Spectroscopy instrumentation for

J.P. Coates, Vibrational Spectroscopy Instrumentation for Infrared and Raman Spectroscopy , Appl. Spectrosc. Rev., 33(4), 267 25 (1998). 

Coates, J. 1997. "Vibrational Spectroscopy Instrumentation for Infrared and Raman Spectroscopy." In G. Ewing, ed. Analytical Instrumentation Handbook (2nd ed.) (pp. 393—555). New York Dekker. 

J Coates. Vibrational spectroscopy Instrumentation for infrared and Raman spectroscopy. Appl Spectrosc Rev 33 267-425, 1998. (Reprinted from Analytical Instrumentation Handbook, New York Marcel Dekker, 1997.)... 

Fadley CS (1974) The International Journal on Theoretical and Experimental Aspects of Electron Spectroscopy Instrumentation for surface studies XPS angular distributions. J Electron Spectrosc Rel Phen 5 725-754... 

There are two fimdamental types of spectroscopic studies absorption and emission. In absorption spectroscopy an atom or molecule in a low-lying electronic state, usually the ground state, absorbs a photon to go to a higher state. In emission spectroscopy the atom or molecule is produced in a higher electronic state by some excitation process, and emits a photon in going to a lower state. In this section we will consider the traditional instrumentation for studying the resulting spectra. They define the quantities measured and set the standard for experimental data to be considered. 

McCreery R L 1996 Instrumentation for dispersive Raman spectroscopy Modern Techniques in Raman Spectroscopy ed J J Laserna (New York Wiley)... 

Time-of-flight mass spectrometers have been used as detectors in a wider variety of experiments tlian any other mass spectrometer. This is especially true of spectroscopic applications, many of which are discussed in this encyclopedia. Unlike the other instruments described in this chapter, the TOP mass spectrometer is usually used for one purpose, to acquire the mass spectrum of a compound. They caimot generally be used for the kinds of ion-molecule chemistry discussed in this chapter, or structural characterization experiments such as collision-induced dissociation. Plowever, they are easily used as detectors for spectroscopic applications such as multi-photoionization (for the spectroscopy of molecular excited states) [38], zero kinetic energy electron spectroscopy [39] (ZEKE, for the precise measurement of ionization energies) and comcidence measurements (such as photoelectron-photoion coincidence spectroscopy [40] for the measurement of ion fragmentation breakdown diagrams). 

Instrument Designs for Infrared Absorption The simplest instrument for IR absorption spectroscopy is a filter photometer similar to that shown in Figure 10.24 for UV/Vis absorption. These instruments have the advantage of portability and typically are used as dedicated analyzers for gases such as ITCN and CO. 

The basic design of instrumentation for monitoring molecular fluorescence and molecular phosphorescence is similar to that found for other spectroscopies. The most significant differences are discussed in the following sections. 

Molecular Fluorescence A typical instrumental block diagram for molecular fluorescence is shown in Figure 10.45. In contrast to instruments for absorption spectroscopy, the optical paths for the source and detector are usually positioned at an angle of 90°. 

The evaluation of instrumentation for molecular UV/Vis spectroscopy is reviewed in the following pair of papers. Altermose, 1. R. Evolution of Instrumentation for UV-Visible Spectrophotometry Parti, /. Chem. Educ. 1986, 63, A216-A223. 

The modern electronic industry has played a very important role in the development of instrumentation based on physical-analytical methods As a result, a rapid boom in the fields of infrared, nuclear magnetic resonance (NMR), Raman, and mass spectroscopy and vapor-phase (or gas-liquid) chromatography has been observed. Instruments for these methods have become indispensable tools in the analytical treatment of fluonnated mixtures, complexes, and compounds The detailed applications of the instrumentation are covered later in this chapter. 

Within the confines of the present volume it is not possible to provide a detailed discussion of instrumentation for atomic fluorescence spectroscopy. An instrument for simultaneous multi-element determination described by Mitchell and Johansson53 has been developed commercially. Many atomic absorption spectrophotometers can be adapted for fluorescence measurements and details are available from the manufacturers. Detailed descriptions of atomic fluorescence spectroscopy are to be found in many of the volumes listed in the Bibliography (Section 21.27). 

Micro-Opto-Electro-Mechanical Systems (MOEMS) will be widely integrated in new astronomical instruments for future Extremely Large Telescopes, as well as for existing lOm-class telescopes. The two major applications are programmable slit masks for Multi-Object Spectroscopy (see Ch. 12) and deformable mirrors for Adaptive Optics systems. Eirst prototypes have shown their capabilities. However, big efforts have stiU to be done in order to reach the requirements and to realize reliable devices. 

The principles of and instrumentation for absorption and fluorescence spectroscopy have been discussed in detail in standard texts (S). 

In the preceding section, we presented principles of spectroscopy over the entire electromagnetic spectrum. The most important spectroscopic methods are those in the visible spectral region where food colorants can be perceived by the human eye. Human perception and the physical analysis of food colorants operate differently. The human perception with which we shall deal in Section 1.5 is difficult to normalize. However, the intention to standardize human color perception based on the abilities of most individuals led to a variety of protocols that regulate in detail how, with physical methods, human color perception can be simulated. In any case, a sophisticated instrumental set up is required. We present certain details related to optical spectroscopy here. For practical purposes, one must discriminate between measurements in the absorbance mode and those in the reflection mode. The latter mode is more important for direct measurement of colorants in food samples. To characterize pure or extracted food colorants the absorption mode should be used. 

Since there are a large number of different experimental laser and detection systems that can be used for time-resolved resonance Raman experiments, we shall only focus our attention here on two common types of methods that are typically used to investigate chemical reactions. We shall first describe typical nanosecond TR spectroscopy instrumentation that can obtain spectra of intermediates from several nanoseconds to millisecond time scales by employing electronic control of the pnmp and probe laser systems to vary the time-delay between the pnmp and probe pnlses. We then describe typical ultrafast TR spectroscopy instrumentation that can be used to examine intermediates from the picosecond to several nanosecond time scales by controlling the optical path length difference between the pump and probe laser pulses. In some reaction systems, it is useful to utilize both types of laser systems to study the chemical reaction and intermediates of interest from the picosecond to the microsecond or millisecond time-scales. 

Although very detailed, fundamental information is available from ultrafast TRIR methods, significant expertise in femtosecond/picosecond spectroscopy is required to conduct such experiments. TRIR spectroscopy on the nanosecond or slower timescale is a more straightforward experiment. Here, mainly two alternatives exist step-scan FTIR spectroscopy and conventional pump-probe dispersive TRIR spectroscopy, each with their own strengths and weaknesses. Commercial instruments for each of these approaches are currently available. 

MHz (55Mn). For 1H MRI experiments, a 25-mm birdcage rf insert was used. For other nuclei, the broadband rf probe supplied with the instrument for high resolution NMR spectroscopy with a saddle-shaped rf coil (6-mm inside diameter) was used with the external aluminum shield removed. 

Instrumentation for fluorescence spectroscopy has been reviewed [8]. For standards in fluorescence spectroscopy, see Miller [138]. Fluorescence detection in HPLC has recently been reviewed [137], Phosphorescence detection of polymer/additive extracts is not being practised. 

The most comprehensive textbook on TEM is that by Williams and Carter (1996). It is written for the microscope operator, and, as well as explaining the use of the instrument for imaging, diffraction and spectroscopy, it also gives an account of the principles of specimen production, and the reader is encouraged to turn to that book for a fuller account of the subject. 

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