We report the first study using active-orbital-based and adaptive CC(;) approaches to describe excited electronic states. These CC(;) methodologies are applied, alongside their completely renormalized (CR) coupled-cluster (CC) and equation-of-motion (EOM) CC counterparts, to recover the ground- and excited-state potential cuts of the water molecule along the O-H bond-breaking coordinate obtained in the parent CC/EOMCC calculations with a full treatment of singles, doubles, and triples (CCSDT/EOMCCSDT). We demonstrate that the active-orbital-based and adaptive CC(;) approaches closely approximate the CCSDT/EOMCCSDT data using significantly reduced computational costs while improving the CR-CC and CR-EOMCC energetics in stretched regions of the O-H bond-breaking potentials.

生成讲解博客的中文版本

生成AI智能校验的中文版本