Photoemission Imaging of 3D Fermi Surface Pairing at the Hidden Order Transition in URu2Si2

We report angle-resolved photoemission spectroscopy (ARPES) experiments probing deep into the hidden order (HO) state of URu2Si2, utilizing tunable photon energies with sufficient energy and momentum resolution to detect the near Fermi surface (FS) behavior. Our results reveal: (i) the full itinerancy of the 5f electrons; (ii) the crucial three-dimensional (3D) k-space nature of the FS and its critical nesting vectors, in good comparison with density-functional theory calculations, and (iii) the existence of hot-spot lines and pairing of states at the FS, leading to FS gapping in the HO phase.

Phonon spectrum, thermal expansion and heat capacity of UO$_2$ from first-principles

We report first-principles calculations of the phonon dispersion spectrum, thermal expansion, and heat capacity of uranium dioxide. The so-called direct method, based on the quasiharmonic approximation, is used to calculate the phonon frequencies within a density functional framework for the electronic structure. The phonon dispersions calculated at the theoretical equilibrium volume agree well with experimental dispersions. The computed phonon density of states (DOS) compare reasonably well with measurement data, as do also the calculated frequencies of the Raman and infrared active modes including the LO/TO splitting. To study the pressure dependence of the phonon frequencies we calculate phonon dispersions for several lattice constants. Our computed phonon spectra demonstrate the opening of a gap between the optical and acoustic modes induced by pressure. Taking into account the phonon contribution to the total free energy of UO$_2$ its thermal expansion coefficient and heat capacity have been {it ab initio} computed. Both quantities are in good agreement with available experimental data for temperatures up to about 500 K.

First-Principles Theory of Multipolar Order in Neptunium Dioxide

We provide a first-principle, materials-specific theory of multipolar order and superexchange in NpO$_2$ by means of a non-collinear local-density approximation +$U$ (LDA+$U$) method. Our calculations offer a precise microscopic description of the triple-$q$-antiferro ordered phase in the absence of any dipolar moment. We find that, while the most common non-dipolar degrees of freedom (e.g., electric quadrupoles and magnetic octupoles) are active in the ordered phase, both the usually neglected higher-order multipoles (electric hexadecapoles and magnetic triakontadipoles) have at least an equally significant effect.