摘要
BaTiO 3 ceramics were synthesized via a conventional solid-state reaction method to investigate the influence of lattice strain induced by tiny content of Fe 3+ doping (1 mol%) on the structural evolution and ferroelectric properties. The incorporation of Fe 3+ introduces a compressive strain field, resulting in a reduced c / a ratio and a disordered domain configuration. Such lattice strain significantly enhances the maximum ferroelectric polarization ( P max ) from 23.2 μC/cm 2 for undoped BaTiO 3 ceramic to 40.6 μC/cm 2 for BaTi 0.99 Fe 0.01 O 3- δ ceramic. This observed enhancement is attributed to a lowered energy barrier for polarization switching and the facilitation of domain wall motion. Phenomenological analysis based on symmetry-related strain-polarization coupling further reveals that the Fe 3+ induced compressive strain mitigates the lattice mismatch stress at domain boundaries and alleviates the strain constraint on polarization switching. These findings clarify the relationship between chemical-doping-induced lattice strain and ferroelectric performance, offering a pathway for the deliberate control of domain structure to achieve high ferroelectric performance in bulk ceramics.
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