Detection REMPI

Plenary 9. J W Nibler et al, e-mail address niblerj chem.orst.edu (CARS and SRS). High resolution studies of high lymg vibration-rotational transitions in molecules excited in electrical discharges and low density monomers and clusters in free jet expansions. Ionization detected (REMPI) SRS or IDSRS. Detect Raman... 

Plenary 11. W Kiefer et al, e-mail address wolfgang.kiefer mail.imi-wue.de (TR CARS). Ultrafast impulsive preparation of ground state and excited state wavepackets by impulsive CARS with REMPI detection in potassium and iodine duners. 

The most widely used of these tecluiiques is resonance-enlianced multiphoton ionization (REMPI) [ ]. A schematic energy-level diagram of the most conunonly employed variant (2 + 1) of this detection scheme is illustrated in the... 

This teclnhque can be used both to pennit the spectroscopic detection of molecules, such as H2 and HCl, whose first electronic transition lies in the vacuum ultraviolet spectral region, for which laser excitation is possible but inconvenient [ ], or molecules such as CH that do not fluoresce. With 2-photon excitation, the required wavelengdis are in the ultraviolet, conveniently generated by frequency-doubled dye lasers, rather than 1-photon excitation in the vacuum ultraviolet. Figure B2.3.17 displays 2 + 1 REMPI spectra of the HCl and DCl products, both in their v = 0 vibrational levels, from the Cl + (CHg) CD reaction [ ]. For some electronic states of HCl/DCl, both parent and fragment ions are produced, and the spectrum in figure B2.3.17 for the DCl product was recorded by monitoring mass 2 (D ions. In this case, both isotopomers (D Cl and D Cl) are detected. 

In the ideal case for REMPI, the efficiency of ion production is proportional to the line strength factors for 2-photon excitation [M], since the ionization step can be taken to have a wavelength- and state-mdependent efficiency. In actual practice, fragment ions can be produced upon absorption of a fouitli photon, or the ionization efficiency can be reduced tinough predissociation of the electronically excited state. It is advisable to employ experimentally measured ionization efficiency line strengdi factors to calibrate the detection sensitivity. With sufficient knowledge of the excited molecular electronic states, it is possible to understand the state dependence of these intensity factors [65]. 

In contrast to the ionization of C q after vibrational excitation, typical multiphoton ionization proceeds via the excitation of higher electronic levels. In principle, multiphoton ionization can either be used to generate ions and to study their reactions, or as a sensitive detection technique for atoms, molecules, and radicals in reaction kinetics. The second application is more common. In most cases of excitation with visible or UV laser radiation, a few photons are enough to reach or exceed the ionization limit. A particularly important teclmique is resonantly enlianced multiphoton ionization (REMPI), which exploits the resonance of monocluomatic laser radiation with one or several intennediate levels (in one-photon or in multiphoton processes). The mechanisms are distinguished according to the number of photons leading to the resonant intennediate levels and to tire final level, as illustrated in figure B2.5.16. Several lasers of different frequencies may be combined. 

As an example, we mention the detection of iodine atoms in their P3/2 ground state with a 3 + 2 multiphoton ionization process at a laser wavelength of 474.3 run. Excited iodine atoms ( Pi/2) can also be detected selectively as the resonance condition is reached at a different laser wavelength of 477.7 run. As an example, figure B2.5.17 hows REMPI iodine atom detection after IR laser photolysis of CF I. This pump-probe experiment involves two, delayed, laser pulses, with a 200 ns IR photolysis pulse and a 10 ns probe pulse, which detects iodine atoms at different times during and after the photolysis pulse. This experiment illustrates a frindamental problem of product detection by multiphoton ionization with its high intensity, the short-wavelength probe laser radiation alone can photolyse the... 

Detection limits in the lOOfg range can be obtained with a tuneable UV laser working at a wavelength of maximum absorption for the compounds of interest. Continuous supersonic beams require high gas loads and combination with a pulsed ionisation technique (e.g. REMPI) is unfavourable in terms of sensitivity. Pulsed valves are a better approach for a GC-UV-MS interface [1021]. 

If we consider only a few of the general requirements for the ideal polymer/additive analysis techniques (e.g. no matrix interferences, quantitative), then it is obvious that the choice is much restricted. Elements of the ideal method might include LD and MS, with reference to CRMs. Laser desorption and REMPI-MS are moving closest to direct selective sampling tandem mass spectrometry is supreme in identification. Direct-probe MS may yield accurate masses and concentrations of the components contained in the polymeric material. Selective sample preparation, efficient separation, selective detection, mass spectrometry and chemometric deconvolution techniques are complementary rather than competitive techniques. For elemental analysis, LA-ICP-ToFMS scores high. 

For ion TOF measurement a probe laser was used to ionize reaction products in the reaction zone. The (1 + F) resonance-enhanced multiphoton ionization (REMPI) method was adapted for H-atom detection. The necessary vacuum ultraviolet (VUV) radiation near 121.6 nm (for Lyman-a transition) can readily be generated by a frequency-tripling technique in a Kr cell.37 The sensitivity of this (1 +1 ) REMPI detection scheme is extremely high owing to the large absorption cross-section of Lyman-a transition,... 

Fig. 1. Detection schemes for H-atoms. Rydberg tagging technique is slightly different from the (1 + l )-REMPI detection scheme in which the H atom is directly ionized Rydberg tagging only pumps the H atom to a high Rydberg state.

The general principle of detection of free radicals is based on the spectroscopy (absorption and emission) and mass spectrometry (ionization) or combination of both. An early review has summarized various techniques to detect small free radicals, particularly diatomic and triatomic species.68 Essentially, the spectroscopy of free radicals provides basic knowledge for the detection of radicals, and the spectroscopy of numerous free radicals has been well characterized (see recent reviews2-4). Two experimental techniques are most popular for spectroscopy studies and thus for detection of radicals laser-induced fluorescence (LIF) and resonance-enhanced multiphoton ionization (REMPI). In the photochemistry studies of free radicals, the intense, tunable and narrow-bandwidth lasers are essential for both the detection (via spectroscopy and photoionization) and the photodissociation of free radicals. 

REMPI provides high detection sensitivity for free radicals similar to that of LIF.4 In the REMPI method, one or more photons typically from a focused laser radiation initially excite the free radicals to an intermediate excited electronic state. The radicals are further excited and ionized by another photon in the same laser pulse (one-color REMPI) or by a photon of different wavelength from another laser beam overlapping in space and time... 

The spectroscopy methods such as LIF and REMPI are utilized not only to detect the free radicals as discussed above, but also to directly measure the internal state distributions of the photoproducts in the photodissociation of free radicals. In this approach, the photochemistry is carried out in the free radical beam under single-collision conditions with well-defined... 

Senkan et al. [34] introduced REMPI analysis technique as a Stage I tool and exemplified its applicability with the example of a dehydrogenation reaction. The principle of this analysis method is based on sample ionization via laser light and subsequent detection of the ionized reactor effluent at dedicated electrodes at the reactor exit. Owing to a number of limitations connected with the analysis technique, it has to be considered of restricted applicability. 

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