Ferroelectric materials with spontaneous polarization‐induced internal electric fields have drawn increasing attention in solar fuel production due to the intrinsic polarized structure. However, the origination of charge separation in these materials at the nano/microlevel is ambiguous owing to the complexity of the multielectric fields. Besides, the observed charge separation ability is far from theoretical expectation. Herein, by spatially resolved surface photovoltage spectroscopy, it is clearly demonstrated that the depolarization field in single‐domain ferroelectric PbTiO3 (PTO) nanoplates is the main driving force for charge separation and it can effectively drive photogenerated electrons and holes to the positive and negative polarization facets, respectively. Moreover, the charge separation ability of PTO nanoplates increases with increasing particle size along the polarization direction, due to the increasing potential difference between the opposite polarization facets. Furthermore, this driving force for charge separation directly contributes to the enhancement of the photocatalytic hydrogen evolution reaction activity in ferroelectrics. Finally, it is proved that the screening field compensates part of the depolarization field and can be diminished by adding a dielectric layer on the ferroelectric surface. These findings demonstrate the importance of increasing the depolarization field and decreasing the screening field for efficient charge separation in ferroelectric semiconductor photocatalysts.

No abstract

Bisimidazole-functionalized cobaltoporphyrin acted as efficient bifunctional catalysts to facilitate the synthesis of cyclic carbonates from epoxides and CO2.