Measurement error due to self-absorption in calibration-free laser-induced breakdown spectroscopy

被引:19
|
作者
Taleb, Aya [1 ,2 ]
Motto-Ros, Vincent [3 ]
Carru, Mauro J. [1 ]
Axente, Emanuel [4 ]
Craciun, Valentin [4 ]
Pelascini, Frederic [2 ]
Hermann, Jorg [1 ]
机构
[1] Aix Marseille Univ, CNRS, LP3, F-13288 Marseille, France
[2] Cetim Grand Est, F-67400 Illkirch Graffenstaden, France
[3] Univ Lyon 1, CNRS, Inst Lumiere Matiere, F-69622 Villeurbanne, France
[4] Natl Inst Laser Plasma & Radiat Phys, Magurele 77125, Romania
基金
欧盟地平线“2020”;
关键词
Elemental analysis; Laser-induced breakdown spectroscopy; Calibration-free; Self-absorption; Error evaluation; INDUCED PLASMA; GROWTH;
D O I
10.1016/j.aca.2021.339070
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Self-absorption of spectral lines is known to lower the performance of analytical measurements via calibration-free laser-induced breakdown spectroscopy. However, the error growth due to this effect is not clearly assessed. Here we propose a method to quantify the measurement error due to self-absorption based on the calculation of the spectral radiance of a plasma in local thermodynamic equilibrium. Validated through spectroscopic measurements for a binary alloy thin film of compositional gradient, the method evidences that measurement performance lowering due to self-absorption depends on the spectral shape of the analytical transition and on the intensity measurement method. Thus, line-integrated intensity measurements of Stark broadened lines enable accurate analysis, even at large optical thickness, if line width and plasma size are precisely known. The error growth due to self-absorption is significantly larger for line shapes dominated by Doppler broadening and for line-center intensity measurements. The findings present a significant advance in compositional measurements via calibration-free laser-induced breakdown spectroscopy, as they enable straightforward selection of most appropriate analytical lines. (c) 2021 Elsevier B.V. All rights reserved.
引用
收藏
页数:7
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