压电
材料科学
铁电性
相界
四方晶系
电场
凝聚态物理
压电系数
电致伸缩
相(物质)
光电子学
复合材料
电介质
物理
量子力学
作者
Oliver Paull,Changsong Xu,Xuan Cheng,Yangyang Zhang,Bin Xu,Kyle P. Kelley,Alex de Marco,Rama K. Vasudevan,L. Bellaïche,Nagarajan Valanoor,Daniel Sando
标识
DOI:10.1038/s41563-021-01098-w
摘要
Piezoelectrics interconvert mechanical energy and electric charge and are widely used in actuators and sensors. The best performing materials are ferroelectrics at a morphotropic phase boundary, where several phases coexist. Switching between these phases by electric field produces a large electromechanical response. In ferroelectric BiFeO3, strain can create a morphotropic-phase-boundary-like phase mixture and thus generate large electric-field-dependent strains. However, this enhanced response occurs at localized, randomly positioned regions of the film. Here, we use epitaxial strain and orientation engineering in tandem—anisotropic epitaxy—to craft a low-symmetry phase of BiFeO3 that acts as a structural bridge between the rhombohedral-like and tetragonal-like polymorphs. Interferometric displacement sensor measurements reveal that this phase has an enhanced piezoelectric coefficient of ×2.4 compared with typical rhombohedral-like BiFeO3. Band-excitation frequency response measurements and first-principles calculations provide evidence that this phase undergoes a transition to the tetragonal-like polymorph under electric field, generating an enhanced piezoelectric response throughout the film and associated field-induced reversible strains. These results offer a route to engineer thin-film piezoelectrics with improved functionalities, with broader perspectives for other functional oxides. Strain in thin films can increase piezoelectric properties, but crystallographic constraints may restrict the enhanced response to localized regions. Here, by combining strain and orientation engineering, a low-symmetry bridging phase of BiFeO3 with enhanced piezoresponse is stabilized uniformly throughout the film.
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