Superconductivity in a two dimensional extended Hubbard model

The Roth's two-pole approximation has been used by the present authors to investigate the role of $d-p$ hybridization in the superconducting properties of an extended $d-p$ Hubbard model. Superconductivity with singlet $d_{x^2-y^2}$-wave pairing is treated by following Beenen and Edwards formalism. In this work, the Coulomb interaction, the temperature and the superconductivity have been considered in the calculation of some relevant correlation functions present in the Roth's band shift. The behavior of the order parameter associated with temperature, hybridization, Coulomb interaction and the Roth's band shift effects on superconductivity are studied.Comment: 14 pages, 8 figures, accepted for publication in European Physical Journal

Specific heat of a non-local attractive Hubbard model

The specific heat of an attractive (interaction $G<0$) non-local Hubbard model is investigated. We use a two-pole approximation which leads to a set of correlation functions. In particular, the correlation function $\ $plays an important role as a source of anomalies in the normal state of the model. Our results show that for a giving range of$G$and$\delta$where$\delta=1-n_T$($n_T=n_{\uparrow}+n_{\downarrow}$), the specific heat as a function of the temperature presents a two peak structure. Nevertehelesss, the presence of a pseudogap on the anti-nodal points$(0,\pm\pi)$and$(\pm\pi,0)$ eliminates the two peak structure, the low temperature peak remaining. The effects of the second nearest neighbor hopping on the specific heat are also investigated.Comment: 5 pages, 7 figure

Magnetic transitions induced by pressure and magnetic field in a two-orbital 5f5f-electron model in cubic and tetragonal lattices

We investigate the onset and evolution of under the simultaneous application of pressure and magnetic field of distinct itinerant N\'eel states using the underscreened Anderson Lattice Model (UALM) which has been proposed to describe $5f$-electron systems. The model is composed by two narrow $f$-bands (of either $\alpha$ or $\beta$ character) that hybridize with a wide $d$-band and local $5f$-electron interactions. We consider both cubic and tetragonal lattices. The N\'eel order parameters $\phi^{\beta}$ and $\phi^{\alpha}$ are assumed to be fixed by an Ising anisotropy. The applied magnetic field $h_z$ is parallel to the anisotropy axis. It has been assumed that the variation of the band width $W$ is sensitive to pressure. In the absence of a magnetic field, the increase of $W$ takes the system from the phase AF$_1$ to another phase AF$_2$. The phase AF$_1$ occurs when $\phi^{\beta}>\phi^{\alpha}>0$ while in the AF$_2$ phase the gaps satisfy $\phi^{\alpha}>\phi^{\beta}>0$. In the presence of a magnetic field $h_z$, the phase AF$_2$ is quickly suppressed and reappears again at intermediate values of the magnetic field while it is predominant at higher magnetic fields. The analysis of the partial density of states close to the phase transition between the phases AF$_1$ and AF$_2$, allows a better understanding the mechanism responsible whereby the transition is induced by an increase in the magnetic field. As a important general result, we found that the magnetic field $h_z$ favours the phase AF$_2$ while the phase AF$_1$ is suppressed. For the tetragonal lattice, the phase AF$_2$ is even more favored when $h_z$ and $c/a$ increases concomitantly, where $c$ and $a$ are the lattice parameters

Attosecond spectroscopy of bio-chemically relevant molecules

Understanding the role of the electron dynamics in the photochemistry of bio-chemically relevant molecules is key to getting access to the fundamental physical processes leading to damage, mutation and, more generally, to the alteration of the final biological functions. Sudden ionization of a large molecule has been proven to activate a sub-femtosecond charge flow throughout the molecular backbone, purely guided by electronic coherences, which could ultimately affect the photochemical response of the molecule at later times. We can follow this ultrafast charge flow in real time by exploiting the extreme time resolution provided by attosecond light sources. In this work recent advances in attosecond molecular physics are presented with particular focus on the investigation of bio-relevant molecules