Detailed wave function analysis for multireference methods: Implementation in the molcas program package and applications to tetracene
journal contributionposted on 16.03.2018 by Felix Plasser, Stefanie A. Mewes, Andreas Dreuw, Leticia Gonzalez
Any type of content formally published in an academic journal, usually following a peer-review process.
© 2017 American Chemical Society. High-level multireference computations on electronically excited and charged states of tetracene are performed, and the results are analyzed using an extensive wave function analysis toolbox that has been newly implemented in the Molcas program package. Aside from verifying the strong effect of dynamic correlation, this study reveals an unexpected critical influence of the atomic orbital basis set. It is shown that different polarized double-ζ basis sets produce significantly different results for energies, densities, and overall wave functions, with the best performance obtained for the atomic natural orbital (ANO) basis set by Pierloot et al. Strikingly, the ANO basis set not only reproduces the energies but also performs exceptionally well in terms of describing the diffuseness of the different states and of their attachment/detachment densities. This study, thus, not only underlines the fact that diffuse basis functions are needed for an accurate description of the electronic wave functions but also shows that, at least for the present example, it is enough to include them implicitly in the contraction scheme.
This paper is based on work supported by the VSC Research Center funded by the Austrian Federal Ministry of Science, Research, and Economy (bmwfw) and by the Austrian Science Fund (FWF) project I2883-N34. SAM gratefully acknowledges funding from the Heidelberg Graduate School for Mathematical and Computational Methods for the Sciences.