Improving the ferroelectric and dielectric properties of barium strontium titanate thin films via local chemical design

Ferroelectric thin films have gained significant attention in recent years due to their potential applications in electronic devices such as ferroelectric memories, phase shifters, filters, and energy storage capacitors. In the present study, a local chemical design strategy was employed to enhance the ferroelectric and dielectric characteristics of Sr0.6Ba0.4TiO3 thin films. The samples were prepared using the chemical solution deposition technique, with Bi3+ ions being introduced into the A-sites. As the concentration of Bi3+ ions increased, both the maximum polarization and the recoverable energy storage density showed a gradual rise, reaching values of 11.77 mu C cm(-2) and 4.19 J cm(-3), respectively, under an applied voltage of 30 V. Notably, the dielectric constant exhibited an enhancement of over 3 times while maintaining a low dielectric loss (<0.06) for the composition of (Sr0.6Ba0.4)(0.7 square 0.1)Bi0.2TiO3 and (Sr0.6Ba0.4)(0.55 square 0.15)Bi0.3TiO3. First-principles calculations demonstrated that substituting Ba2+ and Sr2+ ions with Bi3+ ions in Sr0.6Ba0.4TiO3 thin films led to greater off-center displacements of cations, thereby improving the polarization and dielectric constant. The introduction of Bi3+ ions also significantly stabilized the dielectric constant, with the temperature coefficient of capacitance varying by less than 6.8% over the range of 25-300 degrees C. Furthermore, the dielectric constant exhibited minimal hysteresis, along with high dielectric tunability (>20%) and low dielectric loss (<0.02) under a low applied voltage of 12 V. This study provides a promising approach for enhancing the ferroelectric and dielectric properties of lead-free dielectric materials.