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Fluorine adatoms on graphene induce local changes in electronic and magnetic properties, and subtle correlation effects. We investigate the GGA and GGA+U approaches as possible solutions to describe the magnetic moment and electronic band structure of graphene sheets with fluorine adatoms, and compare to experiments. We show that, due to a lack of strong electronic correlations, GGA fails to reproduce the measured magnetic moment in this structure. In particular, the GGA incorrectly predicts a nonmagnetic ground state with a zero band gap. On the other hand, GGA+U is a computationally efficient tool which provides physically reasonable properties. Using Hubbard U and exchange J parameters of 5 eV and 0.1 eV provides a magnetic moment and optical gap in agreement with experiments. Our results imply that the magnetic moment observed in the experiment is injected by fluorine in carbon pz orbitals throughout the graphene sheet. The spin- orbit coupling (SOC) has almost no influence (ca. 2%) on the magnetism. No Rashba effect is detected and the magnetic moment induced by fluorine strongly dominates the electronic properties. Our findings explain the anisotropic magnetic behavior observed experimentally.
Using computational and theoretical approaches, we investigate the snap-through transition of buckled graphene membranes. Our main interest is related to the possibility of using the buckled membrane as a plate of capacitor with memory (memcapacitor)
In this work, we study structural and vibrational properties of multilayer graphene using density-functional theory (DFT) with van der Waals (vdW) functionals. Initially, we analyze how different vdW functionals compare by evaluating the lattice para
We study a crystallographic etching process of graphene nanostructures where zigzag edges can be prepared selectively. The process involves heating exfoliated single-layer graphene samples with a predefined pattern of antidot arrays in an argon atmos
The single-molecule magnet $mathrm{[Ni(hmp)(MeOH)Cl]_4}$ is studied using both density functional theory (DFT) and the DFT+U method, and the results are compared. By incorporating a Hubbard-U like term for both the nickel and oxygen atoms, the experi
Using the Green functions method we study transport properties of surface electrons in topological insulators in the presence of a correlated random exchange field. Such an exchange field may be due to random magnetization with correlated fluctuation