Tunable hydrogen evolution activity by modulating polarization states of ferroelectric BaTiO3

Abstract

Switchable polarization in ferroelectric catalysts shows promise to overcome the Sabatier limit imposed on traditional catalysts. However, a comprehensive understanding of the polarization effect on electrocatalytic performance remains elusive. In this study, using ferroelectric BaTiO₃ (BTO) as a model system, we report tunable hydrogen evolution reaction (HER) performance governed by polarization states. Based on first-principles calculations, we find that BTO with in-plane polarization shows improved HER activity, in contrast to that with out-of-plane polarization, which is linked to in-plane dipole–dipole interaction at the surface. Interestingly, surface rumpling induced by surface relaxation and polarization states plays an important role in determining surface polarization, which significantly affects the chemical reactivity of surface oxygen. We unravel that the favorable p-band center of surface oxygen is responsible for the enhanced HER activity of in-plane polarized BTO. We further propose the HER catalytic cycle at the BTO surface to break the Sabatier limit via applying controllable polarization states. This work provides an inspiring insight into tunable ferroelectric catalysis by modulating polarization states toward robust HER and beyond.