TY - JOUR
T1 - Breaking the piezoelectricity-coercivity trade-off via local multiphase nanodomain engineering
AU - Xiao, Ruoyu
AU - Song, Kexin
AU - Li, Qian
AU - Guo, Haisheng
AU - Li, Fei
AU - Xu, Zhuo
N1 - Publisher Copyright:
© 2026 Central South University
PY - 2026/10
Y1 - 2026/10
N2 - The pursuit of high-performance piezoelectrics is perpetually constrained by the inherent trade-off between a large piezoelectric coefficient (d33) and a high coercive field (EC); attaining one usually compromises the other. Here, we demonstrate a novel design strategy—local multiphase nanodomain engineering—to break this inverse relationship. In Eu3+-doped Pb(Mg1/3Nb2/3)O3-PbTiO3 (PMN-PT) relaxor ferroelectric single crystals, we achieve an exceptional combination of a giant d33 of 3100 pC/N and a significantly enhanced EC. This contrasts with Nd3+-doped crystals, which exhibit a higher d33 of 3300 pC/N but a reduced EC. Through atomic-resolution microscopy, we directly visualize that the smaller Eu3+ ion promotes the formation of localized tetragonal (T) nanodomains, which act as pinning sites to increase EC, while the coexisting rhombohedral (R) and orthorhombic (O) matrices facilitate polarization rotation, enabling high d33. First-principles calculations reveal that the distinct electronic shielding effects of Eu3+ and Nd3+ dictate the anisotropy of local lattice distortions, steering the formation of different nanodomain structures. Our work transcends conventional doping effects, establishing a foundational strategy for designing advanced ferroelectrics with previously incompatible properties.
AB - The pursuit of high-performance piezoelectrics is perpetually constrained by the inherent trade-off between a large piezoelectric coefficient (d33) and a high coercive field (EC); attaining one usually compromises the other. Here, we demonstrate a novel design strategy—local multiphase nanodomain engineering—to break this inverse relationship. In Eu3+-doped Pb(Mg1/3Nb2/3)O3-PbTiO3 (PMN-PT) relaxor ferroelectric single crystals, we achieve an exceptional combination of a giant d33 of 3100 pC/N and a significantly enhanced EC. This contrasts with Nd3+-doped crystals, which exhibit a higher d33 of 3300 pC/N but a reduced EC. Through atomic-resolution microscopy, we directly visualize that the smaller Eu3+ ion promotes the formation of localized tetragonal (T) nanodomains, which act as pinning sites to increase EC, while the coexisting rhombohedral (R) and orthorhombic (O) matrices facilitate polarization rotation, enabling high d33. First-principles calculations reveal that the distinct electronic shielding effects of Eu3+ and Nd3+ dictate the anisotropy of local lattice distortions, steering the formation of different nanodomain structures. Our work transcends conventional doping effects, establishing a foundational strategy for designing advanced ferroelectrics with previously incompatible properties.
KW - Local multiphase structures
KW - Microstructure characterization
KW - Nanodomain structures
KW - Rare-earth doping
KW - Relaxor ferroelectric single crystal
UR - https://www.scopus.com/pages/publications/105039678208
U2 - 10.1016/j.apmate.2026.100432
DO - 10.1016/j.apmate.2026.100432
M3 - 文章
AN - SCOPUS:105039678208
SN - 2772-834X
VL - 5
JO - Advanced Powder Materials
JF - Advanced Powder Materials
IS - 5
M1 - 100432
ER -