This study employs machine learning to predict emissions of reactive chemical species in plasma systems, suggesting enhanced diagnostic methods.
In this study, an Ar-multi-NTAPPJ system was designed and fabricated to explore its scalability for large-volume processing. Optical emission spectroscopy (OES) measurements were conducted as a function of various operating parameters, including gas flow rate, voltage, duty cycle, and air mixture. The measurements revealed strong emissions from Ar I, originating from fine-structure transitions among the 3p 5 4p → 3p 5 4s levels within the 690-810 nm wavelength range. Additionally, significant emissions were observed from the OH rotational band (A 2 Σ + → X 2 Π) at 309 nm, the N 2 second positive system (C 3 Π u → B 3 Π g ) between 330 nm and 380 nm, and atomic oxygen (2s 2 2p 3 ( 4 S 0 )3p 5 P → 2s 2 2p 3 ( 4 S 0 )3s 5 S 0 ) at 777.5 nm, providing valuable insights into reactive chemical species (RCS) formation. To analyze the influence of operating conditions on these emissions and their impact on reactive species production, a data-driven machine learning (ML) approach was employed, leveraging a combination of dimensionality reduction and supervised learning. Principal component analysis (PCA) was first applied to reduce data dimensionality, enhancing computational efficiency while preserving essential spectral features. Subsequently, two supervised ML models, Random Forest (RF) and Deep Neural Networks (DNN), were trained to map input conditions to predicted emission intensities. To further exploit the predictive capability of these models, a differential evolution optimization strategy was implemented to estimate the optimal combinations of input parameters that maximize specific spectral features, particularly OH(A-X) emission. This study contributes to the development of more efficient and accelerated plasma diagnostic approaches, with the potential for real-time predictions.
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Srikar et al. (2025) studied this question.
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