Analysis of the spectrum of the spin-1 biquadratic antiferromagnetic chain

In questo elaborato vengono discusse le catene di spin-1, modelli quantistici definiti su un reticolo unidimensionale con interazione tra siti primi vicini. Fra la ricca varietà di tipologie esistenti è stato scelto di porre attenzione primariamente sul modello antiferromagnetico con interazione puramente biquadratica. Vengono presentati diversi metodi di classificazione degli autostati di tale modello, a partire dalle simmetrie che ne caratterizzano l’Hamiltoniana. La corrispondenza con altri modelli noti, quali il modello XXZ di spin 1/2, la catena di Heisenberg SU (3) ed i modelli di Potts, è utile ad individuare strutture simmetriche nascoste nel formalismo di spin-1, le quali consentono di ricavare informazioni sullo spettro energetico. Infine, vengono presentati risultati numerici accompagnati da alcune considerazioni sulle modifiche dello spettro quando si aggiunge un termine bilineare alla Hamiltoniana biquadratica.

Ab-initio determination of x-ray absorption near edge structure (xanes) spectra in an ultrasoft and norm conserving pseudopotentials scheme

X-ray absorption spectroscopy (XAS) is a powerful means of investigation of structural and electronic properties in condensed -matter physics. Analysis of the near edge part of the XAS spectrum, the so – called X-ray Absorption Near Edge Structure (XANES), can typically provide the following information on the photoexcited atom: - Oxidation state and coordination environment. - Speciation of transition metal compounds. - Conduction band DOS projected on the excited atomic species (PDOS). Analysis of XANES spectra is greatly aided by simulations; in the most common scheme the multiple scattering framework is used with the muffin tin approximation for the scattering potential and the spectral simulation is based on a hypothetical, reference structure. This approach has the advantage of requiring relatively little computing power but in many cases the assumed structure is quite different from the actual system measured and the muffin tin approximation is not adequate for low symmetry structures or highly directional bonds. It is therefore very interesting and justified to develop alternative methods. In one approach, the spectral simulation is based on atomic coordinates obtained from a DFT (Density Functional Theory) optimized structure. In another approach, which is the object of this thesis, the XANES spectrum is calculated directly based on an ab – initio DFT calculation of the atomic and electronic structure. This method takes full advantage of the real many-electron final wavefunction that can be computed with DFT algorithms that include a core-hole in the absorbing atom to compute the final cross section. To calculate the many-electron final wavefunction the Projector Augmented Wave method (PAW) is used. In this scheme, the absorption cross section is written in function of several contributions as the many-electrons function of the finale state; it is calculated starting from pseudo-wavefunction and performing a reconstruction of the real-wavefunction by using a transform operator which contains some parameters, called partial waves and projector waves. The aim of my thesis is to apply and test the PAW methodology to the calculation of the XANES cross section. I have focused on iron and silicon structures and on some biological molecules target (myoglobin and cytochrome c). Finally other inorganic and biological systems could be taken into account for future applications of this methodology, which could become an important improvement with respect to the multiscattering approach.