Density functional theory study of single-molecule ferroelectricity in Preyssler-type polyoxometalates

A detailed study on the single-molecule ferroelectric property of Preyssler-type polyoxometalates (POMs), [M3+P5W30O110]12− (M = La, Gd, and Lu), is performed by density functional theory calculations. Linked to one H2O molecule, the cation (M3+) encapsulated in the cavity of the Preyssler framework is off-centered, and it generates a permanent dipole, which is essential for a ferroelectric ground state. Accompanied with a 180° rotation of H2O, the switching of M3+ between two isoenergetic sites on both sides of the cavity results in a calculated barrier of 1.15 eV for Gd3+, leading to the inversion of electric polarization. The height of the barrier is in good agreement with the experimentally measured barrier for the Tb3+ ion, whose ionic radius is similar to Gd3+. The total polarization value of the crystal is estimated to be 4.7 µC/cm2 as calculated by the modern theory of polarization, which is quite close to the experimental value. Considering that the order of contributions to the polarization is M3+–H2O > counter-cations (K+) > [P5W30O110]15−, the interconversion of M3+–H2O between the two isoenergetic sites is predicted to be the main origin of ferroelectricity with a polarization contribution of 3.4 µC/cm2; the K+ counter-cations contribute by 1.2 µC/cm2 and it cannot be disregarded, while the framework appears to contribute negligibly to the total polarization. Our study suggests that a suitable choice of M3+–H2O could be used to tune the single-molecule ferroelectricity in Preyssler-type polyoxometalates.