Automated Full-Spectrum Multivariate Calibration for Quantitative Glow Discharge Optical Emission Spectrometry

Glow discharge optical emission spectrometry (GD-OES) enables rapid bulk and depthresolved multi-elemental analysis of solid materials with minimal sample preparation. Conventional quantification, however, relies on preselected analyte emission lines and, if sputtering-rate variations must be compensated, on matrix reference lines or sputtering-rate correction, requiring matrix composition or sputtering rates as input. Modern CCD-based instruments simultaneously record broadband spectra containing thousands of spectral variables, yet most of this information remains unused in conventional calibration based on a few selected lines. Here, we investigate a full-spectrum calibration strategy based on Variable Importance in Projection-selected Partial Least Squares (VIP-PLS) regression for the quantitative determination of individual alloying elements. Al-Si and Cu-Zn alloys were selected as metallurgically and spectrochemically distinct model systems, with Si and Zn as target analytes, respectively. The VIP-PLS models predicted Si and Zn with Root Mean Square Error of Cross-Validation (RMSECV) values of 0.38 wt% and 0.50 wt%, compared with 1.05 wt% and 1.41 wt% for univariate calibration of a single preselected line, and 0.24 wt% and 0.63 wt% for normalized ratio-based calibration using a reference line and the matrix mass fraction. VIP-PLS thus achieved performance comparable to the ratio-based calibration, implicitly compensating for sample-specific intensity variations, such as the sputtering rate, without matrix composition as input and without manual line selection. Time-resolved evaluation further showed that model performance reflects the transient and steady-state stages of the glow discharge, while VIP analysis revealed which spectral features contribute most strongly to the calibration and how they evolve during sputtering. Full-spectrum multivariate calibration therefore provides an automated, spectrum-driven and interpretable route for matrix-specific quantitative GD-OES that exploits information already contained in broadband measurements.

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Publication Details

Journal
ChemRxiv
Published
2026-10-29
DOI
https://doi.org/10.26434/chemrxiv.15011268/v1
Primary Topic
Laser-induced spectroscopy and plasma
Type
preprint
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preprint

Automated Full-Spectrum Multivariate Calibration for Quantitative Glow Discharge Optical Emission Spectrometry

Marius R. Bittermann, Sebastian Recknagel, Silke Richter, Volker Hoffmann et al.
1 links
ChemRxiv
Laser-induced spectroscopy and plasma
preprint

Automated Full-Spectrum Multivariate Calibration for Quantitative Glow Discharge Optical Emission Spectrometry

Marius R. Bittermann, Sebastian Recknagel, Silke Richter, Volker Hoffmann, Jens Riedel, Beatrice Battistella, Carlos Abad
preprint en

Abstract

Glow discharge optical emission spectrometry (GD-OES) enables rapid bulk and depthresolved multi-elemental analysis of solid materials with minimal sample preparation. Conventional quantification, however, relies on preselected analyte emission lines and, if sputtering-rate variations must be compensated, on matrix reference lines or sputtering-rate correction, requiring matrix composition or sputtering rates as input. Modern CCD-based instruments simultaneously record broadband spectra containing thousands of spectral variables, yet most of this information remains unused in conventional calibration based on a few selected lines. Here, we investigate a full-spectrum calibration strategy based on Variable Importance in Projection-selected Partial Least Squares (VIP-PLS) regression for the quantitative determination of individual alloying elements. Al-Si and Cu-Zn alloys were selected as metallurgically and spectrochemically distinct model systems, with Si and Zn as target analytes, respectively. The VIP-PLS models predicted Si and Zn with Root Mean Square Error of Cross-Validation (RMSECV) values of 0.38 wt% and 0.50 wt%, compared with 1.05 wt% and 1.41 wt% for univariate calibration of a single preselected line, and 0.24 wt% and 0.63 wt% for normalized ratio-based calibration using a reference line and the matrix mass fraction. VIP-PLS thus achieved performance comparable to the ratio-based calibration, implicitly compensating for sample-specific intensity variations, such as the sputtering rate, without matrix composition as input and without manual line selection. Time-resolved evaluation further showed that model performance reflects the transient and steady-state stages of the glow discharge, while VIP analysis revealed which spectral features contribute most strongly to the calibration and how they evolve during sputtering. Full-spectrum multivariate calibration therefore provides an automated, spectrum-driven and interpretable route for matrix-specific quantitative GD-OES that exploits information already contained in broadband measurements.

ChemRxiv
Federal Institute For Materials Research and Testing (DE), Leibniz Institute for Solid State and Materials Research (DE), Brandenburg University of Technology Cottbus-Senftenberg (DE)
Laser-induced spectroscopy and plasma
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