The performance of radar absorption of Mn_xFe_3–xO₄/rGO nanocomposites prepared from iron sand beach and coconut shell waste

1.   Introduction

The development of telecommunications technology certainly cannot be separated from the use of electromagnetic waves, one of which is radar (radio detection and ranging) waves. The use of radar waves is superior in military applications ^[1], antenna technology ^[2], and radar wave processing ^[3]. Along with the rapid development of technology, several problems were found due to the use of radar. These problems such as electromagnetic wave pollutions ^[4] and human health problems ^[5] cause electromagnetic wave interference ^[6]. In the last decade, some of the above problems can be overcome by the use of radar absorbing material/RAM ^[7,8]. One example of the application is coating the body of military vehicles such as tanks or military aircraft ^[9]. Radar transmitted from the source is ensured to be absorbed and dissipated by RAM so that it can reduce the results of radar reflection of radar waves from an object ^[10].

Generally, RAM works on the principle of combining a dielectric material and a magnetic material, so that the incoming radar wave will be absorbed through an impedance match to a polarizing effect ^[11,12]. The main ingredients of RAM basically have magnetic and electrical properties that aim to produce magnetic and dielectric losses ^[13]. Magnetic metal powders, ferrites, and nanotubes are some of the magnetic materials that have high adhesion and density ^[14,15]. Ferrimagnetic materials such as Fe₃O₄ based on natural iron sand were chosen as magnetic materials, because they have high saturation magnetization, good flexibility ^[16], heat resistance ^[12], good chemical and thermal stability ^[17], high permeability, and low cost of synthesis ^[18,19]. However, Fe₃O₄ is not sufficient in RAM applications because it only produces a reflection loss (RL) of −5 dB ^[20]. Thus, it is necessary to have a combination of other materials that can increase the dielectric loss value. Efforts to increase the value of dielectric loss in Fe₃O₄ are generally carried out by doping divalent cations such as Mn²⁺. This is important, because it provides an opportunity to improve the dielectric and magnetic properties ^[18,21]. Furthermore, Mn²⁺ has soft magnetic properties which affect the low coercivity field, making it suitable for RAM applications ^[22,23,24].

Regarding the methods used in recent years, several synthesis methods were found, namely solid state reaction ^[25], solvothermal ^[26], ball milling ^[27], sol-gel ^[28], dan co-precipitation ^[29]. From the various synthesis methods, the co-precipitation method has advantages in the form of economic value, easy to perform, fast processing and relatively homogeneous results ^[30,31]. Furthermore, the co-precipitation method can be applied to various materials, including natural materials. In this research, Mn_xFe_3–xO₄ was synthesized by co-precipitation method using natural materials based on iron sand. Iron sand was selected and taken from Bajul Mati Beach because it contains a fairly high magnetite material, which is 90.4% ^[32,33].

To improve the absorption performance of radar waves, a material with better dielectricity is needed. Previous studies reported that Mn_xFe_3–xO₄ materials still have limitations, such as low permittivity and complex permeability ^[24,34]. In addition, one of the main causes of limitations in the application of Mn_xFe_3–xO₄ RAM is the high density value ^[18,35], low stability, and small dielectric loss making it difficult to apply as RAM ^[13].

Carbon-based materials are often used as dielectric materials for RAM purposes because they have advantages such as high electrical conductivity and low density ^[36,37]. Saeed et al. carried out the synthesis of magnetic nano composites/MWCNT and they obtained excellent wave absorption results ^[38]. In another study, Taufiq et al. synthesize magnetic materials combined with activated carbon to increase the value of RL ^[11]. According to the research of Zhao et al., reduced-graphene oxide (rGO) materials can also be combined with magnetic materials for the purpose of increasing reflection loss (RL) ^[39].

Regarding the selection of rGO, the advantages of rGO include materials with good dielectric properties, low density, high surface area and good electrical conductivity ^[40,41], so it is necessary to stabilize the density and dielectric properties of the material from RAM to obtain optimal radar wave absorption capability. Furthermore, the residual and functional group defects cause a polarizing effect that contributes to the increase in the RL value ^[42]. Thus, in this study, the synthesis of rGO based on coconut shell waste material as a precursor with Mn_xFe_3–xO₄ was carried out. The choice of coconut shell used as a dielectric material because it has a carbon element with a content that reaches 80 wt% ^[43], so it is able to absorb radar waves well ^[44]. Meanwhile, rGO has properties in hydroxyl and carboxyl structural defects that support the absorption of radar waves through the principle of surface polarization ^[36,40]. In addition, rGO has a low density and reduces the aggression of Mn_xFe_3–xO₄, making it suitable for use as an antiradar dielectric material ^[45]. The method used for the synthesis of rGO is solid state reaction, because the method is simple. Then, the process of combining Mn_xFe_3–xO₄ (x = 0.25, 0.50, 0.75) with rGO in the form of Mn_xFe_3–xO₄/rGO nano composites through the coprecipitation method. These results present a discussion of the structure, elemental content, morphology, and RAM potential of the Mn_xFe_3–xO₄/rGO nanocomposite.

2.   Materials and methods

2.1.   Materials

The materials used in this study were iron sand obtained from Bajul Mati Beach, Malang as the main component for Fe and coconut shell waste obtained from Malang. Then, the powder of manganese(II) chloride hydrate (MnCl₂∙4H₂O, 99.99%, Sigma-Aldrich, Germany), chloride acid (HCl, 99.99%, Merck, Germany), ammonium hydroxide (NH₄OH, 99.99%, Merck, Germany), ethanol (EtOH, 100%, Merck, Germany), distilled water and ultrafiltered water (MQ).

2.2.   Synthesis of rGO from Coconut Shell Waste

The rGO material was synthesized using the solid-state reaction method. The process began with the cleaned coconut shell which. The coconut shells were washed with distilled water and dried in the sun for 3 d. After drying, the coconut shell was burned to form charcoal. Furthermore, the charcoal was sieved using a 200 mesh sieve to obtain charcoal powder. Then, the sample was carbonated at 400 °C for 5 h.

2.3.   Synthesis of Mn_xFe_3–xO₄/rGO (x = 0.25, 0.50, 0.75)

The Mn_xFe_3–xO₄/rGO nanocomposite was synthesized using the co-precipitation method with the following steps. In general, the Mn_xFe_3–xO₄ synthesis procedure has been corresponded in previous studies ^[21]. At first, the iron sand was washed and dried in the sun to dry. It was then separated using permanent magnets to remove impurities. Next, 20 g of iron sand was dissolved in 58 mL of HCl with a stirring speed of 720 rpm for 30 min at room temperature. The solution was filtered and separated from the residue using filter paper to obtain a solution of FeCl₂ and FeCl₃. Simultaneously, the rGO powder was dispersed into 50 mL of distilled water and sonicated for 2 h at room temperature. Then, each mole fraction, namely: x = 0.25 was 1.36 g, x = 0.50 was 2.72 g, x = 0.75 was 4.09 g MnCl₂∙4H₂O and rGO suspension was added to a mixture of 18 mL of FeCl₂ and FeCl₃ solution. The mixing process was carried out with a stirring speed of 720 rpm which was then titrated with 25 mL of NH₄OH at room temperature. This synthesis process was carried out for 30 min until a black precipitate was produced. The precipitate was washed repeatedly using distilled water until it was odorless with a pH value of 7. Then, each precipitate was filtered using filter paper and dried in an oven at 100 ℃ for 1 h. After drying, 1.5 g of Mn_xFe_3–xO₄/rGO material was compacted with manual pressure to become pellets with a diameter of 0.5 cm and thickness of 1 cm. It was sintered at 400 ℃ for 1 h. The synthesized material was characterized by instruments. The rGO samples were coded as rGO and the Mn_xFe_3–xO₄/rGO samples with various mole fraction x = 0.25, 0.50, 0.75 coded respectively RAM1, RAM2, RAM3 for Mn_0.25Fe_2.75O₄, Mn_0.5Fe_2.5O₄, and Mn_0.75Fe_2.25O₄.

2.4.   Characterization

X-ray diffraction characterization (XRD; PANalytical, X'Pert Pro, Cu-Kα 1.5406 Å) was used to determine the phase, lattice parameters, and crystal size of the samples. Investigation of the lattice parameters, crystal size, and density of Mn_xFe_3–xO₄/rGO was carried out based on the data XRD with refinement rietveld method using Rietica program. Next, identification of microscopic morphology and elemental content was used for Scanning Electron Microscopy (SEM, FEINSPECT-S50) characterization. Particle Size Analyzer (PSA, Mastersizer 3000) was used to identify the particle size of the samples. Then, to study the magnetic properties and absorption ability of the radar waves of the Mn_xFe_3–xO₄/rGO nanocomposite, Vector Network Analyzer (VNA, Advantest R3770, 8–12 GHz (X-Band)) and Permagraph (Magnet Physik Streigroever GmbH) were used to study the magnetic properties and absorption capabilities of radar waves.

3.   Results and discussion

3.1.   Structure of Mn_xFe_3–xO₄/r-GO nanocomposite

XRD patterns of all the samples are displayed in Figure 1. First, the data confirm the presence of only magnetite (PDF No. 19-0629) without any impurities for all samples from other study. In that study, the data of XRD supported by lattice parameter and crystal volume (Figure 2). The diffraction peaks shift to a lower angle as x increases, implying that the lattice parameter increases with Mn²⁺ incorporation ^[21]. Besides, the ionic radius of Mn²⁺ (0.89 Å) is larger than that of Fe²⁺ (0.77 Å) and Fe³⁺ (0.64 Å) ^[46]. Exactly, Mn²⁺ ions were inserted into Fe₃O₄ succesfully by replacing Fe²⁺ or Fe³⁺ ions to form Mn_xFe_3−xO₄ partially. Moreover, the lattice parameters of the Mn_xFe_3–xO₄ with x = 0.25 to 0.50 increased from 8.377 to 8.439 Å.

Figure 1.  XRD patterns (using CuKα radiation) of the (a) Fe₃O₄, rGO, RAM1 sample (Mn_0.25Fe_2.75O₄/rGO) and (b) MnxFe_3–xO₄ (x = 0.25, 0.50, 0.75) (Reprinted from Ref. ^[21] with permission).

DownLoad: Full-Size Img PowerPoint

Figure 2.  Lattice parameter (a) and crystal volume (V = ų) (b) of the Mn_xFe_3–xO₄ (Reprinted from Ref. ^[21] with permission).

DownLoad: Full-Size Img PowerPoint

In this study, the structure of the Mn_xFe_3–xO₄/rGO nanocomposite was successfully characterized. The results of XRD characterization were carried out on samples of iron sand (Mn_xFe_3–xO₄), coconut shell (rGO), and Mn_xFe_3–xO₄/r-GO nanocomposites shown by RAM1 samples (Mn_0.25Fe_2.75O₄/rGO). The XRD Mn_xFe_3–xO₄ diffraction pattern shows that iron sand has formed a crystalline phase consisting of 93.4% magnetite (Fe₃O₄) compound and 6.6% hematite (F₂O₃) compound with a hexagonal structure with space group P63/mmc (reference code: 98-002-9041). In the rGO, the diffraction pattern consists of the main elements of carbon and oxides detected with the chemical formula C₅₀O₁₂H₇₂. Based on Figure 1, the synthesized rGO sample qualitatively shows two amorphous peaks at 2θ = 24° (002) and 43° (001) according to Acharya et al. ^[47] by modified Hummers method and Lavin-Lopez et al. ^[48] by chemical reduction, heat reduction and multiphase reduction methods. This study confirmed that coconut shell was successfully synthesized into rGO material through the solid-state reaction method.

The nanocomposite compound showed a two-phase structure consisting of Mn_xFe_3–xO₄ and rGO compounds. The diffraction pattern of the nanocomposite sample is different compared to the single-phase rGO (a) and Mn_xFe_3–xO₄ (b). Therefore, the two main phases which are Mn_xFe_3–xO₄ and rGO respectively can be identified in the diffraction pattern of the nanocomposite without the appearance of additional diffraction peaks. The Mn_xFe_3–xO₄ (a) pattern appears more than the rGO pattern (b), this is because the amount of Mn_xFe_3–xO₄ content is more than the rGO content.

For sample RAM1, the X-ray diffraction peak was identified from Mn_xFe_3–xO₄/rGO particles at 2θ = 29.9°; 35.2°; 42.9°; 53.3°; 56.6°, and 62.5° which represent Miller indices (220), (311), (400), (422), (511) and (440). The X-ray diffraction pattern of the Mn_xFe_3–xO₄/rGO nanocomposite shows a characteristic spinel ferrite structure and no other phases are formed ^[28,49,50]. The structural study confirms spinel structure formation with Fd3m space group for the 0 ≤ x ≤ 0.5 samples. The combination with rGO did not significantly affect the shift in the X-ray diffraction pattern of Mn_xFe_3–xO₄, which has been clarified by previous studies ^[21,51,52]. The RAM1 sample also shows no rGO peak was found which could be caused by the XRD characterization scan (2θ angle increment) which was too fast. In another report, the disappearance of the X-ray diffraction pattern of rGO caused by the interfacial bonding of Mn_xFe_3–xO₄ with rGO resulted in a separate structure of rGO thus preventing the repetition of rGO ^[18]. This was also clarified by a previous study ^[21]. The hierarchical size of the nanocomposites was explained in detail the particle size with Particle Size Analyzer (PSA).

The sketch of the doping of Mn into Fe₃O₄ can be seen in Figure 3. The composition and cationic distributions of the Mn_xFe_3–xO₄ particles for x composition between 0 and 1 can be analyzed using the following formula in Eq 1 ^[53]:

Figure 3.  The sketch of the doping of Mn into Fe₃O₄.

DownLoad: Full-Size Img PowerPoint

The Mn_xFe_3–xO₄/rGO composite fabrication process was carried out using the co-precipitation method, by first doping Mn on Fe₃O₄ which was reacted with HCl to produce FeCl₂ and FeCl₃. This was carried out to get the same phase, so that the reaction can take place ^[54]. Mn_xFe_3–xO₄/rGO composite preparation through stoichiometric calculations has resulted in composite compounds that have been mixed with the ultrasonic method. Variations in the composition were carried out as many as 3, namely x = 0.25, x = 0.5, and x = 0.75, resulting in 3 (three) samples named consecutively as RAM1, RAM2, and RAM3. The purpose of adding Mn to Fe₃O₄ is to improve the performance of Fe₃O₄ as a radar absorbing material (RAM). In line with the research of Taufiq et al. ^[54]. stated that Fe₃O₄ still has a low absorption ability of radar waves. The reaction that occurs is described in Eq 2.

The iron metal ions (Fe²⁺ and Fe³⁺) enclosed in the square bracket represent those in the octahedral positions, while the other metal ions (Mn²⁺ and Fe³⁺) in the round bracket represent those in the tetrahedral positions depending on the x value. Six oxygen atoms surround the metal ions in the octahedral sites, while four oxygen atoms surround the metal spinel structure can be classified into three types: inverse, ions in the tetrahedral sites. Generally, Fe₃O₄ has an inverted spinel structure ^[54]. In the Mn_xFe_3–xO₄ system, the spinel, which has eight Fe³⁺ ions located in the tetrahedral mixed, and normal spinel. The systems for x = 0.25, 0.5, and 0.75 form mixed spinel structure because Mn²⁺ ions partially shift the Fe³⁺ ions in the tetrahedral positions. Physically, the Mn_xFe_3–xO₄ crystal structure modeled using the Vesta program can be seen in Figure 4 below.

Figure 4.  Crystal Structure of Mn_xFe_3–xO₄.

DownLoad: Full-Size Img PowerPoint

Figure 5 relates the rGO structure modeled using the ChemDraw program. Basically, graphene is composed of thin atoms of 2D sp² carbon layers that form a honeycomb-like structure. Meanwhile GO, which is a graphene derivative, contains sp² and sp³ carbons and binds to a fairly high hydroxyl group (–OH) ^[55,56]. This is very different from rGO which has few oxygen groups and sp³ carbon. Consequently, rGO is more similar to graphene and also has structural defects ^[57].

Figure 5.  The Arrangement of the Atoms of rGO.

DownLoad: Full-Size Img PowerPoint

The curve of the measurement results with PSA can be seen in Figure 6. The particle size characterization of the iron sand sample that has been separated from the non-magnetic material that has been mashed and filtered shows that the raw material has a homogeneous particle size with a single peak with an average value of 531.8 nm (Table 1). This powder was detected to be still in micro size because it still has a size of more than 100 nm. This is because there is still a coagulation process or clumping at the time of measurement, resulting in a precipitate ^[58]. The particle size characterization for the detected rGO samples had an average particle size of 1359 nm. This size is larger than the iron sand sample. The deposition process that occurs in rGO powder is faster than iron sand powder, so the clumping process is faster and is detected as having a larger particle size.

Figure 6.  Size distribution by intensity of rGO (a), Fe₃O₄ (b), Mn_xFe_3–xO₄ x = 0.25 (c), Mn_xFe_3-xO₄ x = 0.5 (d), Mn_xFe_3–xO₄ x = 0.75 (e).

DownLoad: Full-Size Img PowerPoint

Table 1.  Distribution results of samples.

Samples	Distribution results				Z-Avg (nm)
	Size (d.nm)	% Int	σ	%Pd
Fe3O4	369.3	53.3	93.00	25.2	531.8
	194.8	46.7	41.21	21.2
rGO	835.0	100.0	134.9	16.2	1359
Mn0.25Fe2.75O4	416.8	100.0	63.62	15.3	1049
Mn0.5Fe2.5O4	613.9	100.0	110.5	18.0	1432
Mn0.75Fe2.25O4	440.4	100.0	53.65	12.2	1531

---

 | Show Table

DownLoad: CSV

In general, the addition of the composition of Mn and rGO to Fe₃O₄ nanoparticles causes the crystallinity level of Fe₃O₄ to increase teorically ^[12]. This is proven in Figure 6 which shows that the distribution peaks of Mn_xFe₃O₄/rGO in nanocomposites (x = 0.25 to x = 0.75) appear sharper when compared to pure Fe₃O₄. The increase in Mn composition in Mn_xFe_3–xO₄/rGO nanocomposites results in an increase in the intensity of the Mn_xFe_3–xO₄/rGO peak except for x = 0.75 which is lower when compared to x = 0.5. This is because the x = 0.75 particle distribution is lower than other nanocomposites of particle sizes (440.4 nm), but the average of particle size from x = 0.25 to x = 0.75 increase. The increase in particle size is caused by the large number of Mn particles that push Fe. Theoretically, the size of Fe²⁺ and Fe³⁺ ions is larger than that of Mn²⁺ ions. However, when the number of Mn²⁺ ions is more pressing the Fe²⁺ ions will result in clumping, resulting in a larger particle size than before being pushed by Mn²⁺. This phenomenon is theoretically reinforced that in the voltaic series, Mn is to the left of Fe, so it has more reactive properties and is stronger against Fe. The more Mn metal ions push Fe from Fe₃O₄, the larger the particle size of the Mn_xFe_3–xO₄ nanocomposite. This is also confirmed in Table 1 which shows the particle size of the sample.

Uniquely, the Fe₃O₄ available in this work did not produce polymorphs. Polymorphs that are often produced in the synthesis of Fe₃O₄, like α-Fe₂O₃, γ-Fe₂O₃, dan α-Fe₃O₄ ^[59]. This is because the synthesized Fe₃O₄ comes from natural iron sand. Natural iron sand contains stable Fe₂O₃, so it does not cause porosity which causes Fe₂O₃ variations in Fe₃O₄ synthesis ^[54].

The SEM images of Mn_xFe_3–xO₄/rGO nanocomposites with Mn doping composition of x = 0.5 is shown in Figure 7. As shown in Figure 7a, the morphology of the nanocomposites consists of 3 particle shapes namely spheres, chunks, and worm-like structures. Sequentially, these shapes describe the Fe₃O₄ nanoparticles, Mn ^[60,61], and rGO ^[62]. Qualitatively, it is observed that the sphere of Fe₃O₄ tends to agglomerate. The size of Fe₃O₄ nanoparticles is smaller than that of Mn which has relatively irregular chunks. In addition, the Mn surface also shows some agglomeration of Fe₃O₄, while rGO fills the gap between Fe₃O₄ and Mn ^[63]. Illustrated in Figure 5, rGO is a carbon material that is activated with acids to form OH-functional groups, so that the rGO will bind to the positive charge of Fe₃O₄ which causes the Fe₃O₄ to fill the surface of the carbon material. Based on Figure 5a, few rGO surfaces are covered by agglomeration of Fe₃O₄. This is because the density of Fe₃O₄ is higher than that of rGO ^[64]. Figure 5b indicates the morphology of Mn-doped Fe₃O₄ nanoparticles with a magnification of 50,000 and shows that the Fe₃O₄ and Mn nanoparticles are evenly dispersed on the rGO surface. Furthermore, the EDX results show that the composition of heavy elements C, O, and Fe are 28.72, 36.17, and 27.78% and another is Mn, respectively, which confirms the presence of Fe₃O₄ nanoparticles, rGO, and Mn that form Mn_xFe_3–xO₄ composites. The presence of Fe₃O₄ was confirmed by the presence of Fe and O elements. Meanwhile, the rGO were confirmed by the presence of element C, and doping of Mn were confirmed by the presence of element Mn.

Figure 7.  SEM images of Mn_0.5Fe_2.5O₄/rGO with (a) 3000 and (b) 50,000 magnification with the particle size.

DownLoad: Full-Size Img PowerPoint

3.2.   The magnetic properties of Mn_xFe_3–xO₄/rGO

Magnetic properties in the form of hysteresis loops for Mn_xFe_3–xO₄/rGO nanocomposite samples can be seen in Figure 8. All curves show the characteristics of soft and tall soft magnetic hysteresis loops.

Figure 8.  Hysteresis loops of MnxFe_3–xO₄/r-GO with (a) x = 0.25, (b) x = 0.50, and (c) x = 0.75.

DownLoad: Full-Size Img PowerPoint

A summary of the magnetic properties that obtained in this research, can be seen in Table 2.

Table 2.  Magnetic properties of Mn_xFe_3–xO₄/rGO.

Samples	Br (kG)	HcJ (kOe)	Hmax (kOe)
Mn0.25Fe2.75O4	0.12	0.132	14.370
Mn0.5Fe2.5O4	0.11	0.048	12.275
Mn0.75Fe2.25O4	0.10	0.045	8.880

---

 | Show Table

DownLoad: CSV

The sample of Mn_0.25Fe_2.75O₄ had the highest remanent induction (Br), coercivity (H_cJ), and the highest magnetic field strength (H_max) compared to the other samples, 0.12 kg, 0.132 kOe, and 14.370 kOe, respectively. The results of this characterization indicate that the effect of composition affects the magnetic properties. The addition of Mn elements reduces the values of Br, H_cJ, and H_max. Theoretically, Fe has higher magnetic properties than Mn. Thus, when more Mn replaces Fe, the magnetic properties will decrease. However, it must be analyzed further through the results of the reflection loss of the synthesized sample.

3.3.   Reflection loss of Mn_xFe_3–xO₄/rGO

Reflection loss is a characteristic that shows the ability of radar wave absorption from Mn_xFe_3–xO₄/rGO. Reflection loss of each sample has been characterized using VNA with the results of the reflection loss and frequency curves as shown in Figure 9. The results show that there has been absorption of electromagnetic waves in the frequency range between 7–13 GHz with the absorption frequency range at 2–14 GHz. At this frequency, it shows that the Mn_xFe_3–xO₄/r-GO nanocomposite can be applied as a RAM material in the X-Band 8–12 GHz frequency range. Figure 9 shows RL of the Mn_xFe_3–xO₄/rGO nanocomposites at a frequency of 8–12 GHz which were calculated by using Eqs 3 and 4.

Figure 9.  Reflection loss of the Mn_xFe_3–xO₄/rGO nanocomposites with (a) x = 0.25, (b) x = 0.50, (c) x = 0.75.

DownLoad: Full-Size Img PowerPoint

Z_in value was calculated by using Eq 3 below.

where Z_in and Z_in are input and output impedance values. While µ_r and Ɛ_r are the permeability and complex permittivity of the material, c represents the velocity of the radar in a vacuum, f is the frequency of radar, and d is the thickness of the material when tested ^[65].

In Figure 9 for the sample of Mn_0.25Fe_2.75O₄/rGO nanocomposite, absorption of electromagnetic waves has occurred in the frequency range between 8.9–11.5 GHz with the absorption peak frequency at 11.5 GHz of −11.8 dB with a thickness of 1.5 mm adsorption field. Likewise for the Mn_0.5Fe_2.5O₄/rGO nanocomposite sample, absorption occurs in the frequency range between 9–11.3 GHz with the absorption peak frequency at 11.3 GHz of −11.5 dB. Meanwhile, for the Mn_0.75Fe_2.25O₄/r-GO nanocomposite sample, absorption has occurred in the frequency range between 8.8–11.5 GHz with the absorption peak frequency at 11.5 GHz of −1.95 dB.

Fe₃O₄ has an RL of −5.58 dB at a frequency of 10.58 GHz. The low RL value owned by Fe₃O₄ is due to the fact that this sample only consists of magnetic material, thus RAM only absorbs the magnetic part of the radar. In this study, the increase in radar absorption is increased by adding Fe₃O₄ with rGO materials. That is because rGO belongs to good dielectric material. Based on Figure 9, it is noticed that the absorption capability of radar from Mn_xFe_3–xO₄/rGO nanocomposites is stronger than that of Fe₃O₄ nanoparticles. This indicates that the absorption properties of radar increase if added by rGO materials. Physically, this phenomenon occurs since the absorption of radar from Fe₃O₄ nanoparticles only comes from natural resonance and domain wall resonance, so that with the addition of rGO, the dielectric loss properties of the rGO is introduced and the interface polarization between Fe₃O₄ and rGO is introduced. In detail, the RL values of nanocomposites are shown in Table 3. Based on Table 3, it can be seen that the RL values of the Mn_xFe_3–xO₄/rGO nanocomposites are higher than those of MWCNT/Fe₃O₄ ^[66] and ZnFe₂O₄ ^[67]. The addition of dielectric material also causes the absorption bandwidth of the Mn_xFe_3–xO₄/rGO nanocomposites to widen. Differences in composition affect the absorption of Mn_xFe_3–xO₄/rGO nanocomposite RAM material. At composition x = 0.75 is the highest absorption with −11.95 dB.

Table 3.  RL value of the Mn_xFe_3–xO₄/rGO nanocomposites.

Samples	RL (dB)	Ref.
Mn0.25Fe2.75O4/rGO	−11.8	-
Mn0.5Fe2.5O4/rGO	−11.5	-
Mn0.75Fe2.25O4/rGO	−11.95	-
rGO	−5	[52]
rGO	−3.3	[37]
Fe3O4	−3.3	[66]
Fe3O4	−5	[68]
ZnFe2O4	−10.0	[67]
MWCNT/Fe3O4	−10.0	[66]

---

 | Show Table

DownLoad: CSV

Generally, the Mn_xFe_3–xO₄ material in RAM applications acts as a magnetic material. Based on Table 3, the single material is not optimal in absorbing radar waves. Fe₃O₄ material obtained a low RL value of −5 dB ^[68]. The Mn_0.75Fe_2.25O₄/rGO material was able to increase the RL value to −6.95 dB compared to pure Fe₃O₄ ^[17]. This is due to the presence of Mn²⁺ ions which can increase the polarization of the space charge ^[69]. The ability of magnetic loss in Mn_xFe_3–xO₄ material occurs when the direction of the magnetic moment which is relatively antiparallel in the tetrahedral and octahedral regions will be rectified ^[19]. Generally, Mn_xFe_3–xO₄ materials can produce magnetic loss consisting of eddy current loss and natural resonance loss ^[30]. Furthermore, the magnetic loss capability is more dominant due to the eddy current loss phenomenon, as expressed in Eq 5 ^[28].

With C₀ as the value representing the eddy current loss. If depicted in a graph C₀ with f, then the eddy current loss is indicated by a constant value of C₀. In the study of Tajik et al., the Mn_xFe_3–xO₄ material showed a constant C₀ value at frequencies above 8 GHz ^[70]. In another report, Modaresi et al. reported the same ^[28]. Conversely, if the value of C₀ is not constant, it can be indicated that there is a natural resonance loss phenomenon from the magnetic material. The relatively small crystal size has the potential to increase the RL value, which is caused by the exchange length resonance of the magnetic energy of a material ^[55]. Thus, the Mn_xFe_3–xO₄ material can be used as a potential magnetic material in RAM applications.

Furthermore, rGO is a unique material, which refers to its special characteristic which is it can produce dielectric loss. In the report of Liu et al., dielectric materials depend on the phenomenon of dipole and electron polarization ^[37]. Inside an atom, the influence of the electric field from electromagnetic waves will cause electron polarization. If viewed at the molecular level, each molecule has a dipole moment, which when applied by an external electric field will form a charge separation or dipole polarization. In the rGO system, dipole polarization occurs in the structural defects and the presence of various functional groups ^[71]. For example, Qiao et al. representing the interaction of electromagnetic waves with the structural defects of rGO, will result in an asymmetric charge distribution to form a dipole formation ^[72]. This causes the dipole to continue to rotate in electromagnetic waves, which in turn converts electromagnetic wave energy into heat energy ^[73]. In fact, electrons on the surface of rGO can interact with electromagnetic wave energy ^[74]. Consequently, the electrons will migrate and collide with the rGO lattice, where the energy of the electromagnetic waves is converted into heat energy ^[73]. Debye's dipolar relaxation theory is usually used to confirm the ability of dielectric loss, as expressed in Eq 6 ^[28].

Where ε_s and ε_∞ are static permittivity and relative dielectric permittivity. If and are expressed as x and y axes, a semi-circular Cole-Cole graph is formed. According to Chai and colleagues, the presence of a semi-circle pattern indicates a relaxation process, which is caused by the absorption of the electric field from electromagnetic waves ^[67]. Furthermore, Shu et al. reported that the distortion of the semi-circular Cole-Cole graph in the rGO material indicates the presence of polarization ^[74]. Furthermore, based on the previous SEM image of the composite sample in Figure 7, rGO forms cavities and is filled with Mn_xFe_3–xO₄ particles. The presence of cavities in rGO has the potential to increase the value of reflection loss, which is caused by electromagnetic waves undergoing multiple reflections ^[75]. Thus, the rGO material has potential in RAM applications. Although, based on Table 3, the reflection loss value of rGO is still low at −5 dB, so it is necessary to combine it with magnetic materials.

Mn_xFe_3–xO₄ deposition strategy on the surface of rGO is one of the appropriate ways to produce microcurrent networks ^[76]. The mechanism, Mn_xFe_3–xO₄ acts as an electron-hopping bridge between adjacent rGO layers ^[55]. More deeply, electron-hopping is expressed as contact conductivity (σ_contact) as a function of temperature (T) as in Eq 7 ^[76].

Where K_h is the prefactor, U is the barrier potential and k_B is the Boltzmann constant. As the equation above, conductivity is caused by electron-hopping followed by an increase in temperature. The micro current network that is formed will produce a conduction loss ^[55]. The phenomenon of conduction loss is characterized by a decrease in the permittivity value as the frequency increases, which is useful for weakening the energy of electromagnetic waves. However, Cao and colleagues reported that the phenomenon of relaxation or an increase in temperature that is too high causes a conductivity network not to form ^[71]. Consequently, at high frequencies, the dielectric loss capability will decrease. One solution is to adjust the mass composition of rGO with Mn_xFe_3–xO₄. In addition, the presence of interfacial interactions between Mn_xFe_3–xO₄ and rGO has the potential to produce interfacial polarization ^[13]. Physically, the interface interaction accumulates the migration and diffusion of the carrier so as to form a spatial separation consisting of positive and negative charges ^[77]. Consequently, between the boundaries of the Mn_xFe_3–xO₄ and rGO materials, a balance formation is formed in the form of a region of spatial charges and an electric field. However, changing the direction of the electromagnetic wave field can change the charge pattern so that the electromagnetic wave energy will be dissipated ^[78]. Interfacial polarization can also be identified through Debye's dipolar relaxation theory as studied above.

According to Table 3, the Mn_xFe_3–xO₄/rGO composite of the three variations showed fantastic results, namely higher reflection loss values than the single material. The combination of magnetic and dielectric materials provides a synergy effect with good impedance match results (Z ~ 1) ^[79]. Furthermore, this composite system contains a magnetic material, this is in accordance with the results of the reflection loss value obtained from the tests that have been carried out.

Based on the results of the previous research, it was shown that, if the RL value obtained < −15 dB, it indicates that if 96.9% of the radar waves are absorbed by the nanocomposite. Meanwhile, if the RL value obtained < −20 dB, then the absorbed wave is almost 99.0% ^[80]. In this research, the RL value of nanocomposites has a range between −2 to −14 dB or < −20 dB. Thus, it can be concluded that the waves absorbed by nanocomposites in this study are around 96.9–99.0%. Two main aspects affecting the increase of radar absorption by Mn_xFe_3–xO₄/rGO nanocomposites in this study are first, the efficient complementarity between dielectric loss and magnetic loss which is indicated by the relative permittivity and permeability values must be fulfilled ^[68,81]. If Fe₃O₄ nanoparticles stand alone as a compiler of RAM, it can be construed that the resulting RL value is still low. This is due to the large disparity between permeability and permittivity which interferes with impedance matching. Thus, in the Mn_xFe_3–xO₄/rGO system, the Fe₃O₄ nanoparticles act as absorbents of the magnetic parts, and rGO, is as dielectric absorbers of incoming radar. Besides, the rGO also acts as a nucleation site for Fe₃O₄ which prevents or reduces the aggregation of these nanoparticles. Second, there is interfacial polarization between Fe₃O₄-rGO, where multi-interfaces on nanocomposites will produce significant polarization interfaces that will increase the value of dielectric loss at high frequencies ^[65]. This is indicated when the addition of rGO absorption material occurs at a frequency of around 11 GHz. Thus, the development of Mn_xFe_3–xO₄/rGO nanocomposites in this research provides new opportunities for large-scale development for the application of high-performance microwave absorbing materials based on local natural materials through environmentally friendly synthesis.

3.4.   Practical implication and outlook

Uniquely, in this study, reduced-graphene oxide (rGO) synthesized from coconut shell waste has the potential to be developed as a dielectric material from RAM. This is relevant to the data presented in Table 3 that rGO can absorb electromagnetic waves of −5 dB ^[52] added with the findings from this study which combines natural materials of natural iron sand and coconut shell waste, it produces an RL value of −11.95 dB. In general, coconut shell waste is very easy to obtain from the community, especially in Indonesia. Theorically, coconut shell has a high cellulose content, so it contains a high carbon content as well ^[82,83]. Carbon has the ability to absorb electromagnetic waves, so it has the potential to be developed as a dielectric material. Further research on the use of natural materials can be developed towards extracting the potential of the material itself. Natural iron sand can be extracted as a source of Fe₂O₃ which can be synthesized into Fe₃O₄ with benefits as an environmentally friendly magnetic material ^[84], antimicrobial ^[69], and anti-cancer agent ^[79]. Meanwhile, coconut shell waste can be synthesized into rGO with the benefit of being a dielectric material for Radar Absorbing Material (RAM) ^[56], corrosion protection ^[85], and electrochemical sensor ^[70].

4.   Conclusions

The Mn_xFe_3–xO₄/rGO nanocomposites were successfully synthesized by using an environmental precipitation method. Meanwhile, with the addition of rGO in the Mn_xFe_3–xO₄/rGO nanocomposites, their RL increases significantly because the nanocomposites consist of magnetic loss and dielectric loss which increases the radar absorption. Interestingly, the RL value of the Mn_xFe_3–xO₄/rGO nanocomposites ranges from −2.0 to −14.0 dB which shows their radar absorption capability is in the range of 96.9%–99.0%.

Acknowledgments

This work was supported by Faculty of Mathematics and Natural Sciences, Universitas Negeri Malang. The writer was inspired by the special people, like KH. Muhammad Zaini Abdul Ghani, Prof. Effendy, Ph.D, and Prof. Hadi Nur, Ph.D. Special thanks to my best close friend, Muhammad Roy Asrori, S.Pd.

Conflict of Interest

The authors stated that there is no conflict of interest.