arXiv subjects

H. Ågren

Publications and source records attributed to H. Ågren.

6 recordsLinked to original sources

arXiv2020

Interacting Dirac Materials

We investigate the extent to which the class of Dirac materials in two-dimensions provides general statements about the behavior of both fermionic and bosonic Dirac quasiparticles in the interacting regime. For both quasiparticle types, we find common features for the interaction induced renormalization of the conical Dirac spectrum. We perform the perturbative renormalization analysis and compute the self-energy for both quasiparticle types with different interactions and collate previous results from the literature whenever necessary. Guided by the systematic presentation of our results in Table~\ref{Summary}, we conclude that long-range interactions generically lead to an increase of the slope of the single-particle Dirac cone, whereas short-range interactions lead to a decrease. The quasiparticle statistics does not qualitatively impact the self-energy correction for long-range repulsion but does affect the behavior of short-range coupled systems, giving rise to different thermal power-law contributions. The possibility of a universal description of the Dirac materials based on these features is also mentioned.

cond-mat.str-el↗

arXiv2019

Ultra-narrowband selective tunable filters for visible and infrared wavelength ranges

The interaction of non-monochromatic radiation with two types of arrays comprising both plasmonic and dielectric nanoparticles has been studied in detail. We have shown that dielectric nanoparticle arrays provide a complete selective reflection of an incident plane wave within a narrow spectral line of collective lattice resonance with a Q-factor of $10^3$ or larger, whereas plasmonic refractory TiN and chemically stable Au nanoparticle arrays demonstrated high-Q resonances with moderate reflectivity. The spectral position of these resonance lines is determined by the lattice period, as well as the size, shape and material composition of the particles. Moreover, the arrays, with fixed dimensional parameters make it possible to fine-tune the position of a selected resonant spectral line by tilting the array relative to the direction of the incident radiation. These effects provide possibilities for engineering of novel selective tunable optical high-Q filters in a wide range of wavelengths: from visible to middle IR. Several highly refractive dielectric nanoparticle materials with low absorption are proposed for various spectral ranges, such as LiNbO$_3$, TiO$_2$, GaAs, Si, and Ge.

physics.optics↗

arXiv2016

Granular Superconductor in a honeycomb lattice as a realization of Bosonic Dirac Material

We examine the low energy effective theory of phase oscillations in a two-dimensional granular superconducting sheet where the grains are arranged in honeycomb lattice structure. Using the example of graphene we present the evidence for the engineered Dirac nodes in the bosonic excitations: the spectra of the collective bosonic modes cross at the K and K points in the Brillouin zone and form Dirac nodes. We show how two different types of collective phase oscillations are obtained and that they are analogous to the Leggett and the Bogoliubov-Anderson-Gorkov modes in a two-band superconductor. We show that the Dirac node is preserved in the presence of an inter-grain interaction, despite induced changes of the qualitative features of the two collective modes. Finally, breaking the sublattice symmetry by choosing different on-site potentials for the two sublattices leads to a gap opening near the Dirac node, in analogy with Fermionic Dirac materials. Dirac node dispersion of bosonic excitations is thus expanding the discussion of the conventional Dirac cone excitations to the case of bosons. We call this case as a representative of Bosonic Dirac Materials (BDM), similar to the case of Fermionic Dirac materials extensively discussed in the literature.

cond-mat.mes-hall↗

arXiv2012

The electronic structure of poly(pyridine-2,5-diyl) investigated by soft x-ray absorption and emission spectroscopies

The electronic structure of the poly-pyridine conjugated polymer has been investigated by resonant and nonresonant inelastic X-ray scattering and X-ray absorption spectroscopies using synchrotron radiation. The measurements were made for both the carbon and nitrogen contents of the polymer. The analysis of the spectra has been carried out in comparison with molecular orbital calculations taking the repeat-unit cell as a model molecule of the polymer chain. The simulations indicate no significant differences in the absorption and in the non-resonant X-ray scattering spectra for the different isomeric geometries, while some isomeric dependence of the resonant spectra is predicted. The resonant emission spectra show depletion of the π electron bands in line with symmetry selection and momentum conservation rules. The effect is most vizual for the carbon spectra; the nitrogen spectra are dominated by lone pair n orbital emission of σ symmetry and are less frequency dependent.

cond-mat.soft↗

arXiv2012

Resonant inelastic soft-x-ray scattering spectra at the N1s and C1s edges of poly(pyridine-2,5-diyl)

Resonant inelastic scattering measurements of poly(pyridine-2,5-diyl) have been performed at the N1s and C1s edges using synchrotron radiation. For comparison, molecular orbital calculations of the spectra have been carried out with the repeat unit as a model molecule of the polymer chain. The resonant emission spectra show depletion of the p electron bands which is consistent with symmetry selection and momentum conservation rules. The depletion is most obvious in the resonant inelastic scattering spectra of carbon while the nitrogen spectra are dominated by lone pair n orbital emission of s symmetry and are less excitation energy dependent. By comparing the measurements to calculations an isomeric dependence of the resonant spectra is found giving preference to two of the four possible isomers in the polymer.

cond-mat.soft↗

arXiv2012

Competition between decay and dissociation of core-excited OCS studied by X-ray scattering

We show the first evidence of dissociation during resonant inelastic soft X-ray scattering. Carbon and oxygen K-shell and sulfur L-shell resonant and non-resonant X-ray emission spectra were measured using monochromatic synchrotron radiation for excitation and ionization. After sulfur, L2,3 -> π*, σ* excitation, atomic lines are observed in the emission spectra as a consequence of competition between de-excitation and dissociation. In contrast the carbon and oxygen spectra show weaker line shape variations and no atomic lines. The spectra are compared to results from ab initio calculations and the discussion of the dissociation paths is based on calculated potential energy surfaces and atomic transition energies.

physics.chem-ph↗