Chemical Reactions of Silicon Clusters

Details Chemical Reactions of Silicon Clusters Chemical Reactions of Silicon Clusters

1994-05-17

arxiv.org/abs/chem-ph/9405001v1

Physics

Chemical Physics

20 pages + 6 figures, Complete PostScript file is available through anonymous ftp from ramanujan.chem.nyu.edu. The file name i

Scientific paper

10.1063/1.468238

Smalley and co-workers discovered that chemisorption reactivities of silicon clusters vary over three orders of magnitude as a function of cluster size. In particular, they found that \Si{33}, \Si{39}, and \Si{45} clusters are least reactive towards various reagents compared to their immediate neighbors in size. We explain these observations based on our stuffed fullerene model. This structural model consists of bulk-like core of five atoms surrounded by fullerene-like surface. Reconstruction of the ideal fullerene geometry gives rise to four-fold coordinated crown atoms and $\pi$-bonded dimer pairs. This model yields unique structures for \Si{33}, \Si{39}, and \Si{45} clusters without any dangling bonds and thus explains their lowest reactivity towards chemisorption of closed shell reagents. This model is also consistent with the experimental finding of Jarrold and Constant that silicon clusters undergo a transition from prolate to spherical shapes at \Si{27}. We justify our model based on an in depth analysis of the differences between carbon and silicon chemistry and bonding characteristics. Using our model, we further explain why dissociative chemisorption occurs on bulk surfaces while molecular chemisorption occurs on cluster surfaces. We also explain reagent specific chemisorption reactivities observed experimentally based on the electronic structures of the reagents. Finally, experiments on \Si{x}X$_y$ (X = B, Al, Ga, P, As, AlP, GaAs) are suggested as a means of verifying the proposed model. We predict that \Si{x}(AlP)$_y$ and \Si{x}(GaAs)$_y$ $(x = 25, 31, 37; y = 4)$ clusters will be highly inert and it may be possible to prepare macroscopic samples of these alloy clusters through high temperature reactions.

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