Ferroelectric to paraelectric structural transition in LiTaO3 and LiNbO3

The ferroelectric to paraelectric phase transition in LiTaO₃ and in pure as well as Mg-doped LiNbO₃ is investigated theoretically by atomistic calculations in the framework of the density functional theory, as well as experimentally by calorimetry and electrical conductivity measurements. First-principles models within the stochastic self-consistent harmonic approximation (SSCHA) allow to consider anharmonic effects and thus to obtain a realistic estimate of the Curie temperature T₂ of both ferroelectrics. Ab initio molecular dynamics (AIMD) calculations performed on large supercells confirm the Curie temperatures estimated with the SSCHA approach. Moreover, they also suggest that the structural phase transition is a continuous process beginning at temperatures well below T₂. According to AIMD, significant ionic displacements occur already at temperatures of about 100 K and 300 K below T₂ in LiTaO₃ and LiNbO₃, respectively. To asses whether and how far the ionic displacements affect the materials properties, the AIMD results are compared with measurements of the electrical conductivity and of the heat capacity across the phase transition. Our first-principles calculations moreover show that Mg ions, a frequently employed dopant, raise the Curie temperature in LiNbO₃.