Model Study in Chemisorption:Atomic Hydrogen on Beryllium Clusters.

摘要

The interaction between atomic hydrogen and the (0001) surface of Be metal has been studied by ab initio electronic structure theory. Self-consistent-field (SCF) calculations have been performed using minimum,optimized minimum,double zeta and mixed basis sets for clusters as large as 22Be atoms. The binding energy and equilibrium geometry (the distance to the surface) were determined for 4sites. Both spatially restricted (the wavefunction was constrained to transform as one of the irreducible representations of the molecular point group) and unrestricted SCF calculations were performed. Using only the optimized minimum basis set,clusters containing as many as 22beryllium atoms have been investigated. From a variety of considerations,this cluster is seen to be nearly converged within the model used,providing the most reliable results for chemisorption. The site dependence of the frequency is shown to be a geometrical effect depending on the number and angle of the bonds. The diffusion of atomic hydrogen through a perfect beryllium crystal is predicted to be energetically unfavorable. The cohesive energy,the ionization energy and the singlet-triplet separation were computed for the clusters without hydrogen. These quantities can be seen as a measure of the total amount of edge effects. The chemisorptive properties are not related to the total amount of edge effects,but rather the edge effects felt by the adsorbate bonding berylliums. This lack of correlation with the total edge effects illustrates the local nature of the bonding,further strengthening the cluster model for chemisorption. A detailed discussion of the bonding and electronic structure is included. The remaining edge effects for the Be sub 22cluster are discussed. (ERA citation 02:043707)