Photoferroelectric oxides

Giant photovoltaic effect due to bulk photovoltaic effect observed in multiferroic BiFeO3 thin films has triggered a renewed interest on photoferroelectric materials for photovoltaic applications. Tremendous advance has been done to improve power conversion efficiency (up to up to 8.1%) in photoferroelectrics via absorption increase using narrow bandgap ferroelectrics. Other strategies, as it is the more efficient use of ferroelectric internal electric field, are ongoing. Moreover, as a by-product, several progress have been also achieved on photostriction that is the photo-induced deformation phenomenon. Here, we review ongoing and promising routes to improve ferroelectrics photoresponse

Strong enhancement of direct magnetoelectric effect in strained ferroelectric-ferromagnetic thin-film heterostructures

The direct magnetoelectric (ME) effect resulting from the polarization changes induced in a ferroelectric film by the application of a magnetic field to a ferromagnetic substrate is described using the nonlinear thermodynamic theory. It is shown that the ME response strongly depends on the initial strain state of the film. The ME polarization coefficient of the heterostructures involving Terfenol-D substrates and compressively strained lead zirconate titanate (PZT) films, which stabilize in the out-of-plane polarization state, is found to be comparable to that of bulk PZT/Terfenol-D laminate composites. At the same time, the ME voltage coefficient reaches a giant value of 50 V/(cm Oe), which greatly exceeds the maximum observed static ME coefficients of bulk composites. This remarkable feature is explained by a favorable combination of considerable strain sensitivity of polarization and a low electric permittivity in compressively strained PZT films. The theory also predicts a further dramatic increase of ME coefficients at the strain-induced transitions between different ferroelectric phases.Comment: 7 pages, 3 figure

Uniaxial-stress induced phase transitions in [001]c-poled 0.955Pb(Zn1/3Nb2/3)O3-0.045PbTiO3

First-order, rhombohedral to orthorhombic, stress-induced phase transitions have been evidenced by bulk charge-stress measurements and X-ray diffraction derived lattice strain measurements in [001]c-poled PZN-4.5PT. The transitions are induced by uniaxial, compressive loads applied either along or perpendicular to the poling direction. In each case, they occur via rotation of the polar vector in the Cm monoclinic plane and the induced lattice strain is hysteretic yet reversible. Although no depoling is observed in the transverse mode, net depolarization is observed under longitudinal stress which is important for the use of [001]c-poled PZN-PT and PMN-PT single crystals in Tonpilz-type underwater projectors.Comment: To be published in Applied Physics Letters, 16 pages, 3 figure

Phase transitions and ferroelectrics: revival and the future in the field

It appeared worthwhile to us to present a state-of-the-art look at the field of ferroelectrics. We are certainly not attempting to provide a complete review of all aspects of the field of ferroelectrics over the last years but we wish to transport a flavour of the current excitement in the field through the (subjective) choice of four specific examples of current interest: (i) Piezoelectrics and the morphotropic phase boundary, (ii) Multiferroics, (iii) The effect of high pressure on ferroelectrics and (iv) Strain-engineering in ferroelectric oxide thin films. For each topic we will try to work out both current interesting approaches and an outlook into future challenges. Throughout our discussion, the reader is referred to a list of significant review articles, books and papers in the field.Comment: Editorial overview, 31 pages, 4 Figures, 315 Reference

The SrTiO3_3 displacive transition revisited by Coherent X-ray Diffraction

We present a Coherent X-ray Diffraction study of the antiferrodistortive displacive transition of SrTiO$_3$, a prototypical example of a phase transition for which the critical fluctuations exhibit two length scales and two time scales. From the microbeam x-ray coherent diffraction patterns, we show that the broad (short-length scale) and the narrow (long-length scale) components can be spatially disentangled, due to 100 $\mu$m-scale spatial variations of the latter. Moreover, both components exhibit a speckle pattern, which is static on a $\sim$10 mn time-scale. This gives evidence that the narrow component corresponds to static ordered domains. We interpret the speckles in the broad component as due to a very slow dynamical process, corresponding to the well-known \emph{central} peak seen in inelastic neutron scattering.Comment: 4 pages, 3 figures, accepted in PR

Constitutive modeling of the anisotropic behavior of Mullins softened filled rubbers

Original constitutive modeling is proposed for filled rubber materials in order to capture the anisotropic softened behavior induced by general non-proportional pre-loading histo-ries. The hyperelastic framework is grounded on a thorough analysis of cyclic experimental data. The strain energy density is based on a directional approach. The model leans on the strain amplification factor concept applied over material directions according to the Mul-lins softening evolution. In order to provide a model versatile that applies for a wide range of materials, the proposed framework does not require to postulate the mathematical forms of the elementary directional strain energy density and of the Mullins softening evo-lution rule. A computational procedure is defined to build both functions incrementally from experimental data obtained during cyclic uniaxial tensile tests. Successful compari-sons between the model and the experiments demonstrate the model abilities. Moreover, the model is shown to accurately predict the non-proportional uniaxial stress-stretch responses for uniaxially and biaxially pre-stretched samples. Finally, the model is effi-ciently tested on several materials and proves to provide a quantitative estimate of the anisotropy induced by the Mullins softening for a wide range of filled rubbers

Two-step phase changes in cubic relaxor ferroelectrics

The field-driven conversion between the zero-field-cooled frozen relaxor state and a ferroelectric state of several cubic relaxors is found to occur in at least two distinct steps, after a period of creep, as a function of time. The relaxation of this state back to a relaxor state under warming in zero field also occurs via two or more sharp steps, in contrast to a one-step relaxation of the ferroelectric state formed by field-cooling. An intermediate state can be trapped by interrupting the polarization. Giant pyroelectric noise appears in some of the non-equilibrium regimes. It is suggested that two coupled types of order, one ferroelectric and the other glassy, may be required to account for these data.Comment: 27 pages with 8 figures to appear in Phys. Rev.

Phase diagram of Pb(Zr,Ti)O3 solid solutions from first principles

A first-principles-derived scheme, that incorporates ferroelectric and antiferrodistortive degrees of freedom, is developed to study finite-temperature properties of PbZr1-xTixO3 solid solutions near its morphotropic phase boundary. The use of this numerical technique (i) resolves controversies about the monoclinic ground-state for some Ti compositions, (ii) leads to the discovery of an overlooked phase, and (iii) yields three multiphase points, that are each associated with four phases. Additional neutron diffraction measurements strongly support some of these predictions.Comment: 10 pages, 2 figure

Phenomenological theory of phase transitions in epitaxial BaxSr(1-x)TiO3 thin films

A phenomenological thermodynamic theory of BaxSr(1-x)TiO3 (BST-x) thin films epitaxially grown on cubic substrates is developed using the Landau-Devonshire approach. The eighth-order thermodynamic potential for BT single crystal and modified fourth-order potential for ST single crystal were used as starting potentials for the end-members of the solid solution with the aim to develop potential of BST-$x$ solid solution valid at high temperatures. Several coefficients of these potentials for BT were changed to obtain reasonable agreement between theory and experimental phase diagram for BST-x (x > 0.2) solid solutions. For low Ba content we constructed the specific phase diagram where five phases converge at the multiphase point (T_N2 = 47 K, x = 0.028) and all transitions are of the second order. The "concentration-misfit strain" phase diagrams for BST-x thin films at room temperature and "temperature-misfit strain" phase diagrams for particular concentrations are constructed and discussed. Near T_N2 coupling between polarization and structural order parameter in the epitaxial film is modified considerably and large number of new phases not present in the bulk materials appear on the phase diagram.Comment: 8 pages 5 figure

Photostriction in Ferroelectrics from Density Functional Theory

International audienceAn ab initio procedure allowing the computation of the deformation of ferroelectric-based materials under light is presented. This numerical scheme consists in structurally relaxing the system under the constraint of a fixed n e concentration of electrons photoexcited into a specific conduction band edge state from a chosen valence band state, via the use of a constrained density functional theory method. The resulting change in lattice constant along a selected crystallographic direction is then calculated for a reasonable estimate of n e. This method is applied to bulk multiferroic BiFeO 3 and predicts a photostriction effect of the same order of magnitude than the ones recently observed. A strong dependence of photostrictive response on both the reached conduction state and the crystallographic direction (along which this effect is determined) is also revealed. Furthermore, analysis of the results demonstrates that the photostriction mechanism mostly originates from the screening of the spontaneous polarization by the photoexcited electrons in combination with the inverse piezoelectric effect. The coupling of ferroelectric or multiferroic materials with light is currently attracting a lot of attention [1], as, e.g., demonstrated by the above-band-gap photovoltages found in BiFeO 3 (BFO) thin films [2], the search of low band gap materials for photovoltaic applications [3], or the recent development in the so-called hybrid perovskite solar cells [4]. Beyond the photovoltaic effect, there is another coupling between light and properties of ferroelectrics or multiferroics that is of current interest, namely, the so-called photostriction effect, a deformation of the material under illumination [5]. The photostriction phenomenon opens new perspectives for combining several functionalities in future generations of remote switchable devices and is promising for the realization of light-induced actuators [5]. It has been recently observed in BFO under visible light [6,7]. A giant shear strain generated by femtosecond laser pulses was also reported [8,9], and time-resolved synchrotron diffraction reported a shift of the Bragg peak on a picosecond time scale in both bismuth ferrite [10] and lead titanate [11]. However, the microscopic mechanism responsible for photostriction is poorly understood [8,9]. Obviously, having accurate numerical techniques able to tackle photostriction will allow us to " shed some light " on this effect. However, to the best of our knowledge, such numerical tools allowing a systematic study of the photostriction phenomenon and its atomistic origin are not available yet, despite recent attempts to use Density Functional Theory (DFT) as a tool to fit x-ray absorption spectra in pump-probe photostriction experiments [12]. Here, we report the development of an ab initio procedure to compute photostriction from first principles. This procedure not only reproduces the order of magnitude of the observed change of lattice constant in BFO [6], but also reveals that photostriction mostly originates from the combination of the screening of the polarization by the electrons photoejected in the conduction band and the inverse piezoelectric effect. It is also found that photo-striction depends on the precise conduction state the electron is excited into, and on the crystallographic direction along which the effect is studied. In order to realize the difficulty in mimicking photo-striction, let us start by recalling that the Kohn-Sham (KS) implementation of DFT [13] reformulates the many-body problem of interacting electrons into many single-body problems, and " only " guarantees that the model noninter-acting KS Hamiltonian yields the same ground state density and energy as the real interacting Hamiltonian. Such a fact, therefore, leaves the description of unoccupied states within traditional DFT an unanswered question, and the determination of excitation energies remains the privilege of rather costly techniques, such as time-dependent DFT [14] or the GW approximation [15]. However, an alternative formulation of DFT that treats ground and excited states on the same footing has been proposed [16]. In particular, Ref. [16] connected each eigenstate of a real interacting Hamiltonian with the eigenstate of a model noninteracting Hamiltonian through a generalized adiabatic connection (GAC) scheme. The so-called ΔSCF method [17] takes advantage of this GAC scheme, and assumes an one-to-one correspondence between the excited states of a single Kohn-Sham system and the real system [16]. This ΔSCF scheme has proved successful and computationall