RESUMEN
This study proposes a new phase-field (PF) model to simulate the pH-dependent corrosion of iron. The model is formulated based on Bockris's iron dissolution mechanism to describe the pH dependence of the corrosion rate. We also propose a simulation methodology to incorporate the thermodynamic database of the electrolyte solutions into the PF model. We show the applications of the proposed PF model for simulating two corrosion problems: general corrosion and pitting corrosion in pure iron immersed in an acid solution. The simulation results of general corrosion demonstrate that the incorporation of the anodic and cathodic current densities calculated by a Corrosion Analyzer software allows the PF model to simulate the migration of the corroded iron surface, the variation of ion concentrations in the electrolyte, and the electrostatic potential at various pH levels and temperatures. The simulation of the pitting corrosion indicates that the proposed PF model successfully captures the anisotropic propagation of a pit that is affected by the local pH of the electrolyte solution and the aggregation of Cl- ions in the pit.
RESUMEN
Polar states are realized in pseudocubic manganite films fabricated on high-index substrates, in which a Jahn-Teller (JT) distortion remains an active variable. Several types of orbital orders (OOs) were found to develop large optical second harmonics, signaling broken-inversion symmetry distinct from their bulk forms and films on (100) substrates. The observed symmetry lifting and first-principles calculation both indicate that the modified JT q2 mode drives Mn-site off centering, which can be controlled by a magnetic-field-induced phase transition via a coupling of OO and spin orders.
RESUMEN
Photoinduced phase transitions are of special interest in condensed matter physics because they can be used to change complex macroscopic material properties on the ultrafast timescale. Cooperative interactions between microscopic degrees of freedom greatly enhance the number and nature of accessible states, making it possible to switch electronic, magnetic or structural properties in new ways. Photons with high energies, of the order of electron volts, in particular are able to access electronic states that may differ greatly from states produced with stimuli close to equilibrium. In this study we report the photoinduced change in the lattice structure of a charge and orbitally ordered Nd(0.5)Sr(0.5)MnO(3) thin film using picosecond time-resolved X-ray diffraction. The photoinduced state is structurally ordered, homogeneous, metastable and has crystallographic parameters different from any thermodynamically accessible state. A femtosecond time-resolved spectroscopic study shows the formation of an electronic gap in this state. In addition, the threshold-like behaviour and high efficiency in photo-generation yield of this gapped state highlight the important role of cooperative interactions in the formation process. These combined observations point towards a 'hidden insulating phase' distinct from that found in the hitherto known phase diagram.
RESUMEN
Enhancement of the dielectric response of insulators by disorder is theoretically proposed, where the quantum interference of electronic waves through the nanoscale or mesoscopic system and its change due to external perturbations control the polarization. In the disordered case with all the states being localized, the resonant tunneling, which is topologically protected, plays a crucial role, and enhances the dielectric response by a factor 30-40 compared with the pure case. The realization of this idea with accessible materials or structures is also discussed.
