Development of a bond-valence molecular-dynamics model for complex oxides

A simple ten-parameter interatomic potential model is described that is capable of accurately reproducing the static and dynamical properties of complex oxides. The accuracy of this model stems from the crystal-chemical bond-valence theory of ionic and covalent bonding. The development of a specific variant of this model for ferroelectric PbTiO3 sPTd is discussed in detail, and comparison of the model is made with density functional theory computations and with experimental data. Bond-valence molecular dynamics sBVMDd simulations for PT show a ferroelectric transition at 575 K. The BVMD model correctly reproduces the mixed order-disorder and displacive phase transition character, the magnitudes of cation displacements in the ferroelectric and paraelectric phases, and the energy of 180° domain walls. The success of this simple and physically motivated model makes the simulation of extended defects tractable in PT and other complex oxides.