Beams molecular

MBRS Molecular beam spectroscopy [158] A modulated molecular beam hits the surface and the time lag for reaction products is measured Kinetics of surface reactions chemisorption... 

MSS Molecule surface scattering [159-161] Translational and rotational energy distribution of a scattered molecular beam Quantum mechanics of scattering processes... 

A. Schmidt, L. K. Chau, A. Back, and N. R. Armstrong, Epitaxial Phthalocyanine Ultrathin Films Grown by Organic Molecular Beam Epitaxy (OMBE), in Phthalo-cyanines, Vol. 4, C. Leznof and A. P. B. Lever, eds., VCH Publications, 1996. 

The nature of reaction products and also the orientation of adsorbed species can be studied by atomic beam methods such as electron-stimulated desorption (ESD) [49,30], photon-stimulated desoiption (PDS) [51], and ESD ion angular distribution ESDIAD [51-54]. (Note Fig. VIII-13). There are molecular beam scattering experiments such... 

Ref. 205). The two mechanisms may sometimes be distinguished on the basis of the expected rate law (see Section XVni-8) one or the other may be ruled out if unreasonable adsorption entropies are implied (see Ref. 206). Molecular beam studies, which can determine the residence time of an adsorbed species, have permitted an experimental decision as to which type of mechanism applies (Langmuir-Hinshelwood in the case of CO + O2 on Pt(lll)—note Problem XVIII-26) [207,208]. 

This section discusses how spectroscopy, molecular beam scattering, pressure virial coeflScients, measurements on transport phenomena and even condensed phase data can help detemiine a potential energy surface. 

Spectroscopy is the most important experimental source of infomiation on intemiolecular interactions. A wide range of spectroscopic teclmiques is being brought to bear on the problem of weakly bound or van der Waals complexes [94, 95]. Molecular beam microwave spectroscopy, pioneered by Klemperer and refined by Flygare, has been used to detemiine the microwave spectra of a large number of weakly bound complexes and obtain stmctiiral infomiation... 

As with most methods for studying ion-molecule kinetics and dynamics, numerous variations exist. For low-energy processes, the collision cell can be replaced with a molecular beam perpendicular to the ion beam [106]. This greatly reduces the thennal energy spread of the reactant neutral. Another approach for low energies is to use a merged beam [103]. In this system the supersonic expansion is aimed at the tluoat of the octopole, and the ions are passed tluough... 

Several instniments have been developed for measuring kinetics at temperatures below that of liquid nitrogen [81]. Liquid helium cooled drift tubes and ion traps have been employed, but this apparatus is of limited use since most gases freeze at temperatures below about 80 K. Molecules can be maintained in the gas phase at low temperatures in a free jet expansion. The CRESU apparatus (acronym for the French translation of reaction kinetics at supersonic conditions) uses a Laval nozzle expansion to obtain temperatures of 8-160 K. The merged ion beam and molecular beam apparatus are described above. These teclmiques have provided important infonnation on reactions pertinent to interstellar-cloud chemistry as well as the temperature dependence of reactions in a regime not otherwise accessible. In particular, infonnation on ion-molecule collision rates as a ftmction of temperature has proven valuable m refining theoretical calculations. 

Wang L, Lee Y T and Shirley D A 1987 Molecular beam photoelectron spectroscopy of SO2 geometry, spectroscopy, and dynamics of J. Chem. Phys. 87 2489-97... 

Figure A3.7.2. Schematic illustration of crossed molecular beams experimeut for F + H + 2 reaction.

Since this state is so low in energy, it is likely to be populated in the F atom beams typically used in scattering experiments (where pyrolysis or microwave/electrical discharges are used to generate F atoms), so the issue of its reactivity is important. The molecular beam experiments of Lee [43] and Toennies [45] showed no evidence for... 

Flowever, in order to deliver on its promise and maximize its impact on the broader field of chemistry, the methodology of reaction dynamics must be extended toward more complex reactions involving polyatomic molecules and radicals for which even the primary products may not be known. There certainly have been examples of this notably the crossed molecular beams work by Lee [59] on the reactions of O atoms with a series of hydrocarbons. In such cases the spectroscopy of the products is often too complicated to investigate using laser-based techniques, but the recent marriage of intense syncluotron radiation light sources with state-of-the-art scattering instruments holds considerable promise for the elucidation of the bimolecular and photodissociation dynamics of these more complex species. 

Sooies G (ed) 1988 Atomic and Molecular Beam Methods vo s 1 and 2 (New York Oxford University Press)... 

For example, energy transfer in molecule-surface collisions is best studied in nom-eactive systems, such as the scattering and trapping of rare-gas atoms or simple molecules at metal surfaces. We follow a similar approach below, discussing the dynamics of the different elementary processes separately. The surface must also be simplified compared to technologically relevant systems. To develop a detailed understanding, we must know exactly what the surface looks like and of what it is composed. This requires the use of surface science tools (section B 1.19-26) to prepare very well-characterized, atomically clean and ordered substrates on which reactions can be studied under ultrahigh vacuum conditions. The most accurate and specific experiments also employ molecular beam teclmiques, discussed in section B2.3. 

The direct dissociation of diatomic molecules is the most well studied process in gas-surface dynamics, the one for which the combination of surface science and molecular beam teclmiques allied to the computation of total energies and detailed and painstaking solution of the molecular dynamics has been most successful. The result is a substantial body of knowledge concerning the importance of the various degrees of freedom (e.g. molecular rotation) to the reaction dynamics, the details of which are contained in a number of review articles [2, 36, 37, 38, 39, 40 and 41]. 

Lykke K R and Kay B D 1990 State-to-state inelastic and reactive molecular beam scattering from surfaces Laser Photoionization and Desorption Surface Analysis Techniquesvo 1208, ed N S Nogar (Bellingham, WA SPIE) p 1218... 

Panish M B and Temkin H 1993 Gas Source Molecular Beam Epitaxy (New York Springer)... 

Fischer G, Miller R E, Vohralik P F and Watts R O 1985 Molecular beam infrared spectra of dimers... 

On the experimental side, small molecule energy transfer experiments may use molecular beam teclmiques [65. 66 and 67] (see also chapter C3.3 for laser studies). 

Fluendy MAD and Lawley K P 1973 Applications of Molecular Beam Scattering (London Chapman and Hall)... 

To date, the IR-CRLAS studies have concentrated on water clusters (both FI2O and D2O), and methanol clusters. Most importantly, these studies have shown that it is in fact possible to carry out CRLAS in the IR. In one study, water cluster concentrations in the molecular beam source under a variety of expansion conditions were characterized [34]- hr a second study OD stretching bands in (020) clusters were measured [35]. These bands occur between 2300... 

For methanol clusters [36], it was found that the dimer is linear, while clusters of 3 and 4 molecules exist as monocyclic ring structures. There also is evidence that there are two cyclic ring trimer confomiers in the molecular beam. 

Optothemial spectroscopy is a bolonietric method that monitors the energy in a stream of molecules rather than in the light beam. A well collimated molecular beam is directed toward a liquid helium cooled bolometer. There will be energy... 

Scherer J J, Paul J B, O Keefe A and Saykally R J 1997 Cavity ringdown laser absorption spectroscopy history, development, and application to pulsed molecular beams Chem. Rev. 97 25-51... 

---