Suchergebnisse

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) ; Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) ; Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) ; Government of the Russian Federation ; Project CICECO-Aveiro Institute of Materials - national funds through the FCT/MEC ; FEDER under the PT2020 Partnership Agreement ; CNPq: 304604/2015-1 ; CNPq: 400677/2014-8 ; Government of the Russian Federation: 16-02-00821-a ; Government of the Russian Federation: 02. A03.21.0006 ; Project CICECO-Aveiro Institute of Materials - national funds through the FCT/MEC: FCT UID/CTM/50011/2013 ; CNPq: 232241/2014-7 ; Thickness dependence of imprint and polarization dynamics of Pb1-xLax(Zr1-yTiy)(1-x/4)O-3 (PLZT) thin films is reported in this work. Asymmetries in the histograms of the local piezoresponse reveal an imprint effect in the studied films whose origin could be associated to Schottky barriers near the film-substrate interface. Time-resolved spectroscopic measurements shows that the local polarization relaxation follows the exponential dependence . A maximum relaxation time approximate to 2.18s was observed for the 350nm thick film. A similar thickness dependence between grain size, correlation length () and relaxation time () suggest an intrinsic relationship between them.

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) ; Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) ; Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) ; Russian Foundation for Basic Research ; Government of the Russian Federation ; FCT/MEC ; FEDER ; CNPq: 304604/2015-1 ; CNPq: 400677/2014-8 ; CNPq: 232241/2014-7 ; Russian Foundation for Basic Research: 16-02-00821-a ; Government of the Russian Federation: 02.A03.21.0006 ; FCT/MEC: FCT UID/CTM/50011/2013 ; La-modified lead zirconate titanate (PLZT) thin films were prepared to study their physical properties at macro- and nanoscale. Piezoresponse force microscopy (PFM) studies suggest a local imprint behavior at room temperature. Confirmed by P-E hysteresis loops recorded at 180-300K, the imprint effect at room temperature tends to disappear at lower temperatures. In addition, the remanent polarization gradually increases and then decreases after reaching a maximum at around 243K. This behavior suggests the occurrence of a reentrant dipole glass or an activated electric field effect in the studied PLZT films.

We have studied the influence of initial domain structure on piezoelectric and dielectric properties of Sr 0.61 Ba 0.39 Nb 2 O 6 single crystals slightly doped with Ce and Ni. Initial domain structure was created by zero-field cooling, in-field cooling, and partial switching. The difference in the frequency dependences of macroscopic piezoelectric response and temperature dependences of dielectric permittivity for various initial domain structures was revealed. © 2018 Institute of Physics Publishing. All rights reserved. ; Equipment of the Ural Centre for Shared Use "Modern nanotechnology" Ural Federal University was used. The research was made possible by Russian Foundation of Basic Research (project № 16-02- 00821-а) and state task of Ministry of education and science of the Russian Federation (No. 3.4993.2017/6.7). The work was partially supported by Government of the Russian Federation (act 211, agreement 02.A03.21.0006). Part of this work was developed within the scope of the project CICECO-Aveiro Institute of Materials, POCI-01-0145-FEDER-007679 (FCT Ref. UID /CTM /50011/2013), financed by national funds through the FCT/MEC and when appropriate co-financed by FEDER under the PT2020 Partnership Agreement. ; et al.;NT-MDT Spectrum Instruments;Ostec-ArtTool Ltd.;Promenergolab LLC;Russian Foundation for Basic Research;Taylor and Francis Group

Single phase barium titanate–bismuth ferrite ((1-x)BaTiO3-(x)BiFeO3, BTO-BFO) solid solutions were prepared using citric acid and ethylene glycol assisted sol-gel synthesis method. Depending on the dopant content the samples are characterized by tetragonal, tetragonal-pseudocubic, pseudocubic and rhombohedral structure as confirmed by Raman spectroscopy and XRD measurements. An increase of the BFO content leads to a reduction in the cell parameters accompanied by a decrease in polar distortion of the unit cell wherein an average particle size increases from 60 up to 350 nm. Non zero piezoresponse was observed in the compounds with pseudocubic structure while no polar distortion was detected in their crystal structure using X-ray diffraction method. The origin of the observed non-negligible piezoresponse was discussed assuming a coexistence of nanoscale polar and non-polar phases attributed to the solid solutions with high BFO content. A coexistence of the nanoscale regions having polar and non-polar character is considered as a key factor to increase macroscopic piezoresponse in the related compounds due to increased mobility of the domain walls and phase boundaries. © 2020 Elsevier B.V. ; The work has been done in frame of the project TransFerr. This project has received funding from the European Union's Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement No. 778070 . The scanning probe microscopy study was funded by RFBR (grant No. 19-52-04015 ) and BRFFR (grant No. F19RM-008 ). The equipment of the Ural Center for Shared Use "Modern nanotechnology" UrFU was used. Sample structural characterization was funded by RFBR (grant № 18-38-20020 mol_a_ved). M.S. also acknowledges Russian academic excellence project "5–100″ for Sechenov University. This work was developed within the scope of the project CICECO-Aveiro Institute of Materials, refs. UIDB/50011/2020 & UIDP/50011/2020, financed by national funds through the FCT/MEC .

The ferroelectric domain structure of pure Na1/2Bi1/2TiO3 (NBT) and 1 at.% Mn-doped NBT (Mn-NBT) crystals was investigated by piezoresponse force microscopy. The correlation length of the polar regions was found to increase upon Mn substitution. High resolution transmission electron microscopy revealed that the coherency of the lattice across the domain boundaries between polar regions was also enhanced. Selected area electron diffraction showed that Mn favored coexisting 1/2 (ooo) and 1/2 (ooe) oxygen octahedral tiltings, over only 1/2 (ooo) for pure NBT. (C) 2012 American Institute of Physics. [http://dx.doi.org/10.1063/1.3699010] ; National Science Foundation (U.S.). Division of Materials Research. Materials World Network - DMR-0806592 ; United States. Department of Energy - DE-FG02-07ER46480 ; National Natural Science Foundation (China) - 50602047 ; Shanghai Municipal People's Government - 08JC1420500 ; National University of Science and Technology (MISiS). Programme of Creation and Development ; China Scholarship Council

Zirconia- and hafnia-based thin films have attracted tremendous attention in the past decade because of their unexpected ferroelectric behavior at the nanoscale, which enables the downscaling of ferroelectric devices. The present work reports an unprecedented ferroelectric rhombohedral phase of ZrO2 that can be achieved in thin films grown directly on (111)-Nb:SrTiO3 substrates by ion-beam sputtering. Structural and ferroelectric characterizations reveal (111)-oriented ZrO2 films under epitaxial compressive strain exhibiting switchable ferroelectric polarization of about 20.2 μC/cm2 with a coercive field of 1.5 MV/cm. Moreover, the time-dependent polarization reversal characteristics of Nb:SrTiO3/ZrO2/Au film capacitors exhibit typical bell-shaped curve features associated with the ferroelectric domain reversal and agree well with the nucleation limited switching (NLS) model. The polarization-electric field hysteresis loops point to an activation field comparable to the coercive field. Interestingly, the studied films show ferroelectric behavior per se, without the need to apply the wake-up cycle found in the orthorhombic phase of ZrO2. Overall, the rhombohedral ferroelectric ZrO2 films present technological advantages over the previously studied zirconia- and hafnia-based thin films and may be attractive for nanoscale ferroelectric devices. © 2021 American Chemical Society. ; This work was supported by (i) the Portuguese Foundation for Science and Technology (FCT) in the framework of the Strategic Funding Contract UIDB/04650/2020 (ii) DST-SERB, Government of India, through Grant ECR/2017/00006, (iii) Project NECL - NORTE-01-0145-FEDER-022096 and Project UID/NAN/50024/2019. This work was also developed within the scope of the project CICECO-Aveiro Institute of Materials, refs UIDB/50011/2020 and UIDP/50011/2020, financed by national funds through the Portuguese Foundation for Science and Technology/MCTES. R.F.N., M.C.I,. and C.G. acknowledge the financial support from the Romanian Ministry of Education and ...

Ferroelectric materials based on lead zirconate titanate (PZT) are widely used as sensors and actuators because of their strong piezoelectric activity. However, their application is limited because of the high processing temperature, brittleness, lack of conformal deposition, and a limited possibility to be integrated with the microelectromechanical systems (MEMS). Recent studies on the piezoelectricity in the 2-D materials have demonstrated their potential in these applications, essentially due to their flexibility and integrability with the MEMS. In this work, we deposited a few layer graphene (FLG) on the amorphous oxidized Si3N4 membranes and studied their piezoelectric response by sensitive laser interferometry and rigorous finite-element modeling (FEM) analysis. Modal analysis by FEM and comparison with the experimental results show that the driving force for the piezoelectric-like response can be a polar interface layer formed between the residual oxygen in Si3N4 and the FLG. The response was about 14 nm/V at resonance and could be further enhanced by adjusting the geometry of the device. These phenomena are fully consistent with the earlier piezoresponse force microscopy (PFM) observations of the piezoelectricity of the graphene on SiO2 and open up an avenue for using graphene-coated structures in the MEMS. © 1986-2012 IEEE. ; This work was supported in part by the Russian Foundation or Fundamental Research under Grant 16-29-14050, in part by the Ministry of Education and Science of the Russian Federation in the framework of the Increase Competitiveness Program of MISiS under Grant K2-2019-015, in part by the Project CICECO-Aveiro Institute of Materials financed by national funds through the Portuguese Foundation for Science and Technology/MCTES under Grants UIDB/50011/2020 and UIDP/50011/2020, and in part by the Center for Nanophase Materials Sciences, which is a Department of Energy Office of Science User Facility. The work was also supported by Government of the Russian Federation (Act 211, Agreement 02.A03.21.0006) and by the Ministry of Science and Higher Education of the Russian Federation (state task FEUZ-2020-0054). The equipment of the Ural Center for Shared Use "Modern nanotechnology" UrFU was used. The work of Yakov Kopelevich was supported in part by Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) and in part by the Fundação de Amparo à Pesquisa do Estado de S. Paulo (FAPESP) (Brazil).

The physical nature of the ferroelectric (FE), ferrielectric (FEI) and antiferroelectric (AFE) phases, their coexistence and spatial distributions underpins the functionality of antiferrodistortive (AFD) multiferroics in the vicinity of morphotropic phase transitions. Using Landau-Ginzburg-Devonshire (LGD) phenomenology and a semi-microscopic four sublattice model (FSM), we explore the behavior of different AFE, FEI, and FE long-range orderings and their coexistence at the morphotropic phase boundaries in FE-AFE-AFD multiferroics. These theoretical predictions are compared with the experimental observations for dense Bi1-yRyFeO3 ceramics, where R is Sm or La atoms with the fraction 0 ≤ y ≤ 0.25, as confirmed by the X-ray diffraction (XRD) and Piezoresponse Force Microscopy (PFM). These complementary measurements were used to study the macroscopic and nanoscopic transformation of the crystal structure with doping. The comparison of the measured and calculated AFE/FE phase fractions demonstrate that the LGD-FSM approach well describes the experimental results obtained by XRD and PFM for Bi1-yRyFeO3. Hence, this combined theoretical and experimental approach provides further insight into the origin of the morphotropic boundaries and coexisting FE and AFE states in model rare-earth doped multiferroics. © 2021 ; Authors acknowledge Dr. Bobby Sumpter (ORNL) and Reviewers for very useful suggestions and ideas. This material is based upon work (S.V.K.) supported by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, and performed at the Center for Nanophase Materials Sciences, a US Department of Energy Office of Science User Facility. A portion of FEM was conducted at the Center for Nanophase Materials Sciences, which is a DOE Office of Science User Facility (CNMS Proposal ID: 257). A.N.M. work is supported by the National Academy of Sciences of Ukraine (the Target Program of Basic Research of the National Academy of Sciences of Ukraine "Prospective basic research and innovative development of nanomaterials and nanotechnologies for 2020 - 2024″, Project № 1/20-Н, state registration number: 0120U102306). A.N.M., D.V.K., A.D.Y., O.M.F., T.S., V.V.S. and A.L.K. received funding from the European Union's Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie grant agreement No 778070. A.N.M. acknowledges the National Research Foundation of Ukraine. M.V.S. acknowledges financial support from the Ministry of Science and Higher Education of the Russian Federation within the framework of state support for the creation and development of World-Class Research Centers "Digital biodesign and personalized healthcare" №075–15–2020–926. Part of the work (A.L.K.) was supported by the Ministry of Education and Science of the Russian Federation in the framework of the Increase Competitiveness Program of NUST «MISiS» (No. K2–2019–015). V.V.S. and A.L.K. were additionally supported by RFBR and BRFBR, project numbers 20–58–0061 and T20R-359, respectively. Part of this work (A.L.K.) was developed within the scope of the project CICECO-Aveiro Institute of Materials, refs. UIDB/50011/2020 and UIDP/50011/2020, financed by national funds through the FCT/MCTES.