arXiv subjects

M. A. Basith

Publications and source records attributed to M. A. Basith.

At least 19 recordsLinked to original sources

arXiv2024

DyFeO3 electrode material with ultra-wide voltage window for aqueous symmetric supercapacitors

Aqueous supercapacitors (SCs) encounter limitations in operational voltage and energy density due to the low decomposition voltage of water. Here, we fabricate aqueous symmetric supercapacitors (ASSCs) employing DyFeO3 as an electrode material. This hybrid SC in a 0.5 M Na2SO4 aqueous electrolyte exhibits a significantly high working voltage of 2.5 V, with an energy density of 41.81 Wh/kg at a power density of 1250 W/kg, maintaining 94% capacitance retention after 5000 cycles. By incorporating 20% volume of acetonitrile with water in the electrolyte, we extend the potential window to 3.1 V, with an energy density of 84.43 Wh/kg at a power density of 1550 W/kg. The as-fabricated ASSC shows promising stability during a 300-hour float voltage test with almost intact capacitance retention and Coulombic efficiency. For the first time, our study unveils the potential of porous DyFeO3 as an electrode material for advancing ASSCs, featuring an unprecedented ultra-wide voltage window, along with significantly large energy and power densities.

cond-mat.mtrl-sci↗

arXiv2022

Enhanced photocatalytic dye degradation and hydrogen production ability of Bi$_{25}$FeO$_{40}$-rGO nanocomposite and mechanism insight

A comprehensive comparison between Bi$_{25}$FeO$_{40}$-reduced graphene oxide(rGO) nanocomposite and BiFeO$_{3}$-rGO nanocomposite has been performed to investigate their photocatalytic abilities in degradation of Rhodamine B dye and generation of hydrogen by water-splitting. The hydrothermal technique adapted for synthesis of the nanocomposites provides a versatile temperature-controlled phase selection between perovskite BiFeO$_{3}$ and sillenite Bi$_{25}$FeO$_{40}$. Both perovskite and sillenite structured nanocomposites are stable and exhibit considerably higher photocatalytic ability over pure BiFeO$_{3}$ nanoparticles and commercially available Degussa P25 titania. Notably, Bi$_{25}$FeO$_{40}$- rGO nanocomposite has demonstrated superior photocatalytic ability and stability under visible light irradiation than that of BiFeO$_{3}$-rGO nanocomposite. The possible mechanism behind the superior photocatalytic performance of Bi$_{25}$FeO$_{40}$-rGO nanocomposite has been critically discussed.

cond-mat.mtrl-sci↗

arXiv2022

Low temperature synthesis of BiFeO$_{3}$ nanoparticles with enhanced magnetization and promising photocatalytic performance in dye degradation and hydrogen evolution

In this investigation, we have synthesized BiFeO$_{3}$ nanoparticles by varying hydrothermal reaction temperatures from 200 $^{\circ}$C to 120 $^{\circ}$C to assess their visible-light-driven photocatalytic activity along with their applicability for hydrogen production via water splitting. The rhombohedral perovskite structure of BiFeO$_{3}$ is formed for hydrothermal reaction temperature up to 160 $^{\circ}$C, however, for a further decrement of reaction temperature a mixed sillenite phase is observed. The XRD Rietveld analysis, XPS analysis and FESEM imaging ensure the formation of single-phase and well crystalline nanoparticles at 160 $^{\circ}$C reaction temperature with 20 nm of average size. The nanoparticles fabricated at this particular reaction temperature also exhibit improved magnetization, reduced leakage current density and excellent ferroelectric behavior. These nanoparticles demonstrate considerably high absorbance in the visible range with a low bandgap (2.1 eV). The experimentally observed bandgap is in excellent agreement with the calculated bandgap using the first-principles calculations. The favorable photocatalytic performance of these nanoparticles has been able to generate more than two times of solar hydrogen compared to that produced by bulk BiFeO$_{3}$ as well as commercially available Degussa P25 titania. Notably, the experimentally observed bandgap is almost equal for both bulk material and nanoparticles prepared at different reaction temperatures. Therefore, in solar energy applications, the superiority of BFO nanoparticles prepared at 160 $^{\circ}$C reaction temperature may be attributed not only to solely their bandgap but also to other factors, such as reduced particle size, excellent morphology, well crystallinity, large surface to volume ratio, ferroelectricity and so on.

cond-mat.mtrl-sci↗

arXiv2022

First-principles study on phase stability and physical properties of B-site ordered Nd$_{2}$FeCrO$_{6}$ double perovskite

Here, the first-principles predictions on the structural stability, magnetic behavior and electronic structure of B-site ordered double perovskite Nd$_{2}$FeCrO$_{6}$ have been reported. Initially, the ground state of the parent single perovskites NdCrO$_{3}$ and NdFeO$_{3}$ have been studied to determine the relevant Hubbard U parameter to investigate the properties of Nd2CrFeO6. The thermodynamic, mechanical, and dynamic stability analyses suggest the possibility of the synthesis of Nd$_{2}$FeCrO$_{6}$ double perovskite at ambient pressure. The compound shows ferrimagnetic (FiM) nature with 2 $μ$B net magnetic moments and the magnetic ordering temperature has been estimated to be $\sim$265 K. Electronic structure indicates higher probability of direct photon transition over the indirect transition with a bandgap of $\sim$1.85 eV. Additional effect of Nd (4f) spin and spin-orbit coupling (SOC) on the band edges have been found to be negligible for this 4f-3d-3d spin system. This first-principles investigation predicts that due to the ferrimagnetic nature and significantly lower bandgap compared to its antiferromagnetic parent single perovskites, B-site ordered Nd$_{2}$FeCrO$_{6}$ double perovskite could be a promising material for spintronic and visible-light-driven energy applications.

cond-mat.mtrl-sci↗

arXiv2022

Photocatalytic water splitting ability of Fe/MgO-rGO nanocomposites towards hydrogen evolution

Photocatalytic water splitting has greatly stimulated as an ideal technique for producing hydrogen (H$_{2}$) fuel by employing two renewable sources, i.e., water and solar energy. Here, we have adopted a facile hydrothermal approach for the successful synthesis of reduced graphene oxide (rGO) incorporated Fe/MgO nanocomposites followed by thermal treatment at inert atmosphere to investigate their ability for photodegradation and photocatalytic hydrogen evolution via water splitting. Transmission Electron Microscopy images of Fe/MgO-rGO nanocomposite ensured the distribution of Fe/MgO nanoparticles throughout rGO sheets. Notably, all rGO supported nanocomposites, especially the one, thermally treated at 500 $^{o}$C at Argon (Ar) atmosphere has demonstrated significantly higher photocatalytic efficiency towards the photodegradation of a toxic textile dye, rhodamine B, than pristine MgO and commercially available Degussa P25 titania nanoparticles as well as other composites. Under solar irradiation, Fe/MgO-rGO(500) nanocomposite exhibited 86% degradation of rhodamine B dye and generated almost four times higher H$_{2}$ via photocatalytic water splitting compared to commercially available P25 titania nanoparticles. This promising photocatalytic ability of the Fe/MgO-rGO(500) nanocomposite can be attributed to the improved morphological and surface features due to heat treatment at inert atmosphere as well as escalated charge carrier separation with increased light absorption capacity imputed to rGO incorporation.

physics.chem-ph↗

arXiv2021

MoS$_{2}$ nanosheets incorporated α-Fe$_{2}$O$_{3}$/ZnO nanocomposite with enhanced photocatalytic dye degradation and hydrogen production ability

We have synthesized MoS$_{2}$ incorporated $α$-Fe$_{2}$O$_{3}$/ZnO nanocomposites by the hydrothermal process. The effect of incorporating ultrasonically exfoliated MoS$_{2}$ on the photocatalytic performance of $α$-Fe$_{2}$O$_{3}$/ZnO nanocomposites has been demonstrated. Structural, morphological and optical characteristics of the nanomaterials are investigated by performing Rietveld refinement of powder X-ray diffraction patterns, field emission scanning electron microscopy and UV-visible spectroscopy. The photoluminescence spectra of the nanocomposites show that the recombination of photogenerated electron-hole pairs is suppressed due to incorporating MoS$_{2}$ nanosheets. The ultrasonicated MoS$_{2}$ incorporated $α$-Fe$_{2}$O$_{3}$/ZnO nanocomposite shows 91% and 83% efficiency to degrade RhB dye and antibiotic ciprofloxacin under solar illumination. Active species trapping experiments reveal that the hydroxyl radicals play a significant role in RhB degradation. Likewise, the dye degradation efficiency, the amount of hydrogen produced by this nanocomposite via photocatalytic water splitting is also higher as compared to non-ultrasonicated MoS$_{2}$ incorporated $α$-Fe$_{2}$O$_{3}$/ZnO and $α$-Fe$_{2}$O$_{3}$/ZnO nanocomposites as well as Degussa P25 titania nanoparticles. This indicates the promising potential of the incorporation of ultrasonicated MoS$_{2}$ with $α$-Fe$_{2}$O$_{3}$/ZnO nanocomposite for generation of carbon-free hydrogen by water splitting. The substantial increase in the photocatalytic efficiency of $α$-Fe$_{2}$O$_{3}$/ZnO after incorporation of ultrasonicated MoS$_{2}$ can be attributed to its favorable band structure, large surface to volume ratio, effective segregation and migration of photogenerated electron-hole pairs at the interface of heterojunction and the active edge sites provided by few-layer MoS$_{2}$ nanosheets.

physics.app-ph↗

arXiv2021

Sol-gel synthesized double perovskite Gd$_{2}$FeCrO$_{6}$ nanoparticles: Structural, magnetic and optical properties

Lead-free double perovskites are overtaking single perovskites as solar harvesting materials due to their superior stability, excellent catalytic efficiency and minimal toxicity. In this investigation, we have synthesized double perovskite Gd$_{2}$FeCrO$_{6}$ (GFCO) nanoparticles for the first time via a facile sol-gel technique to investigate their structural, magnetic and optical properties. The double perovskite GFCO crystallized in monoclinic structure with P2$_1$/n space group. The Fe/Cr-O bond length was calculated as $\sim$1.95 angstrom from the Raman spectrum which was consistent with the value, $\sim$1.99 angstrom obtained from X-ray diffraction analysis. The average size of the nanoparticles was determined to be $\sim$70 nm by both field emission scanning electron microscopy and transmission electron microscopy. The existence of mixed-valence states of Fe and Cr was confirmed by X-ray photoelectron spectroscopy. The zero-field cooled (ZFC) and field cooled (FC) curves largely diverged below 20 K. A downturn was observed in the ZFC curve at 15 K which corresponds to an antiferromagnetic, Néel transition. The narrow magnetic hysteresis loop recorded at 5 K was nearly saturated and demonstrated an asymmetric shift along the magnetic field axis indicating the concurrence of ferromagnetic and antiferromagnetic domains in GFCO nanoparticles. The UV-visible and photoluminescence spectroscopic analyses unveiled the semiconducting nature of nanostructured GFCO with an optical band gap of 2.0 eV. The as-synthesized thermally stable lead-free GFCO semiconductor might be a potential perovskite material to be employed in photocatalytic and related solar energy applications due to its ability to absorb the visible spectrum of the solar light efficiently

cond-mat.mtrl-sci↗

arXiv2021

Nanostructured LaFeO$_{3}$-MoS$_{2}$ for efficient photodegradation and photocatalytic hydrogen evolution

The fabrication of heterogeneous photocatalysts has received increasing research interest due to their potential applications for the degradation of organic pollutants in wastewater and the evolution of carbon-free hydrogen fuel via water splitting. Here, we report the photodegradation and photocatalytic hydrogen generation abilities of nanostructured LaFeO$_{3}$-MoS$_{2}$ photocatalyst synthesized by facile hydrothermal technique. Prior to conducting photocatalytic experiments, structural, morphological, and optical properties of the nanocomposite were extensively investigated using X-ray diffraction analysis, field emission scanning electron microscopy, and UV-visible spectroscopy, respectively. Nanostructured LaFeO$_{3}$-MoS$_{2}$ photodegraded 96% of rhodamine B dye within only 150 minutes which is considerably higher than that of LaFeO$_{3}$ and commercial Degussa P25 titania nanoparticles. The LaFeO$_{3}$-MoS$_{2}$ nanocomposite also exhibited significantly enhanced photocatalytic efficiency in the decomposition of a colorless probe pollutant, ciprofloxacin eliminating the possibility of the dye-sensitization effect. Moreover, LaFeO$_{3}$-MoS$_{2}$ demonstrated superior photocatalytic activity towards solar hydrogen evolution via water splitting. Considering the band structures and contribution of reactive species, a direct Z-scheme photocatalytic mechanism is proposed to rationalize the superior photocatalytic behavior of LaFeO$_{3}$-MoS$_{2}$ nanocomposite.

physics.app-ph↗

arXiv2021

First-principles calculation of the electronic and optical properties of Gd$_{2}$FeCrO$_{6}$ double perovskite: Effect of Hubbard U parameter

We have synthesized Gd$_{2}$FeCrO$_{6}$ (GFCO) double perovskite which is crystallized in a monoclinic structure with P2$_{1}/$n space group. The UV-visible and photoluminescence spectroscopic analyses confirmed its direct bandgap semiconducting nature. Employing experimentally obtained structural parameters in first-principles calculation, we report the spin-polarized electronic band structure, charge carrier effective mass, density of states, electronic charge density distribution and optical absorption property of the GFCO double perovskite. The effects of on-site d-d Coulomb interaction energy (U$_{eff}$) on the electronic and optical properties were investigated by applying a range of Hubbard U$_{eff}$ parameters from 0 to 6 eV to the Fe-3d and Cr-3d orbitals within the generalized gradient approximation (GGA) and GGA+U methods. When we applied U$_{eff}$ in the range of 1 to 5 eV, both the up-spin and down-spin band structures were observed to be direct. The charge carrier effective masses were also found to enhance gradually from U$_{eff} =$ 1 eV to 5 eV, but, these values were anomalous for U$_{eff} =$ 0 and 6 eV. These results suggest that U$_{eff}$ should be limited within the range of 1 to 5 eV to calculate the structural, electronic and optical properties of GFCO double perovskite. We observed that considering U$_{eff} =$ 3 eV, the theoretically calculated optical band gap 1.99 eV matched well with the experimentally obtained value 2.0 eV. The outcomes of our finding imply that the U$_{eff}$ value of 3 eV most accurately localized the Fe-3d and Cr-3d orbitals of GFCO keeping the effect of self-interaction error from the other orbitals almost negligible. Therefore, we may recommend U$_{eff} =$ 3 eV for first-principles calculation of the electronic and optical properties of GFCO double perovskite that might have potential in photocatalytic and related solar energy applications.

cond-mat.mtrl-sci↗

arXiv2021

Lead-free CsSnCl$_{3}$ perovskite nanocrystals: Rapid synthesis, experimental characterization and DFT simulations

In this investigation, we have synthesized thermally stable cubic CsSnCl$_{3}$ perovskite nanocrystals (crystal size ~300 nm) with better surface morphology by the hot-injection technique. Excellent crystalline quality of these cubic nanocrystals was confirmed by high-resolution transmission electron microscopy imaging. The binding of organic ligands on the surface of the sample was characterized by nuclear magnetic resonance spectroscopy. The UV-visible spectroscopy ensured that CsSnCl$_{3}$ nanocrystals have a direct bandgap of ~2.98 eV which was confirmed by steady-state photoluminescence spectroscopy. The band edge positions calculated by the Mulliken electronegativity approach predicted the potential photocatalytic capability of the nanocrystals which was then experimentally confirmed by the photodegradation of RhB dye under visible and UV-visible irradiation. Our theoretical calculation by employing the generalized gradient approximation (GGA) and GGA + U methods demonstrated 90% accurate estimation of experimentally observed optical bandgap when $U_{eff}$ = 6 eV was considered. The ratio of the effective masses of the hole and electron expressed as D = $m_{h}^{*}/m_{e}^{*}$ was also calculated for $U_{eff}$ = 6 eV. Based on this theoretical calculation and experimental observation of the photocatalytic performance of CsSnCl$_{3}$ nanocrystals, we have proposed a new interpretation of the "D" value: a "D" value of either much smaller or much larger than 1 is the indication of low recombination rate of the photogenerated electron-hole pairs and the high photocatalytic efficiency of a photocatalyst. We believe that this comprehensive investigation may be helpful for the large-scale synthesis of thermally stable cubic CsSnCl$_{3}$ nanocrystals and also for a greater understanding of their potential in photocatalytic, photovoltaics and other prominent optoelectronic applications.

cond-mat.mtrl-sci↗

arXiv2021

Room temperature ferroic orders in Zr and (Zr, Ni) doped SrTiO$_3$

We synthesized strontium titanate SrTiO$_3$ (STO), Zr doped $\text{Sr}_\text{1-x}\text{Zr}_\text{x}\text{Ti}\text{O}_3$ and (Zr, Ni) co-doped $\text{Sr}_\text{1-x}\text{Zr}_\text{x}\text{Ti}_\text{1-y}\text{Ni}_\text{y}\text{O}_3$ samples using solid state reaction technique to report their structural, electrical and magnetic properties. The cubic $Pm$-$3m$ phase of the synthesized samples has been confirmed using Rietveld analysis of the powder X-ray diffraction pattern. The grain size of the synthesized materials was reduced significantly due to Zr doping as well as (Zr, Ni) co-doping in STO. The chemical species of the samples were identified using energy-dispersive X-ray spectroscopy. We observed forbidden first order Raman scattering at 148, 547 and 797 cm$^{-1}$ which may indicate nominal loss of inversion symmetry in cubic STO. The absence of absorption at 500 cm$^{-1}$ and within 600-700 cm$^{-1}$ band in Fourier Transform Infrared spectra corroborates Zr and Ni as substitutional dopants in our samples. Due to 4% Zr doping in $\text{Sr}_\text{0.96}\text{Zr}_\text{0.04}\text{Ti}\text{O}_3$ sample dielectric constant, remnant electric polarization, remnant magnetization and coercivity were increased. Notably, in the case of 4% Zr and 10% Ni co-doping we have observed clearly the existence of both FE and FM hysteresis loops in $\text{Sr}_{0.96}\text{Zr}_{0.04}\text{Ti}_{0.90}\text{Ni}_{0.10}\text{O}_3$ sample. In this co-doped sample, the remnant magnetization and coercivity were increased by $\sim$1 and $\sim$2 orders of magnitude respectively as compared to those of undoped STO. The coexistence of FE and FM orders in (Zr, Ni) co-doped STO might have the potential for interesting multiferroic applications.

cond-mat.mtrl-sci↗

arXiv2020

Fabrication of zinc oxide/graphene-carbon nanotubes nanocomposite with enhanced dye degradation ability

A comparative study between zinc oxide graphene-carbon nanotubes nanocomposite and ZnO nanoparticles was carried out to investigate their abilities in the degradation of Rhodamine B dye. We utilized the Modified Hummer method to prepare the graphene oxide nanosheet. Moreover, graphene-carbon nanotubes had been synthesized from GO and multi-walled carbon nanotubes with a hydroxyl group. The hydrothermal method was employed to fabricate the zinc oxide graphene-carbon nanotubes nanocomposite from ZnO nanoparticles and graphene-carbon nanotubes. During the characterization by X-ray Diffraction (XRD), all the significant peaks of ZnO and zinc oxide graphene-carbon nanotubes nanocomposite were found in the same phase angle. In addition, the final nanocomposite was also characterized by Field Emission Scanning Electron Microscope (FESEM) and Energy Dispersive X-ray Spectroscopy (EDS). Finally, from the dye degradation test, it was apparent that zinc oxide graphene-carbon nanotubes nanocomposite showed superior dye removal ability compared to the ZnO nanoparticles.

cond-mat.mes-hall↗

arXiv2017

Dy doped BiFeO$_3$ : A Bulk Ceramic with Improved Multiferroic Properties Compared to Nano Counterparts

The synthesis as well as structural, multiferroic and optical characterization of Dy doped BiFeO$_3$ multiferroic ceramic are presented. Bulk polycrystalline Bi$_{0.9}$Dy$_{0.1}$FeO$_3$ sample is synthesized by solid state reaction, while their nano counterparts are prepared using ultrasonic probe sonication technique. Significant improvement of phase purity in the as synthesized samples is observed after the doping of Dy both in bulk Bi$_{0.9}$Dy$_{0.1}$FeO$_3$ sample and corresponding nanoparticles as evidenced from Rietveld refinement. Magnetization measurements using SQUID magnetometer exhibit enhanced magnetic properties for Dy doped bulk Bi$_{0.9}$Dy$_{0.1}$FeO$_3$ ceramic compared to their nanostructured counterparts as well as undoped BiFeO$_3$. Within the applied field range, saturation polarization is observed for Bi$_{0.9}$Dy$_{0.1}$FeO$_3$ bulk ceramic only. As a result, intrinsic ferroelectric behavior is obtained just for this sample. Optical bandgap measurements reveal lower bandgap for Dy doped bulk Bi$_{0.9}$Dy$_{0.1}$FeO$_3$ ceramic compared to that of corresponding nanoparticles and undoped BiFeO$_3$. The outcome of this investigation demonstrates the potential of Dy as a doping element in BiFeO$_3$ that provides a bulk ceramic material with improved multiferroic and optical properties compared to those of corresponding nanoparticles which involve rigorous synthesis procedure.

cond-mat.mes-hall↗

arXiv2017

Preparation of high crystalline nanoparticles of rare-earth based complex pervoskites and comparison of their structural and magnetic properties with bulk counterparts

A simple route to prepare Gd$_{0.7}$Sr$_{0.3}$MnO$_3$ nanoparticles by ultrasonication of their bulk powder materials is presented in this article. For comparison, Gd$_{0.7}$Sr$_{0.3}$MnO$_3$ nanoparticles are also prepared by ball milling. The prepared samples are characterized by X-ray diffraction (XRD),field emission scanning electron microscope (FESEM), energy dispersive X-ray (EDX), X-ray photoelectron spectroscope (XPS), and Superconducting Quantum Interference Device (SQUID) magnetometer. XRD Rietveld analysis is carried out extensively for the determination of crystallographic parameters and the amount of crystalline and amorphous phases. FESEM images demonstrate the formation of nanoparticles with average particle size in the range of 50-100 nm for both ultrasonication and 4 hours (h) of ball milling. The bulk materials and nanoparticles synthesized by both ultrasonication and 4 h ball milling exhibit a paramagnetic to spin-glass transition. However, nanoparticles synthesized by 8 h and 12 h ball milling do not reveal any phase transition, rather show an upturn of magnetization at low temperature. The degradation of the magnetic properties in ball milled nanoparticles may be associated with amorphization of the nanoparticles due to ball milling particularly for milling time exceeding 8 h. This investigation demonstrates the potential of ultrasonication as a simple route to prepare high crystalline rare-earth based manganite nanoparticles with improved control compared to the traditional ball milling technique.

cond-mat.mes-hall↗

arXiv2016

Effect of Strontium substitution on the structural and magnetic properties of La1.8Sr0.2MMnO6 (M = Ni, Co) layered manganites

Sr substituted perovskites La1.8Sr0.2MMnO6 (M = Ni, Co) were synthesized using solid state reaction technique to present a systematic study on their morphological, structural and magnetic properties. The average grain size of the as-prepared La1.8Sr0.2NiMnO6 samples are in the range of 0.2-0.7 μm and those for La1.8Sr0.2CoMnO6 manganites are 0.1-2.8 μm, which is significantly less than that of unsubstituted La2NiMnO6 (LNMO) and La2CoMnO6 (LCMO) manganites. The XPS analysis enlightened about phase purity, binding energy and oxygen vacancy of La1.8Sr0.2MMnO6 manganites. The Sr substituted LNMO has revealed a sharp ferromagnetic to paramagnetic phase transition at 160 K which is about 120 K less than that of parent LNMO. The Sr substituted LCMO exhibited such a transition at 220 K which is 8 K less than that of parent LCMO. The temperature dependent magnetization measurements suggest that the effect of Sr on the transition temperature in LNMO is more significant than that of LCMO.

cond-mat.str-el↗

arXiv2016

The 10% Gd and Ti co-doped BiFeO$_3$: A promising multiferroic material

In this investigation, undoped BiFeO$_3$, Gd doped Bi$_{0.9}$Gd$_{0.1}$FeO$_3$, and Gd-Ti co-doped Bi$_{0.9}$Gd$_{0.1}$Fe$_{1-x}$Ti$_x$O$_3$ (x = 0.10, 0.20) materials were synthesized to report their multiferroic properties. The structural analysis and phase identification of these multiferroic ceramics were performed using Rietveld refinement. The Rietveld analysis has confirmed the high phase purity of the 10% Gd-Ti co-doped Bi$_{0.9}$Gd$_{0.1}$Fe$_{0.9}$Ti$_{0.1}$O$_3$ sample compared to that of other compositions under investigation. The major phase of this particular composition is of rhombohedral \textit{R3c} type structure (wt% $>99\%$) with negligible amount of impurity phases. In terms of characterization, we address magnetic properties of this co-doped ceramic system by applying substantially higher magnetic fields than that applied in previously reported investigations. The dependence of temperature and maximum applied magnetic fields on their magnetization behavior have also been investigated. Additionally, the leakage current density has been measured to explore its effect on the ferroelectric properties of this multiferroic system. The outcome of this investigation suggests that the substitution of 10% Gd and Ti in place of Bi and Fe, respectively, in BiFeO$_3$ significantly enhances its multiferroic properties. The improved properties of this specific composition is associated with homogeneous reduced grain size, significant suppression of impurity phases and reduction in leakage current density which is further asserted by polarization vs. electric field hysteresis loop measurements.

cond-mat.mtrl-sci↗

arXiv2016

Saturation magnetization and band gap tuning in BiFeO$_3$ nanoparticles via co-substitution of Gd and Mn

In this investigation, Gd and Mn co-doped Bi$_{0.85}$Gd$_{0.15}$Fe$_{1-x}$Mn$_x$O$_3$ (x=0.0-0.15) nanoparticles have been prepared to report the influence of co-substitution on their structural, optical, magnetic and electrical properties. Due to simultaneous substitution of Gd and Mn in BiFeO$_3$, the crystal structure has been modified from rhombohedral (R3c) to orthorhombic (Pn21a) and the Fe-O-Fe bond angle and Fe-O bond length have been changed. For Mn doping up to 10 % in Bi$_{0.85}$Gd$_{0.15}$Fe$_{1-x}$Mn$_x$O$_3$ nanoparticles, the saturation magnetization (Ms) has been enhanced significantly, however, for a further increase of doping up to 15 %, the Ms has started to reduce again. The co-substitution of Gd and Mn in BiFeO$_3$ nanoparticles also demonstrates a strong reduction in the optical band gap energy and electrical resistivity compared to that of undoped BiFeO$_3$.

cond-mat.mes-hall↗

arXiv2016

Size dependent magnetic and electrical properties of Ba-doped nanocrystalline BiFeO$_3$

Improvement in magnetic and electrical properties of multiferroic BiFeO$_3$ in conjunction with their dependence on particle size is crucial due to its potential applications in multifunctional miniaturized devices. In this investigation, we report a study on particle size dependent structural, magnetic and electrical properties of sol-gel derived Bi$_{0.9}$Ba$_{0.1}$FeO$_3$ nanoparticles of different sizes ranging from $\sim$ 12 to 49 nm. The substitution of Bi by Ba significantly suppresses oxygen vacancies, reduces leakage current density and Fe$^{2+}$ state. An improvement in both magnetic and electrical properties is observed for 10 % Ba-doped BiFeO$_3$ nanoparticles compared to its undoped counterpart. The saturation magnetization of Bi$_{0.9}$Ba$_{0.1}$FeO$_3$ nanoparticles increase with reducing particle size in contrast with a decreasing trend of ferroelectric polarization. Moreover, a first order metamagnetic transition is noticed for $\sim$ 49 nm Bi$_{0.9}$Ba$_{0.1}$FeO$_3$ nanoparticles which disappeared with decreasing particle size. The observed strong size dependent multiferroic properties are attributed to the complex interaction between vacancy induced crystallographic defects, multiple valence states of Fe, uncompensated surface spins, crystallographic distortion and suppression of spiral spin cycloid of BiFeO$_3$.

cond-mat.mes-hall↗