We report the first results of a new instrument for the study of the reactions of naked metal cluster ions using techniques developed by Professor Bondybey to whom this issue is dedicated. Rh6+ ions have been produced using a laser vaporization source and injected into a 3 T Fourier transform ion cyclotron resonance (FT-ICR) mass spectrometer where they are exposed to a low pressure (< 10(-8) mbar) of nitric oxide, NO. This system exhibits abundant chemistry, the first stages of which we interpret as involving the dissociative chemisorption of multiple NO molecules, followed by the liberation of molecular nitrogen. This yields key intermediates such as [Rh6O2]+ and [Rh6O4]+. The formation of the latter, after adsorption of four NO molecules, marks a change in the chemistry observed with further NO molecules adsorbed (presumably molecularly) without further N2 evolution until saturation is apparently reached with the [Rh6O4(NO)7]+ species. We analyse the data in terms of a simple 12-stage reaction mechanism, and we report the relative rate constants for each step. The trends in reactivity are assessed in terms of conceivable structures and the results are discussed where appropriate by comparison with extended surface studies of the same system. Particular attention is paid to the first step in the reaction (Rh6(+) + NO --> [Rh6NO]+) which exhibits distinctly bi-exponential kinetics, an observation we interpret as evidence for two different structural isomers of the Rh6+ cluster with one reacting more than an order of magnitude faster than the other.
The decomposition of nitric oxide on small charged rhodium clusters Rh(n)(+/-) (6 < n < 30) has been investigated by Fourier transform ion cyclotron resonance mass spectrometry. For both cationic and anionic naked clusters, the rates of reaction with NO increase smoothly with cluster size in the range studied without the dramatic size-dependent fluctuations often associated with the reactions of transition-metal clusters. The cationic clusters react significantly faster than the anions and both exhibit rate constants exceeding collision rates calculated by average dipole orientation theory. Both the approximate magnitude and the trends in reactivity are modeled well by the surface charge capture model recently proposed by Kummerlöwe and Beyer. All clusters studied here exhibit pseudo-first-order kinetics with no sign of biexponential kinetics often interpreted as evidence for multiple isomeric structures. Experiments involving prolonged exposure to NO have revealed interesting size-dependent trends in the mechanism and efficiency of NO decomposition: For most small clusters (n < 17), once two NO molecules are coadsorbed on a cluster, N(2) is evolved, generating the corresponding dioxide cluster. By analogy with experiments on extended surfaces, this observation is interpreted in terms of the dissociative adsorption of NO in the early stages of reaction, generating N atoms that are mobile on the surface of the cluster. For clusters where n < 13, this chemistry, which occurs independently of the cluster charge, repeats until a size-dependent, limiting oxygen coverage is achieved. Following this, NO is observed to adsorb on the oxide cluster without further N(2) evolution. For n = 14-16 no single end-point is observed and reaction products are based on a small range of oxide structures. By contrast, no evidence for N(2) production is observed for clusters n = 13 and n > 16, for which simple sequential NO adsorption dominates the chemistry. Interestingly, there is no evidence for the production of N(2)O or NO(2) on any of the clusters studied. A simple general mechanism is proposed that accounts for all observations. The detailed decomposition mechanisms for each cluster exhibit size (and, by implication, structure) dependent features with Rh(13)(+/-) particularly anomalous by comparison with neighboring clusters.
The reactions of gas phase rhodium clusters, Rhn+/- (n<30), with nitrous oxide, N2O, have been investigated under single collision conditions by Fourier transform ion cyclotron resonance mass spectrometry. The only significant reaction observed is the sequential generation of oxides. Absolute rate constants for the reactions of all clusters have been determined and, in the case of the cationic clusters especially, they exhibit large fluctuations as a function of cluster size with local minima observed for n=5, 19, 28. Striking similarities are observed with the variation in rate constants for these clusters in reactions with small hydrocarbons (C. Adlhart and E. Uggerud, J. Chem. Phys., 2005, 123, 214709). Corresponding size effects are also observed but are less marked in the reactions of the anionic clusters. The reactions of several clusters exhibit marked deviations from simple pseudo-first-order kinetics suggesting the presence of multiple isomeric forms: Rh11+, Rh12+ and Rh8- exhibit characteristic biexponential decays which are interpreted in terms of the existence of different structural forms of the cluster which have markedly different reactivity. By contrast, Rh6+, Rh7+ and Rh8+ show rates which apparently increase with time, probably due to collisional activation. Thermalisation of the clusters prior to reaction by exposure to pulses of argon results in changes to the kinetics of these anomalous systems which can be explained in terms of collision induced isomerisation.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.