2014
DOI: 10.1063/1.4886424
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Optimization of confocal laser induced fluorescence in a plasma

Abstract: Laser Induced Fluorescence (LIF) provides measurements of flow speed, temperature, and density of ions or neutrals in a plasma. Traditionally, a LIF measurement requires two ports on a plasma device; one for laser injection and one for emission collection. Proper alignment of LIF optics is time consuming and sensitive to mechanical vibration. We describe a confocal configuration for LIF that requires a single port and requires no alignment. The measurement location is scanned radially by physically moving the … Show more

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Cited by 5 publications
(5 citation statements)
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“…One way to facilitate optical alignment with a moving diagnosed volume is the adaption of a confocal optical assembly [75], focusing the laser beam and the collection optics to the diagnosed volume with a single objective lens. As the injection and collection optical paths are united, confocal LIF setups do not require the alignment of translatable collection optics to the laser's path.…”
Section: Collection Optics and Optical Sensorsmentioning
confidence: 99%
“…One way to facilitate optical alignment with a moving diagnosed volume is the adaption of a confocal optical assembly [75], focusing the laser beam and the collection optics to the diagnosed volume with a single objective lens. As the injection and collection optical paths are united, confocal LIF setups do not require the alignment of translatable collection optics to the laser's path.…”
Section: Collection Optics and Optical Sensorsmentioning
confidence: 99%
“…Previous attempts to measure ion velocity distributions with confocal single-photon LIF have been reported, with longitudinal spatial localization estimated to be approximately 3 cm using an objective focal length of 20 cm. 20 The purpose of this work is to report for the first time, confocal, single-photon LIF measurements that achieve longitudinal spatial localization of the same order of magnitude as conventional LIF methods. The new technique overcomes two major limitations in previous designs: it removes the need for two, spatially separated sightlines required by conventional LIF schemes and extends the short, millimeterscale observing distance limitation of conventional confocal microscopy to hundreds of millimeters.…”
Section: Introductionmentioning
confidence: 99%
“…This widthis about 30% broader than conventional LIF, which has a FWHM of 1.1 mm and encompasses 97.3% of the signal. Previously published state-of-the-art confocal LIF designs exhibit collection regions several centimeters wide, leading to flattened profiles of measured plasma quantities[151]. By comparison, the excellent agreement between the profiles measured confocally and in the conventional way, even on the far side of the core at x > 0 as shown inFig.…”
mentioning
confidence: 65%