Analysis of a Polarizing Michelson Interferometer for Dual Beam Fourier Transform Infrared, Circular Dichroism Infrared, and Reflectance Ellipsometric Infrared Spectroscopies

1981 ◽  
Vol 35 (2) ◽  
pp. 186-193 ◽  
Author(s):  
M. J. Dignam ◽  
M. D. Baker

The properties of a Fourier transform infrared (FT-IR) spectrometer designed around a polarizing Michelson interferometer (PMI) are analyzed with respect to applications in both conventional absorption as well as polarization spectroscopies. The PMI design is that of Martin and Puplett and consists of a metal grid polarizing beam splitter combined with rooftop retromirrors set to rotate the polarization direction in each beam by 90°. If used in conjunction with additional grid polarizers, positioned according to application, the result is an FT-IR instrument that can function both as a dual beam absorption spectrometer and as a polarization spectrometer. Operating in the former mode, the instrument is predicted to achieve speeds comparable to those achievable using a nonpolarizing dual beam Michelson interferometer but to cover a much wider spectral range due to the achromatic nature of metal grid polarizing beam splitters. In the latter mode, it is predicted to give at least double the effective throughput achievable with conventional instruments equipped with external polarization modulating optics, and again to cover a much wider spectral range. It would extend the capability of determining circular dichroism spectra into the far IR (down to ∼3 cm−1) for the first time. With the development of a process for forming a metal grid polarizer of fine spacing (∼0.1 μm) on a KBr substrate, the instrument would be capable of covering the spectral range 25 000 to 3 cm−1 or lower using only two beam splitters, i.e., in two ranges: 25 000 to 450 cm−1 using a KBr-supported metal grid, and 600 to 3 cm−1 or less using an unsupported wire grid.

1994 ◽  
Vol 48 (10) ◽  
pp. 1218-1223 ◽  
Author(s):  
Gang-Chi Chen ◽  
Prasad L. Polavarapu ◽  
Stephen Weibel

Fourier transform infrared (FT-IR) spectrometers are commonly designed with small-area detectors and tight focusing mirrors. Vibrational circular dichroism (VCD) measurements made with such FT-IR instruments contain polarization artifacts, and VCD measurements on both enantiomers (or one enantiomer and racemic mixture) are required in order to reduce these artifacts. This restriction limits the VCD measurements to only those samples for which both enantiomers (or one enantiomer and racemic mixture) are available. Recently a modified design was reported in the literature where the mirrors between sample and detector were replaced with a BaF2 lens, and a larger-area detector was substituted for the smaller-area counterpart. These modifications successfully alleviated some of the artifact problems. This design, however, is not suitable for polarizing interferometers, where polarizations exiting the interferometer are to be preserved to a high degree of purity. In addition, it is not clear whether the throughput enhancement advantage realized with a larger-area detector completely offsets the disadvantage from increased noise with detector area. Furthermore, BaF2 lenses reduce the broad range routinely available on an FT-IR instrument. Here we report a new design that replaces all the mirrors at the exit port of the interferometer with two KBr lenses and retains the full spectral range (4000–400 cm−1) of mid-infrared FT-IR spectrometers. VCD measurements obtained with small- (1 × 1 mm) and large- (4 × 4 mm) area detectors are found to have similar signal quality.


1990 ◽  
Vol 44 (1) ◽  
pp. 5-7 ◽  
Author(s):  
N. Ragunathan ◽  
N. S. Lee ◽  
T. B. Freedman ◽  
L. A. Nafie ◽  
C. Tripp ◽  
...  

Fourier transform infrared (FT-IR) vibrational circular dichroism (VCD) has been observed for the first time with the use of a polarizing Michelson interferometer (PMI). VCD spectra have been recorded for (–)- α-pinene between 900 and 1350 cm−1 at 4 cm−1 resolution with excellent signal-to-noise ratio. The FT-VCD spectra are virtually the same as those recorded for (–)- α-pinene under the same conditions with the use of the more conventional double modulation FT-IR approach.


1988 ◽  
Vol 42 (1) ◽  
pp. 32-38 ◽  
Author(s):  
Petr Malon ◽  
Timothy A. Keiderling

Using a newly constructed FT-IR vibrational circular dichroism (VCD) instrument, we have found that elimination of the ellipsoidal collection mirror before the detector and its replacement by a lens leads to a significant improvement in the absorption artifact problem seen previously in FT-IR/VCD. In the mid-IR region, we have been able to measure VCD of a single enantiomer for molecules such as α-pinene, 3-methylcyclohexanone, and dimethyltartrate. More importantly, this reduction in artifact level brings the FT-IR/VCD band shape of some particularly-difficult-to-measure bands, such as carbonyl stretches, into better agreement with those found in dispersive measurements. These results imply that the dispersive results are reliable, though of lower resolution than those obtained with the use of FT-IR/VCD.


1986 ◽  
Vol 40 (5) ◽  
pp. 628-632 ◽  
Author(s):  
Donald L. Beduhn ◽  
Robert L. White

A dual-beam Fourier transform infrared spectrometer (FT-IR) is described. Sensitivity improvement, photometric accuracy, and instrument stability are evaluated by comparing dual-beam spectra with conventional single-beam spectra. Dual-beam FT-IR data acquisitions require an order of magnitude less measurement time than single-beam acquisitions for spectra of comparable signal-to-noise ratios. Application of dual-beam FT-IR for analysis of a highly transmitting sample is discussed. Single fiber analysis without masking and without an infrared microscope is described.


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