A thorough Investigation of Rare-Earth Dy3+ Substituted Cobalt-Chromium Ferrite and Its Magnetoelectric Nanocomposite.

The stoichiometric compositions of a ferrite system with a chemical formula CoCr0.5DyxFe1.5-xO4 where x = 0.0, 0.025, 0.05, 0.075 and 0.1 were prepared by the sol-gel auto-combustion method. The structural, morphological and magnetic properties were studied by the X-ray diffraction (XRD), infra-red spectroscopy (IR), scanning electron microscopy, transmission electron microscopy and vibrating sample magnetometer. XRD analysis confirmed the cubic spinel structure of the prepared samples without the presence of any impurity and secondary phases. Selected area electron diffraction and IR measurements gives further confirmation to the XRD observations. Considering that strain mechanism, elastic properties and cation distribution play a major role for controlling the magnetic properties and therefore these properties were precisely evaluated through reliable methodologies such as XRD and IR data. The cation distribution was determined by the X-ray diffraction data which are further supported by the magnetization studies. Magnetoelectric properties of CoCr0.5DyxFe1.5-xO4 + BaTiO3 have also been investigated. The mechanisms involved are discussed in the manuscript.

Interface-Driven Multiferroicity in Cubic BaTiO3-SrTiO3 Nanocomposites.

Perovskite multiferroics have drawn significant attention in the development of next-generation multifunctional electronic devices. However, the majority of existing multiferroics exhibit ferroelectric and ferromagnetic orderings only at low temperatures. Although interface engineering in complex oxide thin films has triggered many exotic room-temperature functionalities, the desired coupling of charge, spin, orbital and lattice degrees of freedom often imposes stringent requirements on deposition conditions, layer thickness and crystal orientation, greatly hindering their cost-effective large-scale applications. Herein, we report an interface-driven multiferroicity in low-cost and environmentally friendly bulk polycrystalline material, namely cubic BaTiO3-SrTiO3 nanocomposites which were fabricated through a simple, high-throughput solid-state reaction route. Interface reconstruction in the nanocomposites can be readily controlled by the processing conditions. Coexistence of room-temperature ferromagnetism and ferroelectricity, accompanying a robust magnetoelectric coupling in the nanocomposites, was confirmed both experimentally and theoretically. Our study explores the 'hidden treasure at the interface' by creating a playground in bulk perovskite oxides, enabling a broad range of applications that are challenging with thin films, such as low-power-consumption large-volume memory and magneto-optic spatial light modulator.

Impact of Sm3+ and Er3+ Cations on the Structural, Optical, and Magnetic Traits of Spinel Cobalt Ferrite Nanoparticles: Comparison Investigation.

In this study, we investigated a comparison of the structure, morphology, optic, and magnetic (room temperature (RT)) features of Er3+ and Sm3+ codoped CoFe2O4 (CoErSm) nanospinel ferrite (NSFs) (x ≤ 0.05) synthesized via hydrothermal (H-CoErSm NSFs) and sonochemical (S-CoErSm NSFs) approaches. The formation of all products via both synthesis methods has been validated by X-ray powder diffraction (XRD) and scanning electron microscopy (SEM), along with energy-dispersive X-ray (EDX) and transmission electron microscopy (TEM) techniques. The single phase of the spinel structure (except for the Hyd sample with x = 0.03) was evidenced by XRD analysis. The D XRD (crystallite size) values of H-CoErSm and S-CoErSm NSFs are in the 10-14.7 and 10-16 nm ranges, respectively. TEM analysis presented the cubic morphology of all products. A UV-visible percent diffuse reflectance (DR %) study was performed on all products, and E g (direct optical energy band gap) values varying in the 1.32-1.48 eV range were projected from the Tauc plots. The data of RT magnetization demonstrated that all prepared samples are ferromagnetic in nature. M-H data revealed that rising the contents of cosubstituent elements (Sm3+ and Er3+ ions) caused an increase in M s (saturation magnetization) and H c (coercive field) in comparison to pristine samples. Although concentration dependence is significant (x > 0.02), no strict regularity (roughly fluctuating) has been ruled out in M s values for doped samples prepared via the hydrothermal method. However, sonochemically prepared samples demonstrated that M s values increase with increasing x up to x = 0.04 and then decrease with the further rise in cosubstituent Sm3+ and Er3+ ions. The calculated values of M s and H c were found to be greater in H-CoErSm NSFs compared to those in S-CoErSm NSFs. The present investigation established that the distribution of cations and the variation in crystallite/particle sizes are efficient to control the intrinsic properties of all samples.

Structural, Magnetic, and Mossbauer Parameters' Evaluation of Sonochemically Synthesized Rare Earth Er3+ and Y3+ Ions-Substituted Manganese-Zinc Nanospinel Ferrites.

The effect of Er3+ and Y3+ ion-co-substituted Mn0.5Zn0.5Er x Y x Fe2-2x O4 (MZErYF) (x ≤ 0.10) spinel nanoferrites (SNFs) prepared by a sonochemical approach was investigated. Surface and phase analyses were carried out using SEM, TEM, and XRD. Hyperfine parameters were determined by fitting room-temperature (RT) Mossbauer spectra. Magnetic field-dependent magnetization data unveiled the superparamagnetic nature at RT and ferrimagnetic nature at 10 K. RT saturation magnetization (M S) and calculated magnetic moments (n B) are 34.84 emu/g and 1.47 µB, respectively, and have indirect proportionalities with increasing ion content. M S and n B data have a similar trend at 10 K including remanent magnetizations (M r). The measured coercivities (H C) are between 250 and 415 Oe. The calculated squareness ratios are in the range of 0.152-0.321 for NPs and assign the multidomain nature for NPs at 10 K. The extracted effective magnetocrystalline constants (K eff) have an order of 104 erg/g except for Mn0.5Zn0.5Er0.10Y0.10Fe1.80O4 SNFs that has 3.37 × 105 erg/g. This sample exhibits the greatest magnetic hardness with the largest magnitude of H C = 415 Oe and an internal anisotropy field H a = 1288 Oe among all magnetically soft NPs.

TiO2-Doped Ni0.4Cu0.3Zn0.3Fe2O4 Nanoparticles for Enhanced Structural and Magnetic Properties.

TiO2 (0-10 wt %)-doped nanocrystalline Ni0.4Cu0.3Zn0.3Fe2O4 (Ni-Cu-Zn) ferrites were synthesized using the sol-gel route of synthesis. The cubic spinel structure of the ferrites having the Fd3m space group was revealed from the analysis of Rietveld refined X-ray diffraction (XRD) data. The secondary phase of TiO2 with a space group of I41/amd was observed within the ferrites with doping, x > 3 wt %. The values of lattice parameter were enhanced with the addition of TiO2 up to 5 wt % and reduced further for the highest experimental doping of 10 wt %. Field emission scanning electron microscopy (FESEM) images exhibit the spherical shape of the synthesized particles with some agglomeration, while the compositional purity of prepared ferrite samples was confirmed by energy-dispersive X-ray spectroscopy (EDX) and elemental mapping. The cubic spinel structure of the prepared ferrite sample was confirmed by the Raman and Fourier transform infrared (FTIR) spectra. UV-visible diffuse reflectance spectroscopy was utilized to study the optical properties of the ferrites. The value of band gap energy for the pristine sample was less than those of the doped samples, and there was a decrement in band gap energy values with an increase in TiO2 doping, which specifies the semiconducting nature of prepared ferrite samples. A magnetic study performed by means of a vibrating sample magnetometer (VSM) demonstrates that the values of saturation magnetization of the ferrites decrease with the addition of TiO2 content, and all investigated ferrites show the characteristics of soft magnetic materials at room temperature. The Mössbauer study confirms the decrease in the magnetic behavior of the doped ferrites due to the nonmagnetic secondary phase of TiO2.

Dynamical magnetic behavior of anisotropic spinel-structured ferrite for GHz technologies.

We have fabricated a high quality magnetic Ni0.5Zn0.5Fe2O4 ferrite powder/polymer composite sheet consisting of common and environmentally friendly elements only. The sheet was then tested for its dynamic permeability by irradiating with electromagnetic waves with frequencies up to 50 GHz. Two different originally developed methods were used for the high-frequency permeability measurements, a short-circuited microstrip line method and a microstrip line-probe method. It is challenging to measure the dynamic permeability of magnetic thin films/sheets beyond 10 GHz because of the low response signal from these materials. However, the two methods produced essentially equivalent results. In the frequency dependent permeability profile, the maximum position of the profile, [Formula: see text], shifted towards higher frequencies upon increasing an applied (strong) static external magnetic field, [Formula: see text]. A linear relationship between [Formula: see text] and [Formula: see text] for the entire range of [Formula: see text] was observed even at small [Formula: see text]. In general, the spinel-structured Ni-based ferrites exhibit low magnetic anisotropy, but the present sample showed a uniaxial-anisotropic behavior in the parallel direction of the sheet. Our Ni0.5Zn0.5Fe2O4 powder/polymer composite sheet thus exhibits high performance at GHz frequencies, and should be applicable e.g. as an anisotropic electromagnetic wave-interference material.

Impact of Tm3+ and Tb3+ Rare Earth Cations Substitution on the Structure and Magnetic Parameters of Co-Ni Nanospinel Ferrite.

Tm-Tb co-substituted Co-Ni nanospinel ferrites (NSFs) as (Co0.5Ni0.5) [TmxTbxFe2-2x]O4 (x = 0.00-0.05) NSFs were attained via the ultrasound irradiation technique. The phase identification and morphologies of the NSFs were explored using X-rays diffraction (XRD), selected area electron diffraction (SAED), and transmission and scanning electronic microscopes (TEM and SEM). The magnetization measurements against the applied magnetic field (M-H) were made at 300 and 10 K with a vibrating sample magnetometer (VSM). The various prepared nanoparticles revealed a ferrimagnetic character at both 300 and 10 K. The saturation magnetization (Ms), the remanence (Mr), and magneton number (nB) were found to decrease upon the Tb-Tm substitution effect. On the other hand, the coercivity (Hc) was found to diminish with increasing x up to 0.03 and then begins to increase with further rising Tb-Tm content. The Hc values are in the range of 346.7-441.7 Oe at 300 K to 4044.4-5378.7 Oe at 10 K. The variations in magnetic parameters were described based on redistribution of cations, crystallites and/or grains size, canting effects, surface spins effects, super-exchange interaction strength, etc. The observed magnetic results indicated that the synthesized (Co0.5Ni0.5)[TmxTbxFe2-x]O4 NSFs could be considered as promising candidates to be used for room temperature magnetic applications and magnetic recording media.

Synthesis of Dy-Y co-substituted manganese­zinc spinel nanoferrites induced anti-bacterial and anti-cancer activities: Comparison between sonochemical and sol-gel auto-combustion methods.

This study described the beneficial properties of ultrasonic irradiation approach to synthesize the spinel-type Dy-Y co-substituted Mn-Zn nanospinel ferrites (NSFs). We have used two different approaches like citrate sol-gel combustion and ultrasonic irradiation routes to produced series of Mn0.5Zn0.5Fe2-2x(DyxYx)O4 (0.0 ≤ x ≤ 0.05) NSFs (DyY-MnZn NSFs). The structure and morphology of NSFs X-was examined by using XRD, EDX, SEM and TEM methods. We have found that spinel ferrites and hematite phase in DyY-MnZn NSFs produced by citrate sol-gel, while DyY-MnZn NSFs created by ultrasonic irradiation contain a pure phase of spinel ferrite. TEM analysis revealed the spherical nanoparticles with fairly uniform size. We have also analyzed the biological applications of DyY-MnZn NSFs prepared by both methods (ultrasonication and sol-gel) by examining their anti-cancer and anti-bacterial (Escherichia coli and Staphylococcus aureu) activities. We have found that both methods produced inhibitory actions on colon cancer cells (HCT-116) and bacterial cells, whereas, no inhibitory action was observed when examined on normal and non-cancerous cells (HEK-293).

Structural, mechanical, dielectric properties and magnetic interactions in Dy3+-substituted Co-Cu-Zn nanoferrites.

Sol-gel-synthesized Co-Cu-Zn ferrite nanoparticles diluted with Dy3+ ions were investigated in terms of their structural, morphological, elastic, magnetic and dielectric properties. X-ray diffraction patterns showed the formation of a single-phase cubic spinel structure. As the concentration of Dy3+ ions was increased, the lattice length gradually increased from 8.340 to 8.545 Å, obeying Vegard's law. The Williamson-Hall (W-H) method was employed to observe the change in the lattice strain. Crystallite size obtained from W-H plots followed a pattern similar to that observed using the Scherrer equation. The cation distribution suggested a strong preference of Dy3+ ions for the octahedral B site while Cu2+ and Fe3+ ions were distributed over both A and B sites. The microstructures of the samples were visualized using transmission electron microscopy. Mechanical properties such as stiffness constant, longitudinal and transverse wave velocities, Young's modulus, bulk modulus, rigidity modulus, Poisson's ratio and Debye temperature were investigated by acquiring infrared spectra recorded in the range of 300 to 800 cm-1. Replacement of Fe3+ ions with the strongly magnetic Dy3+ ions increased the saturation magnetization and coercivity. Dielectric constant increased with Dy3+ substitution but decreased with applied frequency.

Interface-Charge Induced Giant Electrocaloric Effect in Lead Free Ferroelectric Thin-Film Bilayers.

Conventional refrigeration methods based on compression-expansion cycles of greenhouse gases are environmentally threatening and cannot be miniaturized. Electrocaloric effects driven by electric fields are especially well suited for implementation of built-in cooling in portable electronic devices. However, most known electrocaloric materials present poor cooling performances near room temperature, contain toxic substances, and require high electric fields. Here, we show that lead-free ferroelectric thin-film bilayers composed of (Bi0.5Na0.5)TiO3-BaTiO3 (BNBT) and Ba(Zr0.2Ti0.8)O3-(Ba0.7Ca0.3)TiO3 (BCZT) display unprecedentedly large electrocaloric effects of ∼23 K near room temperature under moderate electric bias. The giant electrocaloric effect observed in BNBT/BCZT bilayers, which largely surpasses the sum of the individual caloric responses measured in BNBT and BCZT, is originated from the presence of compositional bound charges at their interface. Our discovery of interface charge-induced giant electrocaloric effects indicates that multilayered oxide heterostructures hold tremendous promise for developing highly efficient and scalable solid-state cooling applications.

Ni0.4Cu0.2Zn0.4TbxFe2-xO4 nanospinel ferrites: Ultrasonic synthesis and physical properties.

The Fe3+ ions were replace with Tb3+ ions as highly paramagnetic rare earth element within the structure of Ni0.4Cu0.2Zn0.4Fe2O4 nano-spinel ferrites (NSFs). The structural, magnetic, spectroscopic and optic properties have been studied in details. All products have been synthesized via ultrasonic approach via Qsonica ultrasonic homogenizer, frequency: 20 kHz and power: 70 W for 60 min. No annealing or calcination process was applied for any product. The microstructural analysis of products has been done via X-ray powder diffractometry (XRD) which presented the cubic spinel structure with nanosized distribution of all. The cubic morphology of all products were confirmed by both HR-TEM and FE-SEM. Optical band gap (Eg) values were assessed by applying %DR (percent diffuse reflectance) analysis and Kubelka-Munk theory. The Tauc schemes showed that Eg values are in a narrow range (1.87-1.98 eV). The quadrupole splitting, line width, hyperfine magnetic field, isomer shift values and cation distribution have been determined from 57Fe Mossbauer analysis. The magnetic properties of various nanoparticles have been obtained from VSM (vibration sample magnetometer) measurements at 10 and 300 K (RT). The magnetic results revealed superparamagnetic and soft ferromagnetic traits at 10 and 300 K, respectively. Ms (saturation magnetization) and Mr (remanence) initially increase with increasing Tb3+ substituting level up to x = 0.06 then diminish for further x values. Hc (coercivity) shows an opposite variation tendency of Ms and Mr. The observed magnetic traits are deeply discussed in relation with the structure, morphology, magnetic moments and cation distributions.

Structural, magnetic, optical properties and cation distribution of nanosized Co0.7Zn0.3TmxFe2-xO4 (0.0 ≤ x ≤ 0.04) spinel ferrites synthesized by ultrasonic irradiation.

This study expressed the influence of Tm substitution on the structural, optical and magnetic properties of Co-Zn spinel ferrites (Co0.7Zn0.3TmxFe2-xO4 (0.0 ≤ x ≤ 0.04)). The different compositions were synthesized by sonochemical method using Qsonica ultrasonic homogenizer, frequency: 20 kHz and power: 70 W for 60 min. XRD patterns proved the presence of single-phase spinel ferrites with crystallites size in the 8-10 nm range. Cation distribution approved the occupancy of octahedral (B) site by Tm. The morphology and the elements stoichiometry are obtainable through FE-SEM, EDX and elemental mapping. Optical band gap (Eg) values were estimated via DR % (percent diffuse reflectance) investigations and Kubelka-Munk theory. Tauc plots revealed that direct Eg values are ranging between 1.49 and 1.68 eV. The analyses of magnetization versus magnetic field, M(H), were performed. The following magnetic parameters like saturation magnetization Ms, squareness ratio (SQR = Mr/Ms), magnetic moment nB, coercivity Hc and remanence Mr have been evaluated. M(H) curves revealed the superparamagnetic (SP) at RT and ferromagnetic property at 10 K. It was showed that the Tm3+ substitutions significantly affect the magnetic properties of host spinel ferrites. An increasing trend in the Ms, Mr, Hc, and nB values was noticed for lower Tm3+ substitution content.

Sonochemical synthesis and physical properties of Co0.3Ni0.5Mn0.2EuxFe2-xO4 nano-spinel ferrites.

Nanoparticles (NPs) of composition Co0.3Ni0.5Mn0.2EuxFe2-xO4, where 0.00 ≤ x ≤ 0.10 (hereafter called CNMEuF) were synthesized by sonochemical approach using UZ SONOPULS HD 2070 ultrasonic homogenizer (frequency of 20 kHz and power of 70 W). As-synthesized samples were characterized thoroughly to determine the effects of europium ions (Eu3+) substitution on their structure, morphology and magnetic traits. Structural analyses of the synthesized NPs confirmed their high purity and crystalline cubic phases. Percent diffuse reflectance (%DR) data and Kubelka-Munk theory were exploited to evaluate the optical band gap energies of the studied CNMEuF NPs. Values of optical band gap energies obtained from the Tauc plots were observed in the range of 1.47-1.58 eV. The hysteresis loops (at room temperature and 10 K) of synthesized NPs were analyzed to determine their magnetic properties. These NPs disclosed superparamagnetic and hard ferrimagnetic character at room temperature and 10 K, respectively. With exception, the sample with x = 0.10 revealed soft ferrimagnetic behavior at 10 K. Eu3+ doping was shown to have significant influence on the structure and magnetic attributes of the proposed CNMEuF NPs. Values of various magnetic parameters of proposed compositions were reduced with the increase in Eu3+ dopant contents.

Sonochemical synthesis of Eu3+ substituted CoFe2O4 nanoparticles and their structural, optical and magnetic properties.

Magnetic, optic and microstructural properties of ultrasonically synthesized CoEuxFe2-xO4 (x ≤ 0.1) nanoferrites (NFs) have been examined in this study. After sonochemical synthesis, XRD and FT-IR analyses confirmed the purity, the structure (cubic spinel structure and Fd3m space group) and the spectral properties of the spinel ferrite samples. The spherical morphology and chemical compositions of the products were observed via transmission and scanning electron microscopes along with EDX and elemental mapping. Percent diffuse reflectance (%DR) was used for optical investigation. Optical band gaps (Eg) were estimated utilizing Kubelka-Munk theory and Tauc equation. Eg values are in a narrow band of 1.34 to 1.44 eV. The magnetic parameters like Ms (saturation magnetization), SQR = Mr/Ms (squareness ratio), nB (magnetic moment), Hc (coercivity) and Mr (remanence) have been evaluated by analyzing measurements of magnetization versus magnetic field performed at room (RT; T = 300 K) and low (T = 10 K) temperatures. It is showed that the different produced CoEuxFe2-xO4 (0.00 ≤ x ≤ 0.10) nanospinel ferrites present superparamagnetic (SPM) nature at RT. At low temperature, the various produced CoEuxFe2-xO4 (x ≤ 0.08) nanospinel ferrites display ferrimagnetic (FM) nature. With exception, the x = 0.10 sample exhibit SPM behavior at T = 10 K. It is noticed that the Eu3+ substitutions alter in a significant way on the magnetic data. A decreasing trend in the Ms, Mr and nB values was noted with Eu3+ substitutions.

Structural, magnetic, optical properties and cation distribution of nanosized Ni0.3Cu0.3Zn0.4TmxFe2-xO4 (0.0 ≤ x ≤ 0.10) spinel ferrites synthesized by ultrasound irradiation.

In this study, Tm3+ ion substituted NiCuZn nanospinel ferrites, Ni0.3Cu0.3Zn0.4TmxFe2-xO4 (0.0 ≤ x ≤ 0.10), have been synthesized sonochemically. The structural, spectroscopic, morphological, optic and magnetic investigation of the samples were done by X-ray powder diffractometry (XRD), Fourier transform infrared spectrophotometry (FT-IR), UV-Vis diffused reflectance (%DR) spectrophotometry, transmission and scanning electron microscopies (TEM and SEM) along with EDX, Vibrating sample magnetometry (VSM), respectively. The purity of prepared products were confirmed via XRD, FT-IR, EDX and elemental mapping analyses. The analyses of magnetization versus M(H) (applied magnetic field) were performed at 300 and 10 K. The following magnetic parameters like Ms (saturation magnetization), SQR = Mr/Ms (squareness ratio), nB(magnetic moment), Hc (coercivity) and Mr (remanence) have been discussed. M(H) loops revealed superparamagnetic property at RT and soft ferromagnetic nature at 10 K. It is showed that the Tm3+ substitutions significantly affect the magnetizations data. A decreasing trend in the Ms, Hc, Mr, and nB values was detected with Tm3+ substitution.

Structural, optical and magnetic properties of Tm3+ substituted cobalt spinel ferrites synthesized via sonochemical approach.

Co-Tm nano-spinel ferrite with chemical formula CoTmxFe2-xO4 (0.0 ≤ x ≤ 0.08) NPs were prepared via sonochemical approach. X-ray powder diffraction patterns, microscopic images (SEM and TEM) and infrared spectra proved the formation of Co spinel ferrite. The effect of Tm3+ substituted on spinal structure was evaluated by lattice parameters, tetrahedral and octahedral bond length and cationic distribution. The band gap energy (Eg) of samples were estimated by performing UV-Vis percent diffuse reflectance (% DR) and applying the Kubelka-Munk theory. Eg values are in an interval between 1.33 eV and 1.64 eV. The analyses of magnetization were performed at room (300 K; RT) and low (10 K) temperatures. Different magnetic parameters including coercivity Hc, saturation magnetization Ms, remanence Mr, squareness ratio (SQR = Mr/Ms) and magnetic moment nB were deduced and discussed. The results showed superparamagnetic (SPM) nature at RT for x = 0.00 and 0.02 samples. However, the other products exhibit ferromagnetic (FM) nature. At 10 K, all synthesized NPs display FM behavior. An amazing increase in the magnitudes of Ms, Mr and Hc was observed at 10 K in comparison to RT, which is principally due to the reduced thermal fluctuations of magnetic moments at lower temperatures. The Tm3+ substitution affects considerably the magnetizations data. An enhancement in the Ms, Mr, and nB was detected on increasing the Tm3+ concentration. The SQR values at RT are found to be smaller than 0.5 postulating a single domain nature with uniaxial anisotropy for all produced ferrites. However, SQRs are in the range 0.66-0.76 at 10 K, suggesting the multi magnetic domain at low temperature, except the x = 0.02 product where the SQR = 0.47 indicating the single magnetic domain. The obtained magnetic results were investigated deeply with relation to structural and microstructural properties.

Impact of La3+ and Y3+ ion substitutions on structural, magnetic and microwave properties of Ni0.3Cu0.3Zn0.4Fe2O4 nanospinel ferrites synthesized via sonochemical route.

In the current study, Ni0.4Cu0.2Zn0.4La x Y x Fe2-x O4 (x = 0.00 - 0.10) nanospinel ferrites (NSFs) were fabricated via an ultrasonic irradiation route. The creation of single phase of spinel nanoferrites (NSFs) was investigated by X-ray powder diffractometry (XRD) and selected area diffraction pattern (SAED). The cubic morphology of all samples was confirmed by scanning and transmission electron microscopies (SEM and TEM) respectively. The UV-Vis investigations provided the direct optical energy band gap values in a narrow photon energy interval of 1.87-1.92 eV. The 57Fe Mössbauer spectroscopy analysis explained that the hyperfine magnetic fields of Octahedral (Oh) and Tetrahedral (Td) sites decreased with substitution. The paramagnetic properties of NPs decrease with increase of content of doped ions. Investigations of magnetic properties reveal a superparamagnetic nature at 300 K and soft ferromagnetic trait at 10 K. The M s (saturation magnetization) and M r (remanence) decrease and the H c (coercivity) increases slightly with La3+ and Y3+ substitution. The observed magnetic traits are deeply discussed in relation with the morphology, structure, magnetic moments and cation distributions. The microwave characterization of the prepared NSFs showed that, dissipation (i.e., absorption) of incoming microwave energy occurs at a single frequency, for each sample, lying between 7 and 10.5 GHz. The reflection losses (RL) at these frequencies range from -30 to -40 dB and the mechanism of which is explained in the framework of dipolar relaxation and spin rotation. The best microwave properties were obtained with a LaY concentration of x = 0.08 having an RL of -40 dB @ 10.5 GHz and an absorption bandwidth of 8.4 GHz @ -10 dB. With these high values of RL and absorbing bandwidth, LaY doped NiCuZn NSF products would be promising candidates for radar absorbing materials in the X-band.

Polycrystalline to preferred-(100) single crystal texture phase transformation of yttrium iron garnet nanoparticles.

Nanocrystalline Ce-substituted yttrium iron garnet (YIG) powders of different compositions, Y3-x Ce x Fe5O12 (0 ≤ x ≤ 2.0), were synthesized by a combination of sol-gel auto-combustion and solid-state synthesis techniques. The as-obtained powder samples were sintered at 1150 °C for 10 h. The garnet structure formation is confirmed by the X-ray diffraction pattern, which shows that the calculated lattice parameter increased for x = 1.0 and shows a decreasing trend for x ≥ 1.0 with the addition of cerium ions. The lattice parameter increased from 12.38 Å to 12.41 Å for x ≤ 1.0 whereas it decreased from 12.412 Å to 12.405 Å with the cerium composition for x > 1.0. The average particle size determined by high resolution transmission electron microscopy is in the range of 50 to 90 nm and found to increase with the substitution of cerium ions in YIG. The room temperature magnetic parameters such as saturation magnetization, coercivity and remanence magnetization are greatly affected by the substitution of cerium ions. The values of saturation magnetization decrease from 25.5 to 15 emu g-1 whereas coercivity increases from 1 to 28 Oe with the substitution of cerium ions. The pure YIG sample shows polycrystalline nature that changed towards a single-crystal structure leading to a preferred-(100) orientation with the Ce substitution. The change from a ring to a spotty pattern observed in SAED confirmed the crystalline phase transformation and is well supported by HRTEM and magnetic measurements. The behavior of magnetic and electrical properties is well supported by the poly- and single-crystalline nature of YIG and Ce-YIG, respectively. The crystal structure transformation in YIG brought about by Ce substitution could unveil enormous opportunities in the preparation of single-crystal materials from their polycrystalline counterparts.

Au quantum dots engineered room temperature crystallization and magnetic anisotropy in CoFe2O4 thin films.

For the first time, this work presents a novel room temperature time-effective concept to manipulate the crystallization kinetics and magnetic responses of thin films grown on amorphous substrates. Conventionally, metal-induced crystallization is adopted to minimize the crystallization temperature of the upper-layer thin film. However, due to the limited surface area of the continuous metal under-layer, the degree of crystallization is insufficient and post-annealing is required. To expose a large surface area of the metal under-layer, we propose a simple and novel approach of using an Au nanodots array instead of a continuous metallic under-layer to obtain crystallization of upper-layer thin films. Spinel cobalt ferrite (CFO) thin film as a 'model' was deposited on an Au nano-dots array to realize this methodology. Our findings revealed that the addition of quantum-sized Au nano-dots as a metal under-layer dramatically enhanced the crystallization of the cobalt ferrite upper layer at room temperature. The appearance of major X-ray diffraction peaks with high intensity and well-defined crystallized lattice planes observed via transmission electron microscopy confirmed the crystallization of the CFO thin film deposited at room temperature on 4 nm-sized Au nano-dots. This crystallized CFO thin film exhibits 18-fold higher coercivity (Hc = 4150 Oe) and 4-fold higher saturation magnetization (Ms = 262 emu cm-3) compared to CFO deposited without the Au under-layer. The development of this novel concept of room-temperature crystallization without the aid of additives and solvents represents a crucial breakthrough that is highly significant for exploring the green and energy-efficient synthesis of a variety of oxide and metal thin films.

Controllable dynamics of oxygen vacancies through extrinsic doping for superior catalytic activities.

Due to its strong redox ability, high stability, cost effectiveness and non-toxicity, cerium oxide (CeO2) has been extensively researched as an active photocatalyst material. The underlying photocatalytic reactions are mostly associated with the transportation of oxygen ions through vacancies, but the actual transport phenomenon had not been clearly understood. In this work, gadolinium (Gd) is sequentially doped into CeO2 to investigate how extrinsic doping can modulate oxygen vacancies in CeO2 and influence photocatalytic activities. From our investigations, it was found that the Gd doping may induce structural symmetry breaking leading to a pure CeO2 fluorite structure that transforms mobile oxygen vacancies into clustered or immobile vacancies. When the vacancies were set as "mobile" (for Gd doping levels ≤15 at%), maximum photocatalytic activities were obtained. In contrast, suppressed photocatalytic efficiencies were noted for higher Gd doping levels (20 at% or more). The results reported in this research may provide an extra degree of freedom in the form of extrinsic doping to configure the oxygen vacancy defects and their mobility to achieve better catalytic efficiencies.