4.5 Article

Cepstral analysis for baseline-insensitive absorption spectroscopy using light sources with pronounced intensity variations

Journal

APPLIED OPTICS
Volume 59, Issue 26, Pages 7865-7875

Publisher

OPTICAL SOC AMER
DOI: 10.1364/AO.399405

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Funding

  1. Air Force Research Laboratory [FA930019-P-1506]
  2. Air Force Office of Scientific Research [FA9550-17-1-0224]
  3. National Science Foundation [1842166DGE]
  4. National Aeronautics and Space Administration [PLANET18R-0018]

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This paper presents a data-processing technique that improves the accuracy and precision of absorption-spectroscopy measurements by isolating the molecular absorbance signal from errors in the baseline light intensity (I-o) using cepstral analysis. Recently, cepstral analysis has been used with traditional absorption spectrometers to create a modified form of the time-domain molecular free-induction decay (m-FID) signal, which can be analyzed independently from I-o. However, independent analysis of the molecular signature is not possible when the baseline intensity and molecular response do not separate well in the time domain, which is typical when using injection-current-tuned lasers [e.g., tunable diode and quantum cascade lasers (QCLs)] and other light sources with pronounced intensity tuning. In contrast, the method presented here is applicable to virtually all light sources since it determines gas properties by least-squares fitting a simulated m-FID signal (comprising an estimated Io and simulated absorbance spectrum) to the measured m-FID signal in the time domain. This method is insensitive to errors in the estimated Io, which vary slowly with optical frequency and, therefore, decay rapidly in the time domain. The benefits provided by this method are demonstrated via scanned-wavelength direct-absorption-spectroscopy measurements acquired with a distributed-feedback (DFB) QCL. The wavelength of a DFB QCL was scanned across the CO P(0,20) and P(1,14) absorption transitions at 1 kHz to measure the gas temperature and concentration of CO. Measurements were acquired in a gas cell and in a laminar ethylene-air diffusion flame at 1 atm. The measured spectra were processed using the new m-FID-based method and two traditional methods, which rely on inferring (instead of rejecting) the baseline error within the spectral-fitting routine. The m-FID-based method demonstrated superior accuracy in all cases and a measurement precision that was approximate to 1.5 to 10 times smaller than that provided using traditional methods. (C) 2020 Optical Society of America

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