In situ temperature-dependent Raman-scattering experiments under an external dc electric field E have been performed on PbSc 0:5 Ta [110]. This indicates that the actual polar B-cation shifts are along the cubic body diagonals, implying a rhombohedral structure of the polar nanoregions. The T ? ðEÞ-dependence reveals that the local structural distortions associated with locally coupled polar displacements of B-site cations reach saturation near 0.5 kV/cm. When Pb 2þ is partially replaced by Ba 2þ , the strong increase of T ? with E occurs if the electric field is applied along the [110] direction. This indicates that the substitution disorder on the A-site lowers the symmetry of the polar nanoregions to orthorhombic or monoclinic. The T ? ðEÞ dependence determined from the B-cation localized mode shows saturation near 2.0 kV/cm, indicating that the zero-field structural state of PST-Ba exhibits less coupled polar shifts of B-site cations as compared to that of PST. According to the E-dependence of the Raman scattering near 55 cm À1 , for both compounds the overall response of the Pb system to the external electric field in the vicinity of T ? ðEÞ resembles antiferroelectric behavior, which along with the fact that the coupling between the B-site cations is ferroelectric, suggests that the polar nanoregions in Pb-based relaxors are ferrielectric in nature.