Investigation of a near-surface laser plasma by the method of intraresonator laser spectroscopy

Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 53, No. 6, pp. 919–927, December, 1990.     

Intracavity UV-range laser spectrometer

We suggest a variant, which has already been implemented, of a selective intracavity laser spectrometer with intracavity nonlinear optical conversion of the frequency range of generated multimode radiation. The apparatus provides a means for transition into the UV spectral range (shorter than 300 nm) to carry out direct recording and quantative investigation of strong resonance lines of atomic absorption, which earlier were beyond the reach of the intracavity method. We measured selective absorption in spectral lines of a number of metals: FeI 296.690 nm, TiI 294.200 nm, and GaI 287.424 nm. Institute of Molecular and Atomic Physics, National Academy of Sciences of Belarus, 70 F. Skorina Ave., Minsk, 220072, Belarus; e-mail: Ild@imaph.bas-net.by. Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 66, No. 6, pp. 875–879, November–December, 1999.     

A high-resolution cw dye laser spectrometer

The construction and utilization of a high-resolution cw dye laser spectrometer is described. The laser incorporates pressure tuned intra-cavity etalons enabling the single mode output laser frequency to be tuned more than one nm in a continuous scan. In the scan the laser jumps from one cavity mode to the next in ～ 50 MHz steps. In comparison to molecular Doppler widths this mode jumping is negligible. As an example of the use of the instrument, a high-resolution absorption spectrum of molecular iodine between the sodium D lines is presented. A unique frequency counter provides the calibration of the absorption spectrum.     

All-semiconductor laser driven terahertz time-domain spectrometer

We present a terahertz time-domain spectrometer pumped by an all-semiconductor femtosecond laser system which emits 600 fs long optical pulses at 830 nm. Standard LT-GaAs antennas are used to generate and coherently detect THz radiation with a bandwidth of 1.4 THz. The measured time traces are in good agreement with simulations based on the Drude–Lorentz model. Spectroscopic measurements on polymers with different additive contents as well as THz imaging were carried out to confirm the successful operation of the spectrometer. Our approach holds great potential for the development of cost-effective, rugged and portable THz spectrometers for a variety of applications.     

Photoacoustic spectrometer based on a DFB-diode laser

We have developed a photoacoustic spectrometer based on a distributed feedback diode laser. The laser can be tuned continuously over 700 GHz enabling both the precise determinations of absorption line parameters such as the pressure broadening coefficient and pressure shift as well as sensitive concentration measurements.     

Optical heterodyne Herriott-type multipass laser absorption spectrometer

We present a Herriott-type multipass laser absorption spectrometer enhanced by optical heterodyne detection. The proposal is demonstrated by measuring the spectra of water vapor molecule in the region from 12247.6873 to 12249.6954 cm-1. Compared with direct absorption spectroscopy, the signal-to-noise ratio is improved nearly one magnitude of factor by combining with the optical heterodyne spectroscopy and extra weak absorption lines are observed. The minimum detectable absorption is estimated at 4.36×10-8 cm-1 and the measured line shape dominated by Doppler broadening can be precisely recovered by direct transformation of experimental optical heterodyne spectral profile.     

On-line computer controlled cw dye laser spectrometer for laser isotope separation

An on-line cw dye laser multichannel spectrometer is described, which can be controlled by FORTRAN. Automatic tuning of a dye laser to the wavelength of maximum excitation selectivity for photochemical isotope separation is achieved. Applying the system to the selective photoaddition of iodine chloride ICl to acetylene, an enrichment factor of³⁷Cl in the photoproduct C₂H₂ICl of β=100±5 was obtained. Both stable chlorine isotopes can be enriched to more than 97% purity in a single step, starting from natural samples in both cases.