New tools for the systematic analysis and visualization of electronic excitations

• Verfasst von: Plasser, Felix [VerfasserIn]
• Verfasst von: Wormit, Michael [VerfasserIn]
• Verfasst von: Dreuw, Andreas [VerfasserIn]
• Titel: New tools for the systematic analysis and visualization of electronic excitations
• Titelzusatz: I. Formalism
• Verf.angabe: Felix Plasser, Michael Wormit, and Andreas Dreuw
• Fussnoten: Gesehen am 11.12.2017
• Titel Quelle: Enthalten in: The journal of chemical physics
• Jahr Quelle: 2014
• Band/Heft Quelle: 141(2014,13) Artikelnummer 024106, 13 Seiten
• ISSN Quelle: 1089-7690
• DOI: doi:10.1063/1.4885819
• Datenträger: Online-Ressource
• Sprache: eng
• K10plus-PPN: 1566246946

Abstract

A variety of density matrix based methods for the analysis and visualization of electronic excitations are discussed and their implementation within the framework of the algebraic diagrammatic construction of the polarization propagator is reported. Their mathematical expressions are given and an extensive phenomenological discussion is provided to aid the interpretation of the results. Starting from several standard procedures, e.g., population analysis, natural orbital decomposition, and density plotting, we proceed to more advanced concepts of natural transition orbitals and attachment/detachment densities. In addition, special focus is laid on information coded in the transition density matrix and its phenomenological analysis in terms of an electron-hole picture. Taking advantage of both the orbital and real space representations of the density matrices, the physical information in these analysis methods is outlined, and similarities and differences between the approaches are highlighted. Moreover, new analysis tools for excited states are introduced including state averaged natural transition orbitals, which give a compact description of a number of states simultaneously, and natural difference orbitals (defined as the eigenvectors of the difference density matrix), which reveal details about orbital relaxation effects.