Molybdenum carbide, nitride, and sulfide clusters were created via laser ablation in the presence of dilute and neat reactive carrier gases. Distributions of the neutral products were characterized by time-of-flight mass spectrometry after photoionization with 193 nm radiation. The carbide clusters show an increase in ion intensity up to Mo 8 C 12 at which point there is a sharp drop in intensity. The latter suggests that the Mo 8 C 12 neutral or ion is particularly stable, which we attribute to a Met-Car-like structure analogous to that observed for other early transition-metal carbides. Carbide clusters containing 10−23 Mo atoms exhibit a Mo x C x +3 stoichiometry, while those containing >23 Mo atoms are closer to Mo x C x +2, indicative of near cubic nanocrystallite structures. At low mass (Mo x, x ≤ 6), cluster ions produced in expansions of ammonia gas contained up to three nitrogen atoms; however, heavier species (Mo x, x ≤ 40) appear to be pure molybdenum metal clusters. The mass distributions for the sulfide clusters indicate a “magic number” structure at Mo 6 S 4 + which is attributed to a stable structure previously observed for the [Cu 6 S 4 ] - anion. Also, the dependence of cluster distributions on the fluence of the ionizing laser was investigated to gain insight on the observed cluster ion distributions using a simple, qualitative kinetic model.
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Lightstone et al. (2003) studied this question.
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