Electron-phonon interaction and ultrafast photoemission from doped monolayer MoS.

We have examined the effect of electron-phonon coupling on photoluminescence and ultrafast response of electron doped monolayer MoS, using a combination of density functional theory, time dependent density functional theory, and many-body theory. For small doping (∼1-3%) of interest here, the electron-phonon coupling parameter is modest (∼0.1-0.

Plasmon Excitations in Mixed Metallic Nanoarrays.

Features of the surface plasmon from macroscopic materials emerge in molecular systems, but differentiating collective excitations from single-particle excitations in molecular systems remains elusive. The rich interactions between single-particle electron-hole and collective electron excitations produce phenomena related to the chemical physics aspects within the atomic array. We study the plasmonic properties of atomic arrays of noble (Au, Ag, and Cu) and transition-metal (Pd, Pt) homonuclear chains using time-dependent density functional theory and their Kohn-Sham transition contributions.

Optical generation of collective plasmon modes in small gold chains induced by doping transition-metal impurities.

Our examination of the optical properties of small gold chains containing up to 24 atoms doped with a transition metal (TM) atom (Ni, Rh, Fe), using the time-dependent density functional theory, show the splitting of the collective plasmon peak. We associate the additional peak with a local plasmonic mode which corresponds to charge oscillations around the potential created by the d orbitals of the impurity atoms. The effect is almost independent of the position of the TM atom in the chain, as long as it is not at the chain edge.

Dynamical mean-field theory for molecules and nanostructures.

Dynamical mean-field theory (DMFT) has established itself as a reliable and well-controlled approximation to study correlation effects in bulk solids and also two-dimensional systems. In combination with standard density-functional theory (DFT), it has been successfully applied to study materials in which localized electronic states play an important role. It was recently shown that this approach can also be successfully applied to study correlation effects in nanostructures.

A DFT + DMFT approach for nanosystems.

We propose a combined density-functional-theory-dynamical-mean-field-theory (DFT + DMFT) approach for reliable inclusion of electron-electron correlation effects in nanosystems. Compared with the widely used DFT + U approach, this method has several advantages, the most important of which is that it takes into account dynamical correlation effects. The formalism is illustrated through different calculations of the magnetic properties of a set of small iron clusters (number of atoms 2 ≤ N ≤ 5).