Potential energy surfaces of MH2 (M = Co, Fe, and Cu)

• Published in: The Journal of chemical physics 1984-08, Vol.81 (3), p.1373-1382
• Main Authors: Siegbahn, P. E. M., Blomberg, M. R. A., Bauschlicher, C. W., Jr
• Format: Article
• Language: English
• Subjects: Atomic and molecular collision processes and interactions; Atomic and molecular physics; Exact sciences and technology; Inorganic And Physical Chemistry; Interatomic and intermolecular potentials and forces, potential energy surfaces for collisions; Physics
• ISSN: 0021-9606; 1089-7690
• DOI: 10.1063/1.447771

In many important catalytic processes, the dissociation of the hydrogen molecule is a fundamental step, and the chemisorption of dihydrogen by metal surfaces has been studied. However, quantitative results from theoretical treatments are not very encouraging. Blomberg and Siegbahn (1983) have found that the negative binding energy for NiH2 obtained with the aid of the commonly used Hartree-Fock approximation differs greatly from the result found on the basis of a more sophisticated calculation, including electron correlation. Another study showed the great importance of d orbitals in the dissociation process. A study, similar to the one on NH2, has been conducted for three other metals, including cobalt, iron, and copper. The present investigation is concerned with the results of this study. The potential surfaces of CoH2, FeH2, and CuH2 are discussed, taking into account the lowest atomic states, the bent low spin complex, the bent high spin saddle points, and the linear states.