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Application of Calcium Hexaferrite as Microwave Absorbing Material: Review

N. M. Gahane1*, Y.D. Choudhari2, P. J. Chaware2 and K.G. Rewatkar2

1Department of Physics, Hislop College, Nagpur, India.

2Department of Physics, Dr. Ambedkar college, Deeksha Bhoomi, Nagpur-10, India.

Corresponding Author E-mail:nmgahane@gmail.com

DOI : http://dx.doi.org/10.13005/msri/200105

Article Publishing History
Article Received on : 24 Jan 2023
Article Accepted on : 24 Feb 2023
Article Published : 27 Feb 2023
Plagiarism Check: Yes
Reviewed by: Dr. Piyush J. Patel
Second Review by: Dr. Guruswamy B
Final Approval by: Dr. Srinivasa C. V
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ABSTRACT: Many studies have been conducted on Spinel, Garnet, and Hexa-ferrites in single and multi-doped concentrations. This article is an attempt to review the researcher's work on Ca, Ba, and Sr hexaferrite by substituting a variety of various ions such as Al, La, Sn, Zr, Co, Cr, and Ir. This review paper investigates M-type (Ca, Sr, Ba) Hexa-ferrites with a space group of P63/mmc that were synthesized using various techniques and characterized by XRD for crystallographic information, SEM and TEM for surface morphology, VSM for magnetic behaviour, and Vector Network Analyzer (VNA) for microwave absorption properties. Changes in a material's chemical composition affect features such as coercivity, saturation magnetization, and Curie temperature, as well as managing these properties and utilizing these compounds in the field of microwave absorption properties and magnetic field industry. KEYWORDS: Coercivity; Hexaferrite; Saturation magnetization; SEM; XRD; VNA

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Gahane N. M, Choudhari Y. D, Chaware P. J, Rewatkar K. G. Application of Calcium Hexaferrite as Microwave Absorbing Material: Review. Mat. Sci. Res. India; 20(1).


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Gahane N. M, Choudhari Y. D, Chaware P. J, Rewatkar K. G. Application of Calcium Hexaferrite as Microwave Absorbing Material: Review. Mat. Sci. Res. India; 20(1). Available from: https://bit.ly/3IB5vAn


Introduction

Numerous studies have been conducted since the invention of radar to create radar-absorbing materials. This material is beneficial for antenna pattern shaping, radar cross reduction, and EMI reduction. The radar absorbing materials work by absorbing radar electromagnetic radiation 1. The magnetic and dielectric properties of the materials influence the absorption of the E-M wave. The absorbing material must have the lowest reflectance throughout the largest bandwidth; the weight and size of the absorbing material are also critical for radar. Radar absorption materials are divided into two types: conductive materials and magnetic materials 2. Hexa-ferrites and carbonyl iron are used in magnetic radar absorbers. Hexaferrite is a type of hard ferrite that is a permanent magnet that retains its magnetism after being magnetized and has a high coercivity and remanence after magnetization 3. Certain ferrites are further split into the following groups: M, W, Y, Z, and X compounds. Each of them possesses a unique crystalline phase via which absorption materials have been absorbed in the MHz and GHz band ranges 4. The performance of a material is determined by its structure and physical qualities. Changing the chemical makeup of an absorber can result in significant changes in chemical and physical properties across a wide range of frequency bands 5. There have been no publications published on M-type barium ferrites or strontium ferrites, although there have been a few studies on the microwave absorption magnetic characteristics of calcium hexaferrite. As a result, we took up the review paper for calcium hexaferrite 6.

Table 1: Classification of hexaferrite

Hexaferrite type

Combination

Molecular formula

Structural Staking

M

M

CaFe12O19

RSR*S*

Y

Y

CaSrFe12O19

TSTSTS

W

M+S

CaCo2Fe16O27

RSSR R*S*S*

Z

M+Y

Ca3 Co2Fe24O41

RSTSR*S*T*S*

X

2M+S

Ba2 Co2Fe28O46

RSR*S*S*

Table 2: Crystallographic site of hexaferrite

Sub lattice

Coordination

Block

No of ions

Spin orientations

2a

Octahedral

S

one

2b

Pseudo-tetrahedral

R

one

4fIV

tetrahedral

S

two

4fIV

Octahedral

R

two

12K

Octahedral

R-S

six

Experimental Technique

The sol-gel technique, coprecipitation method, hydrothermal method, and solid-state method are easy chemical ways for economically producing hexagonal ferrites. These techniques are effective for regulating the grain size and morphology of ferrite particles 7. When creating a ferrite powder, we pay close attention to the following factors: Heat treatment, chemicals used in beginning powders, powder stoichiometry Using these crucial components, the Ca hexaferrite material was substituted with Mg-Ti, and several hexaferrite samples were generated using the citrate sol-gel method 8. Between the frequencies of 12 and 20 GHz, the microwave absorption characteristics of calcium hexaferrite replaced by Mg-Ti were investigated. Similarly, the Ca substituted Sr hexaferrite was produced using a standard solid-state reaction approach 9, before being applied in magnetic media and absorbing microwaves. For the field of high-density recording media, the Sn-Zr substituted Ca hexaferrite was synthesized using the sol-gel auto combustion process with urea as a fuel 10. The Co-Sn and Sn-Zr substituted Ca hexaferrite with the chemical formulas Ca(Co-Sn) xFe12-2xO19 and Ca(Co-Zr) xFe12-xO19 for x= 0 to 5 were synthesized by sol-gel technique 11. The M Type Ba hexaferrite substituted by Ca generated by microemulsion and a stearic acid sol-gel method is useful in the storage media industry. Previously, Ir-Co substituted Ca hexaferrite with the chemical formula CaFe12-2xIrxCoxO19, which was manufactured using the chemical-coprecipitation process 12. The microwave absorption capabilities of calcium and strontium hexaferrite substituted with Co and Ti by boll milling technique and solid-state reaction were investigated at frequencies ranging from 8.4 GHz to 12.4 GHz. A ceramic approach was used to create the Cu-Ti and Al-Co substituted M Type Ca hexaferrite for x=0 to 5 and x=2 to 5 13,14.

Results and discussions

XRD  Report

The sol-gel method, solid-state reaction, ceramic process, and coprecipitation method were all used to successfully synthesis the M-type Calcium hexaferrite nanoparticle. X-ray diffraction studies reveal the creation of a hexagonal structure with a space group of P63/mmc and planes (107), (114), (203), and (204 (108) 15. The lattice parameters were discovered to be in the range of a = 5-6 and c = 22-24. The Debye-Scherer formula was used to determine the particle’s averaged crystallite size 16. The TEM pictures revealed that the produced ferrites nanoparticles were spherical with a size distribution between 20 and 60 nm, which corresponded to the particle size determined by XRD. Due to unit cell elongation, bigger La, Mg–Ti, Sn–Zr, Cu-Ti, Co-Ti, Co-Sn, and Co-Al ions are replaced by smaller Fe ions 17,18.

Figure 1: XRD image of M-type hexaferrite

Click here to View Figure

Table 3: Lattice parameter, particle size of Hexaferrite

Hexaferrite material

a

(Å)

c

(Å)

crystalline size

(nm)

Volume

Å3

Ca(Co–Sn)0.2Fe11.6O19

5.843

21.516

56.17

636.137

SrFe12O19

5.641

22.322

54.17

654.345

CaLa0.7Fe11.3O19

5.621

22.361

24

635.24

VSM Report

The magnetic properties of the material, such as saturation magnetization, coercivity (Hc), and Retentivity (Mr), proved its hard ferrite nature. When a material is used for storage, its coercivity is important 19. As the concentration of replacing ions in the material increases/decreases, if the coercivity is low, it becomes a soft magnet; if the coercivity is high, it becomes a hard magnet. The Fe3+ ions in the M-type hexaferrite composition are dispersed in five separate crystallographic locations: three up-spin sites (2a, 12k, and 2b) and two down-spin sites (4f1 and 4f2) along the c axis 20. The saturation magnetization and coercivity were observed to decrease with increasing Mg-Ti concentrations, while  increased with increasing Al concentrations using hysteresis loops 21. The activation energy and dc electrical resistivity of ferrite samples increased with increasing Al concentration at room temperature. In the presence of surfactants, Ba-Ca hexaferrite exhibited low coercivity 22.    

Figure 2: VSM Graph of M-type hexaferrite.

Click here to View Figure

Table 4: Ms, Mr of M-type Hexaferrite.

Hexaferrite material

a

(Å)

c

(Å)

crystalline size

(nm)

Volume

Å3

Ca(Co–Sn)0.2Fe11.6O19

5.843

21.516

56.17

636.137

SrFe12O19

5.641

22.322

54.17

654.345

CaLa0.7Fe11.3O19

5.621

22.361

24

635.24

The appearance of non-magnetic anions in the tetrahedral and octahedral positions was frequently responsible for the low Curie temperature. Sites 2a and 2b, 12k, and 4f have been occupied by non-magnetic ions such as magnesium, titanium, copper, and aluminum 23.

 SEM 

SEM images of fragmented surfaces of La substituted sintered Ca hexaferrite are shown in the figure. The micrograph demonstrates that the particle size is reduced as a result of La replacement. Hexaferrite of calcium was used in place of the original substance. The index of crystallinity was derived from the following relationship 24. A micrograph gives us the average particle size of D, while a Scherer equation tells us the average crystalline size of r. The pinning effect and particle growth inhibition may be caused by a little amount of unsubstituted La2O3 in the sample 25

Figure 3: SEM Micrograph of CaLaXFe12-xO19

Click here to View figure

Microwave Absorbing Property

The reflection loss (RL) of hexaferrite materials was used to investigate their microwave absorption capabilities; as a result, the preceding formula can be used to calculate reflection loss

Where f is the microwave frequency, d is the absorber layer thickness, and c is the velocity of an electromagnetic wave in a vacuum. and u are the complex relative permittivity and permeability, respectively, while Zin is the absorber’s input impedance 26. The microwave absorption property of material was tested between 3 and 12 GHz, which requires a low matching thickness, low reflection loss, and a wide absorption bandwidth. When it comes to storing electric and magnetic energy, the real portions of complex permittivity (ε′) and permeability (u′) are used, while the shadowy portions of complex permittivity (ε′′) and permeability (u′′) have been used to express the dissipation of magnetic and electrical energy 27. It is useful for microwave absorption if the absorbers have large imaginary portions of both complex permittivity and permeability, as reflection loss is impacted by impedance. As a result, to accomplish impedance matching, the real components (ε′ and μ′) must be as identical as possible 28. The imaginary parts of Ba hexaferrite are very close to one and zero, while the real parts are close to 2–27. For frequencies between 2 and 18 gigahertz, has a very minor change, this indicates that it has a very low dielectric loss 29.

Table 5: Reflection loss, layer size of Hexaferrite.

Material

Layer Size (Mm)

Frequency Range(Ghz)

Reflection Loss (Db)

Reference

Ba hexaferrite (BaFe12O19)

2mm-3mm

8-14.8

-30 to -17

[17] [31] [35]

Sr hexaferrite (SrFe12O19)

1mm-2mm

8-12

-16 to -8

[20] [26]

Ca hexaferrite

(CaFe12O19)

2mm- 3 mm

8- 20

-39 to -.9

[1][9]

 Whenever the RL is below -10 decibels, only 10% of the electromagnetic radiation has mirrored, whereas 90% of the electromagnetic energy consumed. The effective absorption bandwidth is established for a certain frequency range when RL is less than -10 dB 30. When the thickness of the absorber is changed, the greatest absorption peaks shift to a lower frequency 31. The electrical test demonstrates the bandgap calculation for the material, which effectively provides a significant choice for microwave absorption. The detailed energy calculation is performed as follows:

Figure 4: Reflection loss of M-type hexaferrite

Click here to View figure

Table 6: Electrical parametric value of sample.

Sample

Band Gap

Eg (ev)

Resistivity

(at RT 340C)

Transition

Tem.  K)

Volume

(A3)

Ca0.7Sr0.3Fe12O19

0.380

2.212*107

409

644.242

SrFe12O19

0.23

2.322*107

413

654.345

CaLa0.7Fe11.3O19

0.24

2.33*107

408

635.24

When it comes to matching width, there is a frequency at which the two pieces of information peer. When replacing magnetic Fe3 with non-magnetic ions, the matching frequency drops almost exponentially, which would conflict with a drop in the anisotropy field as the substitution level progress 32. The reflection coefficient of Ca hexaferrite decreased with increasing applied field frequency, as seen in figure 5. The Sr-Ca hexaferrite possesses low conductivity, low dielectric constant (ε′′), and dielectric loss tangent (tan δ).

Figure 5: Variation of dielectric with frequency

Click here to View Figure

Conclusion

Ca hexaferrite has a very fascinating subject of research for scientists because of its data storage and microwave uses. The substitution of various ions in Ca hexaferrite resulted in promising modifications in the electrical, magnetic, and physical characteristics, indicating that the researcher can manufacture new M-type hexaferrite with improved attributes through impurity substitution. The current review concludes that calcium hexaferrite is suitable for microwave absorption and a very good replacement for barium and strontium hexaferrite, as it exhibits extremely similar features Ba and Sr. There is numerous research that must be conducted utilizing various methods of preparation of Ca hexaferrite, with varied ferrite compositions, to determine the effect of preparation procedures on the properties of ferrite. The energy band gap of La-substituted powders and sintered pellets is evaluated using the four-probe method, which demonstrates that the sample’s resistivity and energy bandgap decrease as the conversion rate for lanthanum rises. The Scherer formula is used to determine particle size. Lanthanum substitution increases with particle size. The temperature-recorded M-H curves revealed that large values of Ms, Mr, and Hc were obtained for all Ca1-xSrxFe12O19 nanoribbons and that they increased with ribbon-width broadening. Specifically, the best Ms and Hc were around 67.9 emu/g and 7.31 kOe.

Acknowledgment

The author would thankful for the Department of Nanoscience and Nanotechnology Dr. Ambedkar College, Nagpur for providing synthesis and electrical characterizations and VMV college for proving the setup for random measurement of Energy band gap using electronic setup

Conflict of Interest

The author wouldn’t have any conflict of interest with other authors. This is finding with the sample; the result may be changed with combinational concentration

Funding Source

The author(s) received no financial support for the research, authorship, and/or publication of this article.

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