Abstract
Carbon spheres (CS)@MnO2 core-shell nanocomposites, with MnO2 nanoflakes uniformly coating at the surface of CS cores, were successfully synthesized by a facile water-bathing method. MnO2 amounts is estimated to be 24.7 wt% in CS@MnO2 nanocomposites. A high dielectric loss value and an electromagnetic shielding effectiveness of 16‒23 dB were observed for the CS@MnO2 in the frequency range of 8‒18 GHz, which is mainly attributed to the enhanced absorption loss. The incorporation of the CS with MnO2 improves the electrical conductivity. Meanwhile, the electromagnetic impendence matching has been significantly ameliorated. Moreover, the increasing interfaces between the CS and MnO2 facilitate the microwave attenuation as well. Thus, the electromagnetic shielding performances were greatly enhanced. Our findings provide an effective methodology for the synthesis of the CS@MnO2 core-shell nanocomposite for potential electromagnetic applications.
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Introduction
In recent years, the rapid development of electromagnetic wave communications and radar systems urgently expect the excellent electromagnetic interference (EMI) shielding or absorbing materials to fulfill the rising demands in environmental protection devices, anti-electromagnetic interference (EMI) coatings and self-concealing technologies1. Generally, two mechanisms for EMI shielding are widely acceptable, e.g., electromagnetic reflection and absorption. Regard to the electromagnetic wave (EMW) shields, the absorber plays a crucial role in improving the electromagnetic performances, which strongly depends on the crystallinity, morphology and granulometry of the absorber. Traditional absorbers, such as ferrites and conductive polymers, could make a strong absorption. However, the complicated morphological tailoring is needed. Besides, the thicknesses are often too thick for practical applications2. Comparatively, carbon materials have been extensively investigated in EMI shielding applications with the advantages of low density, excellent chemical resistance and diverse microstructures3. Yet, the high reflective characteristic of carbon materials caused by their larger conductivity and permittivity hampers their performances as effective EMW absorbers4.
More recently, core-shell structures have caught great interests as an effective route to improve the chemical homogeneity and hence enhance the functionality of the composite5. For instance, Dong et al. reported that polyaniline (PANi) coated Ni nanocomposites presented dual dielectric relaxation to improve the microwave absorption of Ni nanoparticulates. With a PANi content of 15.6 wt%, the nanocomposite exhibited an effective absorption bandwidth (reflection loss (RL) < −10 dB) in the range of 4.2‒18 GHz with a thickness of 2 to 6 mm6. The research from Singh et al. also indicated that the decoration of Co/Ni to single walled carbon nanotubes (SWCNTs) delivered an enhanced EMI shielding performance7. Similarly, Du et al. wrapped Fe3O4 microspheres with carbon shells, which displayed a wide absorption bandwidth of about 14 GHz (4.0‒18 GHz) with a variation in shell thickness from 1.5 to 5.0 mm8.
In this sense, it is highly speculated that coating carbon materials with a less conductive dielectric could be an effective strategy to improve the electromagnetic performances of carbon materials by modulating the impedance matching between carbon material and free space. Moreover, the core-shell structures introduce large specific surface areas and interfaces, which will arise more polarization effects to improve the EMI shielding properties9.
As a typical transition metal oxide, manganese dioxide (MnO2) has been intensively studied in the fields of catalyst, batteries and electrochemical capacitor electrodes, due to its unique advantages including natural abundance, cheap precursors, easy synthesis, and thermal stability10,11,12. Significantly, MnO2 has been proved to be a competitive candidate for EMW absorptions and shields13,14,15. Nevertheless, the weak electrical conductivity and poor magnetic loss requires morphological tailoring, ion doping or incorporating with conductive components to improve its electrochemical or electromagnetic properties16,17. Previously, our group synthesized α-MnO2 nanostructures using a facile water-bathing method. It was found that the MnO2/paraffin wax composites possessed great EMW absorption properties in the frequency range of 2‒18 GHz14, even in the low frequency range at low temperature18. Wang et al. hydrothermally synthesized MnO2 hollow microspheres consisted of MnO2 nanoribbons, showing enhanced EMW attenuation with an effective absorption bandwidth of about 4 GHz (14.0–18 GHz) in a thickness of 3 mm19. Ramaprabhu et al. reinforced polyvinylidene fluoride (PVDF) with both 5 wt.% MnO2 nanotubes (MNTs) and 1 wt.% functionalized multiwalled carbon nanotubes (f-MWCNT), which showed a EMI shielding effectiveness of ~20 dB in the whole X-band frequency range20.
In view of the above considerations, we design a core-shell nanostructure with relatively high conductivity carbon sphere (CS) core and MnO2 nanoflakes shell, which will provide better impedance matching as well as good EMW absorption based on MnO2, CS and their synergistic effects. The unique CS@MnO2 core-shell structure is expected to exhibit better electromagnetic performances. In brief, we successfully prepared CS@MnO2 core-shell nanostructure using a facile water-bathing method. The micro-structures are thoroughly characterized and then the EMI shielding performances are examined in the frequency range of 8‒18 GHz. Finally, possible explanations are discussed in great details.
Results and Discussions
Phase crystallinity
The crystal structure and phase purity of the as-prepared products were identified by XRD and Raman spectra. Figure 1a shows the typical XRD pattern of the samples including CS, MnO2 and CS@MnO2. All the detected diffraction peaks can be indexed to monoclinic potassium birnessite MnO2 (JCPDS 80–1098) regardless CS, which consists of 2D edge-shared [MnO6] octahedral layers with K+ cations and water molecules in the interlayer space21. Four diffraction peaks at 2θ of 12.6°, 25.2°, 37.3° and 65.6° correspond to the (001), (002), (\(\overline{1}\) 11) and (020) basal reflections of MnO2, while the diffraction peaks at 11.6° and 24° are indexed to the diffraction of carbon materials3. Besides, no characteristic peaks of impurities are detected. The broadened peaks imply that the MnO2 is composed of small nanocrystals, which will be supported by the following TEM analysis.
To further compare the difference of MnO2 and CS@MnO2, the Raman spectra were obtained (Fig. 1b). The Raman peaks at 495, 567 and 636 cm−1 are derived from the birnessite-type MnO2, which belongs to Ag spectroscopic species originating from the breathing vibrations of [MnO6] octahedra within a birnessite-type framework. Generally, two Raman peaks at 567 cm−1 and 636 cm−1 are viewed as ν 3(Mn-O) stretching vibration and the symmetric stretching vibration ν 2(Mn-O) in [MnO6]22. Importantly, the Raman spectrum of CS@MnO2 appears similar features with pure MnO2, except a slight shift for the ν 2(Mn-O) stretching frequency, which is ascribed to the interaction between the MnO2 and carbon materials23. Characteristic D band and G band peaks at 1354 cm−1 and 1592 cm−1, confirm the existence of the CS in the composites, which agrees well with previous reports11,21.
To estimate the MnO2 amounts in CS@MnO2 nanocomposite, a TGA analysis has been performed in air. Totally, the weight loss of 76.3 wt% is clearly observed from room temperature to 400 °C in Fig. 2, indicating the complete consumption of CS at about 400 °C21,24. Therefore, the MnO2 amounts is estimated to be 24.7 wt% in the CS@MnO2 composites.
Microstructures
The TEM and HRETM images of the CS@MnO2 and MnO2 nanostructures are displayed in Fig. 3. From Fig. 3a and b, it can be seen that the CS core (about 300 nm in diameter in the inset of Fig. 3a) is uniformly covered with a layer of about several nanometers in thickness. The MnO2 coating is in the form of tiny nanoflakes. As is known, carbon spheres synthesized with hydrothermally treated glucose usually have large functional groups on their surfaces, which produces plentiful active sites to favor MnO2 coating25,26. Figure 3c illustrates the MnO2 shell in CS@MnO2 by HRTEM, which reveals the interplanar spacings of 0.69 nm and 0.28 nm, matching well with the (001) and (200) crystal planes of birnessite MnO2. In the case of pure MnO2, the MnO2 is in the form of nanoflakes with dimensions of 30–50 nm (Fig. 3d). The HRTEM shows the interplanar spacings of 0.66 nm and 0.34 nm, as depicted in Fig. 3e, corresponding to the (001) and (200) planes of birnessite MnO2.
In short, these analyses confirm the formation of CS@MnO2 core-shell structure by a facile water-bathing method. The unique structure of CS@MnO2 makes it a favorable candidate for electromagnetic shielding.
Electromagnetic results
As we all know, the electromagnetic shielding performances are closely associated with their dielectric (\({\varepsilon }_{{\rm{r}}}={\varepsilon ^{\prime} }_{{\rm{r}}}-{\rm{j}}{\varepsilon ^{\prime\prime} }_{{\rm{r}}}\)) and magnetic (\({\mu }_{{\rm{r}}}={\mu ^{\prime} }_{{\rm{r}}}-{\rm{j}}{\mu ^{\prime\prime} }_{{\rm{r}}}\)) properties, as plotted in Fig. 4. It is found a decreasing ε r with the increasing frequency from 8 to 18 GHz for the CS@MnO2 (Fig. 4a). On the contrary, an increasing μ r is observed for the same sample (Fig. 4b). Nevertheless, both the ε r and μ r values of pure MnO2 are almost maintained. For instance, the real part of ε r decreases from 25.5 at 8 GHz to 15.2 at 18 GHz, while the imaginary part drops from 36.1 at 8 GHz to 20.4 at 18 GHz, which may be favorable to the electromagnetic shielding performances. Particularly, great difference is observed in imaginary parts of μ r between MnO2 and CS@MnO2, as shown in Fig. 4b. Compared to the almost steady imaginary μ r values (1.05–1.20) of MnO2, the CS@MnO2 shows negative imaginary μ r from −0.09 to −0.21. This phenomenon is not common in ordinary materials; however, it has been intensively reported for certain designed nanostructures such as hollow cobalt nanochains27, Fe/Al2O3 28, and Ni/Al2O3 29.
To investigate the electromagnetic loss characteristics of the CS@MnO2 core-shell composites, the dielectric and magnetic dissipation factors tanδ e = ε″/ε′ and tan δ m = μ″/μ′ are calculated, as expressed in Fig. 4. The values of tanδ e for CS@MnO2 (>1.3) are much larger than pure MnO2 (0.03‒0.06), which comes from the synergic results of electronic polarization, interfacial polarization, dipole relaxation and natural resonance. Besides, the unique core-shell structure is also beneficial to the great tanδ e 7. Under an external electromagnetic field, the charges accumulate at the interfaces between the MnO2 tiny dendrites and the carbon spheres to form enormous diploes, hence it could contribute to the dielectric loss by causing pronounced interfacial polarization. Owing to the surface anisotropy field, the materials in nano-scale may produce higher anisotropy energy to favor dielectric loss30. Moreover, great performances in electrochemical and electromagnetic fields31,32,33 were reported for MnO2 nanostructures with sheet- or flake-like shapes because of larger specific surface areas and better surficial activities.
As to tanδ m , pure MnO2 shows a tanδ m less than 0.02, while the CS@MnO2 composite gives negative values due to its negative imaginary μ r, as demonstrated in Fig. 4d. Similar to tanδ e , two obvious peaks at around 10 GHz and 14 GHz for both MnO2 and CS@MnO2 are also observed, which is related to the resonances in ε r 1,34. Based on the above results, CS@MnO2 core-shell is believed to exhibit excellent electromagnetic shielding performances over pure MnO2 in terms of higher dielectric and magnetic loss properties.
EMI shielding effectiveness
The shielding effectiveness (SE) towards EMI was calculated by the relation:
According to the Schelkunoff’s Equation, the SE based on transmission line theory is expressed as1,7:
Where, SE A, SE R and SE M represent shielding contributions from absorption, reflection and multiple reflection, respectively. Generally, the SE M can be ignored for all practical purposes when the SE is larger than 10 dB, and SE R and SE A are thus given using the following equations2:
Where, T and R are the transmission coefficient and reflection coefficient, which is obtained by the following equations35,36,
Where the E in, E re and E tr are the electric intensity of the incident, reflected and transmission waves, respectively.
The obtained SE of MnO2 nanoflakes and CS@MnO2 core-shell nanostructure with a thickness of 2 mm are shown in Fig. 5. Compared to the small SE values of MnO2 (11.3‒12.3 dB) (Fig. 5b), CS@MnO2 displays an increasing SE from 16.2 dB to 22.8 dB as the frequency increasing from 8 GHz to 18 GHz, indicating an improvement of the shielding proficiency of the incident EMW from 85% to 93% (Fig. 5a). The SE mainly arises from SE A, especially at high frequency bands. For example, the SE A values at 8 GHz and 18 GHz are 12.4 and 22.5 dB, which accounts for 76.5% and 98.7% of the total SE. The excellent EMI shielding properties of CS@MnO2 is plausibly explained by the unique core-shell structure and the synergistic effect. Because of the poor conductivity of MnO2, a better impedance matching with the air is achieved. In the case of carbon materials, great EMW reflection on the surface may occur due to the impedance mismatching caused by the relatively higher electrical conductivity. When the incident EMW transmits into the CS@MnO2 core-shell nanostructure, the better impedance matching between the air and MnO2 will guide the wave into the interior of the structure to reach the carbon surface. The EMW is partially attenuated by the electric loss from carbon core. On the other hand, the reflected wave from the CS surface is absorbed again by the MnO2 shell. Hence, the effective complementarities between the dielectric loss and the magnetic loss, originating from the synergistic effect of the CS cores and the MnO2 nanoflaky shells, also endow CS@MnO2 with a better absorption37. As listed in Table 1, the SE values are clearly comparable to those reported MnO2-based EMI shielding materials.
To completely explore the underlying electromagnetic mechanisms of the CS@MnO2 core-shell nanostructure, the electrical conductivity (σ), the dielectric polarization as well as magnetization are totally examined. Based on the measured electromagnetic parameters, the frequency dependent electrical conductivity of the pure MnO2 and CS@MnO2 are calculated from Equation (7), as displayed in Fig. 6a.
Conductivity of 0.06–0.24 S/m is obtained for pure MnO2 from 8 GHz to 18 GHz. However, bigger electrical conductivity (about 16–20.11 S/m) of CS@MnO2 is indicated in Fig. 6a at the same frequency range.
The electromagnetic attenuation coefficient (α) is calculated based on ε r and μ r values by the Equation (8).
here, f and c are the frequency and electromagnetic wave velocity in free space, respectively. Although both samples show increasing α values with frequency, the CS@MnO2 core-shell structure clearly show much higher values, as shown in Fig. 6b, suggesting a suitable explanation of excellent SE.
In order to explore the intrinsic dielectric and magnetic response, the Debye dielectric relaxation model is adopted to analyze the mechanisms of the dielectric loss. According to the Debye dipolar relaxation, the dielectric permittivity in complex form can be expressed as38:
where f is the frequency, τ is the relaxation time, ε s and ε ∞ are the dielectric constant in static and optical frequency, respectively. Accordingly, the relationship between ε′ and ε″ is further expressed as following39:
Therefore, the curve of ε′ versus ε″ is a single semicircle, denoting as Cole–Cole semicircle. Each semicircle generally corresponds to one type of Debye relaxation process. From Fig. 7a, three semicircles are detected for the CS@MnO2, expressing several dielectric loss mechanisms such as interfacial polarization, space charge polarization besides dielectric relaxation. Moreover, the conductance loss caused by the improved electrical conductivity may also contribute greatly38. The Cole–Cole semicircle curve of pure MnO2, as is in Fig. 7b, exhibits distorted and complicated shape, implying the existence of diverse dielectric loss processes40.
As discussed above, magnetic loss also plays significant role in the electromagnetic attenuation process. In particular, the contributions of eddy current loss, as approximately described by Equation (11)41, to magnetic loss is studied.
where, d and μ 0 are the particle diameter and the magnetic permeability of free space. For a magnetic material, the parameter C 0 = μ″(μ′)−2(f)−1 is often used to determine its eddy current loss domination. As shown in Fig. 8, the C 0 fluctuates markedly in the range of 8‒18 GHz, indicating complicated loss mechanisms other than only eddy current loss, such as magnetic hysteresis loss, domain-wall displacement loss and natural resonance41. The better magnetic loss of the CS@MnO2 could be ascribed to its unique core-shell structure. Liu et al. reported that the high-frequency performances of magnetic composites were enhanced by the separation of conductive particles with an insulating shell42. The incorporation of CS with MnO2 nanoflaky particles improves the electrical conductivity greatly, and thus results in larger eddy current densities, which produce significant eddy losses in an alternating electromagnetic field. Moreover, the time lag of the magnetization vector causes magnetic loss as well. As the frequency increases, the motion of the magnetization cannot keep up with the alternation of the applied electromagnetic field, leading to the increase of the imaginary μ r, and thus the magnetic loss42, as shown in Fig. 4.
Taken together, we could imagine the possible electromagnetic shielding mechanism for the CS@MnO2 core-shell based on the native natures of CS and MnO2 and the synergistic effect. When an incident EMW arrives at the surface of the CS@MnO2 composites, most incident wave will transmit through the thin MnO2 shell due to the improved impendence matching. At the interface between CS and MnO2, partial wave is attenuated by CS in the form of dielectric loss and magnetic eddy loss. The rest is reflected back to the shell again and attenuated by the MnO2 nanoflakes. Moreover, CS provides places for tiny MnO2 nanoflakes coating, enormous interfaces exists between the CS core and MnO2 shell, producing large amounts of polarization sites. These active sites, along with the dangling bonded atoms as well as unsaturated coordinations, derive remarkable interface polarization and obvious attenuation43. Last but not least, the eddy currents from natural resonance contribute significantly towards better absorption performances7 due to enhanced surface anisotropy of the tiny MnO2. Our results suggest that the CS@MnO2 core-shell composite can be taken as a potential EMI shielding material with absorption as the dominant shielding efficiency.
Conclusions
In summary, CS@MnO2 core-shell structured composite with MnO2 (24.7 wt%) nanoflakes coated on the surface of the carbon sphere cores has been developed with a facile water-bathing method. The CS@MnO2 composite shows enhanced dielectric loss and EMI shielding performances in the frequency range of 8‒18 GHz. A shielding effectiveness of 16‒23 dB is obtained with a thickness of 2 mm. It is found that the shielding efficiency is dominantly from absorption. The incorporation of MnO2 nanoflaky shells with spherical carbon cores ameliorates the electrical conductivity and the impendence matching of the CS@MnO2 composites. Thus, the electromagnetic shielding properties are greatly improved.
Methods
Synthesis of CS@MnO2 core-shell composites
All chemicals were purchased from commercial sources with chemical grade and used without any further purification.
CS was prepared according to a typical hydrothermal method. Typically, 50 mL glucose solution with the concentration of 0.5 mol/L was transferred into a Teflon-lined autoclave and the hydrothermal reaction was conducted at 180 °C for 10 h. After cooled down to room temperature naturally, the brown product was collected by centrifugation and washed several times with water and absolute ethanol, and then dried at 100 °C for 10 h.
To produce the MnO2 coating, 0.1 g as-prepared CS was dispersed in 100 mL deionized water with the aid of ultrasonication for 2 h. Then 0.6 g KMnO4 was dissolved into the previous solution with vigorous magnetic stirring for 30 min. Thereafter, the mixture solution was reacted at 80 °C for 6 h in a water-bathing. The obtained suspension was centrifuged and repeatedly washed with water and absolute ethanol, then dried at 60 °C. For comparison, another sample was obtained following the same method without CS.
Crystal and morphology characterizations
The crystal structures were investigated by powder X-Ray diffraction (XRD) on Rigaku TTR-III diffractometer with the Cu kα radiation (λ = 0.15418 nm) in the diffraction range of 2θ = 10–80°. The Raman spectra were recorded on a Reinshaw inVia Raman microscope with a power output of 3 mW under the laser excitation of 514 nm. The thermal decomposition analysis was determined on an American TA Q500 TGA thermal analyzer in air with a heating rate of 10 °C/min. The morphologies of the samples were observed by transmission electron microscopy (TEM, JEM-2100) with an accelerating voltage of 200 kV. To make a uniform dispersion of the products, the samples for TEM analysis were pretreated by dispersing it in absolute alcohol with a few seconds sonication and then dropped on a copper grid supported with amorphous carbon film.
Electromagnetic characterization
The dielectric permittivity and magnetic permeability, as well as the electromagnetic S parameters (S 11, S 12, S 21 and S 22) were measured at room temperature from 8 to 18 GHz by a vector network analyzer (VNA, Agilent Technologies, N5230A). The product was uniformly mixed with paraffin wax in mass ratios of 50 wt% and pressed into a 2-mm-thick ring sample with an inner diameter of 3.04 mm and outer diameter of 7.00 mm.
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Acknowledgements
This work is financially supported by the Natural Science Foundation of China (Grant No. 11564042) and the Application Basic Research Fund of Yunnan Province (Grant No. 2014FB110).
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H.T.G. and C.J.D. conceived and designed the research. H.Y.W. and Z.F.Z. performed the experiments and characterizations. H.T.G., C.J.D. and G.C. prepared the manuscript and analyzed the experimental results. Y.D.W. discussed the experimental results and the manuscript construction.
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Wang, H., Zhang, Z., Dong, C. et al. Carbon spheres@MnO2 core-shell nanocomposites with enhanced dielectric properties for electromagnetic shielding. Sci Rep 7, 15841 (2017). https://doi.org/10.1038/s41598-017-16059-0
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DOI: https://doi.org/10.1038/s41598-017-16059-0
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