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Effect of (Nd, Ni) co-doped on the multiferroic and photocatalytic properties of BiFeO{sub 3}
Highlights: • Sol–gel synthesis. • Saturation magnetization and ferroelectricity increases in Ni co-doped samples. • Conduction mechanism is different in Nd doped and (Nd, Ni) co-doped samples. • Samples show good photocatalytic activity in the presence of H{sub 2}O{sub 2}. - Abstract: Bi{sub 0.95}Nd{sub 0.05}Fe{sub 1−x}Ni{sub x}O{sub 3} (x = 0, 0.01, 0.03 and 0.05) samples are synthesized by solgel method. The phase and crystal structure of the samples are confirmed by X-ray diffraction studies, Rietveld refinement is performed to calculate the structural parameters. The reflectance spectra show bands in UV and visible region and the optical band gap is calculated using Kulbeka–Munk function. The magnetization and leakage current density are strongly influenced by doping. Different conduction mechanisms are observed in Nd doped and Ni co-doped samples. All the samples exhibit ferroelectric nature at various frequencies. Photocatalytic activities of the samples are determined by the degradation of methylene blue dye in the presence of visible light and H{sub 2}O{sub 2} which shows samples are good photo-Fenton like catalyst.
Study of the structural and magnetic phase-transitions and multiferroic properties in BiFeO3-Ba0.95Ca0.05TiO3 solid solutions
Highlights: • The detailed structural analysis has been done for (1-x) BiFeO{sub 3}-xBa{sub 0.95}Ca{sub 0.05}TiO{sub 3} (0.1 ≤ x ≤ 0.9). • The detailed magnetic behavior has been studied for (1-x) BiFeO{sub 3}-xBa{sub 0.95}Ca{sub 0.05}TiO{sub 3} (0.1 ≤ x ≤ 0.9). • The dielectric constant (ε') and the dielectric loss (ε'') versus frequency curves have been fitted by using Cole-Cole dispersion formula and non-Debye relaxation behavior has been found. • The weak magnetodielectric response (MD) has been found. • The non saturating P-E loops have been found for 0.7 ≤ x ≤ 0.9 samples. - Abstract: We synthesized (1-x) BiFeO{sub 3}-x Ba{sub 0.95}Ca{sub 0.05}TiO{sub 3} solid solutions for 0.1 ≤ x ≤ 0.9, using a solid-state-reaction. The XRD analysis reveals that a composition-driven rhombohedral-to-cubic and a cubic-to-tetragonal phase-transition occur at x ≈ 0.4 and x ≈ 0.7, respectively. The experiments show that BaCaTiO{sub 3}-substitution suppresses the spiral spin-structure, which leads to net magnetization. The samples have been found to exhibit magnetic order for 0.1 ≤ x ≤ 0.7 and paramagnetic behavior for x ≥ 0.8. The electrical conductivity increases with increasing frequency of the applied electric field. The dielectric measurements suggest a non-Debye type relaxation. The samples show magneto-dielectric response (MD) upto x = 0.5, with the highest MD of 11.61% at 10 kHz for x = 0.3. The maximum attainable remanent polarization (P{sub r}) ∼ 5.24 μC/cm{sup 2} was observed for x = 0.7.
Constraining Data Mining with Physical Models: Voltage- and Oxygen Pressure-Dependent Transport in Multiferroic Nanostructures
Development of new generation electronic devices requires understanding and controlling the electronic transport in ferroic, magnetic, and optical materials, which is hampered by two factors. First, the complications of working at the nanoscale, where interfaces, grain boundaries, defects, and so forth, dictate the macroscopic characteristics. Second, the convolution of the response signals stemming from the fact that several physical processes may be activated simultaneously. Here, we present a method of solving these challenges via a combination of atomic force microscopy and data mining analysis techniques. Rational selection of the latter allows application of physical constraints and enables direct interpretation of the statistically significant behaviors in the framework of the chosen physical model, thus distilling physical meaning out of raw data. We demonstrate our approach with an example of deconvolution of complex transport behavior in a bismuth ferrite–cobalt ferrite nanocomposite in ambient and ultrahigh vacuum environments. Measured signal is apportioned into four electronic transport patterns, showing different dependence on partial oxygen and water vapor pressure. These patterns are described in terms of Ohmic conductance and Schottky emission models in the light of surface electrochemistry. Finally and furthermore, deep data analysis allows extraction of local dopant concentrations and barrier heights empowering our understanding of the underlying dynamic mechanisms of resistive switching.
Real-Space Infrared Spectroscopy of Ferroelectric Domain Walls in Multiferroic h -(Lu,Sc)FeO 3
Herein we employ synchrotron-based near-field infrared spectroscopy to image the phononic properties of ferroelectric domain walls in hexagonal ( h ) Lu 0.6 Sc 0.4 FeO 3 , and we compare our findings with a detailed symmetry analysis, lattice dynamics calculations, and prior models of domain-wall structure. Rather than metallic and atomically thin as observed in the rare-earth manganites, ferroelectric walls in h -Lu 0.6 Sc 0.4 FeO 3 are broad and semiconducting, a finding that we attribute to the presence of an A -site substitution-induced intermediate phase that reduces strain and renders the interior of the domain wall nonpolar. Mixed Lu/Sc occupation on the A site also provides compositional heterogeneity over micron-sized length scales, and we leverage the fact that Lu and Sc cluster in different ratios to demonstrate that the spectral characteristics at the wall are robust even in different compositional regimes. This work opens the door to broadband imaging of physical and chemical heterogeneity in ferroics and represents an important step toward revealing the rich properties of these flexible defect states.
Multiferroics: Focusing light on flexoelectricity
Here, the photocurrent generated at the boundary between structural phases of bismuth ferrite reveals information on the coupling between mechanical and electrical phenomena.
Manipulating magnetoelectric energy landscape in multiferroics
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A family of ionic supersalts with covalent-like directionality and unconventional multiferroicity
Ionic crystals composed of elemental ions such as NaCl are non-polar due to directionless ionic bonding interactions. Here, we show that these can develop polarity by changing their building blocks from elemental ions to superalkali and superhalogen cluster-ions, which mimic the chemistry of alkali and halogen atoms, respectively. Due to the non-spherical geometries of these cluster ions, corresponding supersalts form anisotropic polar structures with ionic bonding, yet covalent-like directionality, akin to sp 3 hybridized systems. Using density functional theory and extensive structure searches, we predict a series of stable ferroelectric/ferroelastic supersalts, PnH 4 MX 4 (Pn = N, P; M = B, Al, Fe; X = Cl, Br) composed of superalkali PnH 4 and superhalogen MX 4 ions. Unlike traditional ferroelectric/ferroelastic materials, the cluster-ion based supersalts possess ultra-low switching barrier and can endure large ion displacements and reversible strain. In particular, PH 4 FeBr 4 exhibits triferroic coupling of ferroelectricity, ferroelasticity, and antiferromagnetism with controllable spin directions via either ferroelastic or 90-degree ferroelectric switching.
Reversible control over the distribution of chemical inhomogeneities in multiferroic BiFeO3
Abstract Despite the appeal of flawless order, semiconductor technology has demonstrated that implanting inhomogeneities into single-crystalline materials is pivotal for modern electronics. However, the influence of the local arrangement of chemical inhomogeneities on the material’s functionalities is underexplored. In this work, we control the distribution of chemical inhomogeneities in La 3+ -substituted ferroelectric BiFeO 3 thin films. By means of a stress- and composition-driven phase transition, we trigger the formation of a lattice of La 3+ -rich and La 3+ -poor layers. This ordering correlates with the emergence of an antipolar phase. An electric field restores the original ferroelectric phase and re-randomizes the distribution of the La 3+ inhomogeneities. Leveraging these insights, we tune the polar/antipolar phase coexistence to set the net polarization of La 0.15 Bi 0.85 FeO 3 to any desired value between its saturation limits. Finally, we control the net polarization response in device-compliant capacitor heterostructures to show that inhomogeneity-distribution control is a valuable tool in the design of functional oxide electronics.
Thermal multiferroics in all-inorganic quasi-two-dimensional halide perovskites
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Topologically protected magnetoelectric switching in a multiferroic
Not provided.
Hidden Magnetic States Emergent Under Electric Field, In A Room Temperature Composite Magnetoelectric Multiferroic
The ability to control a magnetic phase with an electric field is of great current interest for a variety of low power electronics in which the magnetic state is used either for information storage or logic operations. Over the past several years, there has been a considerable amount of research on pathways to control the direction of magnetization with an electric field. More recently, an alternative pathway involving the change of the magnetic state (ferromagnet to antiferromagnet) has been proposed. In this paper, we demonstrate electric field control of the Anomalous Hall Transport in a metamagnetic FeRh thin film, accompanying an antiferromagnet (AFM) to ferromagnet (FM) phase transition. This approach provides us with a pathway to “hide” or “reveal” a given ferromagnetic region at zero magnetic field. By converting the AFM phase into the FM phase, the stray field, and hence sensitivity to external fields, is decreased or eliminated. Using detailed structural analyses of FeRh films of varying crystalline quality and chemical order, we relate the direct nanoscale origins of this memory effect to site disorder as well as variations of the net magnetic anisotropy of FM nuclei. Our work opens pathways toward a new generation of antiferromagnetic – ferromagnetic interactions for spintronics.