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Dipten Bhattacharya

Publications and source records attributed to Dipten Bhattacharya.

At least 19 recordsLinked to original sources

Enhanced negative capacitance in La-doped Pb(Zr$_{0.4}$Ti$_{0.6}$)O$_3$ ferroelectric capacitor from tuning of bias voltage pulse

We report a remarkable bias voltage dependent specific negative capacitance in multidomain La-doped Pb(Zr$_{0.4}$Ti$_{0.6}$)O$_3$ (PLZT) ferroelectric capacitors. The specific negative capacitance maximizes at a specific bias voltage because of emergence of maximum domain-wall density during ``switching" of the domains. Domain configuration changes from such an ``optimum" state if higher or lower bias voltage is applied at a much faster or slower rate. Phase-field simulation using time-dependent Ginzburg-Landau equation corroborates the experimental results and shows dependence of the domain-wall length during switching on the bias voltage amplitude and its maximization at a specific bias voltage amplitude. Interestingly, the radius of curvature of the resulting polarization ($P$) versus voltage ($V$) hysteresis loop at the coercive voltage ($V_C$), as well, turns out to be depending on the bias voltage. All these results indicate a close correlation among the bias voltage pulse profile (amplitude and time scale), domain-wall length during switching, shape of the resulting ferroelectric hysteresis loop, and the transient negative capacitance. It may have important ramifications both in the context of physics behind negative capacitance in a multidomain ferroelectric capacitor and devices being developed by exploiting its advantages.

cond-mat.mtrl-sci

Evidence of spin reorientation transition below 150 K from magnetic force microscopy in a ferromagnetic BiFeO$_3$ thin film

We investigated the magnetic transitions in BiFeO$_3$ at low temperature (5-300 K) and observed nearly 90$^o$ rotation of magnetic domains (imaged by vertical magnetic force microscopy) across 150 K in an epitaxial thin film of thickness $\sim$36 nm. It offers a clear evidence of spin reorientation transition. It also corroborates the transition observed below $\sim$150 K in the zero-field-cooled and field-cooled magnetization versus temperature data. The field-driven 180$^o$ domain switching at room temperature, on the other hand, signifies presence of ferromagnetism. Since bulk antiferromagnetic BiFeO$_3$ does not exhibit such a transition, this observation in ferromagnetic thin film of BiFeO$_3$ indicates a radical effect because of epitaxial strain. Density functional theory based first-principles calculations too reveal that combined in- and out-of-plane epitaxial strain induces magnetic transition from G- to C-type structure in BiFeO$_3$.

cond-mat.mtrl-sci

Charge-transfer-driven enhanced room-temperature ferromagnetism in BiFeO$_3$/Ag nanocomposite

We report observation of more than an order of magnitude jump in saturation magnetization in BiFeO$_3$/Ag nanocomposite at room temperature compared to what is observed in bare BiFeO$_3$ nanoparticles. Using transmission electron microscopy together with energy dispersive x-ray spectra (which maps the element concentration across the BiFeO$_3$/Ag interface) and x-ray photoelectron spectroscopy, we show that both the observed specific self-assembly pattern of BiFeO$_3$ and Ag nanoparticles and the charge transfer between Ag and O are responsible for such an enormous rise in room-temperature magnetization. The BiFeO$_3$/Ag nanocomposites, therefore, could prove to be extremely useful for a variety of applications including biomedical.

cond-mat.mtrl-sci

Room-temperature multiferroicity in GaFeO$_3$ thin film grown on (100)Si substrate

Room-temperature magnetoelectric multiferroicity has been observed in c-axis oriented GaFeO$_3$ thin films (space group $Pna2_1$), grown on economic and technologically important (100)Si substrates by pulsed laser deposition technique. Structural analysis and comprehensive mapping of Ga:Fe ratio across a length scale range of 10$^4$ reveal coexistence of epitaxial and chemical strain. It induces formation of finer magnetic domains and large magnetoelectric coupling - decrease in remanent polarization by $\sim$21\% under $\sim$50 kOe. Magnetic force microscopy reveals presence of both finer ($<$100 nm) and coarser ($\sim$2 $μ$m) magnetic domains. Strong multiferroicity in epitaxial GaFeO$_3$ thin films, grown on (100)Si substrate, brighten the prospect of their integration with Si-based electronics and could pave the way for development of economic and more efficient electromechanical, electrooptic or magnetoelectric sensor devices.

cond-mat.mtrl-sci

Room-temperature surface multiferroicity in Y$_2$NiMnO$_6$ nanorods

We report observation of surface-defect-induced room temperature multiferroicity - surface ferromagnetism ($M_S$ at 50 kOe $\sim$0.005 emu/g), ferroelectricity ($P_R$ $\sim$2 nC/cm$^2$), and significantly large magnetoelectric coupling (decrease in $P_R$ by $\sim$80\% under $\sim$15 kOe field) - in nanorods (diameter $\sim$100 nm) of double perovskite Y$_2$NiMnO$_6$ compound. In bulk form, this system exhibits multiferroicity only below its magnetic transition temperature $T_N$ $\approx$ 70 K. On the other hand, the oxygen vacancies, formed at the surface region (thickness $\sim$10 nm) of the nanorods, yield long-range magnetic order as well as ferroelectricity via Dzyloshinskii-Moriya exchange coupling interactions with strong Rashba spin-orbit coupling. Sharp drop in $P_R$ under magnetic field indicates strong cross-coupling between magnetism and ferroelectricity as well. Observation of room temperature magnetoelectric coupling in nanoscale for a compound which, in bulk form, exhibits multiferroicity only below 70 K underscores an alternative pathway for inducing magnetoelectric multiferroicity via surface defects and, thus, in line with magnetoelectric property observed, for example, in domain walls or boundaries or interfaces of heteroepitaxially grown thin films which do not exhibit such features in their bulk.

cond-mat.mtrl-sci

Electric-field-driven resistive transition in multiferroic SrCo$_2$Fe$_{16}$O$_{27}$/Sr$_3$Co$_2$Fe$_{24}$O$_{41}$composite

We report observation of electric-field-driven resistive transition at a characteristic threshold field $E_{th}(T)$ across a temperature range 10-200 K in an off-stoichiometric composite of (~80 vol%) W- and (~20 vol%) Z-type hexaferrites. The dielectric constant $ε$ and the relaxation time constant $τ$ too exhibit anomalous jump at $E_{th}(T)$. The $E_{th}(T)$, the extent of jump in resistivity ($Δρ$), and the hysteresis associated with the jump [$ΔE_{th}(T)$] are found to decrease systematically with the increase in temperature ($T$). Several temperature-driven phase transitions have also been noticed in low and high resistive states (LRS and HRS). The temperature-driven conduction turns out to be governed by activated hopping of small polarons at all the phases with electric ($E$) and magnetic ($H$) field dependent activation energy $U(E,H)$. Interestingly, as the temperature is raised, the $E$-driven conduction at a fixed temperature evolves from $\textit{Ohmic}$ to $\textit{non-Ohmic}$ across 10-200 K and within 110-200 K, $ρ$ follows three-dimensional variable range hopping (3D-VRH) with stretched exponential $\sim$ $exp[(E_0/E)^4]$ or power law $\sim$ $(E_0/E)^m$ ($m$ varies within $\sim$0.6-0.7 and $\sim$0.6-0.8 at LRS and HRS, respectively) dependence depending on the localization length ($ζ_E$) to diffusion length ($d_E$) ratio associated with $E$-driven conduction. The $ρ(E,T)$ follows universal scaling only at LRS within 10-110 K but not at higher temperature or at HRS. The entire set of observations has been discussed within the framework of structural evolution of the point-defect (cation vacancies or oxygen excess) network. This comprehensive map of esoteric $ρ-E-T-H$ and $ε-E-T-H$ patterns provides insights on defect driven effects in a composite useful for tuning both the resistive transition and multiferroicity.

cond-mat.str-el

Nonmonotonic magnetic field dependence of remanent ferroelectric polarization in reduced-graphene-oxide-BiFeO$_3$ nanocomposite

In a nanocomposite of reduced graphene oxide (RGO) and BiFeO$_3$ (BFO), the remanent ferroelectric polarization is found to follow nonmonotonic magnetic field dependence at room temperature as the applied magnetic field is swept across 0-20 kOe on a pristine sample. The remanent ferroelectric polarization is determined both from direct electrical measurements on an assembly of nanoparticles and powder neutron diffraction patterns recorded under 0-20 kOe field. The nanosized ($\sim$20 nm) particles of BFO are anchored onto the graphene sheets of RGO via Fe-C bonds with concomitant rise in covalency in the Fe-O bonds. The field-dependent competition between the positive and negative magnetoelectric coupling arising from magnetostriction due to, respectively, interface and bulk magnetization appears to be giving rise to the observed nonmonotonic field dependence of polarization. The emergence of Fe-C bonds and consequent change in the magnetic and electronic structure of the interface region has influenced the coupling between ferroelectric and magnetic properties remarkably and thus creates a new way of tuning the magnetoelectric properties via reconstruction of interfaces in nanocomposites or heterostructures of graphene/single-phase-multiferroic systems.

cond-mat.mtrl-sci

Large structure-dependent room temperature exchange bias in self-assembled BiFeO3 nanoparticles

We studied the magnetic properties of self-assembled aggregates of BiFeO3 nanoparticles (~ 20-40 nm). The aggregates formed two different structures - one with limited and another with massive cross-linking - via `drying-mediated self-assembly' process following dispersion of the nanoparticles within different organic solvents. They exhibit large coercivity H_C (>1000 Oe) and exchange bias field H_E (~ 350-900 Oe) in comparison to what is observed in isolated nanoparticles (H_C ~ 250 Oe; H_E ~ 0). The H_E turns out to be switching from negative to positive depending on the structure of the aggregates with |H_E| being larger. The magnetic force microscopy reveals the magnetic domains (extending across 7-10 nanoparticles) as well as the domain switching characteristics and corroborate the results of magnetic measurements. Numerical simulation of the `drying-mediated-self-assembly' process shows that the nanoparticle-solvent interaction plays an important role in forming the `nanoparticle aggregate structures' observed experimentally. Numerical simulation of the magnetic hysteresis loops, on the other hand, points out the importance of spin pinning at the surface of nanoparticles as a result of surface functionalization of the particles in different suspension media. Depending on the concentration of pinned spins at the surface pointing preferably along the easy-axis direction - from greater than 50\% to less than 50% - H_E switches from negative to positive. Quite aside from bulk sample and isolated nanoparticle, nanoparticle aggregates - resulting from surface functionalization - therefore, offer remarkable tunability of properties depending on structures.

cond-mat.mes-hall

Effect of surface pinning on magnetic nanostuctures

Magnetic nanostructures are often considered as highly functional materials because they exhibit unusual magnetic properties under different external conditions. We study the effect of surface pinning on the core-shell magnetic nanostuctures of different shapes and sizes considering the spin-interaction to be Ising-like. We explore the hysteresis properties and find that the exchange bias, even under zero field cooled conditions, increases with increase of, the pinning density and the fraction of up-spins among the pinned ones. We explain these behavior analytically by introducing a simple model of the surface. The asymmetry in hysteresis is found to be more prominent in a inverse core-shell structure, where spin interaction in the core is antiferromagnetic and that in the shell is ferromagnetic. These studied of inverse core-shell structure are extended to different shapes, sizes, and different spin interactions, namely Ising, XY- and Heisenberg models in three dimension. We also briefly discuss the pinning effects on magnetic heterostructures.

cond-mat.mes-hall

Origin of Ferroelectricity in Orthorhombic LuFeO$_3$

We demonstrate that small but finite ferroelectric polarization ($\sim$0.01 $μ$C/cm$^2$) emerges in orthorhombic LuFeO$_3$ ($Pnma$) at $T_N$ ($\sim$600 K) because of commensurate (k = 0) and collinear magnetic structure. The synchrotron x-ray and neutron diffraction data suggest that the polarization could originate from enhanced bond covalency together with subtle contribution from lattice. The theoretical calculations indicate enhancement of bond covalency as well as the possibility of structural transition to the polar $Pna2_1$ phase below $T_N$. The $Pna2_1$ phase, in fact, is found to be energetically favorable below $T_N$ in orthorhombic LuFeO$_3$ ($albeit$ with very small energy difference) than in isostructural and nonferroelectric LaFeO$_3$ or NdFeO$_3$. Application of electric field induces finite piezostriction in LuFeO$_3$ via electrostriction resulting in clear domain contrast images in piezoresponse force microscopy.

cond-mat.str-el

Nonmonotonic particle-size-dependence of magnetoelectric coupling in strained nanosized particles of BiFeO$_3$

Using high resolution powder x-ray and neutron diffraction experiments, we determined the off-centered displacement of the ions within a unit cell and magnetoelectric coupling in nanoscale BiFeO$_3$ ($\approx$20-200 nm). We found that both the off-centered displacement of the ions and magnetoelectric coupling exhibit nonmonotonic variation with particle size. They increase as the particle size reduces from bulk and reach maximum around 30 nm. With further decrease in particle size, they decrease precipitously. The magnetoelectric coupling is determined by the anomaly in off-centering of ions around the magnetic transition temperature ($T_N$). The ions, in fact, exhibit large anomalous displacement around the $T_N$ which is analyzed using group theoretical approach. It underlies the nonmonotonic particle-size-dependence of off-centre displacement of ions and magnetoelectric coupling. The nonmonotonic variation of magnetoelectric coupling with particle size is further verified by direct electrical measurement of remanent ferroelectric hysteresis loops at room temperature under zero and $\sim$20 kOe magnetic field. Competition between enhanced lattice strain and compressive pressure appears to be causing the nonmonotonic particle-size-dependence of off-centre displacement while coupling between piezo and magnetostriction leads to nonmonotonicity in the variation of magnetoelectric coupling.

cond-mat.mtrl-sci

Determination of intrinsic ferroelectric polarization in lossy improper ferroelectric systems

We measured the intrinsic hysteretic polarization in lossy improper and nanoferroelectric systems where the nonhysteretic polarization and leakage are large and the relaxation takes place over a broader time scale. We used different measurement protocols such as standard single triangular voltage pulse, a pulse train of PUND (Positive Up Negative Down), and an even more complicated pulse train of fourteen voltage pulses and compared the results obtained. We show that a protocol which sends a train of fourteen pulses is more appropriate for extracting relaxed (i.e., time scale independent) and intrinsic remanent polarization for these samples. We also point out that it is possible to select and design an appropriate measurement protocol depending on the magnitude of polarization and leakage of the system.

cond-mat.str-el

Reply to the Comment on "Superspin Glass Mediated Giant Spontaneous Exchange Bias in BiFeO$_3$-Bi$_2$Fe$_4$O$_9$ Nanocomposite [Phys. Rev. Lett. 110, 107201 (2013)]"

In this article we reply to the concerns raised by Harres $\textit{et al}$. [Phys. Rev. Lett. (to be published)] about some of the results reported in our original paper [T. Maity $\textit{et al}$. Phys. Rev. Lett. $\textbf{110}$, 107201 (2013)]. We show that the magnetic hysteresis loops are not minor and both path dependency of exchange bias and presence of superspin glass phase in the nanocomposite are indisputable.

cond-mat.str-el

Large magnetoelectric coupling in nanoscale BiFeO$_3$ from direct electrical measurements

We report the results of direct measurement of remanent hysteresis loops on nanochains of BiFeO$_3$ at room temperature under zero and $\sim$20 kOe magnetic field. We noticed a suppression of remanent polarization by nearly $\sim$40\% under the magnetic field. The powder neutron diffraction data reveal significant ion displacements under a magnetic field which seems to be the origin of the suppression of polarization. The isolated nanoparticles, comprising the chains, exhibit evolution of ferroelectric domains under dc electric field and complete 180$^o$ switching in switching-spectroscopy piezoresponse force microscopy. They also exhibit stronger ferromagnetism with nearly an order of magnitude higher saturation magnetization than that of the bulk sample. These results show that the nanoscale BiFeO$_3$ exhibits coexistence of ferroelectric and ferromagnetic order and a strong magnetoelectric multiferroic coupling at room temperature comparable to what some of the type-II multiferroics show at a very low temperature.

cond-mat.str-el

Room temperature multiferroicity in orthorhombic LuFeO$_3$

From the measurement of dielectric, ferroelectric, and magnetic properties we observe simultaneous ferroelectric and magnetic transitions around $\sim$600 K in orthorhombic LuFeO$_3$. We also observe suppression of the remanent polarization by $\sim$95\% under a magnetic field of $\sim$15 kOe at room temperature. The extent of suppression of the polarization under magnetic field increases monotonically with the field. These results show that even the orthorhombic LuFeO$_3$ is a room temperature multiferroic of type-II variety exhibiting quite a strong coupling between magnetization and polarization.

cond-mat.str-el

Origin of the asymmetric exchange bias in BiFeO$_3$-Bi$_2$Fe$_4$O$_9$ nanocomposite

We show from detailed magnetometry across 2-300 K that the BiFeO$_3$-Bi$_2$Fe$_4$O$_9$ nanocomposite offers a unique spin morphology where superspin glass (SSG) and dilute antiferromagnet in a field (DAFF) coexist at the interface between ferromagnetic Bi$_2$Fe$_4$O$_9$ and antiferromagnetic BiFeO$_3$. The coexisting SSG and DAFF combine to form a local spin texture which gives rise to a path-dependent exchange bias below the spin freezing temperature ($\sim$29K). The exchange bias varies depending on the protocol or path followed in tracing the hysteresis loop. The exchange bias has been observed below blocking temperature (T$_B$$\sim$60K) of the superparamagnetic Bi$_2$Fe$_4$O$_9$. The conventional exchange bias (CEB) increases nonmonotonically as temperature decreases. The magnitude of both exchange bias (H$_E$) and coercivity (H$_C$) increase with decrease in temperature and are found to be asymmetric below 20K depending on the path followed in tracing the hysteresis loop and bias field. The local spin texture at the interface between ferromagnetic and antiferromagnetic particles generates a nonswitchable unidirectional anisotropy along the negative direction of the applied field. The influence of this texture also shows up in "asymmetric" jumps in the hysteresis loop at 2 K which smears off at higher temperature. The role of the interface spin texture in yielding the path dependency of exchange bias is thus clearly delineated.

cond-mat.str-el

Large magnetocapacitance in electronic ferroelectric manganite systems

We have observed a sizable positive magnetocapacitance ($\sim$$5-90\%$) in perovskite Pr$_{0.55}$Ca$_{0.45}$MnO$_3$ and bilayer Pr(Sr$_{0.1}$Ca$_{0.9}$)$_2$Mn$_2$O$_7$ system under 5T magnetic field across 20-100 K below the magnetic transition point T$_N$. The magnetodielectric effect, on the other hand, exhibits a crossover: (a) from positive to negative for the perovskite system and (b) from negative to positive for the bilayer system over the same temperature range. The bilayer Pr(Sr$_{0.1}$Ca$_{0.9}$)$_2$Mn$_2$O$_7$ system exhibits a sizable anisotropy as well. We have also noticed the influence of magnetic field on the dielectric relaxation characteristics of these systems. These systems belong to a class of improper ferroelectrics and are expected to exhibit charge/orbital order driven ferroelectric polarization below the transition point T$_{CO}$. Large magnetocapacitance in these systems shows typical multiferroic behavior even though the ferroelectric polarization is small in comparison to that of other ferroelectrics.

cond-mat.str-el

Spontaneous exchange bias in a nanocomposite of BiFeO$_3$-Bi$_2$Fe$_4$O$_9$

We have observed a large as well as path-dependent spontaneous exchange bias (H$_{SEB}$) ($\sim$30-60 mT) in a nanocomposite of BiFeO$_3$-Bi$_2$Fe$_4$O$_9$ across 5-300 K when it is measured in an unmagnetized state following zero-field cooling and appropriate demagnetization. The path dependency yields a variation in the exchange bias depending on the sign of the starting field and the path followed in tracing the hysteresis loop. The asymmetry thus observed - $Δ$H$_{SEB}$ - is found to be decreasing nonmonotonically across 5-300 K with a peak around 200 K. The $Δ$H$_{SEB}$ together with large H$_{SEB}$ could have significant ramification in tuning the exchange bias driven effects and consequent applications.

cond-mat.mtrl-sci