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تسجيل مستخدم جديدThe crystalline structure of orthorhombic SrRuO$_3$: Application of hybrid scheme to the density functionals revised for solids
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The crystalline structure of ground-state orthorhombic SrRuO$_3$ is reproduced by applying hybrid density functional theory scheme to the functionals based on the revised generalized-gradient approximations for solid-state calculations. The amount of Hartree-Fock (HF) exchange energy is varied in the range of $5-20%$ in order to systematically ascertain the optimum value of HF mixing which in turn ensures the best correspondence to the experimental measurements. Such investigation allows to expand the set of tools that could be used for the efficient theoretical modelling of, for example, only recently stabilized phases of SrRuO$_3$.
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By investigating the crystalline structure of ground-state orthorhombic SrRuO$_3$, we present a benchmark study of some of the most popular density functional theory (DFT) approaches from the local density approximation (LDA), generalized-gradient ap
proximation (GGA), and hybrid functional families. Recent experimental success in stabilizing tetragonal and monoclinic phases of SrRuO$_3$ at room temperature sheds a new light on the ability to accurately describe geometry of this material by applying first-principles calculations. Therefore, our work is aimed to analyse the performance of different DFT functionals and provide some recommendations for future research of SrRuO$_3$. A comparison of the obtained results to the low-temperature experimental data indicates that revised GGAs for solids are the best choice for the lattice constants and volume due to their nice accuracy and low computational cost. However, when tilting and rotation angles appear on the scene, a combination of the revised GGAs with the hybrid scheme becomes the most preferable option. It is important to note that a worse performance of LDA functional is somewhat compensated by its realistic reproduction of electronic and magnetic structure of SrRuO$_3$, making it a strong competitor if the physical features are also taken into account.
We assess the performance of recent density functionals for the exchange-correlation energy of a nonmolecular solid, by applying accurate calculations with the GAUSSIAN, BAND, and VASP codes to a test set of 24 solid metals and non-metals. The functi
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One of the standard generalized-gradient approximations (GGAs) in use in modern electronic-structure theory, PBE, and a recently proposed modification designed specifically for solids, PBEsol, are identified as particular members of a family of funct
ionals taking their parameters from different properties of homogeneous or inhomogeneous electron liquids. Three further members of this family are constructed and tested, together with the original PBE and PBEsol, for atoms, molecules and solids. We find that PBE, in spite of its popularity in solid-state physics and quantum chemistry, is not always the best performing member of the family, and that PBEsol, in spite of having been constructed specifically for solids, is not the best for solids. The performance of GGAs for finite systems is found to sensitively depend on the choice of constraints steaming from infinite systems. Guidelines both for users and for developers of density functionals emerge from this work.
A SrRuO$_3$ (SRO) thin film and its heterostructure have brought much attention because of the recently demonstrated fascinating properties, such as topological Hall effect and skyrmions. Critical to the understanding of those SRO properties is the s
tudy of the spin configuration. Here, we conduct resonant soft x-ray scattering (RSXS) at oxygen K-edge to investigate the spin configuration of a 4 unit-cell SRO film that was grown epitaxially on a single crystal SrTiO$_3$. The RSXS signal under a magnetic field (~0.4 Tesla) clearly shows a magnetic dichroism pattern around the specular reflection. Model calculations on the RSXS signal demonstrate that the magnetic dichroism pattern originates from a Neel-type chiral spin structure in this SRO thin film. We believe that the observed spin structure of the SRO system is a critical piece of information for understanding its intriguing magnetic and transport properties.
A recent study of Mejia-Rodriguez and Trickey [Phys. Rev. A 96, 052512 (2017)] showed that the deorbitalization procedure (replacing the exact Kohn-Sham kinetic-energy density by an approximate orbital-free expression) applied to exchange-correlation
functionals of the meta-generalized gradient approximation (MGGA) can lead to important changes in the results for molecular properties. For the present work, the deorbitalization of MGGA functionals is further investigated by considering various properties of solids. It is shown that depending on the MGGA, common orbital-free approximations to the kinetic-energy density can be sufficiently accurate for the lattice constant, bulk modulus, and cohesive energy. For the band gap, calculated with the modified Becke-Johnson MGGA potential, the deorbitalization has a larger impact on the results.
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