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Christian Pellerin

Publications and source records attributed to Christian Pellerin.

4 recordsLinked to original sources

New developments in planar array infrared spectroscopy.

A planar array infrared (PA-IR) spectrograph offers several advantages over other infrared approaches, including high acquisition rate and sensitivity. However, it suffers from some important drawbacks, such as a limited spectral range and a significant curvature of the recorded spectral images, which still need to be addressed. In this article, we present new developments in PA-IR spectroscopy that overcome these drawbacks. First, a data processing method for the correction of the curvature observed in the spectral images has been developed and refined. In addition, a dual-beam instrument that allows the simultaneous recording of two independent spectral images has been developed. These two improvements have been combined to demonstrate the real-time background correction capability of PA-IR instruments. Finally, the accessible spectral range of the PA-IR spectrograph has been extended to cover simultaneously the methylene stretching (3200-2800 cm(-1)) and the finger-print (2000-1000 cm(-1)) spectral regions.

Algorithms↗

Acquisition of mid-infrared spectra from nonrepeatable events with sub-100-micros temporal resolution using planar array infrared spectroscopy.

A novel method is presented that is capable of collecting time-resolved vibrational spectroscopic information with sub-100-micros temporal resolution. Unlike previous step scan FT-IR approaches, the phenomena under study do not necessarily need to be repeatable. The methodology described herein is based on the planar array infrared (PA-IR) technique, which utilizes a spectrograph for wavelength dispersion and a mid-infrared focal plane array (FPA) detector for simultaneous detection of multiple wavelengths. Unlike previous PA-IR approaches, a rolling mode FPA is employed. This unique data readout mode, where data are read out of the array two rows at a time, is exploited to generate increased temporal resolution. The capabilities of this technique are demonstrated using the example of the electric field-induced Freedericksz transition of a nematic liquid crystal. It is shown that the orientational dynamics of a single transition can be tracked over a spectral range of 154 cm(-)(1) with a temporal resolution of 99.17 micros while requiring a total experimental time of less than 1 s.

Journal Article↗

A faster approach to infrared rheo-optics using a planar array infrared spectrograph.

Infrared rheo-optics combines dynamic mechanical analysis with infrared spectroscopy to provide molecular level information about the segmental reorientation and the changes in local environment associated with the dynamic deformation of polymers. Up to now, the application of this technique has been limited by the amount of time necessary to perform the experiments. In this article, we demonstrate that the use of a planar array infrared (PA-IR) spectrograph can accelerate the acquisition time by as much as two orders of magnitude while maintaining a signal-to-noise ratio (SNR) similar to that obtained using step-scan Fourier transform infrared (FT-IR) spectrometry, and by more than three orders of magnitude at the expense of a reduced SNR. The advantages and drawbacks of this new technique are discussed.

Elasticity↗

Performance and application of a new planar array infrared spectrograph operating in the mid-infrared (2000-975 cm(-1)) fingerprint region.

A no-moving-part planar array infrared spectrograph (PA-IR) equipped with a 256 x 256 mercury cadmium telluride (MCT) focal plane array has been designed and constructed. The performance of the instrument, whose frequency range extends from 2000-975 cm(-1), has been assessed in terms of resolution, bandwidth, and signal-to-noise ratio. The PA-IR spectrograph is able to record spectra with an 8.7 ms time resolution and has peak-to-peak noise levels as low as 2.4 x 10(-4) A.U. As a demonstration of the potential of PA-IR, the dynamics of reorientation of a liquid crystalline sample exposed to a single electric field pulse has been studied. It was shown that PA-IR can be used for the simultaneous acquisition of two orthogonally polarized spectra. The advantages and limitations of PA-IR, step-scan Fourier transform infrared (FT-IR), and ultrarapid-scanning FT-IR for real-time studies of reversible and irreversible phenomena are thoroughly discussed.

Polymers↗