Thermal Instability and Microstructure of Strontium M-type Hexaferrite Nanoparticles Synthesized by Citrate Approach

The dried gel of SrFe12O19, prepared by citrate approach, was investigated by means of infrared spectroscopy （ IR ）, thermogravimetric analysis （ TG ）, differential scanning calorimetry （ DSC ）, X- ray diffraction（ XRD ） techniques, energy dispersive spectroscopy（ EDS ）, and transmission electron microscopy（ TEM ）. The thermal instability and the thermal decomposition of low-temperature strontium M-type hexaferrite crystallized at about 600℃ were confirmed for the first time by XRD method. The decomposition of the low-temperature strontium M-type hexaferrite took place at about 688.6℃ determined by DSC investigation. The low-temperature strontium M-type hexaferrite nanopartieles were decomposed into SrFeO2.5 with an orthorthombic cell and Fe2O3 with a tetragonal cell as well as possibl α-Fe2O3 . The agglomerated particles with sizes less than 200 nm obtained at 800℃ were plesiomorphous to strontium M-type hexaferrite. The thermally stable strontium M-type hexaferrite nanopartieles with sizes less than 100um cotdd take place at 900 ℃ . Up to 1000 ℃ , the phose transformotion to form strontium M-type hexaferrite was ended, the calcinations with the sizes more than 1μm were composed of α-Fe2O3 and strontium M-type hexaferrite. The method of distinguishing γ-Fe2O3 with a spinel structure from Fe2O3 with tetragonal cells by using powder XRD method was proposed. Fe2O3 with tetragonal cells to be crystallized before the crystallization of thermally stable strontium M-type hexaferrite was confirmed for the first time. The reason why α- Fe2O3 as an additional phase appears in the calcinations is the cationic vacancy of stroutium M-type hexaferrite , SrFe12-x□O19 （0≤x ≤0.5）.

Impact of In^(3+) cations on structure and electromagnetic state of M-type hexaferrites

The solid solutions of In^(3+) doped M-type strontium hexaferrites were produced using a conventional solid-state reaction method,and Rietveld analysis of the neutron diffraction patterns was conducted.In^(3+) cations occupy octahedral (4f_(Ⅵ)and 12 k) and tetrahedral (4f_(Ⅳ)) positions (SG=P6_(3)/mmc(No.194)).The average particle size is 837–650 nm.Curie tempearature (T_(C)) of the compounds monotonically decreased down to~520 K with increasing x.A frustrated magnetic state was detected from ZFC and FC magnetizations.saturation magnetization (M_(s)) and effective magnetocrystalline anisotropy coefficient (k_(eff)) were determined using the law of approach to saturation.A real permittivity (ε″) maximum of~3.3 at~45.5 GHz and an imaginary permittivity (ε′) of~1.6 at~42.3 GHz were observed for x=0.1.A real permeability (μ′) maximum of~1.5 at~36.2 GHz was observed for x=0.Aμ″imaginary permeability maximum of~0.8 at~38.3 GHz was observed for x=0.1.The interpretation of the results is based on the type of dielectric polarization and the natural ferromagnetic resonance features.

Influence of cerium ions on structure-dependent magnetic properties of Ba-Sr M-type hexaferrite nanocrystals

The present study is a systematic effort to investigate the structure-sensitive magnetic parameters of Ce^(3+) substituted Ba-Sr hexaferrite nanocrystals chemically formulated as Ba_(0.5)Sr_(0.5)Ce_(x)Fe_(12-x)O_(19) where x=0.0-0.2 with Δx=0.05.The hexaferrite powders were prepared using the sol-gel self-ignition route and structurally characterized by means of powder X-ray diffraction and Fourier transform infrared spectroscopy.The creation of the M-type hexaferrite phase within the synthesized samples was revealed from the Rietveld refinement of the X-ray diffractograms.The occurrence of a secondary phase of CeO_(2) was revealed within the hexaferrites for the substitution,x> 0.The refined X-ray diffraction data were utilized to compute the lattice parameters,X-ray density,and lattice parameter ratio.The crystal structure plotted from the refined XRD data reveals the occupancy of the ions at different lattice sites.The XPS data of the hexaferrite were analyzed to confirm the oxidation states of the constituent elements.The nanocrystalline nature of the hexaferrites was revealed from the crystallite sizes calculated using Scherer's formula.The analysis of FTIR spectra confirms that only a fraction of Ce^(3+)accommodated in the lattice and the remaining Ce content reside in the form of the CeO_(2) phase.The morphology of the hexaferrites was analyzed from the FESEM profiles of the ferrite samples.The magnetic behavior study was performed by analyzing the Curie temperature,hysteresis loops,and hyperfine interactions by means of susceptibility,V.S.M,and Mossbauer spectroscopy,respectively.The hexaferrites with increasing coercivity,decreasing saturation magnetization,and decreasing Curie temperature are reported in the study.The substituted Ce^(3+)ions inhibit the grain growth and create lattice imperfections giving rise to hexaferrites with tuned magnetic parameters suitable for different applications.

Co-Doped Rare-Earth (La, Pr) and Co-Al Substituted M-Type Strontium Hexaferrite: Structural, Magnetic, and Mossbauer Spectroscopy Study

The present study investigates the influence of La3+ and Pr3+ doping on the structural, magnetic properties, and hyperfine fields of Sr0.7RE0.3Fe12-2x CoxAlxO19, (RE: La3+ and Pr3+, x = 0.0 - 0.8) hexaferrite compounds prepared via auto-combustion technique. The XRD analysis shows a linear decrease in a and c lattice and unit cell volume contraction with the content x. The room temperature magnetic study shows that for the Pr3+ doped Sr0.7Pr0.3Fe12-2x CoxAlxO19 (Pr3+-SrM), the magnetization value monotonically decreases while for La3+ doped Sr0.7La0.3Fe12-2xCoxAlxO19 (La3+-SrM) magnetization value shows a noticeable increase in magnetization value with x. The coercivity of the Pr3+-SrM compound was observed to decrease while that of the La3+-SrM compound showed a marked 40% increase at x = 0.2 (~5829 Oe) in comparison to undoped SrFe12O19 (~3918 Oe). A difference in Curie temperature was also observed, with Tc ~ 525°C at x = 0.4 for Pr3+-SrM and Tc = 505°C for x = 0.4 for La3+-SrM compound. The observed differences in magnetic properties have been explained on the basis of the site occupancy of Co2+ and Al3+ in the presence of rare-earth ions. The presence of non-magnetic rare-earth ion, La3+, improved saturation magnetization, and coercivity and deemed suitable replacement for Sr2+. The hyperfine parameters namely quadrupole shift showed a decrease with the La3+ or Pr3+ doping independent of (Co2+-Al3+) ions doping. Overall, the Mossbauer analysis suggests that the (Co2+-Al3+) impurities prefer occupancy at 2a site.

Tailoring the optical and magnetic properties of La-BaM hexaferrites by Ni substitution

We investigate the impact of Ni insertion on the structural,optical,and magnetic properties of Ba_(0.8)La_(0.2)Fe_(12-x)Ni_(x)O_(19)hexaferrites(Ni substituted La-BaM hexaferrites).Samples were prepared using the conventional co-precipitation method and sintered at 1000℃for 4 hours to assist the crystallization process.An analysis of the structure of the samples was carried out using an x-ray diffraction(XRD)spectrometer.The M-type hexagonal structure of all the samples was confirmed using XRD spectra.The lattice parameters a and c were found to be in the ranges of 5.8925±0.001 nm–5.8952±0.001 nm and 23.2123±0.001 nm–23.2219±0.001 nm,respectively.The M-type hexagonal nature of the prepared samples was also indicated by the presence of corresponding FT-IR bands and Raman modes in the FT-IR and Raman spectra,respectively.EDX results confirmed the successful synthesis of the samples according to the required stoichiometric ratio.A UV-vis spectrometer was used to record the absorption spectra of the prepared samples in the wavelength range of 200 nm–1100 nm.The optical energy bandgap of the samples was found to be in the range of 1.21 eV–3.39 eV.The M–H loops of the samples were measured at room temperature at an applied magnetic field range of 0 kOe–60 kOe.A high saturation magnetization of 99.92 emu/g was recorded in the sample with x=0 at a microwave operating frequency of 22.2 GHz.This high value of saturation magnetization is due to the substitution of La3+ions at the spin-up(12k,2a,and 2b)sites.The Ni substitution is proven to be a potential candidate for the tuning of the optical and magnetic parameters of M-type hexaferrites.Therefore,we suggest that the prepared samples are suitable for use in magneto-optic applications.

Microstructure and microwave electromagnetic properties of Dy^(3+)-doped W-type hexaferrites

Ba 1 x Dy x Co 2 Fe 16 O 27 （x = 0.00, 0.05, 0.10, 0.15, and 0.20） was prepared by the solid-state method. The phase structure was studied using powder X-ray diffraction （XRD）, the electromagnetic properties were measured, and the reflection loss of Dy 3＋ -doped ferrite material was calculated using electromagnetic parameters by the transmission line theory. All XRD patterns showed the single phase of the magnetoplumbite barium ferrite without other intermediate phase when x ≤ 0.15. The values of ε ′ and ε ″ increased slightly with Dy 3＋ ions doping. The values of μ″ and μ′ were improved with Dy 3＋ doping, exhibiting excellent microwave magnetic performance. The reasons have also been discussed using the electromagnetic theory. Dy substitution could increase microwave-absorbing performance and broaden frequency band （reflection loss （RL） -10 dB）, and the absorbing peak shifted to high-frequency position. When x = 0.2, ferrite layer exhibited the most excellent microwave-absorbing performance at a thin matching thickness of 1.5 mm. The peak value of RL was around -15 dB, and the frequency band （RL -10 dB） was about 7 GHz （from 8 to 15 GHz）.

Magnetoelectric effects in multiferroic Y-type hexaferrites Ba(0.3)Sr(1.7)CoxMg(2-x)Fe(12)O(22)

Y-type hexaferrites with tunable conical magnetic structures are promising single-phase multiferroics that exhibit large magnetoelectric effects. We have investigated the influence of Co substitution on the magnetoelectric properties in the Y-type hexaferrites Ba(0.3)Sr(1.7)CoxMg(2-x)Fe(12)O(22)(x = 0.0, 0.4, 1.0, 1.6). The spin-induced electric polarization can be reversed by applying a low magnetic field for all the samples. The magnetoelectric phase diagrams of BaBa(0.3)Sr(1.7)CoxMg(2-x)Fe(12)O(22) are obtained based on the measurements of magnetic field dependence of dielectric constant at selected temperatures. It is found that the substitution of Co ions can preserve the ferroelectric phase up to a higher temperature, and thus is beneficial for achieving single-phase multiferroics at room temperature.

Preparation and Characterization of W-Type Hexaferrite Doped with La^(3+)

A series of W-type ferrites with the composition ofBal-xLaxCo2Fe16O27（where, x =0.0, 0.05, 0.10, 0.15, 0.20 and 0.25） were prepared by solid-state reaction method. The structure transformations of the ferrites were examined by XRD, DTA-TG and XPS, and the microwave-absorbing properties were investigated by evaluating the permeability and permittivity of materials（μτ,ετ, ）. The results showed that the phase-transition temperature increased with the addition of La^3＋ content, and a single-phase was formed at 1250℃ at last. Microwave properties were obviously improved as a result of the substitution of La^3＋ for Ba^2＋ at the frequency range of 0.5 - 18.0 GHz.

Evolution of structure and physical properties in Al-substituted Ba-hexaferrites

The investigations of the crystal and magnetic structures of the BaFe12_xAlxO19 （x = 0.1-1.2） solid solutions have been performed with powder neutron diffractometry. Magnetic properties of the BaFe12_xAlxOt9 （x = 0.1-1.2） solid solutions have been measured by vibration sample magnetometry at different temperatures under different magnetic fields. The atomic coordinates and lattice parameters have been Rietveld refined. The invar effect is observed in low temperature range （from 4.2 K to 150 K）. It is explained by the thermal oscillation anharmonicity of atoms. The increase of microstress with decreasing temperature is found from Rietveld refinement. The Curie temperature and the change of total magnetic moment per formula unit are found for all compositions of the BaFet2_xAlxO19 （x = 0.1-1.2） solid solutions. The magnetic structure model is proposed. The most likely reasons and the mechanism of magnetic structure formation are discussed.

Preparation and microwave hexaferrites by a sol-gel process

s Ba_4Zn_zCo_(2-z)Fe_(36)O_(60) hexaferrites with Z = 2.0, 1.5, 1.0, 0.5, and0.0 were prepared by a citrate Sol-gel process. The complex dielectric constant and complexpermeability of hexaferrite-paraffin wax composites were measured in the range from 0.1 to 6.0 GHz.Measured results showed that both the complex dielectric constant and the dielectric loss exhibitedno significant change as the measuring frequency increasing except for the sample with Z = 0.0. Thereal part of permeability decreased with increasing frequency for all samples in the whole measuringfrequency range, and the natural resonance phenomena were observed in all μ″ spectrum but Co_2U.The results also indicate that the content of zinc closely affects the microwave properties ofBa_4Zn_zCo_(2-z)Fe_(36)O_(60) ferrites, and the greater the zinc content, the lower the naturalresonance frequency is.

Synthesis and Magnetic Properties of Conventional and Microwave Calcined Strontium Hexaferrite Powder

Powders of strontium hexaferrite (SrFe12O19 - SrF) have been prepared by the sol-gel process. The prepared precursor was calcined in two different calcination techniques, using conventional furnace and microwave furnace. Thermal analysis studies showed exothermic and endothermic reaction peak at room temperature to 1200°C. An investigation of SrFe12O19 crystalline powder from the structural and magnetic aspect is performed using X-ray diffraction (XRD), High resolution scanning electron microscopy (HR-SEM) and vibrating sample magnetometer (VSM). The average particle diagonal size of SrFe12O19 powder was 80 - 100 nm in conventional and 40 - 70 nm in microwave calcinations respectively. XRD result showed the formation of SrFe12O19 of the sample calcined at 900oC with Fe/Sr: D-Fructose ratio = 12.

Radiation Losses in the Microwave X Band in Al-Cr Substituted Y-Type Hexaferrites

We present a study on radiation losses in the microwave X band in Al-Cr substituted Y-type hexaferrites, namely Ba2Mg2Alx/2Crx/2Fe12-xO22 （x = 0, 0.5 and 1.0）. The study is performed by means of a vector network analyzer, Fourier transform infrared spectroscopy, a vibrating sample magnetometer and x-ray powder diffraction. Ba2Mg2Fe12O22 hexaferrite shows radiation loss of -37.25dB （99.999% loss） at frequency 9.81 GHz, which can be attributed to its high value of saturation magnetization, i.e., 22.08emu/g. Moreover, we obtain that magnetic properties have strong influence on the radiation losses.

Impact of Co^(2+)substitution on structure and magnetic properties of M-type strontium ferrite with different Fe/Sr ratios

Ion substitution has significantly improved the performance of ferrite magnets,and cobalt remains a key area of research.Studies on the mechanism of Co^(2+)in strontium ferrite,especially SrFe_(2n-x)Co_(x)O_(19-d)(n=6.1-5.4;x=0.05-0.20)synthesized using the ceramic method,showed that Co^(2+)preferentially enters the lattice as the Fe/Sr ratio decreases.This results in a decrease in the lattice constants a and c due to oxygen vacancies and iron ion deficiency.The impact of Co substitution on morphology is minor compared to the effect of the Fe/Sr ratio.As the Fe/Sr ratio decreases and the Co content increases,the saturation magnetization decreases.The magnetic anisotropy field exhibits a nonlinear change,generally increasing with higher Fe/Sr ratios and Co content.These changes in the performance of permanent magnets are attributed to the absence of Fe^(3+)ions at the 12k+2a and 2b sites and the substitution of Co^(2+)at the 2b site.This suggests that by adjusting the Fe/Sr ratio and appropriate Co substitution,the magnetic anisotropy field of M-type strontium ferrite can be effectively optimized.

Magnetic and microwave absorbing properties of M-type barium ferrite/graphene oxide composite microwave absorber

In order to improve the absorbing properties of M- type barium ferrite absorbing materials, M-type barium ferrite/graphene oxide composites with different graphene oxide contents were synthesized by the sol-gel autocombustion method. X-ray diffraction （XRD）, a scanning electronic microscopy （ SEM ）, a physical properties measurement system （PPMS-9）, and a vector network analyzer were used to analyze their structure, surface morphology, magnetic and absorbing properties, respectively. The results show that the absorbing band of the composite absorbing material is widened and the absorbing strength is increased compared with the pure M-type barium ferrite. The sample with the content of doped graphene oxide of 3% has the minimum reflectivity at 10 to 18 GHz frequencies. Hence, the doped graphene oxide effectively improves the absorbing properties of M-type barium ferrite.

Absorption-Dominant mmWave EMI Shielding Films with Ultralow Reflection using Ferromagnetic Resonance Frequency Tunable M-Type Ferrites

Although there is a high demand for absorption-dominant electromagnetic interference(EMI) shielding materials for 5G millimeter-wave(mmWave) frequencies, most current shielding materials are based on reflection-dominant conductive materials. While there are few absorption-dominant shielding materials proposed with magnetic materials, their working frequencies are usually limited to under 30 GHz. In this study, a novel multi-band absorption-dominant EMI shielding film with M-type strontium ferrites and a conductive grid is proposed. This film shows ultralow EMI reflection of less than 5% in multiple mmWave frequency bands with sub-millimeter thicknesses, while shielding more than 99.9% of EMI. The ultralow reflection frequency bands are controllable by tuning the ferromagnetic resonance frequency of M-type strontium ferrites and composite layer geometries. Two examples of shielding films with ultralow reflection frequencies, one for 39 and 52 GHz 5G telecommunication bands and the other for 60 and 77 GHz autonomous radar bands, are presented. The remarkably low reflectance and thinness of the proposed films provide an important advancement toward the commercialization of EMI shielding materials for 5G mmWave applications.

Factors of Impacting the Coprecipitation Process for Synthesizing CoTi-substitued Barium M-type Ferrite Ultrafine Powder

The effect of pH values on synthesizing single-phase CoTi-substituted barium M-type ferrite ultrafine powders,and BaCoTiFe- 10O- 19, was investigated employing corrosion versus pH plot (E-pH plot) for metal element, thermodynamic calculation, and co-dump coprecipitation. The pH values of complete coprecipitation of all Fe 3+, Ti 4+, Co 2+ and Ba 2+ cations are 9-12 and higher than 7.9 on the basis of E-pH plot analysis and thermodynamic calculation, respectively. The minimum pH value necessary to the formation of single-phase BaCoTiFe- 10O- 19 is 8.5 in the light of the co-dump coprecipitation.These results indicate that the coprecipitation process for synthesizing CoTi-substituted barium M-type ferrite ultrafine powders is simultaneously influenced by synergetic coprecipation effect of cations and coordination effect of Cl-anions. The test time of the minimum pH value corresponding to forming a series of single-phase CoTi-substituted barium M-type ferrite ultrafine powders,and BaCo-xTi-xFe- 12-2xO- 19, may be significantly reduced by using the effects of two new factors on the coprecipitation process.

EXPERIMENTAL AND THEORETICAL RESEARCH OF ELECTRON EMISSION MECHANISM OF M-TYPE CATHODES

With the most advanced Synchronous Radiation Photoelectron Spectrum(SRPS),the emission mechanism of M-type cathodes has been investigated from the perspective of chemical state.Based on the experimental results of SRPS analysis,a new model of the electron emission mechanism for M-type cathode is discussed.The main topics in this paper include the research status of electron emission mechanism of M-type cathodes;the advantages of SRPS technology;the distribution of oxygen chemical state on the cathode surface and the evolvement of oxygen chemical state during activation process;the relation between barium chemical state and osmium(Os)-coating;surplus barium and its formula;the characteristics of Os,and other noble metal coatings;the relation between film characteristics and emission performance of cathodes,the inhibition effects to the emission for Platinum(Pt)-coated cathode,etc.At the end of this paper,electron emission mechanism of M-type cathode is summarized and foreseen.

Synthesis and Microwave Electromagnetic Properties of M-type Hexagonal FerriteBaTiCoFe_(10)O_(19)

An M-type hexagonal ferrite BaTiCoFe10 O19 was prepared by solid phase reaction by a partial 2Fe3+→Ti4+ Co2+ substitution. The morphology observation and phase identification of BaTiCoFe10O19 were carried out by SEM and XRD, and its X-ray powder diffraction data was reported in this paper for the first time. Further, the microwave electromagnetic properties of BaTiCoFe10O19 were measured and discussed.

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