Optimally enhanced optical emission in laserinduced breakdown spectroscopy by combining spatial confinement and dual-pulse irradiation

Similar documents
Enhancement of optical emission from laserinduced plasmas by combined spatial and magnetic confinement

Accuracy improvement of quantitative analysis by spatial confinement in laser-induced breakdown spectroscopy

Generation of high-temperature and low-density plasmas for improved spectral resolutions in laser-induced breakdown spectroscopy

The importance of longer wavelength reheating in dual-pulse laser-induced breakdown spectroscopy

Quantitative Analysis of Carbon Content in Bituminous Coal by Laser-Induced Breakdown Spectroscopy Using UV Laser Radiation

Outline. LIBS Background. LIBS Developments. LIBS Overview. Atomic Emission Spectroscopy

JAAS Accepted Manuscript

Title duration on laser ablation in liqui. Rightc 2009 Elsevier B.V. All rights res

Single pulse laser-induced breakdown spectroscopy of bulk aqueous solutions at oceanic pressures: interrelationship of gate delay and pulse energy

Measurements of plasma temperature and electron density in laser-induced copper plasma by time-resolved spectroscopy of neutral atom and ion emissions

A Fundamental Study of Laser-Induced Breakdown Spectroscopy Using Fiber Optics for Remote Measurements of Trace Metals

Influence of laser energy on the electron temperature of a laser induced Mg plasma

Chapter 4 LIBS system: Performance evaluation and optimization of conditions for quantitative analysis

Time-Resolved Emission Spectroscopic Study of Laser-Induced Steel Plasmas

EFFECT OF LASER INTENSITY AND DYNAMICS OF PLASMA ON LASER INDUCED BREAKDOWN SPECTROSCOPY

International Journal of Scientific and Research Publications, Volume 5, Issue 5, May ISSN Osayuwamen Ogboghodo

Measurements of egg shell plasma parameters using laser-induced breakdown spectroscopy

Temporally resolved laser induced plasma diagnostics of single crystal silicon effects of ambient pressure

THEORETICAL ASPECT OF ENHANCEMENT AND SATURATION IN EMISSION FROM LASER PRODUCED PLASMA

Time-resolved ultraviolet laser-induced breakdown spectroscopy for organic material analysis

Elemental analysis by microwave-assisted laser-induced breakdown spectroscopy: Evaluation on ceramics

Design, construction and assessment of a field-deployable laser-induced breakdown spectrometer for remote elemental sensing

Measurements of Deuterium Retention and Surface Elemental Composition with Double Pulse Laser Induced Breakdown Spectroscopy

Investigation of fundamental mechanisms related to ambient gas heating and hydrodynamics of laser-induced plasmas

Laser heating of noble gas droplet sprays: EUV source efficiency considerations

Development of advanced optical techniques for verification measurements Igor Jovanovic University of Michigan

Correction of Matrix Effects in Quantitative Elemental Analysis With Laser Ablation Optical Emission Spectrometry

Spectrochimica Acta Part B

Evaluation of laser-induced breakdown spectroscopy (LIBS) as a new in situ chemical sensing technique for the deep ocean

Determination of Cl/C and Br/C ratios in pure organic solids using laser-induced plasma spectroscopy in near vacuum ultraviolet{

Controlling Graphene Ultrafast Hot Carrier Response from Metal-like. to Semiconductor-like by Electrostatic Gating

Remote Femtosecond Laser Induced Breakdown Spectroscopy (LIBS) in a Standoff Detection Regime

Assessment of the Upper Particle Size Limit for Quantitative Analysis of Aerosols Using Laser-Induced Breakdown Spectroscopy

OPTICAL DETECTION OF SLOW EXCITED NEUTRALS IN PLASMA- ASSISTED EXCIMER LASER ABLATION

Chemical warfare detection by LIBS

Laser Ablation for Chemical Analysis: 50 Years. Rick Russo Laser Damage Boulder, CA September 25, 2012

Achievement of local thermodynamic equilibrium for ns laser-induced plasmas on aluminium sample at different wavelengths

Effect of applying static electric field on the physical parameters and dynamics of laser-induced plasma

Comparative study of two new commercial echelle spectrometers equipped with intensified CCD for analysis of laser-induced breakdown spectroscopy

LASER-INDUCED BREAKDOWN SPECTROSCOPY FOR REAL TIME AND ONLINE ELEMENTAL ANALYSIS

Analytical capability of LIBS method for carbon detection

Chamber Development Plan and Chamber Simulation Experiments

Remote laser-induced plasma spectrometry for elemental analysis of samples of environmental interest

Visualization of Xe and Sn Atoms Generated from Laser-Produced Plasma for EUV Light Source

Study of the Matrix Effect on the Plasma Characterization of Heavy Elements in Soil Sediments using LIBS with a Portable Echelle Spectrometer

Development of an Alternating Electric Field Accelerator for Laser-Ablation Plasma Acceleration

Introduction to laser-based combustion diagnostics

Remote Raman & Fluorescence Capabilities for Chemical Detection at University of Hawaii

EMISSION SPECTRA OF LASER-INDUCED PLASMAS AT THE ELEMENTAL ANALYSIS OF SOLIDS: MEASUREMENT AND MODELING RESULTS

Analysis by laser-induced breakdown spectroscopy of complex solids, liquids, and powders with an echelle spectrometer

Comparisons between LIBS and ICP/OES

Work Piece Identification based on Plasma Emission Analysis for Customized Laser Processing

Differential Spectral Imaging of the CN Violet Band in Laser-Induced Plasmas on TNT Simulant Molecules

Underwater Raman Sensor for Detecting High Explosives and Homemade Explosives (HMEs)

Approach to Detection in Laser-Induced Breakdown Spectroscopy

Glass surface modification using Nd:YAG laser in SF 6 atmospheres

BRET C. WINDOM UNIVERSITY OF FLORIDA

UNDERWATER LIBS INVESTIGATIONS SETUP FOR METALS IDENTIFICATION

Richard Miles and Arthur Dogariu. Mechanical and Aerospace Engineering Princeton University, Princeton, NJ 08540, USA

Laser matter interaction

Oceanic Applications of Laser Induced Breakdown Spectroscopy: Laboratory Validation

No. 9 Experimental study on the chirped structure of the construct the early time spectra. [14;15] The prevailing account of the chirped struct

Self-channeling of Femtosecond Laser Pulses for Rapid and Efficient Standoff Detection of Energetic Materials

MICHAEL J. WITTE 1 AND CHRISTIAN G. PARIGGER 1,a

The role of laser wavelength on plasma generation and expansion of ablation plumes in air

Remote Femtosecond Laser Induced Breakdown Spectroscopy (LIBS) in a Standoff Detection Regime

Nanosecond Broadband Spectroscopy For Laser-Driven Compression Experiments

LASER-INDUCED BREAKDOWN SPECTROSCOPY INFRARED EMISSION FROM INORGANIC AND ORGANIC SUBSTANCES

LIBSlab ANALYZERS ANALYZERS

The application of spectrum standardization method for carbon analysis in coal using laser-induced breakdown spectroscopy

Laser-produced extreme ultraviolet (EUV) light source plasma for the next generation lithography application

Multi-diagnostic comparison of femtosecond and nanosecond pulsed laser plasmas

Spectroscopic Studies of Soft X-Ray Emission from Gadolinium Plasmas

Title. Author(s)Takeuchi, Masato; Sasaki, Koichi. CitationApplied physics A: Materials science & processing, 1. Issue Date Doc URL.

Laser-Induced Breakdown Spectroscopy: Application to Nuclear Waste Management Seong Yong Oh, Fang Yu Yueh, Jagdish P.

Behavior and Energy States of Photogenerated Charge Carriers

Answers to questions on exam in laser-based combustion diagnostics on March 10, 2006

DISCHARGE CHARACTERISTICS OF A LASER-ASSISTED PLASMA THRUSTER

Dynamics of carbon and tungsten colliding plumes

Highly Efficient and Anomalous Charge Transfer in van der Waals Trilayer Semiconductors

This article appeared in a journal published by Elsevier. The attached copy is furnished to the author for internal non-commercial research and

Optimization of laser-produced plasma light sources for EUV lithography

Assessment of Threshold for Nonlinear Effects in Ibsen Transmission Gratings

Mandatory Assignment 2013 INF-GEO4310

DIAGNOSTIC OF A LASER-INDUCED OPTICAL BREAKDOWN BASED ON HALF-WIDTH AT HALF AREA OF H LINES , H , AND H

Plume expansion and stoichiometry in the growth of multi-component thin films using dual-laser ablation

Spatially and temporally resolved temperature measurements of plasma generated in percussion drilling with a diode-pumped Nd:YAG laser

MAPPING OF ATOMIC NITROGEN IN SINGLE FILAMENTS OF A BARRIER DISCHARGE MEASURED BY TWO PHOTON FLUORESCENCE SPECTROSCOPY (TALIF)

dating of geological samples by laser ablation ICPMS

LASER ABLATION SYNTHESIS OF ZINC OXIDE CLUSTERS:

Femtosecond laser rapid fabrication of large-area rose-like micropatterns on freestanding flexible graphene films

Magnetic Assisted Laser Micromachining for Highly Reflective Metals

Magnetic fields applied to laser-generated plasma to enhance the ion yield acceleration

HYPER-RAYLEIGH SCATTERING AND SURFACE-ENHANCED RAMAN SCATTERING STUDIES OF PLATINUM NANOPARTICLE SUSPENSIONS

Direct measurement of spectral phase for ultrashort laser pulses

Electron Density Measurements of Argon Surface-Wave Discharges

GA A25842 STUDY OF NON-LTE SPECTRA DEPENDENCE ON TARGET MASS IN SHORT PULSE LASER EXPERIMENTS

Portable LIBS system for determining the composition of multilayer structures on objects of cultural value

Spectroscopic Diagnostics of Laser Plasma Plume of Aluminum

Growth and collapse of laser-induced bubbles in glycerol water mixtures

Transcription:

University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Faculty Publications from the Department of Electrical and Computer Engineering Electrical & Computer Engineering, Department of 1-16-2012 Optimally enhanced optical emission in laserinduced breakdown spectroscopy by combining spatial confinement and dual-pulse irradiation L. B. Guo Huazhong University of Science and Technology, University of Nebraska-Lincoln B. Y. Zhang University of Nebraska-Lincoln X. N. He University of Nebraska-Lincoln C. M. Li Huazhong University of Science and Technology, University of Nebraska-Lincoln Y. S. Zhou University of Nebraska-Lincoln See next page for additional authors Follow this and additional works at: http://digitalcommons.unl.edu/electricalengineeringfacpub Part of the Computer Engineering Commons, and the Electrical and Computer Engineering Commons Guo, L. B.; Zhang, B. Y.; He, X. N.; Li, C. M.; Zhou, Y. S.; Wu, T.; Park, J. B.; Zeng, X. Y.; and Lu, Yongfeng, "Optimally enhanced optical emission in laser-induced breakdown spectroscopy by combining spatial confinement and dual-pulse irradiation" (2012). Faculty Publications from the Department of Electrical and Computer Engineering. 232. http://digitalcommons.unl.edu/electricalengineeringfacpub/232 This Article is brought to you for free and open access by the Electrical & Computer Engineering, Department of at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Faculty Publications from the Department of Electrical and Computer Engineering by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln.

Authors L. B. Guo, B. Y. Zhang, X. N. He, C. M. Li, Y. S. Zhou, T. Wu, J. B. Park, X. Y. Zeng, and Yongfeng Lu This article is available at DigitalCommons@University of Nebraska - Lincoln: http://digitalcommons.unl.edu/ electricalengineeringfacpub/232

Optimally enhanced optical emission in laserinduced breakdown spectroscopy by combining spatial confinement and dual-pulse irradiation L. B. Guo, 1,2 B. Y. Zhang, 2 X. N. He, 2 C. M. Li, 1,2 Y. S. Zhou, 2 T. Wu, 1 J. B. Park, 2 X. Y. Zeng, 1 and Y. F. Lu 2,* 1 Wuhan National Laboratory for Optoelectronics (WNLO), College of Optoelectronics Science and Engineering, Huazhong University of Science and Technology, Wuhan, Hubei 430074, China 2 Department of Electrical Engineering, University of Nebraska-Lincoln, Lincoln, NE 68588-0511, USA *ylu2@unl.edu Abstract: In laser-induced breakdown spectroscopy (LIBS), a pair of aluminum-plate walls were used to spatially confine the plasmas produced in air by a first laser pulse (KrF excimer laser) from chromium (Cr) targets with a second laser pulse (Nd:YAG laser at 532 nm, 360 mj/pulse) introduced parallel to the sample surface to re-excite the plasmas. Optical emission enhancement was achieved by combing the spatial confinement and dual-pulse LIBS (DP-LIBS), and then optimized by adjusting the distance between the two walls and the interpulse delay time between both laser pulses. A significant enhancement factor of 168.6 for the emission intensity of the Cr lines was obtained at an excimer laser fluence of 5.6 J/cm 2 using the combined spatial confinement and DP-LIBS, as compared with an enhancement factor of 106.1 was obtained with DP-LIBS only. The enhancement mechanisms based on shock wave theory and reheating in DP- LIBS are discussed. 2012 Optical Society of America OCIS codes: (300.6365) Spectroscopy, laser induced breakdown; (350.5400) Plasmas. References and links 1. L. J. Radziemski and D. A. Cremers, Laser Induced Plasma and Applications, (Marcel Dekker, New York, 1989). 2. U. Panne, R. E. Neuhauser, M. Theisen, H. Fink, and R. Niessner, Analysis of heavy metal aerosols on filters by laser-induced plasma spectroscopy, Spectrochim. Acta, B At. Spectrosc. 56(6), 839 850 (2001). 3. L. M. Cabalín and J. J. Laserna, Surface stoichiometry of manganin coatings prepared by pulsed laser deposition as described by laser-induced breakdown spectrometry, Anal. Chem. 73(6), 1120 1125 (2001). 4. A. C. Samuels, F. C. DeLucia, Jr., K. L. McNesby, and A. W. Miziolek, Laser-induced breakdown spectroscopy of bacterial spores, molds, pollens, and protein: initial studies of discrimination potential, Appl. Opt. 42(30), 6205 6209 (2003). 5. N. J. McMillan, R. S. Harmon, F. C. De Lucia, and A. M. Miziolek, Laser-induced breakdown spectroscopy analysis of minerals: Carbonates and silicates, Spectrochim. Acta, B At. Spectrosc. 62B(12), 1528 1536 (2007). 6. F. C. De Lucia, Jr., J. L. Gottfried, and A. W. Miziolek, Evaluation of femtosecond laser-induced breakdown spectroscopy for explosive residue detection, Opt. Express 17(2), 419 425 (2009). 7. F. Hilbk-Kortenbruck, R. Noll, P. Wintjens, H. Falk, and C. Becker, Analysis of heavy metals in soils using laser-induced breakdown spectrometry combined with laser-induced fluorescence, Spectrochim. Acta, B At. Spectrosc. 56(6), 933 945 (2001). 8. R. Noll, H. Bette, A. Brysch, M. Kraushaar, I. Mönch, L. Peter, and V. Sturm, Laser-induced breakdown spectrometry applications for production control and quality assurance in the steel industry, Spectrochim. Acta, B At. Spectrosc. 56(6), 637 649 (2001). 9. X. K. Shen, J. Sun, H. Ling, and Y. F. Lu, Spatial confinement effects in laser-induced breakdown spectroscopy, Appl. Phys. Lett. 91(8), 081501 (2007). 10. J. Gruber, J. Heitz, H. Strasser, D. Bäuerle, and N. Ramaseder, Rapid in-situ analysis of liquid steel by laserinduced breakdown spectroscopy, Spectrochim. Acta, B At. Spectrosc. 56(6), 685 693 (2001). 11. R. E. Neuhauser, U. Panne, and R. Niessner, Laser-induced plasma spectroscopy (LIPS): a versatile tool for monitoring heavy metal aerosols, Anal. Chim. Acta 392(1), 47 54 (1999). 12. B. J. Marquardt, B. M. Cullum, T. J. Shaw, and S. M. Angel, Fiber optic probe for determining heavy metals in solids based on laser-induced plasmas, Proc. SPIE 3105, 203 212 (1997). (C) 2012 OSA 16 January 2012 / Vol. 20, No. 2 / OPTICS EXPRESS 1436

13. C. M. Davies, H. H. Telle, and A. W. Williams, Remote in situ analytical spectroscopy and its applications in the nuclear industry, Anal. Bioanal. Chem. 355(7-8), 895 899 (1996). 14. K. Y. Yamamoto, D. A. Cremers, M. J. Ferris, and L. E. Foster, Detection of metals in the environment using a portable laser-induced breakdown spectroscopy instrument, Appl. Spectrosc. 50(2), 222 233 (1996). 15. D. Anglos, Laser-induced breakdown spectroscopy in art and archaeology, Appl. Spectrosc. 55(6), 186A 205A (2001). 16. M. Corsi, G. Cristoforetti, M. Hidalgo, S. Legnaioli, V. Palleschi, A. Salvetti, E. Tognoni, and C. Vallebona, Application of laser-induced breakdown spectroscopy technique to hair tissue mineral analysis, Appl. Opt. 42(30), 6133 6137 (2003). 17. A. K. Knight, N. L. Scherbarth, D. A. Cremers, and M. J. Ferris, Characterization of laser-induced breakdown spectroscopy (LIBS) for application to space exploration, Appl. Spectrosc. 54(3), 331 340 (2000). 18. J. Scaffidi, W. Pearman, J. C. Carter, and S. M. Angel, Observations in collinear femtosecond-nanosecond dualpulse laser-induced breakdown spectroscopy, Appl. Spectrosc. 60(1), 65 71 (2006). 19. J. Scaffidi, J. Pender, W. Pearman, S. R. Goode, B. W. Colston, Jr., J. C. Carter, and S. M. Angel, Dual-pulse laser-induced breakdown spectroscopy with combinations of femtosecond and nanosecond laser pulses, Appl. Opt. 42(30), 6099 6106 (2003). 20. R. E. Russo, X. L. Mao, J. J. Gonzalez, and S. S. Mao, Femtosecond laser ablation ICR-MS, J. Anal. At. Spectrom. 17(9), 1072 1075 (2002). 21. X. K. Shen, H. Wang, Z. Q. Xie, Y. Gao, H. Ling, and Y. F. Lu, Detection of trace phosphorus in steel using laser-induced breakdown spectroscopy combined with laser-induced fluorescence, Appl. Opt. 48(13), 2551 2558 (2009). 22. X. N. He, W. Hu, C. M. Li, L. B. Guo, and Y. F. Lu, Generation of high-temperature and low-density plasmas for improved spectral resolutions in laser-induced breakdown spectroscopy, Opt. Express 19(11), 10997 11006 (2011). 23. A. M. Popov, F. Colao, and R. Fantoni, Enhancement of LIBS signal by spatially confining the laser-induced plasma, J. Anal. At. Spectrom. 24(5), 602 604 (2009). 24. A. M. Popov, F. Colao, and R. Fantoni, Spatial confinement of laser-induced plasma to enhance LIBS sensitivity for trace elements determination in soils, J. Anal. At. Spectrom. 25(6), 837 848 (2010). 25. L. B. Guo, C. M. Li, W. Hu, Y. S. Zhou, B. Y. Zhang, Z. X. Cai, X. Y. Zeng, and Y. F. Lu, Plasma confinement by hemispherical cavity in laser-induced breakdown spectroscopy, Appl. Phys. Lett. 98(13), 131501 (2011). 26. S. Singha, Z. Hu, and R. J. Gordon, Ablation and plasma emission produced by dual femtosecond laser pulses, J. Appl. Phys. 104(11), 113520 (2008). 27. J. Uebbing, J. Brust, W. Sdorra, F. Leis, and K. Niemax, Reheating of a laser-produced plasma by a second pulse laser, Appl. Spectrosc. 45(9), 1419 1423 (1991). 28. A. De Giacomo, M. Dell Aglio, O. De Pascale, and M. Capitelli, From single pulse to double pulse ns-laserinduced breakdown spectroscopy under water: elemental analysis of aqueous solutions and submerged solid samples, Spectrochim. Acta, B At. Spectrosc. 62(8), 721 738 (2007). 29. X. K. Shen, J. Sun, H. Ling, and Y. F. Lu, Spectroscopic study of laser-induced Al plasmas with cylindrical confinement, J. Appl. Phys. 102(9), 093301 (2007). 30. L. B. Guo, W. Hu, B. Y. Zhang, X. N. He, C. M. Li, Y. S. Zhou, Z. X. Cai, X. Y. Zeng, and Y. F. Lu, Enhancement of optical emission from laser-induced plasmas by combined spatial and magnetic confinement, Opt. Express 19(15), 14067 14075 (2011). 31. D. K. Killinger, S. D. Allen, R. D. Waterbury, C. Stefano, and E. L. Dottery, Enhancement of Nd:YAG LIBS emission of a remote target using a simultaneous CO( 2) laser pulse, Opt. Express 15(20), 12905 12915 (2007). 32. F. F. Chen, Introduction to Plasma Physics, (Plenum, New York, 1974). 1. Introduction Over the last few decades, laser-induced breakdown spectroscopy (LIBS) has been demonstrated as a promising and useful element analysis technique [1 8]. By focusing a powerful pulsed laser beam onto a sample surface, a hot luminous spark, forming a plasma, is generated, emission from the plasma used to identify and quantify within the sample. LIBS offers a simple and fast method of elemental analysis. The ability to form a plasma on unprocessed samples makes LIBS an amazingly versatile diagnostic tool [9 11]. It is one of the few techniques that can be used for non-contact elemental analysis, making LIBS uniquely suited to measurements of hazardous materials and materials in difficult-to-reach locations [12,13]. In recent years, LIBS has been successfully applied in many areas such as civilian and military environmental monitoring, cultural heritage analysis and characterization, biological and medical identification, and even space exploration [14 17]. Despite its obvious advantages, one of the major shortcomings of LIBS is its low detection sensitivity. Continuous studies have been made to improve the sensitivity of LIBS. These studies have led to investigations such as dual-pulse excitation and various plasma confinements [18 25]. The methods mentioned above have improved the detection sensitivity in LIBS though individual enhancement approaches. Further improvement of LIBS sensitivity will rely on (C) 2012 OSA 16 January 2012 / Vol. 20, No. 2 / OPTICS EXPRESS 1437

combination of these approaches. For example, dual-pulse LIBS (DP-LIBS) can be combined with spatial confinement of plasmas to effectively improve the sensitivity of LIBS. In DP- LIBS using orthogonal geometry, the first pulse is introduced onto the sample surface and the second pulse is focused parallel to the surface to reheat the plasma ablated by the first pulse. An increase in optical emission from the re-excited plasma can be observed [26 28]. At the same time, along with the generation and expansion of the laser-induced plasma in air by the first pulse, a shock wave is produced. The shock wave will be reflected back when it encounters some obstacles to compress the plasma plume [29]. The collision rate among the particles will be increased within the compressed plasma, resulting in an increase in the number of atoms at high-energy states, and hence, enhancing the emission intensity. Either dual-pulse excitation or plasma confinement was employed separately in previous studies. For instance, we [30] studied the enhancement of optical emission plasmas confined with the combination of spatial and magnetic confinements, resulting in a maximum enhancement factor of only 24 for pure metallic Cr sample. Killinger et al. [31] reported the enhancement of plasmas using a simultaneous CO 2 laser pulse, resulting in an increase of 60x for the Al atomic lines at 308 nm. In this study, our aim was to further improve the enhancement effects by the spatial confinement and dual-pulse in LIBS. Laser-induced plasmas with shock waves were produced and confined between a pair of parallel walls. The plasma plumes in LIBS were also investigated to study the evolution of the plasmas. 2. Experimental methods 2.1 Experiment setup Fig. 1. Schematic diagram of the experiment setup. The schematic diagram of the experimental setup of the spatially confined DP-LIBS is shown in Fig. 1. The experiments were performed in ambient air. A KrF excimer laser (Lambda Physik, Compex 205, wavelength: 248 nm, pulse duration: 23 ns) was used for the first laser pulse to generate plasmas. The laser beam was reflected both by a reflector (Reflector 1) and a dichroic mirror, respectively. The dichroic mirror is reflective to the laser beam but transparent to the other wavelengths studied. The laser beam was then focused onto a chromium (Cr) sample, which was sandwiched by a pair of aluminum (Al) parallel walls, by an UV-grade quartz lens (L1) of 15 cm focal length. The laser beam was slightly focused to a spot size of about 2.6 0.5 mm 2 to reach a laser fluence of 5.6 J/cm 2. Plasma plumes with a size of several millimeters were generated between the walls. A Q-switched Nd:YAG laser operating at 532 nm (Continuum, Powerlite Precision II 8010, pulse duration of 6 ns) with a (C) 2012 OSA 16 January 2012 / Vol. 20, No. 2 / OPTICS EXPRESS 1438

pulse energy of 360 mj/pulse was introduced in parallel to the sample surfaces to reheat the plasmas generated by the first pulse. Both lasers were synchronized by a digital delay generator (Stanford Research System DG535, 5 ps delay resolution). The pulse repetition rate was set to 10 Hz. The Nd:YAG laser was focused by a convex lens (Lens 3 with f/10 cm focal length). The spatial position of the second pulse was adjusted by the Reflector 2 and Lens 3. The Nd:YAG laser was focused to a spot with a diameter of about 1 mm, around 2 mm above the sample surfaces. To avoid over ablation, the Cr target was mounted on a motorized translation stage, so that a new surface was exposed at each shot. 2.2 Spectral measurements The optical emission from plasmas was coupled to an optical fiber by Lens 1 and another UVgrade quartz lens (Lens 2 with f/6 cm focal length). The optical fiber, with a core diameter of 100 μm, was coupled to a spectrometer (Andor Tech., Shamrock 303i) with three gratings of 150, 600, and 2400 lines/mm. The grating of 2400 lines/mm, with a spectral resolution of 0.04 nm at 435 nm, was used in this study. A 512 512 pixel intensified charge-coupled device (ICCD) (Andor Tech., istar, DH-712) was attached to the exit focal plane of the spectrometer. The gate delay and width of the ICCD was adjusted so that the spectra at different time delays after the laser pulse can be obtained. Plasma reheating with different interpulse delays was studied to obtain the optimal enhancement. The spectrometer started to acquire spectra at 3 μs after the first-pulse plasma. For all experiments, the excimer laser was fired first to produce a plasma. The Nd:YAG laser at 532 nm was fired second for plasma reheating. The purity of the Cr targets is 99.95%. Fig. 2. Time-integrated spectra from Cr targets with combined walls and dual pulse (solid curve), with dual-pulse laser (short dashed curve) and with excimer laser only (short dotted curve). Excimer laser fluence: 5.6 J/cm 2 ; Nd:YAG laser pulse energy: 360 mj/pulse. 3. Results and discussion 3.1 Time-integrated OES from the pure Cr targets The time-integrated emission spectra of the laser-induced Cr plasmas in a spectral range of 419-432 nm were recorded with the presence of the walls in the DP-LIBS, (solid curves), DP- LIBS only (dashed curves), and excimer laser only (dotted curves), as shown in Fig. 2. The distance between the two flat walls was 13 mm. All the spectra were averaged over 30 shots to reduce the standard deviation. The time delay between the excimer laser and Nd:YAG laser was 0 μs. The gate delay and width of the ICCD detector was 3 and 30 μs, respectively. The emission intensities for the Cr atomic lines (425.44, 427.48, and 428.97 nm) were all (C) 2012 OSA 16 January 2012 / Vol. 20, No. 2 / OPTICS EXPRESS 1439

obviously enhanced in the DP-LIBS with and without the presence of the walls, comparing to the excimer laser only. Enhancement factors of about 8 and 6 were obtained in the DP-LIBS with and without the walls. This clearly shows the difference cases with and without the walls in the DP-LIBS. The transition configuration for the three Cr atomic lines is 3d 5 ( 6 S)4s - 3d 5 ( 6 S)4p, where the 3d 5 ( 6 S)4s is the ground state of the Cr atom. Fig. 3. Emission intensity of Cr atomic lines (425.44 nm) as a function of time delay, using both dual-pulse and walls (square dots and solid curve), using dual-pulse (circle dots and short dashed curve) and excimer only (triangle dots and short dotted curve), at excimer laser fluence of 5.6 J/cm 2, Nd:YAG laser: 360 mj/pulse. 3.2 Temporal evolution of emission intensities for Cr atomic lines from the pure Cr target A better understanding of the process of plasma emission enhancement with walls in the DP- LIBS was obtained. Figure 3 shows the temporal evolution of the emission intensities of the Cr atomic line (425.44 nm) in DP-LIBS with the walls (square dots and solid curve), DP- LIBS without the walls (circle dots and short dashed curve), and LIBS using excimer laser only (triangle dots and short dotted). The time delay between the excimer laser and Nd:YAG laser was 9 μs. The ICCD started to acquire spectra from 3 μs after the first laser pulse and ended at 63 μs, with a gate width of 2 μs and a step of 2 μs. There were two significant enhancement peaks in the DP-LIBS with the walls. The two peaks occurred during the time periods from 7 to 17 μs and from 19 to 47 μs, while only one peak occurred from 7 to 17 μs in under DP-LIBS without the walls for comparison. The first peak was due to the enhancement by the reheating of Nd:YAG laser, whereas the second enhancement peak was due to the spatial confinement of the plasmas. Dual-pulse enhancement factors of about 12 (with aluminum walls) and 10 (without aluminum walls) have been acquired in DP-LIBS. (C) 2012 OSA 16 January 2012 / Vol. 20, No. 2 / OPTICS EXPRESS 1440

Fig. 4. Emission intensity for Cr atomic lines (All with 425.44 nm) as a function of time delay. The distance between the walls are 11 mm, 13 mm, 15 mm, and 17 mm, at excimer laser fluence of 5.6 J/cm 2, Nd:YAG laser: 360 mj/pulse. 3.3 The optimization of the distance between the plate-walls To optimize the distance between the two walls in the DP-LIBS, Fig. 4 shows the evolutions of the emission intensity as a function of the time delay with different wall distances of 11 (square dots and curve), 13 (circle dots and curve), 15 (pentagon dots and curve), and 17 mm (triangle dots and curve), respectively. The intensity of LIBS using excimer laser only (diamond dots and curve) was also plotted for comparison. It is observed that the emission intensities were all enhanced although the enhancement factor depends on the wall distance. The maximum enhancement factor of the second peak decreased with a longer time delay as the wall distance increased. This is because the energy of the shock wave dissipates quickly with distance, and the traveling time increases as the wall distance increases. The best distance between the two flat walls is 11 mm. 3.4 The optimization of the interpulse delay time between the excimer laser and Nd:YAG laser After the optimization of the wall distance, the time delay between the excimer laser and Nd:YAG laser pulses was adjusted to further optimize the enhancement effects. Figure 5(a) shows the temporal evolution of DP-LIBS spectra with walls with an interpulse delay of 17 μs. The first spectrum was acquired with a delay of 3 μs after the first pulse and a gate width of 2 μs, and the following spectra were acquired with an increment of 2 μs. In Figs. 5(b) - 5(d), time-integrated LIBS spectra of Cr lines from reheating were compared with the firstpulse LIBS spectra to show the enhancement with different interpulse delays. As indicated in Figs. 5(b) - 5(d), after reheating of the plasmas, the intensity of LIBS spectra of Cr lines increased significantly compared with first-pulse LIBS spectra. Time-integrated LIBS spectra from the plasma of the Cr targets were acquired under first-pulse only condition [3 μs after plasma generation (dashed lines)] and with reheating [2 μs after second pulse (solid lines)] at different interpulse delays: Figs. 5(b) 17, (c) 25, and (d) 33 μs. It is shown that the strongest emission intensity of the Cr atomic lines appeared with an interpulse delay of 25 μs, significantly higher than shorter or longer interpulse delays. (C) 2012 OSA 16 January 2012 / Vol. 20, No. 2 / OPTICS EXPRESS 1441

Fig. 5. (a) Temporal evolution of DP-LIBS spectra with 50 μs interpulse delay; time-integrated LIBS spectra of plasmas from a Cr target under first-pulse only condition [3 μs after plasma generation (dashed lines)] and with reablation [2 μs after second pulse (solid lines)] at different interpulse delays of (b) 17, (c) 25, and (d) 33 μs. At excimer laser fluence of 5.6 J/cm 2, Nd:YAG laser: 360 J/pulse. Table 1. The enhancement factors of emission intensity for Cr atomic lines (425.44 nm) in the DP-LIBS with and without walls Experiments Interpulse delay: (μs). ICCD gate delay: (μs). Start to acquire from the second pulse. ICCD gate width: (μs). Enhancement factor VS. Excimer laser only DP-LIBS only 25 2 2 106.1 DP-LIBS with walls 25 2 2 168.6 Therefore, the optimized interpulse delay time for DP-LIBS with confining walls is 25 μs. under the best interpulse delay of 25 μs, as is shown in Table 1, the Cr line (425.44 nm) recorded by the spectrometer were acquired from 2 μs after the second-pulse plasma and with a gate width of 2 μs, the enhancement factor reached 168.6 when adding walls in DP-LIBS, while the enhancement factor was 106.1 only in DP-LIBS without confining walls. The reason can be explained by the combination of both spatial confinement of plasmas and dual-pulse reheating. When the plasma is generated by the first laser, the drastically increased pressure around the plasma induces a localized shock wave. The shock wave usually spreads out at a speed higher than the ordinary sound wave. When it reaches the walls, the shock wave is reflected by the parallel walls and travels back to the plasma center. Thus, the plasma is confined to a smaller size with increased emission intensity [32]. At the same time, the second laser pulse enters to reheat the plasma which is confined by the shock wave. As a result, the confined plasma is re-excited by the second laser pulse, leading to an increased number of excited atoms within the plasma, and consequently, temperature at the center of the plasma (C) 2012 OSA 16 January 2012 / Vol. 20, No. 2 / OPTICS EXPRESS 1442

increases. Therefore, the LIBS spectra of the Cr plasmas with combined spatial confinement of plasmas and dual-pulse LIBS can be further enhanced, resulting in a high sensitivity. 4. Conclusions In summary, the enhancement effects of optical emission in DP-LIBS with spatial confinement was studied. The significant enhancements in the atomic lines from Cr plasmas were observed. By the optimization of the distance between two Al walls and the interpulse delay time, the maximum enhancement factor for Cr atomic lines reached 168.6, as compared with an enhancement factor of 106.1 for DP-LIBS without Al walls. It is obvious that the combined enhancement effects of confinement walls and dual-pulse in LIBS is much stronger than that of DP-LIBS only. The results of this study provide a new pathway in improving the sensitivity of LIBS. Acknowledgment This research work was financially supported by National Natural Science Foundation China (grant number 51128501) and National Science Foundation (CMMI 0900419 and CMMI 1126208). (C) 2012 OSA 16 January 2012 / Vol. 20, No. 2 / OPTICS EXPRESS 1443