Double monochromator

Most available infrared instruments use the Littrow mount for the prism, the beam being reflected from a plane mirror behind the pnsm and thus returning it through the prism a second time. This doubles the dispersion produced. Actually, a double-pass system is also used so that the beam goes through the pnsm four times. Other design modifications include those with single beam and double monochromator, double beam and double monochromator, and related combinations, See also Infrared Radiation. 

The mechanics of HREELS is now manageable using personal computer based spectrometer control. Typical spectral resolution of modern instruments is 1- 5 meV. At the lower end of this range physical effects due to natural vibrational line widths are observable. In the early days of HREELS (which extend to the present, because many of the older spectrometers are still in use), single-pass cylindrical (127°) capacitor spectrometers, both fixed and with a movable analyser or monochromator, double-pass cylindrical (127°) capacitor analysers, spherical capacitor spectrometers and even some dual-use photoelectron spectrometers with enhanced resolution ranges were used, with spectral resolution in the 7-12 meV range. 

Due to the rather stringent requirements placed on the monochromator, a double or triple monocln-omator is typically employed. Because the vibrational frequencies are only several hundred to several thousand cm and the linewidths are only tens of cm it is necessary to use a monochromator with reasonably high resolution. In addition to linewidth issues, it is necessary to suppress the very intense Rayleigh scattering. If a high resolution spectrum is not needed, however, then it is possible to use narrow-band interference filters to block the excitation line, and a low resolution monocln-omator to collect the spectrum. In fact, this is the approach taken with Fourier transfonn Raman spectrometers. 

Infrared instruments using a monochromator for wavelength selection are constructed using double-beam optics similar to that shown in Figure 10.26. Doublebeam optics are preferred over single-beam optics because the sources and detectors for infrared radiation are less stable than that for UV/Vis radiation. In addition, it is easier to correct for the absorption of infrared radiation by atmospheric CO2 and 1420 vapor when using double-beam optics. Resolutions of 1-3 cm are typical for most instruments. 

A dispersive element for spectral analysis of PL. This may be as simple as a filter, but it is usually a scanning grating monochromator. For excitation spectroscopy or in the presence of much scattered light, a double or triple monochromator (as used in Raman scattering) may be required. 

A modern laser Raman spectrometer consists of four fundamental components a laser source, an optical system for focusing the laser beam on to the sample and for directing the Raman scattered light to the monochromator entrance slit, a double or triple monochromator to disperse the scattered light, and a photoelectric detection system to measure the intensity of the light passing through the monochromator exit slit (Fig. 7). 

Fig. 10. Scattered light including ghosts appearing in a single, double, and triple monochromator. Although scattered light plunges to the square root in a double monochromator, interference with Raman spectra still occurs occasionally. In a triple monochromator, instrumental scatter has never been known to interfere with Raman scatter...

A detachable monochromator (19) developed by Spex Industries, was another approach in minimizing stray light. It is a modified Czerny-Turner spectrograph which can be coupled to the exit slit of a double monochromator and function as a variable bandpass, variable frequency filter. This accessory, while providing the versatility of a triple monochromator, does not add much mechanical and optical complexity and can be removed when not wanted. 

SI(220) double crystal monochromator was used with entrance slit (1 mm high 20 m from the source point) chosen to give a bandpass of 2 eV at the Pt edge, 11,563.7 eV.( ) The operation of the catalyst... 

The probability of Raman scattering is quite small. This normally requires the use of intense laser sources and concentrated samples. A high-resolution double or triple monochromator is used to separate the Raman lines from the intense Raleigh line. 

In Raman measurements [57], the 514-nm line of an Ar+ laser, the 325-nm line of a He-Cd laser, and the 244-nm line of an intracavity frequency-doubled Ar+ laser were employed. The incident laser beam was directed onto the sample surface under the back-scattering geometry, and the samples were kept at room temperature. In the 514-nm excitation, the scattered light was collected and dispersed in a SPEX 1403 double monochromator and detected with a photomultiplier. The laser output power was 300 mW. In the 325- and 244-nm excitations, the scattered light was collected with fused silica optics and was analyzed with a UV-enhanced CCD camera, using a Renishaw micro-Raman system 1000 spectrometer modified for use at 325 and 244 nm, respectively. A laser output of 10 mW was used, which resulted in an incident power at the sample of approximately 1.5 mW. The spectral resolution was approximately 2 cm k That no photoalteration of the samples occurred during the UV laser irradiation was ensured by confirming that the visible Raman spectra were unaltered after the UV Raman measurements. 

HREELS experiments [66] were performed in a UHV chamber. The chamber was pre-evacuated by polyphenylether-oil diffusion pump the base pressure reached 2 x 10 Torr. The HREELS spectrometer consisted of a double-pass electrostatic cylindrical-deflector-type monochromator and the same type of analyzer. The energy resolution of the spectrometer is 4-6 meV (32-48 cm ). A sample was transferred from the ICP growth chamber to the HREELS chamber in the atmosphere. It was clipped by a small tantalum plate, which was suspended by tantalum wires. The sample was radia-tively heated in vacuum by a tungsten filament placed at the rear. The sample temperature was measured by an infrared (A = 2.0 yum) optical pyrometer. All HREELS measurements were taken at room temperature. The electron incident and detection angles were each 72° to the surface normal. The primary electron energy was 15 eV. 

The typical experimental setup (here the experiment established at beamline G3/ HASYLAB [12] is shown) is outlined in Figure 5. The white synchrotron radiation is monochromatized by a double crystal monochromator using the Ge (311) reflection... 

The first laser Raman spectra were inherently time-resolved (although no dynamical processes were actually studied) by virtue of the pulsed excitation source (ruby laser) and the simultaneous detection of all Raman frequencies by photographic spectroscopy. The advent of the scanning double monochromator, while a great advance for c.w. spectroscopy, spelled the temporary end of time resolution in Raman spectroscopy. The time-resolved techniques began to be revitalized in 1968 when Bridoux and Delhaye (16) adapted television detectors (analogous to, but faster, more convenient, and more sensitive than, photographic film) to Raman spectroscopy. The advent of the resonance Raman effect provided the sensitivity required to detect the Raman spectra of intrinsically dilute, short-lived chemical species. The development of time-resolved resonance Raman (TR ) techniques (17) in our laboratories and by others (18) has led to the routine TR observation of nanosecond-lived transients (19) and isolated observations of picosecond-timescale events by TR (20-22). A specific example of a TR study will be discussed in a later section. 

Fourier transform spectrometer or double-beam spectrophotometer incorporating prism or grating monochromator, thermal or photon detector, alkali halide cells. 

X-ray Instrumentation. All experiments were performed at the Cornell High Energy Synchrotron Source (CHESS) operated at 5.8 GeV (Stations A-3, B and C-2). Monochromatic radiation was obtained with a Si (220) double crystal monochromator. In order to eliminate higher harmonics, 50% detunning was typically employed. ... 

The design of a conventional atomic absorption spectrometer is relatively simple (Fig. 3.1), consisting of a lamp, a beam chopper, a burner, a grating monochromator, and a photomultiplier detector. The design of each of these is briefly considered. The figure shows both single and double beam operation, as explained below. 

Figure 3.1 Schematic diagram of an AAS spectrometer. A is the light source (hollow cathode lamp), B is the beam chopper (see Fig. 3.2), C is the burner, D the monochromator, E the photomultiplier detector, and F the computer for data analysis. In the single beam instrument, the beam from the lamp is modulated by the beam chopper (to reduce noise) and passes directly through the flame (solid light path). In a double beam instrument the beam chopper is angled and the rear surface reflective, so that part of the beam is passed along the reference beam path (dashed line), and is then recombined with the sample beam by a half-silvered mirror.

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