FT-ICR study on hydrogenation of niobium cluster cations Nb-n(+) (n=2-15) in seeded supersonic jet and multiple-collision-induced dissociation of NbnHm+ hydrides

Hydrogenation of niobium cluster cations Nb-n(+) (n=2-15) in a seeded super sonic jet of H-2/He and multiple-collision-induced dissociation (MCID) of t he resulting NbnHm+ hydrides have been studied using a Fourier transform io n cyclotron resonance (FT-ICR) mass spectrometer. The nascent NbnHm+ hydrid es trapped in the FT-ICR cell have broad m distributions with no apparent p revalence of odd or even m. A pulse of argon applied to the trapped cluster s causes a dramatic squeezing of the initial m distribution (through the co llision-induced removal of weakly bound H-2 molecules), favoring several pa rticular hydrides for each cluster size n, e.g., Nb7H8+, Nb7H11+, and Nb7H1 2+ for n=7. The maximum m values of these stable hydrides are close to the stoichiometric composition of NbH2 for the clusters with n < 13, and approa ch that of NbH at larger n. The hydrides observed in our experiments are di fferent from the products of the Nb-n(+)+H-2 reactions performed in the FT- ICR cell at room temperature, which show only even and strongly n-dependent m values. The MCID of the NbnHm+ clusters occurs through the sequential de sorption of H-2 molecules yielding NbnH+ and Nb-n(+) as final dissociation products for odd and even m, respectively. Based on the experiments on the MCID of Nb12H18+, an explanation is suggested for different reactivities of the Nb-12(+) clusters toward H-2 in the ICR and fast-flow-reactor experime nts. (C) 1999 American Institute of Physics. [S0021-9606(99)00448-1].