Browsing by Author "Droghetti, Andrea"

Now showing 1 - 4 of 4
  • Thumbnail Image
    Item
    DFT+SIGMA2 method for electron correlation effects at transition metal surfaces
    Droghetti, Andrea; Radonjić, Miloš M.; Halder, Anita; Rungger, Ivan; Chioncel, Liviu
    We present a computational approach for electronically correlated metallic surfaces and interfaces, which combines density functional and dynamical mean-field theory using a multiorbital perturbative solver for the many-body problem. Our implementation is designed to describe ferromagnetic metallic thin films on a substrate. The performances are assessed in detail for a Fe monolayer on a W(110) substrate, a prototypical nanoscale magnetic system. Comparing our results to photoemission data, we find qualitative and quantitative improvements in the calculated spectral function with respect to the results of density functional theory within the local spin density approximation. In particular, the spin splitting of the d states is drastically reduced and, at the same time, their spectral width becomes narrower. The method is, therefore, able to account for the main correlation effects in the system.
  • Thumbnail Image
    Item
    Dynamical mean-field theory for spin-dependent electron transport in spin-valve devices
    Droghetti, Andrea; Radonjić, Miloš M.; Chioncel, Liviu; Rungger, Ivan
    We present a combination of density functional theory and dynamical mean-field theory (DMFT) for comput-ing the electron transmission through two-terminal nanoscale devices. The method is then applied to metallic junctions presenting alternating Cu and Co layers, which exhibit spin-dependent charge transport and the giant magnetoresistance (GMR) effect. The calculations show that the coherent transmission through the 3d states is greatly suppressed by electron correlations. This is mainly due to the finite lifetime induced by the electron-electron interaction and is directly related to the imaginary part of the computed many-body DMFT self-energy. At the Fermi energy, where in accordance with the Fermi-liquid behavior the imaginary part of the self-energy vanishes, the suppression of the transmission is entirely due to the shifts of the energy spectrum induced by electron correlations. Based on our results, we finally suggest that the GMR measured in Cu/Co heterostructures for electrons with energies about 1 eV above the Fermi energy is a manifestation of dynamical correlation effects.
  • Thumbnail Image
    Item
    Enhancing Electron Correlation at a 3d Ferromagnetic Surface
    Janas, David, Maximilian; Droghetti, Andrea; Ponzoni, Stefano; Cojocariu, Iulia; Jugovac, Matteo; Vitaliy Feyer; Radonjić, Miloš M.; Rungger, Ivan; Chioncel, Liviu; Zamborlini, Giovanni; Cinchetti, Mirko
    Spin-resolved momentum microscopy and theoretical calculations are combined beyond the one-electron approximation to unveil the spin-dependent electronic structure of the interface formed between iron (Fe) and an ordered oxygen (O) atomic layer, and an adsorbate-induced enhancement of electronic correlations is found. It is demonstrated that this enhancement is responsible for a drastic narrowing of the Fe d-bands close to the Fermi energy (E-F) and a reduction of the exchange splitting, which is not accounted for in the Stoner picture of ferromagnetism. In addition, correlation leads to a significant spin-dependent broadening of the electronic bands at higher binding energies and their merging with satellite features, which are manifestations of a pure many-electron behavior. Overall, adatom adsorption can be used to vary the material parameters of transition metal surfaces to access different intermediate electronic correlated regimes, which will otherwise not be accessible. The results show that the concepts developed to understand the physics and chemistry of adsorbate-metal interfaces, relevant for a variety of research areas, from spintronics to catalysis, need to be reconsidered with many-particle effects being of utmost importance. These may affect chemisorption energy, spin transport, magnetic order, and even play a key role in the emergence of ferromagnetism at interfaces between non-magnetic systems.
  • No Thumbnail Available
    Item
    Predicting the conductance of strongly correlated molecules: the Kondo effect in perchlorotriphenylmethyl/Au junctions
    Appelt, Wilhelm H.; Droghetti, Andrea; Chioncel, Liviu; Radonjić, Miloš; Muñoz, Enrique T.; Kirchner, Stefan; Vollhardt, Dieter; Rungger, Ivan
    Stable organic radicals integrated into molecular junctions represent a practical realization of the single-orbital Anderson impurity model. Motivated by recent experiments for perchlorotriphenylmethyl (PTM) molecules contacted to gold electrodes, we develop a method that combines density functional theory (DFT), quantum transport theory, numerical renormalization group (NRG) calculations and renormalized super-perturbation theory (rSPT) to compute both equilibrium and non-equilibrium properties of strongly correlated nanoscale systems at low temperatures effectively from first principles. We determine the possible atomic structures of the interfaces between the molecule and the electrodes, which allow us to estimate the Kondo temperature and the characteristic transport properties, which compare well with experiments. By using the non-equilibrium rSPT results we assess the range of validity of equilibrium DFT + NRG-based transmission calculations for the evaluation of the finite voltage conductance. The results demonstrate that our method can provide qualitative insights into the properties of molecular junctions when the molecule-metal contacts are amorphous or generally ill-defined, and that it can further give a fully quantitative description when the experimental contact structures are well characterized.