2006
DOI: 10.1103/physrevlett.96.127602
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Polar Domains in Lead Titanate Films under Tensile Strain

Abstract: Thin films of PbTiO3, a classical ferroelectric, have been grown under tensile strain on single-crystal substrates of DyScO3. The films, of only 5 nm thickness, grow fully coherent with the substrate, as evidenced by synchrotron x-ray diffraction. A mapping of the reciprocal space reveals intensity modulations (satellites) due to regularly spaced polar domains in which the polarization appears rotated away from the substrate normal, characterizing a low-symmetry phase not observed in the bulk material. This co… Show more

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Cited by 138 publications
(130 citation statements)
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“…A closer observation near the phase transitions reveals two noticeable changes in the signature of the Raman spectra: the disappearance of several stronger modes at ∼ 820 • C and the complete disappearance of all the modes above 1000 • C. This temperature behavior implies that BFO maintains its room temperature structure up to ∼ 820 • C, indicating the a structural (ferroelectric) phase transition, in agreement with the earlier investigations on BFO bulk single crystal and polycrystalline samples [24]. Note that thin films of BFO show first order phase transitions as in bulk, whereas STO and PbTiO 3 PTO are known to be first order in bulk but second order in thin films [25,26].…”
Section: Resultssupporting
confidence: 90%
“…A closer observation near the phase transitions reveals two noticeable changes in the signature of the Raman spectra: the disappearance of several stronger modes at ∼ 820 • C and the complete disappearance of all the modes above 1000 • C. This temperature behavior implies that BFO maintains its room temperature structure up to ∼ 820 • C, indicating the a structural (ferroelectric) phase transition, in agreement with the earlier investigations on BFO bulk single crystal and polycrystalline samples [24]. Note that thin films of BFO show first order phase transitions as in bulk, whereas STO and PbTiO 3 PTO are known to be first order in bulk but second order in thin films [25,26].…”
Section: Resultssupporting
confidence: 90%
“…With increasing film thickness, the effect of depolarization field becomes weaker and elastic strain energy increases and thus ferroelastic domains form to relax the strain energy. Such a domain structure transition from the depolarization field energydriven 180° domains to the elastic energy-driven 71° domains is further supported by a coexistence substrates, where 180° domains have been observed in ultrathin films (to compensate the large depolarization field) 26 and periodic c/a domain structures have been observed in relatively thicker films to compensate the increasing elastic energy. 44,45 As noted above, such domain structures can play an important role in the evolution of material…”
mentioning
confidence: 69%
“…In dislocation-free epitaxial films, the strain is usually relieved by changing the system symmetry 23,24 or through the formation of ferroelastic domains 25 . Large flexoelectric polarizations have been reported for dislocation-free but ferroelastically twinned films with large elastic strain gradients causing a rotation of the polarization 21 ; in this case, the flexoelectric polarization were comparable to the spontaneous polarization of archetypal ferroelectrics evidencing that strain-engineered polar rotations can be an alternative pathway to enhancing piezoelectricity via the generation of ferroelectrics with tailored polarization 26,27 .…”
Section: Textmentioning
confidence: 99%