performed using the optofluidic prism. First, parallel light beam scanning is achieved with a constant deviation angle of 10° and a tuning range of 60 μm using the asymmetric prism. The detected output light intensity is increased by 65.7%. Second, light dispersion is experimentally demonstrated using 488-nm and 633-nm laser beams. The two laser beams become distinguishable with a deviation angle difference of 2.5° when the apex angle of the prism reaches 116°.     

Fluorescent liquid-core/air-cladding waveguides towards integrated optofluidic light sources

We have demonstrated fluorescent liquid-core/air-cladding (LA) waveguides suitable for use as integrated optofluidic light sources. These waveguides were fabricated by conventional soft lithography using poly(dimethylsiloxane) (PDMS). Two-phase stratified flows of air and ethylene glycol with fluorescent dye were generated along the PDMS channel. Compared to the liquid-core/liquid-cladding (L(2)) waveguide, the larger refractive index contrast of the LA waveguide resulted in stronger optical confinement. Specifically, the larger refractive index contrast led to experimentally achievable captured fractions (the amount of light to be coupled into the liquid core) as high as 22.8% and the measured propagation losses as low as 0.14 dB cm(-1). Furthermore, in our LA waveguides, diffusional mixing of the core and cladding fluids did not occur and the size of the core stream could be reversibly tuned simply by adjusting the flow rates of the two contiguous phases.     

Highly sensitive optofluidic chips for biochemical liquid assay fabricated by 3D femtosecond laser micromachining followed by polymer coating

The demand for increased sensitivity in the concentration analysis of biochemical liquids is a crucial issue in the development of lab on a chip and optofluidic devices. We propose a new design for optofluidic devices for performing highly sensitive biochemical liquid assays. This design consists of a microfluidic channel whose internal walls are coated with a polymer and an optical waveguide embedded in photostructurable glass. The microfluidic channel is first formed by three-dimensional femtosecond laser micromachining. The internal walls of the channel are then coated by the dipping method with a polymer that has a lower refractive index than water. Subsequently, the optical waveguide is integrated with the microfluidic channel. The polymer coating on the internal walls permits the probe light, which is introduced by the optical waveguide, to propagate along the inside of the microfluidic channel. This results in a sufficiently long interaction length between the probe light and a liquid sample in the channel and thus significantly improves the sensitivity of absorption measurements. Using the fabricated optofluidic chips, we analyzed protein in bovine serum albumin to concentrations down to 7.5 mM as well as 200 nM glucose-D.     

Concentration-dependent energy transfer studies in ternary dye mixture of Stilbene-420, Coumarin-540 and Nile Blue

The energy transfer studies in the case of ternary dye mixture [Stilbene-420 (donor)+Coumarin-540 (intermediator)+Nile Blue (acceptor)] have been done and discussed through optical gain characteristics at various acceptor concentrations under nitrogen laser excitation. The concentration of the other two dyes were kept constant. It is observed that the concentration of the acceptor dye plays a very critical role in energy transfer dye laser (ETDL) as small change in its concentration varies the intensity of the laser output in the red region by large amount. Also, the highest laser output in the red region is obtained when the concentration of the acceptor dye is slightly higher than that of the intermediator dye. The present studies are helpful in deciding the optimum concentration of the acceptor dye to be used in ternary dye mixture for maximum gain and tuning range. The ternary dye mixture under study provides an ETDL tuning range up to 700 nm.     

An integrated optofluidic platform for Raman-activated cell sorting

We report on integrated optofluidic Raman-activated cell sorting (RACS) platforms that combine multichannel microfluidic devices and laser tweezers Raman spectroscopy (LTRS) for delivery, identification, and simultaneous sorting of individual cells. The system allows label-free cell identification based on Raman spectroscopy and automated continuous cell sorting. Two optofluidic designs using hydrodynamic focusing and pinch-flow fractionation are evaluated based on their sorting design and flow velocity effect on the laser trapping efficiency at different laser power levels. A proof-of-principle demonstration of the integrated optofluidic LTRS system for the identification and sorting of two leukemia cell lines is presented. This functional prototype lays the foundation for the development of a label-free cell sorting platform based on intrinsic Raman markers for automated sampling and sorting of a large number of individual cells in solution.     

First Highly Efficient and Photostable E and C Derivatives of 4,4‐Difluoro‐4‐bora‐3a,4a‐diaza‐s‐indacene (BODIPY) as Dye Lasers in the Liquid Phase,Thin Films,and Solid‐State Rods

A new library of E‐ and C‐4,4‐difluoro‐4‐bora‐3a,4a‐diaza‐s‐indacene (BODIPY) derivatives has been synthesized through a straightforward protocol from commercially available BODIPY complexes, and a systematic study of the photophysical properties and laser behavior related to the electronic properties of the B‐substituent group (alkynyl, cyano, vinyl, aryl, and alkyl) has been carried out. The replacement of fluorine atoms by electron‐withdrawing groups enhances the fluorescence response of the dye, whereas electron‐donor groups diminish the fluorescence efficiency. As a consequence, these compounds exhibit enhanced laser action with respect to their parent dyes, both in liquid solution and in the solid phase, with lasing efficiencies under transversal pumping up to 73 % in liquid solution and 53 % in a solid matrix. The new dyes also showed enhanced photostability. In a solid matrix, the derivative of commercial dye PM597 that incorporated cyano groups at the boron center exhibited a very high lasing stability, with the laser emission remaining at the initial level after 100 000 pump pulses in the same position of the sample at a 10 Hz repetition rate. Distributed feedback laser emission was demonstrated with organic films that incorporated parent dye PM597 and its cyano derivative. The films were deposited onto quartz substrates engraved with appropriate periodical structures. The C derivative exhibited a laser threshold lower than that of the parent dye as well as lasing intensities up to three orders of magnitude higher.     

High-throughput optofluidic platforms for mosaicked microfibers toward multiplex analysis of biomolecules

We describe high-throughput optofluidic platforms for mosaic-patterned microfibers by generating stratified laminar flows. An inert carrier liquid flow near PDMS channel walls conveyed a photopolymerizable liquid which permitted stable production of microfibers with particular morphologies and compositional patterns. Finally, mosaicked microfibers were prepared with desired configurations toward multiplex biomolecular analysis.     

Optofluidic microsystem with quasi-3 dimensional gold plasmonic nanostructure arrays for online sensitive and reproducible SERS detection

Practical applications of chemical and biological detections through surface-enhanced Raman scattering (SERS) require high reproducibility, sensitivity, and efficiency, along with low-cost, straightforward fabrication. In this work, we integrated a poly-(dimethylsiloxane) (PDMS) chip with quasi-3D gold plasmonic nanostructure arrays (Q3D-PNAs), which serve as SERS-active substrates, into an optofluidic microsystem for online sensitive and reproducible SERS detections. The Q3D-PNA PDMS chip was fabricated through soft lithography to ensure both precision and low-cost fabrication. The optimal dimension of the Q3D-PNA in PDMS was designed using finite-difference time-domain (FDTD) electromagnetic simulations with a simulated enhancement factor (EF) of 1.6 × 10⁶. The real-time monitoring capability of the SERS-based optofluidic microsystem was investigated by kinetic on/off experiments through alternatively flowing Rhodamine 6G (R6G) and ethanol in the microfluidic channel. A switch-off time of ∼2 min at a flow rate of 0.3 mL min⁻¹ was demonstrated. When applied to the detection of low concentration malathion, the SERS-based optofluidic microsystem with Q3D-PNAs showed high reproducibility, significantly improved efficiency and higher detection sensitivity via increasing the flow rate. The optofluidic microsystem presented in this paper offers a simple and low-cost approach for online, label-free chemical and biological analysis and sensing with high sensitivity, reproducibility, efficiency, and molecular specificity.     

Hydrodynamically tunable optofluidic cylindrical microlens

In this work, we report the design, fabrication, and characterization of a tunable optofluidic microlens that focuses light within a microfluidic device. The microlens is generated by the interface of two co-injected miscible fluids of different refractive indices, a 5 M CaCl(2) solution (n(D) = 1.445) and deionized (DI) water (n(D) = 1.335). When the liquids flow through a 90-degree curve in a microchannel, a centrifugal effect causes the fluidic interface to be distorted and the CaCl(2) solution bows outwards into the DI water portion. The bowed fluidic interface, coupled with the refractive index contrast between the two fluids, yields a reliable cylindrical microlens. The optical characteristics of the microlens are governed by the shape of the fluidic interface, which can be altered by simply changing the flow rate. Higher flow rates generate a microlens with larger curvature and hence shorter focal length. The changing of microlens profile is studied using both computational fluid dynamics (CFD) and confocal microscopy. The focusing effect is experimentally characterized through intensity measurements and image analysis of the focused light beam, and the experimental data are further confirmed by the results from a ray-tracing optical simulation. Our investigation reveals a simple, robust, and effective mechanism for integrating optofluidic tunable microlenses in lab-on-a-chip systems.     

Difluoro-boron-triaza-anthracene: a laser dye in the blue region. Theoretical simulation of alternative difluoro-boron-diaza-aromatic systems

The synthesis, photophysical and laser properties of a difluoro-boron-triaza-anthracene (BTAA) compound are analyzed in the present paper. The molecular structure of this dye is an anthracene-like core with N atoms at 4a, 9 and 10a positions where two of them (4a and 10a) are linked through a BF(2)-bridge group. This structure is reminiscent of aza-BODIPY dye with an s-indacene core, BODIPY being one of the most commonly used laser dye family in the Vis region. The main absorption and emission bands of the new dye are localized in the blue part of the Vis region of the electromagnetic radiation, a spectral region practically unexploited by the BODIPY chromophore. Moreover, the new dye presents a higher laser efficiency and photostability than other commercial laser dyes operating in the same spectral region. In order to look for new molecular structures with potential laser emission covering the whole Vis spectral region, the spectroscopic properties of other different chromophoric systems based on BF(2)-linking aromatic groups are theoretically simulated by quantum mechanical calculations.     

Energy transfer distributed feedback dye laser using Rhodamine B-Acid blue 7 dye mixture

The characteristics of energy transfer distributed feedback dye laser (ETDFDL) are studied both theoretically and experimentally in a mixture of Rhodamine B and Acid blue 7 dyes pumped by 532 nm Nd:YAG laser. The behaviour of donor and acceptor DFDL, the dependence of their pulse width and output power on pump power and donor-acceptor concentrations are studied. Experimentally, the tunability is achieved over the spectral range 565-680 nm using a prism dye cell arrangement. The output energy of DFDL is measured at the emission peaks of donor and acceptor for different pump powers and donor-acceptor concentrations. The output pulse of DFDL is found to be as narrow as 40-ps duration, which is nearly 100-fold shorter than the pump pulse. The pulse linewidth is of the order of 0.1 A.     

Comparing spiro-OMeTAD and P3HT hole conductors in efficient solid state dye-sensitized solar cells

Two hole conductor materials, spiro-OMeTAD and P3HT, were compared in solid-state dye-sensitized solar cells. Two organic dyes containing one anchor unit (D35) or two anchor units (M3) were used in the comparison. Absorbed photon to current conversion efficiency close to unity was obtained for the devices with spiro-OMeTAD. Energy conversion efficiencies of 4.7% and 4.9% were measured for the devices with spiro-OMeTAD and the dyes D35 and M3, respectively. For the devices using the P3HT hole conductor the results were rather different comparing the two dye molecules, with energy conversion efficiencies of 3.2% and 0.5% for D35 and M3, respectively. Photo-induced absorption measurements suggest that the regeneration of the dyes, and the polymer infiltration, is not complete using P3HT, while spiro-OMeTAD regenerates the dyes efficiently. However, the TiO(2)/D35/P3HT system shows rather high energy conversion efficiency and electrochemical oxidation of the dyes on TiO(2) indicates that D35 have a more efficient dye to dye hole conduction than M3, which thereby might explain the higher performance. The dye hole conduction may therefore be of significant importance for optimizing the energy conversion in such hybrid TiO(2)/dye/polymer systems.     

Diffusion driven optofluidic dye lasers encapsulated into polymer chips

Lab-on-a-chip systems made of polymers are promising for the integration of active optical elements, enabling e.g. on-chip excitation of fluorescent markers or spectroscopy. In this work we present diffusion operation of tunable optofluidic dye lasers in a polymer foil. We demonstrate that these first order distributed feedback lasers can be operated for more than 90 min at a pulse repetition rate of 2 Hz without fluidic pumping. Ultra-high output pulse energies of more than 10 μJ and laser thresholds of 2 μJ are achieved for resonator lengths of 3 mm. By introducing comparatively large on-chip dye solution reservoirs, the required exchange of dye molecules is accomplished solely by diffusion. Polymer chips the size of a microscope cover slip (18 × 18 mm(2)) were fabricated in batches on a wafer using a commercially available polymer (TOPAS(?) Cyclic Olefin Copolymer). Thermal imprinting of micro- and nanoscale structures into 100 μm foils simultaneously defines photonic resonators, liquid-core waveguides, and fluidic reservoirs. Subsequently, the fluidic structures are sealed with another 220 μm foil by thermal bonding. Tunability of laser output wavelengths over a spectral range of 24 nm on a single chip is accomplished by varying the laser grating period in steps of 2 nm. Low-cost manufacturing suitable for mass production, wide laser tunability, ultra-high output pulse energies, and long operation times without external fluidic pumping make these on-chip lasers suitable for a wide range of lab-on-a-chip applications, e.g. on-chip spectroscopy, biosensing, excitation of fluorescent markers, or surface enhanced Raman spectroscopy (SERS).     

Optical trapping of microparticles using silicon nitride waveguide junctions and tapered-waveguide junctions on an optofluidic chip

We study optical trapping of microparticles on an optofluidic chip using silicon nitride waveguide junctions and tapered-waveguide junctions. We demonstrate the trapping of single 1 μm-sized polystyrene particles using the evanescent field of waveguide junctions connecting a submicrometer-sized input-waveguide and a micrometer-sized output-waveguide. Particle trapping is localized in the vicinity of the junction. We also demonstrate trapping of one and two 1μm-sized polystyrene particles using tapered-waveguide junctions connecting a submicrometer-sized singlemode input-waveguide and a micrometer-sized multimode output-waveguide. Particle trapping occurs near the taper output end, the taper center and the taper input end, depending on the taper aspect ratio.     

Two-photon laser photochemistry of a coumarin laser dye

Irradiation of 7-dimethylamino-4-methylcoumarin (1), a commercially available laser dye, in ethanol solution with the focused output of an XeCl excimer laser at 308 nm resulted in the formation of yellow oligomeric material derived from the ethanol solvent. The efficiency of formation of the yellow material was shown to be dependent on the intensity of the laser light, indicating that the photochemistry involved absorption of two photons. The oligomeric material is proposed to be a substance which interferes with stimulated emission in coumarin dye lasers. In addition, acetaldehyde and several gaseous products, principally hydrogen and butane, were formed. A product resulting from the coupling of 1 with the ethanol solvent was also isolated and characterized. Excimer laser irradiation of 1 in methanol yielded formaldehyde, hydrogen and solvent oligomers, while irradiation of 1 in benzene resulted in the formation of a black precipitate. The non-oligomeric products are similar to those observed from the direct irradiation of the solvent in the vacuum-UV region. A mechanism is proposed for the observed photochemistry in which 1 absorbs, sequentially, two photons from the laser pulse, resulting in the formation of a highly excited state which then transfers energy to the solvent.     

SnO2/SiO2 and Sn/Sb-oxide/SiO2 gel-derived composites. Part 1: Structural evolution from a Mössbauer study

The lasing photostability of the red perylimide dye (RPD) in various solid matrices was measured under frequency-doubled Nd:YAG laser excitation. The RPD: composite glass laser intensity decayed to 50% of its initial value after approximately 20,000 pump pulses of 13 mJ/pulse. The output of RPD:ormosil glass and RPD:PMMA glass lasers decayed to 50% of their initial value after 1,200 and 1,000 pump pulses of the same energy, respectively. For rhodamine-6G:silica-gel and rhodamine-6G:ormosil glass lasers, the 50% decay occurred already after 1,000 and 300 pulses, respectively. The decay was non-exponential, suggesting that the dye bleaching was not a single-photon process. The average laser output decay rates increased linearly with the pump energy. Singlet-singlet excited state absorption of the RPD dye in the solid matrices was also measured between 550 and 730 nm. At ～600 nm the cross section was ～2×10^?16 cm²/molecule. The excited-state absorption competes with the lasing, and is a main factor that limits the laser efficiency.     

Tuning the lasing wavelength of dye-doped chiral nematic liquid crystal by fluid flow

The influence of hydrodynamic flow on the lasing wavelength and stability of the laser emission average power of a dye-doped chiral liquid crystalline (DDCLC) structure is studied. Multiple lasing peaks at equidistant wavelengths are observed, which are originating from multiple domains that are induced by the hydrodynamic flow of the DDCLC. A simultaneous blue shift over 4 nm for all lasing peaks is observed after increasing the flow velocity to 0.3 mm/s for cells with a thickness of 10 μm. It is observed that the CLC flow dramatically increases the stability of the laser emission compared to conventional cells because dye bleaching and LC molecular reorientation due to pumping beam is reduced.     

Photostablity and amplified spontaneous emission in dye-activated new organic-inorganic hybrid material

This paper reports on the lasing action of some dyes (pyrromethene 597, pyrromethene 567 and Rhodamin B) incorporated into a new organic-inorganic hybrid material. The amplified spontaneous emission (ASE) was studied under 532 nm, laser excitation in transverse pumping configuration for the prepared rod samples. The influence of the dye concentration on the amplified spontaneous emission peak wavelengths, the output energies, the gain and the energy conversion efficiencies were studied. Relatively high efficiencies (up to ∼64%) were obtained with good photostabilities where a decrease to ∼30% of the initial amplified spontaneous emission output energy were observed after pumping by 60,000 shots at relatively high repetition rate (10 Hz) and energy (15 mJ).     

Optofluidic variable-focus lenses for light manipulation

This paper presents a planar optofluidic lens for light manipulation utilizing a combination of optofluidic biconvex lens with micromixer. Three light manipulation techniques including tunable optical diverging, collimating and focusing are realized by altering the refractive index of the optofluidic variable-focus lenses formed by solid polydimethylsiloxane (PDMS) walls and tunable liquid lens body. The optical power from the laser input can be increased or decreased with the tuning of the variable-focus lenses' refractive indexes. The optical power adjustment capabilities are demonstrated and characterized. The combinations of benefits of all lens' optical manipulation capabilities, greater mechanical stability, significant increase of optofluidic device's life time and seamless integration with other lab-on-a-chip functionalities provide a promising and versatile optofluidic compartment to integrate with lab-on-a-chip excitation and sensing applications. Optofluidic lens-including system for tunable fluorescence sensing is demonstrated showing 186% increase in detected fluorescence intensity.     

High power CW (16W) and pulse (145W) laser diodes based on quantum well heterostructures

We suggested and experimentally confirmed the effective method of internal optical loss reduction by high order mode suppression in a separate confinement quantum well laser heterostructure with asymmetric ultra thick waveguide. Manufacturing of InGaAs/GaAs/AlGaAs laser heterostructure with a 1.7 microm-thick asymmetric waveguide allowed attaining super low value of internal optical loss alphai=0.34 cm-1 preserving high efficiency and fundamental transverse mode operation. Record-high 16 W continuous wave (CW) and 145 W pulse room temperature front facet output optical power and 74% wallplug efficiency were attained in 100-microm-aperture 1.06-microm-emitting laser diodes with 3 mm cavity length.