SPECTROSCOPIC CONSTANTS OF SIH2, GEH2, SNH2, AND THEIR CATIONS AND ANIONS FROM DENSITY-FUNCTIONAL COMPUTATIONS

Local (LSD) and nonlocal (NLSD) spin density calculations using differ ent exchange-correlation functionals have been performed to determine equilibrium geometries, harmonic vibrational frequencies (omega e) ion ization potentials (IP), electron affinities (EA) dipole moments (mu), and singlet-triplet energy gaps (Delta E(ST)) of SiH2, GeH2, and SnH2 . Geometrical structures as well as vibrational frequencies are in agr eement with the available experimental data and compare favorably with the most sophisticated post-Hartree-Fock computations performed until now. Both computed Ips (9.15 and 9.25 eV for SiH2 and GeH2, respectiv ely) and EA of SiH2 (1.17 eV) compare favorably with experimental data (9.17, 9.21, and 1.2 eV). Accurate values are obtained also for singl et-triplet energy gaps. We report for the first time the electron affi nities of all neutral systems and the spectroscopic constants of the c ations and anions. (C) 1995 John Wiley & Sons, Inc.