TY - JOUR
T1 - Enhanced electromechanical performance of Si-modified lead-free BiFeO3-BaTiO3 ceramics for high-temperature piezoelectric applications
AU - Alrobei, Hussein
AU - Habib, Muhammad
AU - Ali, Shoaib
AU - Malik, Rizwan Ahmed
AU - Iqbal, Muhammad Javid
AU - Iqbal, Qamar
AU - Essa, Fadl A.
AU - Omara, Z. M.
N1 - Publisher Copyright:
© 2025 Alrobei et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
PY - 2025/3
Y1 - 2025/3
N2 - Environmental pollution generated by industrial wastes are deteriorating land, water, and marine life, which raises major concerns about climate change. Since environmentally friendly piezoelectric materials can generate clean energy by applying mechanical forces, they are seen as viable agents for industrial applications. In recent research work, the Si-modified 0.70Bi1.03FeO3-0.30BaTiO3 (BF30BT) environmentally friendly piezoceramics were synthesized using a solid-state method followed by a thermal quenching process. The crystalline structure, microstructure, and electromechanical characteristics were explored as a function of Si for both dopants (BC; before calcination) and additives (AC; after calcination). The result of pure BF30BT ceramic reveals a dominant rhombohedral phase exhibiting a d33 of 251 pC/N with a higher TC of 560 °C. The Si-doping gradually transformed the predominant rhombohedral phase to the rhombohedral-tetragonal mixed phase asymmetry as a result a good balance was achieved among d33 (209 pC/N), Qm (32.6), and kp (0.32%) with a high TC (465 °C). A giant-induced electric field bipolar strain of 0.39% corresponding to a large-signal piezoelectric coefficient d33 * ≈ 750 pm/V was perceived in Si-doped BF30BT ceramic. The defect dipoles by acceptor doping play an essential role in the enhancement of piezoelectricity. The defect dipole aligns in the spontaneous polarization and also offers restoring force for domain switching leading to high asymmetric electrostrain. This study provides a good design benchmark for a new generation of eco-friendly large-strain actuator piezoceramics.
AB - Environmental pollution generated by industrial wastes are deteriorating land, water, and marine life, which raises major concerns about climate change. Since environmentally friendly piezoelectric materials can generate clean energy by applying mechanical forces, they are seen as viable agents for industrial applications. In recent research work, the Si-modified 0.70Bi1.03FeO3-0.30BaTiO3 (BF30BT) environmentally friendly piezoceramics were synthesized using a solid-state method followed by a thermal quenching process. The crystalline structure, microstructure, and electromechanical characteristics were explored as a function of Si for both dopants (BC; before calcination) and additives (AC; after calcination). The result of pure BF30BT ceramic reveals a dominant rhombohedral phase exhibiting a d33 of 251 pC/N with a higher TC of 560 °C. The Si-doping gradually transformed the predominant rhombohedral phase to the rhombohedral-tetragonal mixed phase asymmetry as a result a good balance was achieved among d33 (209 pC/N), Qm (32.6), and kp (0.32%) with a high TC (465 °C). A giant-induced electric field bipolar strain of 0.39% corresponding to a large-signal piezoelectric coefficient d33 * ≈ 750 pm/V was perceived in Si-doped BF30BT ceramic. The defect dipoles by acceptor doping play an essential role in the enhancement of piezoelectricity. The defect dipole aligns in the spontaneous polarization and also offers restoring force for domain switching leading to high asymmetric electrostrain. This study provides a good design benchmark for a new generation of eco-friendly large-strain actuator piezoceramics.
UR - http://www.scopus.com/inward/record.url?scp=86000313402&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0318768
DO - 10.1371/journal.pone.0318768
M3 - Article
C2 - 40053560
AN - SCOPUS:86000313402
SN - 1932-6203
VL - 20
JO - PLoS ONE
JF - PLoS ONE
IS - 3 March
M1 - e0318768
ER -