Author Affiliations
1East China Normal University, State Key Laboratory of Precision Spectroscopy, Shanghai, China2Chongqing Institute of East China Normal University, Chongqing Key Laboratory of Precision Optics, Chongqing, China3University of Shanghai for Science and Technology, School of Optical-Electrical and Computer Engineering, Engineering Research Center of Optical Instrument and System (Ministry of Education), Shanghai Key Laboratory of Modern Optical System, Shanghai, China4China Academy of Space Technology (Xi’an), National Key Laboratory of Science and Technology on Space Microwave, Xi’an, Shaanxi, China5Shanghai Research Center for Quantum Sciences, Shanghai, China6Chongqing Institute for Brain and Intelligence, Guangyang Bay Laboratory, Chongqing, Chinashow less
Fig. 1. (a) Photo of plasma-grating excited fluid jet stream. (b) Schematic of the spatial configuration of three filaments generated by pulses A, B, and C. The parallel structure represents plasma gratings generated by the nonlinear interactions of coplanar filaments A, B, and/or C. (c) Schematic of the top view of the plasma grating interacting with the fluid jet.
Fig. 2. Time evolution of a typical F-GIBS spectrum: evolution of (a) a typical F-GIBS with the detection delay and (b) the intensity and SNR of Cu I 324.7 nm excited by F-GIBS.
Fig. 3. F-GIBS signals of Cu I 324.7, Cr I 425.4, and Na I 588.9 nm attained under different interpulse delays.
Fig. 4. Top view of the noncollinear interaction area between pulses A and B to create plasma gratings (a) without and (b) with the third filament (pulse C) entering the plasma grating at 50 ps delay, respectively. The plasma grating fluorescence photos are shown in the inset pictures.
Fig. 5. Top view of the noncollinear interaction area between the ahead pulse C ( delay) and plasma grating inducing by pulses A and B.
Fig. 6. Top view of the noncollinear coplanar filament interaction area as the three filaments are synchronized.
Fig. 7. Comparison of FIBS, GIBS, and F-GIBS at different delays (0 and ) in aqueous solutions for spectral lines of (a) Cu, (b) Cr, (c) H, and (d) Na elements.
Line | to (eV) | | | 0 ps | 50 ps | −50 ps | Cu I 324.7 nm | 0.000 to 3.816 | 3.19 | 26.38 | 70.36 | 77.71 | Cu I 327.4 nm | 0.000 to 3.785 | 5.11 | 28.33 | 75.31 | 87.62 | Cr I 425.4 nm | 0.000 to 2.913 | 22.03 | 92.80 | 145.77 | 174.98 | Cr I 427.4 nm | 3.086 to 5.986 | 18.08 | 94.72 | 154.52 | 177.99 | Cr I 428.9 nm | 0.000 to 2.889 | 20.59 | 99.11 | 152.71 | 195.18 | Na I 588.9 nm | 0.000 to 2.104 | 4.51 | 6.75 | 8.87 | 12.44 | Na I 589.5 nm | 0.000 to 2.102 | 3.58 | 5.91 | 7.19 | 11.21 |
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Table 1. The enhancement factors of various spectral lines attained by GIBS and F-GIBS excitation protocols versus FIBS.