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50     Cha pte r  T h ree


                  Figure 3-10d shows the image of the focused beam using a L 2
               lens with trifluoroethanol (n = 1.29) as the cladding liquid and ben-
                                       d
               zothiazole as the core liquid. Due to the higher contrast in refractive
               index between the core and the cladding, the focal distance achieved
               was smaller. The quality of the beam was visibly worse than the
               case when the index of the cladding liquid was matched to that of PDMS
               (Fig. 3-10b and c). The streaks in the light beam were due to scattering
               of light from the rough channel wall.
                        2
               3-5-3 L  Light Sources
               We developed various on-chip fluidic light sources based on the L 2
               waveguide systems for optical detection and spectroscopic analysis
               in integrated microanalytical systems (μTAS). In these systems, the
               liquid cores contain fluorescent dyes, excited by incident light from
               an external halogen bulb or a pump laser. Although external excita-
               tion sources are still necessary, integration of fluorescent light sources
               during device fabrication removes both the need for insertion and
               alignment of optical-fiber light sources and the constraints on chan-
               nel size imposed by fiber optics.
               Broadband Fluorescent Light Source
               The construction of a microfluidic broadband light source is similar
               to that of a L  waveguide [13]. Solutions of multiple fluorescent dyes
                          2
               form the core streams, sandwiched by cladding streams with lower
               index of refraction. Excitation of these dyes by an external halogen
               bulb results in a broadband optical output with wavelength ranging
               from 450 to 750 nm.
                  Simultaneous use of multiple fluorophores in a common solution,
                          2
               in a single L  light source, is not possible, because of energy transfer
               from fluorophores emitting at shorter wavelength to fluorophores
               emitting at longer wavelength. Spatial separation of the fluorophores
               in different streams circumvents this problem. One design uses a cas-
               cade (series) of single-core, dye light sources of increasing absorption
               energy to generate a combined broadband output (Fig. 3-11a and b).
               The second approach uses a parallel array of single-core, dye light
               sources (Fig. 3-11c and d). The spectral content of the light output for
               both cascade and array light sources can be controlled through the
               choice of flow rates and dyes. Output intensity from these light sources
               is comparable to standard fiberoptic spectrophotometer light sources.

                2
               L  Microfluidic Dye Laser
               Details about different microfluidic dye lasers can be found in
               Chap.10. Here we describe the use of L  waveguide for dye laser [14].
                                               2
               The construction of a microfluidic dye laser is similar to that of a L 2
               waveguide. Solutions of fluorescent dye act as the gain media. They
               form the core streams, sandwiched by cladding streams with lower
               index of refraction, in a microchannel of length 5 to 20 mm where the
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