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Vibrational emission analysis of the CN molecules in laser-induced breakdown spectroscopy of organic compounds
Affiliation:1. State Key Lab of Electrical Insulation and Power Equipment, Xi''an Jiaotong University, Xi''an 710049, PR China;2. BAM Federal Institute for Materials Research and Testing, Richard-Willstätter-Straße 11, Berlin 12489, Germany;1. The University of Tennessee/University of Tennessee Space Institute, Center for Laser Applications, 411 B.H. Goethert Parkway, Tullahoma, TN 37388-9700, USA;2. Hornkohl Consulting, Tullahoma, TN 37388, USA;1. Homi Bhabha National Institute, Indira Gandhi Centre for Atomic Research, Kalpakkam 603102, India;2. Materials Chemistry & Metal Fuel Cycle Group, Indira Gandhi Centre for Atomic Research, Kalpakkam 603102, India;3. Raja Ramanna Fellow, Indira Gandhi Centre for Atomic Research, Kalpakkam 603102, India
Abstract:Laser-induced breakdown spectroscopy (LIBS) of organic materials is based on the analysis of atomic and ionic emission lines and on a few molecular bands, the most important being the CN violet system and the C2 Swan system. This paper is focused in molecular emission of LIBS plasmas based on the CN (B2Σ–X2Σ) band, one of the strongest emissions appearing in all carbon materials when analyzed in air atmosphere. An analysis of this band with sufficient spectral resolution provides a great deal of information on the molecule, which has revealed that valuable information can be obtained from the plume chemistry and dynamics affecting the excitation mechanisms of the molecules. The vibrational emission of this molecular band has been investigated to establish the dependence of this emission on the molecular structure of the materials. The paper shows that excitation/emission phenomena of molecular species observed in the plume depend strongly on the time interval selected and on the irradiance deposited on the sample surface. Precise time resolved LIBS measurements are needed for the observation of distinctive CN emission. For the organic compounds studied, larger differences in the behavior of the vibrational emission occur at early stages after plasma ignition. Since molecular emission is generally more complex than that involving atomic emission, local plasma conditions as well as plume chemistry may induce changes in vibrational emission of molecules. As a consequence, alterations in the distribution of the emissions occur in terms of relative intensities, being sensitive to the molecular structure of every single material.
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