Vertical detachment energies of ammonia cluster anions using self-interaction-corrected methods

Peter Ufondu; Po-Hao Chang; Tunna Baruah; Rajendra R Zope

doi:10.1063/5.0139728

Vertical detachment energies of ammonia cluster anions using self-interaction-corrected methods

J Chem Phys. 2023 Apr 28;158(16):164308. doi: 10.1063/5.0139728.

Authors

Peter Ufondu¹, Po-Hao Chang¹, Tunna Baruah¹, Rajendra R Zope¹

Affiliation

¹ Department of Physics, University of Texas at El Paso, El Paso, Texas 79968, USA.

PMID: 37096854
DOI: 10.1063/5.0139728

Abstract

Systems with weakly bound extra electrons impose great challenges to semilocal density functional approximations (DFAs), which suffer from self-interaction errors. Small ammonia clusters are one such example of weakly bound anions where the extra electron is weakly bound. We applied two self-interaction correction (SIC) schemes, viz., the well-known Perdew-Zunger and the recently developed locally scaled SIC (LSIC) with the local spin density approximation (LSDA), Perdew-Burke-Ernzerhof (PBE) generalized gradient approximation (GGA), and the SCAN meta-GGA functionals to calculate the vertical detachment energies (VDEs) of small ammonia cluster anions (NH3)n-. Our results show that the LSIC significantly reduces the errors in calculations of VDE with LSDA and PBE-GGA functionals leading to better agreement with the reference values calculated with coupled cluster singles and doubles with perturbative triples [CCSD(T)]. Accurate prediction of VDE as an absolute of the highest occupied molecular orbital (HOMO) is challenging for DFAs. Our results show that VDEs estimated from the negative of HOMO eigenvalues with the LSIC-LSDA and Perdew-Zunger SIC-PBE are within 11 meV of the reference CCSD(T) results. The LSIC method performs consistently well for the VDE estimates, from both the total energy differences and the absolute HOMO eigenvalues.