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Optimal emission enhancement in orthogonal double-pulse laser-induced breakdown spectroscopy

  • R. Sanginés
  • , V. Contreras
  • , H. Sobral*
  • , A. Robledo-Martinez
  • *Corresponding author for this work

    Research output: Contribution to journalArticleScientificpeer-review

    23 Citations (Scopus)

    Abstract

    Abstract Orthogonal double-pulse (DP) laser-induced breakdown spectroscopy (LIBS) was performed using reheating and pre-ablative configurations. The ablation pulse power density was varied by two orders of magnitude and the DP experiments were carried out for a wide range of interpulse delays. For both DP-LIBS schemes, the signal enhancement was evaluated with respect to the corresponding single-pulse (SP) LIBS as a function of the interpulse delay. The reheating scheme shows a sharp maximum signal enhancement of up to 200-fold for low ablative power densities (0.4 GW cm<sup>- 2</sup>); however, for power densities larger than 10 GW cm<sup>- 2</sup> this configuration did not improve the SP outcome. On the other hand, a more uniform signal enhancement of about 4-6 was obtained for the pre-ablative scheme nearly independently of the used ablative power density. In terms of the signal-to-noise ratio (SNR) the pre-ablative scheme shows a monotonic increment with the ablative power density. Whereas the reheating configuration reaches a maximum at 2.2 GW cm<sup>- 2</sup>, its enhancement effect collapses markedly for fluencies above 10 GW cm<sup>- 2</sup>.

    Original languageEnglish
    Article number4935
    Pages (from-to)139-145
    Number of pages7
    JournalSpectrochimica Acta - Part B Atomic Spectroscopy
    Volume110
    DOIs
    Publication statusPublished - 6 Jul 2015
    Publication typeA1 Journal article-refereed

    Keywords

    • Double-pulse
    • Emission enhancement
    • LIBS

    Publication forum classification

    • Publication forum level 1

    ASJC Scopus subject areas

    • Instrumentation
    • Atomic and Molecular Physics, and Optics
    • Analytical Chemistry
    • Spectroscopy

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