Comparison of How Graphite and Shungite Affect Thermal, Mechanical, and Dielectric Properties of Dielectric Elastomer-Based Composites

: The aim of this work involved comparing the effect graphite and shungite have on the properties of dielectric elastomer-based materials. For this reason, dielectric elastomer–Sylgard (S) was ﬁlled with 1, 3, 5, 10, and 15 wt.% of graphite (G) and shungite (Sh). The structure of the obtained materials was studied by means of scanning electron microscopy and atomic force microscopy. The inﬂuence of the introduced additives on the thermal stability of the obtained composites was evaluated using thermogravimetry. Moreover, the mechanical properties and the dielectric constant of the elastomer with an addition of graphite and shungite were determined. Obtained results allowed us to establish that the presence of graphite as well as shungite signiﬁcantly inﬂuences mechanical as well as dielectric properties. Additionally, the optimum mass of additives, allowing to increase the dielectric constant without the signiﬁcant decrease of strain at break, was indicated. In the case of materials containing graphite, regardless of the ﬁller content (1–15 wt.%), the mechanical as well as the dielectric properties are improved, while in the case of composites with an addition of shungite exceeding the 5 wt.% of ﬁller content, a reduced tensile strength was observed.


Introduction
Dielectric elastomers, also called electrostrictive polymers, belong to the group of so-called intelligent materials that exhibit particular mechanical properties once affected by an electric current. Dielectric elastomers are characterized by much higher values of generated deformations and forces than most other smart materials, such as magnetic alloys with shape memory or piezoelectric materials. In that respect, their parameters are similar to muscles, hence their colloquial name, "artificial muscles". Thanks to their electrostrictive deformation capacity, these materials enable the design and construction of elements of executive robots such as robotic manipulators [1].
The basic principle according to which the dielectric elastomers operate mainly involves converting electrical energy into mechanical energy. It should be mentioned that they are characterized by high mechanical strength, hence the wide possibility of their use in various industries. This type of electroactive polymers also displays promising levels of performance in scavenging ambient mechanical energy. Therefore the technology has the potential to be an alternative to electromagnetism-based solutions [2,3]. The application mentioned above can result in a decrease in carbon dioxide emissions and consequently contribute to the achievement of the NetZero effect [4]. It should be stressed, however, that the NetZero effect is a more complex problem encompassing gas emissions not only consisting of polylactide, and both graphite and shungite were studied. Based on the obtained results, it was observed that in the case of filler contents of up to 10 wt.%, the changes in mechanical properties were insignificant.
The aim of this work is to analyze the effect of different amounts (between 1 and 15 wt.%) of graphite and shungite on structural, thermal, mechanical, and dielectric properties. Considering the properties of both carbonaceous fillers characterized above, introducing them into PDMS is likely to provide valuable insight into possible applications of the obtained materials. The comparison of changes in the properties mentioned above, caused by either of the fillers, can help determine the desired and effective type and amount of carbonaceous material.

Formation of PDMS-Based Composites
In the first stage, 10 g of component A of Sylgard was dissolved in 40 g of n-hexane. Subsequently, the appropriate amount of carbonaceous filler was introduced into the mixture (the mass of filler constituting 1, 3, 5, 10, and 15 wt.% of mass component A). With the aim to obtain a uniform distribution of graphite and shungite in the polymer matrix, an ultrasound mixer was applied. After 30 min of mixing, the Sylgard B component was added. It should be noted that the weight ratio of component A to component B was 10. After 30 min of mixing, the resulting samples were placed in square, polystyrene Petri dishes and left in a dryer at a temperature of 70 • C for five days.

Composites Characterization Methods
The morphology of the obtained composites containing carbonaceous filler was analyzed using the Quanta 3D FEG SEM/FIB scanning electron microscope. SE signal detection with a 1.2-nm resolution capability was applied.
The element mapping of the used fillers was studied by using scanning electron microscope (SEM 1430 VP, LEO Electron Microscopy Ltd., Oberkochen, Germany) connected with an energy dispersive X-ray spectrometer (EDX) Quantax 200 (Bruker AXS, Karlsruhe, Germany).
The morphology and structure of the obtained composites was evaluated by means of an atomic force microscope Veeco SPM (Digital Instrument). The size of the scan area was 5 µm × 5 µm. The roughness parameters were square (R q ) and arithmetical mean deviation of the assessed profile (R a ) as well as (R max ) calculated using Nanoscope software (Veeco Metrology, Inc., Santa Barbara, CA, USA). The definition as well as the equations describing the roughness parameters have been presented in our previous work [42].
The influence of carbonaceous filler on the thermal stability of the obtained composites was analyzed using the SDT 2960 Simultaneous TGA-DTA by TA Instruments. The samples were studied in an air atmosphere in a temperature range between 25 • C and 600 • C with a heating rate of 10 • C/min.
The mechanical properties were carried out in accordance with the PN EN ISO 527-1:2012 and PN EN ISO 527-2:2012 standards: The dimensions of the samples were determined using the ZKM 02-150 microscope.
The dielectric properties of the materials were measured by applying a specially designed laboratory stand. The active elements of the laboratory stand were 4.02 mm thick with copper plate electrodes with a working surface of 50.00 mm in diameter. After deter- mining the dimensions of the electrodes using a digital sensor for absolute measurement with a resolution of 0.01 mm from Mitutoyo and a digital micrometer with a resolution of 0.001 mm from Mahr, they were galvanically connected to the measuring leads in a non-interfering manner.
The measurements of the dielectric properties were carried out with the Dual Display LCR DE-5000 analyzer with an AC voltage of 600 mV and a frequency range of 10 2 to 10 5 Hz at room (23 • C) temperature. The capacitance of the device, resulting from placing the tested sample between the electrodes, was measured with an accuracy of 0.01 pF.

Morphology and Topography of Carbonaceous Fillers
In the first stage, the morphology of the fillers used in the study and the obtained composites, consisting of PDMS and the carbonaceous additives mentioned above, was analyzed. For this reason, scanning electron microscopy (SEM) was used and the obtained results have been presented in respective figures. In Figure 1A,B the structure of graphite has been depicted. It is well known that graphite is formed of layers connected by weak van der Waals forces [29]. Taking into account the presented images ( Figure 1A,B), the layered structure can be clearly observed. According to the literature [17], the thickness of individual flakes is about 50 nm. The structure of graphite was also described by Kranauskaite [27] where similar, typical diameters of graphite have been indicated.
with copper plate electrodes with a working surface of 50.00 mm in diameter. After determining the dimensions of the electrodes using a digital sensor for absolute measurement with a resolution of 0.01 mm from Mitutoyo and a digital micrometer with a resolution of 0.001 mm from Mahr, they were galvanically connected to the measuring leads in a non-interfering manner.
The measurements of the dielectric properties were carried out with the Dual Display LCR DE-5000 analyzer with an AC voltage of 600 mV and a frequency range of 10 2 to 10 5 Hz at room (23 °C) temperature. The capacitance of the device, resulting from placing the tested sample between the electrodes, was measured with an accuracy of 0.01 pF.

Morphology and Topography of Carbonaceous Fillers
In the first stage, the morphology of the fillers used in the study and the obtained composites, consisting of PDMS and the carbonaceous additives mentioned above, was analyzed. For this reason, scanning electron microscopy (SEM) was used and the obtained results have been presented in respective figures. In Figure 1A,B the structure of graphite has been depicted. It is well known that graphite is formed of layers connected by weak van der Waals forces [29]. Taking into account the presented images ( Figure 1A,B), the layered structure can be clearly observed. According to the literature [17], the thickness of individual flakes is about 50 nm. The structure of graphite was also described by Kranauskaite [27] where similar, typical diameters of graphite have been indicated. The morphology of shungite is presented in Figure 2A The morphology of shungite is presented in Figure 2A,B. It can be seen that shungite particles are significantly smaller compared to those observed in graphite. In shungite, contrary to graphite, the difference in size between individual particles is much greater and, according to the literature [43], ranges from 400 to 500 nm. The SEM analysis of shungite was also presented in the work of Diyuk [44] where the grains of separate compounds were observed.
In turn, in Figure 3, mapping images obtained by means of scanning electron microscopy with energy dispersive X-ray analysis (SEM-EDX) have allowed for a comparison of composition of the carbonaceous fillers used in the study. It can be seen that shungite particles are significantly smaller compared to those observed in graphite. In shungite, contrary to graphite, the difference in size between individual particles is much greater and, according to the literature [43], ranges from 400 to 500 nm. The SEM analysis of shungite was also presented in the work of Diyuk [44] where the grains of separate compounds were observed.
In turn, in Figure 3, mapping images obtained by means of scanning electron microscopy with energy dispersive X-ray analysis (SEM-EDX) have allowed for a comparison of composition of the carbonaceous fillers used in the study.  Table 1 provides insight into the composition of graphite and shungite. The type of basic, chemical elements and their quantity in the prepared samples were determined by energy dispersive spectroscopy. The composition of graphite is in line with the results obtained by Siburian et al. [45] and Ogbu et al. [46]. Taking into account the presented data, it can clearly be seen that in the case of graphite, the quantity of carbon is more than four times higher in comparison with shungite. In the case of shungite, the chemical elements such as carbon, oxygen, residual amount of ferrum, silicon, as well as compounds based on oxygen and silicon, in particular SiO2, have been detected. The composition of shungite was described also in the work of Obradovic et al. [31].  It can be seen that shungite particles are significantly smaller compared to those observed in graphite. In shungite, contrary to graphite, the difference in size between individual particles is much greater and, according to the literature [43], ranges from 400 to 500 nm. The SEM analysis of shungite was also presented in the work of Diyuk [44] where the grains of separate compounds were observed.
In turn, in Figure 3, mapping images obtained by means of scanning electron microscopy with energy dispersive X-ray analysis (SEM-EDX) have allowed for a comparison of composition of the carbonaceous fillers used in the study.  Table 1 provides insight into the composition of graphite and shungite. The type of basic, chemical elements and their quantity in the prepared samples were determined by energy dispersive spectroscopy. The composition of graphite is in line with the results obtained by Siburian et al. [45] and Ogbu et al. [46]. Taking into account the presented data, it can clearly be seen that in the case of graphite, the quantity of carbon is more than four times higher in comparison with shungite. In the case of shungite, the chemical elements such as carbon, oxygen, residual amount of ferrum, silicon, as well as compounds based on oxygen and silicon, in particular SiO2, have been detected. The composition of shungite was described also in the work of Obradovic et al. [31]. The analysis of images ( Figure 3) in connection with the data presented in Table 1 provides insight into the composition of graphite and shungite. The type of basic, chemical elements and their quantity in the prepared samples were determined by energy dispersive spectroscopy. The composition of graphite is in line with the results obtained by Siburian et al. [45] and Ogbu et al. [46]. Taking into account the presented data, it can clearly be seen that in the case of graphite, the quantity of carbon is more than four times higher in comparison with shungite. In the case of shungite, the chemical elements such as carbon, oxygen, residual amount of ferrum, silicon, as well as compounds based on oxygen and silicon, in particular SiO 2 , have been detected. The composition of shungite was described also in the work of Obradovic et al. [31].

Morphology and Topography of Sylgard and Its Composites
In Figure 4, the surface of PDMS with and without the addition of graphite has been shown. Results obtained by means of the SEM technique clearly indicate that the addition of graphite does not significantly influence the morphology of the obtained composites. It has been noted that at 10,000× magnification, the surface of composites seems to be smooth, without scratches and pores. However, an increase in color intensity with an increase of graphite content can be observed. Moreover, some small impurities on the surface, probably formed during the preparation of samples for SEM analysis, are also visible.

Morphology and Topography of Sylgard and Its Composites
In Figure 4, the surface of PDMS with and without the addition of graphite has been shown. Results obtained by means of the SEM technique clearly indicate that the addition of graphite does not significantly influence the morphology of the obtained composites. It has been noted that at 10,000× magnification, the surface of composites seems to be smooth, without scratches and pores. However, an increase in color intensity with an increase of graphite content can be observed. Moreover, some small impurities on the surface, probably formed during the preparation of samples for SEM analysis, are also visible.

SG5 SG3
Energies 2022, 15, x FOR PEER REVIEW 7 of 22 The comparison of surface morphology of PDMS and its composites filled with shungite has been presented in Figure 5. The addition of shungite in the range between 1 and 10 wt.% does not cause significant changes in the morphology of the analyzed materials. The surface of composites SSh1, SSh3, SSh5, and SSh10 seems to be uncovered by any cracks, holes, or pores. However, it can be clearly observed that in the case of the sample containing 15 wt.% of shungite, the aggregates of filler cause differentiation of the surface morphology of the obtained material. The comparison of surface morphology of PDMS and its composites filled with shungite has been presented in Figure 5. The addition of shungite in the range between 1 and 10 wt.% does not cause significant changes in the morphology of the analyzed materials. The surface of composites SSh1, SSh3, SSh5, and SSh10 seems to be uncovered by any  The comparison of surface morphology of PDMS and its composites filled with shungite has been presented in Figure 5. The addition of shungite in the range between 1 and 10 wt.% does not cause significant changes in the morphology of the analyzed materials. The surface of composites SSh1, SSh3, SSh5, and SSh10 seems to be uncovered by any cracks, holes, or pores. However, it can be clearly observed that in the case of the sample containing 15 wt.% of shungite, the aggregates of filler cause differentiation of the surface morphology of the obtained material.

SSh3 SSh5
Energies 2022, 15, x FOR PEER REVIEW 8 of 22 Cross-sections of pure polymer matrix and PDMS filled with both carbonaceous fillers are presented in Figures 6 and 7. It can be clearly seen that while the surface of the obtained materials seems to be characterized by universally dispersed additives, the crosssections reveal different dispersions of graphite and shungite introduced into the system. In the case of a sample with an addition of 1 wt.% of graphite, the filler seems to be uniformly distributed throughout the entire mass of the obtained composite. The increase in the amount of additive (3 and 5 wt.%) allows to obtain films where the graphite is deposited mostly in the upper level of the materials. The addition of 10 and 15 wt.% of graphite leads to the dispersion of filler throughout the entire mass of Sylgard. Cross-sections of pure polymer matrix and PDMS filled with both carbonaceous fillers are presented in Figures 6 and 7. It can be clearly seen that while the surface of the obtained materials seems to be characterized by universally dispersed additives, the cross-sections reveal different dispersions of graphite and shungite introduced into the system. In the case of a sample with an addition of 1 wt.% of graphite, the filler seems to be uniformly distributed throughout the entire mass of the obtained composite. The increase in the amount of additive (3 and 5 wt.%) allows to obtain films where the graphite is deposited mostly in the upper level of the materials. The addition of 10 and 15 wt.% of graphite leads to the dispersion of filler throughout the entire mass of Sylgard. The same tendency is observed in relation to composites containing shungite. In the case of materials consisting of Sylgard and 1, 10, and 15 wt.% of carbonaceous filler, shungite is evenly dispersed in the polymer matrix. However, in the case of 3 and 5 wt.% of filler content in the elastomer-based composites, the agglomerates of shungite are observed near the top layer of the studied materials. It is apparent that the dispersion of the analyzed fillers significantly depends on the quantity of the compound used in the process. Cross-sections of pure polymer matrix and PDMS filled with both carbonaceous fillers are presented in Figures 6 and 7. It can be clearly seen that while the surface of the obtained materials seems to be characterized by universally dispersed additives, the crosssections reveal different dispersions of graphite and shungite introduced into the system. In the case of a sample with an addition of 1 wt.% of graphite, the filler seems to be uniformly distributed throughout the entire mass of the obtained composite. The increase in the amount of additive (3 and 5 wt.%) allows to obtain films where the graphite is deposited mostly in the upper level of the materials. The addition of 10 and 15 wt.% of graphite leads to the dispersion of filler throughout the entire mass of Sylgard.

SG3 SG5
Energies 2022, 15, x FOR PEER REVIEW 9 of 22 To compare the obtained results with the data published by other researchers, scientific papers devoted to the study of polymeric materials containing carbonaceous fillers were studied. Unfortunately, there are no publications presenting a cross-section of composites filled with graphite or shungite. The only fractographs were included in the work of Voigt et al. [47] where the melamine-formaldehyde-based laminates with an addition of 3 wt.% of shungite were analyzed. The characteristics of the polymeric matrix used in this study, as well as the quality of the image, preclude a viable comparison of the obtained results.
In an aim to analyze the topography of the obtained materials and to establish the effect of carbonaceous fillers on the roughness of the studied composites, atomic force microscopy was used. The AFM images of pure Sylgard and its composites with an addition of carbonaceous fillers, graphite and shungite, are shown in Figures 8 and 9, respectively.  obtained results.
In an aim to analyze the topography of the obtained materials and to establish the effect of carbonaceous fillers on the roughness of the studied composites, atomic force microscopy was used. The AFM images of pure Sylgard and its composites with an addition of carbonaceous fillers, graphite and shungite, are shown in Figures 8 and 9, respectively. In the case of samples containing up to 5 wt.% of graphite as well as shungite, no significant changes in the R a and R q parameters have been observed. The data in Table 2 indicate that the values of average surface roughness (R a ) and root mean square surface roughness (R q ) range from about 1 to 5 nm. The increase in quantity of both fillers (10 and 15 wt.%) leads to a huge increase in values of all analyzed roughness parameters: R a , R q , and R max .
The other fact that must be taken into account is that the introduction of shungite caused more significant changes in the topography of the obtained composites than graphite, with a notable exception of the sample containing 5 wt.% of the filler. When comparing the SG5 and SSh5 samples, the average surface roughness and root mean square surface roughness are characterized by lower values in the case of materials modified by means of shungite. On summarizing the obtained results, it can clearly be seen that surfaces that seem to be smooth in SEM analysis are characterized by higher roughness parameters.  In the case of samples containing up to 5 wt.% of graphite as well as shungite, no significant changes in the Ra and Rq parameters have been observed. The data in Table 2 indicate that the values of average surface roughness (Ra) and root mean square surface roughness (Rq) range from about 1 to 5 nm. The increase in quantity of both fillers (10 and 15 wt.%) leads to a huge increase in values of all analyzed roughness parameters: Ra, Rq, and Rmax.

Influence of Graphite and Shungite on Thermal Stability of the Obtained Composites
Thermal stability is extremely important in the case of electroactive materials. For this reason, the thermal properties of the incorporated carbonaceous fillers and their effect on thermal stability of the obtained composites were established by means of thermogravimetric analysis (TG). Thermal stability of both fillers and composites as well as pure elastomer was discussed based on the temperature values corresponding to 5, 10, 30, and 50% mass loss (Table 3). In Figure 10, the changes of shungite and graphite mass along with the increase in temperature are shown. The other fact that must be taken into account is that the introduction of shungite caused more significant changes in the topography of the obtained composites than graphite, with a notable exception of the sample containing 5 wt.% of the filler. When comparing the SG5 and SSh5 samples, the average surface roughness and root mean square surface roughness are characterized by lower values in the case of materials modified by means of shungite. On summarizing the obtained results, it can clearly be seen that surfaces that seem to be smooth in SEM analysis are characterized by higher roughness parameters.

Influence of Graphite and Shungite on Thermal Stability of the Obtained Composites
Thermal stability is extremely important in the case of electroactive materials. For this reason, the thermal properties of the incorporated carbonaceous fillers and their effect on thermal stability of the obtained composites were established by means of thermogravimetric analysis (TG). Thermal stability of both fillers and composites as well as pure elastomer was discussed based on the temperature values corresponding to 5, 10, 30, and 50% mass loss (Table 3). In Figure 10, the changes of shungite and graphite mass along with the increase in temperature are shown.   Taking into account both fillers used in the study, it can be clearly seen that graphite is more resistant to temperature changes. In the case of graphite, the mass loss at temperature 600 • C does not exceed 3%, while shungite loses 5% and 10% at temperatures of 546.7 • C and 584.7 • C, respectively. According to the literature, the first stage of decomposition of shungite (about 1%) is related to the presence of moisture while at approx. 500 • C, sulfur evaporation can be observed [34]. Moreover in the cited work of Fujita et al. [34], it was established that heating shungite above 500 • C leads to the production of silicon carbide and changing carbon to CO 2 .
In Figure 11A,B the effect of carbonaceous fillers on thermal stability of Sylgard-based composites can be observed. The values of temperature at 5, 10, 30, and 50% mass loss for all studied films have been presented in Table 4.
In the case of pure Sylgard, its decomposition was described in the work of Johnson et al. [48]. It was indicated that the initial stage of thermal degradation is connected with the decomposition of [Si(CH 3 ) 2 O] n and the dehydration of polymer. The obtained results, concerning the obtained Sylgard-based composites, indicate that the thermal stability of studied materials is strongly related to the type and amount of the filler introduced into the system. In the case of materials containing carbonaceous fillers, it was established that regardless of the amount of the applied additive, the temperatures at 5%, 30%, and 50%, mass loss increased in comparison to neat Sylgard. It is interesting, however, that in the case of 10% mass loss, the temperature of composites is higher than in the case of pure elastomer only after introduction of 10 and 15 wt.% of fillers.
Taking into account both fillers used in the study, it can be clearly seen that graphite is more resistant to temperature changes. In the case of graphite, the mass loss at temperature 600 °C does not exceed 3%, while shungite loses 5% and 10% at temperatures of 546.7 °C and 584.7 °C, respectively. According to the literature, the first stage of decomposition of shungite (about 1%) is related to the presence of moisture while at approx. 500 °C, sulfur evaporation can be observed [34]. Moreover in the cited work of Fujita et al. [34], it was established that heating shungite above 500 °C leads to the production of silicon carbide and changing carbon to CO2.
In Figure 11A,B the effect of carbonaceous fillers on thermal stability of Sylgardbased composites can be observed. The values of temperature at 5, 10, 30, and 50% mass loss for all studied films have been presented in Table 4. Furthermore, it can be clearly noticed that despite graphite being more thermally stable compared to shungite, composites containing shungite are more resistant at high temperatures. The most significant increase in thermal stability was observed in the case of material consisting of Sylgard and 15 wt.% of shungite. Obtained results suggest the formation of char at the surface of the decomposed materials containing shungite. Taking into account that shungite is mostly composed of silica, it is reasonable to assume that char accumulating on the surface forms a barrier between the polymer and measurement atmosphere. Analyzing the available literature, it can be concluded that there is little information devoted to the thermal stability of elastomers with an addition of carbonaceous fillers. For this reason, it makes use of graphite and shungite to improve the thermal properties of elastomeric materials, which an extremely interesting research issue.

Mechanical Properties
In the case of electroactive materials, where the shape shifts result from a change in electrical voltage, mechanical properties seem to be essential. In particular, strength and elasticity count among the features that significantly depend on the type and quantity of the filler used in the procedure. For this reason, the changes in tensile strength and elongation at the break of obtained composites containing carbonaceous additives have been studied. In Figure 12A,B, the tensile strength of pure PDMS and its composites containing graphite and shungite respectively has been shown. All samples containing graphite have displayed higher values of tensile strength in comparison to pure Sylgard. The SG1 sample containing the smallest amount of graphite (1 wt.%) proved to be most resistant to stretching among all of the composites tested. The tensile strength of this sample reached a value more than twice as high as the one recorded in relation to pure Sylgard. In the case of the remaining samples: SG3, SG5, SG10, and SG15, as the amount of graphite in the polymer matrix increased, decreased values of tensile stress in comparison with the SG1 sample have been recorded. It should be stressed, however, that the tensile stress for the remaining composites has achieved significantly higher values than in the case of pure Sylgard. The same tendency was observed in the work of Sarath et al. [49], where exfoliated graphite was introduced into silicone rubber. A decrease in tensile strength observed in the case of materials filled with 10 and 15 wt.% of graphite can suggest a weakening of the interfacial bonding between All samples containing graphite have displayed higher values of tensile strength in comparison to pure Sylgard. The SG1 sample containing the smallest amount of graphite (1 wt.%) proved to be most resistant to stretching among all of the composites tested. The tensile strength of this sample reached a value more than twice as high as the one recorded in relation to pure Sylgard. In the case of the remaining samples: SG3, SG5, SG10, and SG15, as the amount of graphite in the polymer matrix increased, decreased values of tensile stress in comparison with the SG1 sample have been recorded. It should be stressed, however, that the tensile stress for the remaining composites has achieved significantly higher values than in the case of pure Sylgard. The same tendency was observed in the work of Sarath et al. [49], where exfoliated graphite was introduced into silicone rubber. A decrease in tensile strength observed in the case of materials filled with 10 and 15 wt.% of graphite can suggest a weakening of the interfacial bonding between the additive and polymer matrix after introducing an increased amount of filler [50]. The obtained results are consistent with the data published in the work ofŻenkiewicz et al. [41] where a significant decrease in σ was observed in relation to filler contents up to 10 wt.% of graphite. The same tendency was observed by Kalaitzidou et al. [51], who reported that at low loading level, the mechanical properties of polypropylene filled with graphite were significantly improved.
In the case of materials containing shungite, the changes in tensile strength have been completely different than in composites comprising Sylgard and graphite.
The samples SSh1, SSh3, and SSh5, have achieved higher tensile strength values than the sample without the addition of shungite. The sample containing 5 wt.% of shungite, however, showed the highest tensile strength, while in the case of materials containing graphite, the addition of only as little as 1 wt.% of the carbonaceous filler has allowed to obtain a similar value of tensile strength. Moreover, it should be stressed that after introducing 10 and 15 wt.% of shungite into the polymer matrix, a drastic reduction in the value of tensile stress was observed. It is well known that the introduction of different fillers into the PDMS matrix, in the majority of cases, increases durability by impeding polymer chain mobility. Based on the results published by Solovieva et al. [39] and presented in this work, it can clearly be seen that the addition of shungite improves molecular mobility.
In Figure 13A,B, elongation at the break of Sylgard and its composites filled with graphite and shungite respectively has been presented. In both cases, including materials consisting of the dielectric matrix and graphite as well as composites containing shungite, an increase in elongation at break has been observed. Analyzing the results encompassing the elongation at break values of samples containing graphite ( Figure 13A), a contrary tendency, compared to the tensile strength of the tested composites, can be noticed. The SG15 sample, containing 15 wt.% of graphite, is characterized by the highest value of elongation at break (140 ± 7%). This observation confirms the most significant flexibility among all of the studied composites containing graphite.  Summarizing the results presented in Figures 12A and 13A, it is possible to observe an increase in the flexibility and tensile strength of the studied materials containing graphite, regardless of its amount. However, it has to be stressed that in the case of tensile strength, the best results were achieved for composites filled with 1 wt.% of graphite, while the highest value of deformation at break were recorded in relation to material with an addition of 15 wt.% of the carbonaceous additive.
The incorporation of shungite into Sylgard results in a significant increase in the elongation at break values of all studied composites. As can be observed, the sample containing 15 wt.% of shungite was characterized by an elongation at break value more Summarizing the results presented in Figures 12A and 13A, it is possible to observe an increase in the flexibility and tensile strength of the studied materials containing graphite, regardless of its amount. However, it has to be stressed that in the case of tensile strength, the best results were achieved for composites filled with 1 wt.% of graphite, while the The incorporation of shungite into Sylgard results in a significant increase in the elongation at break values of all studied composites. As can be observed, the sample containing 15 wt.% of shungite was characterized by an elongation at break value more than twice as high as the value recorded in the case of pure Sylgard. The effect of shungite on the mechanical properties was analyzed in the work of Solovieva et al. [39] as well as Garishin et al. [52]. While determining the influence of the shungite addition on mechanical properties, they have established that the introduced carbonaceous filler consists of phases that differ in polarity. For this reason, considering the bipolarity of shungite, its compatibility and potential to mix with almost all types of materials has been explained.
In summary, the obtained results allow for presenting the dependence of mechanical properties on used carbonaceous fillers. It needs to be stressed that in the case of materials, tensile strength as well as elongation at break increase throughout the entire load range (1-15 wt.%) of the introduced graphite, while exceeding 5 wt.% of shungite results in a decrease in tensile strength.

Dielectric Properties
The polymer capacity (C) representing the electric charge that can be deposited in a capacitor was determined at frequencies between 10 2 and 10 5 Hz and used to discuss the influence of graphite and shungite addition into poly(dimethylsiloxane) elastomer on its dielectric properties. According to the formula C = ε r C p , the capacity of a flat capacitor filled with a dielectric (C) with the same dimensions as the air capacitor is ε r -times higher than C p (the capacity of the air capacitor). Thus, changes in C values can be expressed as changes in ε r -dielectric constant of the tested capacitor. In Table 5, values of dielectric constant (ε r ) and dielectric loss (ϕ) of all tested materials are summarized. Analysis of the presented data leads to the conclusion that both applied fillers result in a substantial improvement of the dielectric properties of the elastomer matrix, represented by an increase of ε r values. The higher the filler content, the higher dielectric constant. Simultaneously, dielectric loss also increases in comparison to the neat Sylgard sample (S) however, ϕ values are still relatively low.
The dependence of ε r vs. wt.% of filler can be explained through the accumulation of charge carriers in the internal surface of the PDMS matrix. According to the Maxwell-Wagner-Sillars model, under an external electric field, the charge carriers can easily migrate to the grains, and these grains accumulated at the grain boundaries [53].
As a result of this process, large polarization is produced, and high dielectric constants are observed [54]. The higher the charge carriers' content, the higher polarization, and finally, the higher ε r values. Similar behavior was observed earlier by Prasanna et al. [19] for polyaniline/exfoliated graphite flakes (PANI/EGF), by Li et al. [20] for polyvinylidene fluoride/graphite nanosheets (PVDF/GNs), and by Torgut et al. [25] for 2-hydroxyethyl methacrylate-co-N-isopropylacrylamide/graphite (poly(NIPAM-co-HEMA)/G) composites. The increase in ε r values with increasing wt.% of G and Sh in the composite can be also due to formation of conducting pillars of both fillers in the PDMS matrix.
The data collected in Table 5 indicate a slight decrease of dielectric constant (ε r ) with the increase in frequency. This decrease is due to the reduction of space charge polarization effect, typical behavior of dielectric materials, also known as dielectric dispersion [17,55]. Poly(dimethylsiloxane) is a high molecular polymer of a chain-like structure. Under the external electric field, it will produce polarization. This phenomenon is limited due to the presence of chain bonds. When the frequency increases, the unidirectional duration of the electric field shortens, the degree of polarization is small, and the charge induced by polarization is less, so the dielectric constant decreases with the increase of frequency [56]. Similar observations have already been made by Li et al. [17] for polyvinylidene fluoride/expanded graphite composites and attributed to the mismatch of interfacial polarization of composites to the external electric field at elevated frequencies.
It can also be noted that for each particular additive content, and each frequency applied, the dielectric constants of SG composites are noticeably higher than those of SSh. At 1 kHz (Figure 14), 10 wt.% graphite incorporation caused a 144.9 × ε r increase, while the addition of shungite resulted in a 111.9× increase in the same modification conditions. It is a fact that both graphite and shungite belong to the group of conducting fillers however, they substantially differ in carbon content (Table 1). While graphite consists mainly of carbon (82.8 wt.%), carbon constitutes only 15.19 wt.% of shungite. According to the data provided by Obradović et al. [31], Solovieva et al. [39], and mapping SEM/EDX images (Figure 3), the main constituents of shungite are silicon, iron, aluminum, calcium, sulfur, and magnesium oxides. Moreover, based on Table 1, it can be assumed that SiO2 is the most represented oxide in shungite, among others. The dielectric constant of different It is a fact that both graphite and shungite belong to the group of conducting fillers however, they substantially differ in carbon content (Table 1). While graphite consists mainly of carbon (82.8 wt.%), carbon constitutes only 15.19 wt.% of shungite. According to the data provided by Obradović et al. [31], Solovieva et al. [39], and mapping SEM/EDX images (Figure 3), the main constituents of shungite are silicon, iron, aluminum, calcium, sulfur, and magnesium oxides. Moreover, based on Table 1, it can be assumed that SiO 2 is the most represented oxide in shungite, among others. The dielectric constant of different oxides is relatively low: 3.9 for SiO 2 and 9 for Al 2 O 3 [57,58], and what is essential, is lower than that of graphite (ε r = 10 ÷ 15). Even if shungit also consists of highly dielectric iron oxide with ε r (α-Fe 2 O 3 ) = 30, its content is relatively low. Thus, it can be concluded that the differences in the dielectric constants of SG and SSh composites come primarily from the composition of both additives.
The dielectric properties of the polymer composites can also vary depending on the size and shape of the conductive filler, the volume fraction, the method of preparation, and the interaction between the filler material and polymer [25,59,60]. As the method of composite preparation in the case of both G and Sh fillers is analogous, it is worth noting the substantial differences in the size and shape of G and Sh presented in Figures 1 and 2 (shungite particles are significantly smaller than graphite), which can affect the additive dispersion and the final ε r values.
The comparison of presented results (Table 5) with those presented in the literature [17,19,20,61,62] show that both G and Sh are more efficient additives for ε r improvement than polydopamine/silicon dioxide/graphite oxide nanohybrid (PDA@SiO 2 @GO) filler and acts similarly to exfoliated graphite flakes (EGf) added to polyaniline (PANI), graphite sheets (GN), and expanded graphite (EG) added to polyvinylidene fluoride (PVDF).
As the problem of dielectric elastomers modification can be related to the deterioration of the breakdown strength, it is worth noting that in the case of the studied fillers, both G and Sh additives improved the tensile strength value. Lower σ values than those indicated for pure Sylgard, exhibit only SSh10 and SSh15 samples.

Conclusions
In the study two carbonaceous fillers, graphite and shungite, were used in order to alter the properties of Sylgard-based composites. Obtained results indicate that the dispersion of graphite, as well as shungite, in the PDMS matrix, significantly depends on the amount of the filler used in the procedure.
Taking into account the thermal stability of the obtained composites, it was established that even though graphite is characterized by more significant thermal resistance, improved thermal stability was observed in the case of the PDMS-based composites with the addition of shungite. The obtained results suggest that this phenomenon could be related to the higher content of silicon in the molecular composition of shungite, which can form a protective layer on the surface of the polymer during decomposition at high temperatures.
The comparison of mechanical properties of the tested composites revealed that the addition of graphite in the entire load range of the additive improved both tensile strength and flexibility of the obtained composites. The increase in the values of tensile strength and elongation at break of the Sylgard-graphite composites are most likely the result of a larger specific surface area and smaller size of graphite particles in comparison with shungite. Studied composites were characterized by an improved dielectric constant after introducing both of the carbonaceous fillers. The observed increase of ε r is significantly connected with an accumulation of charge carriers in the internal surface of Sylgard. Moreover, the changes in dielectric constant can likely result from the presence of conducting pillars within both fillers in the PDMS matrix.
In summary, the obtained results reveal that both carbonaceous fillers, graphite and shungite, allow to obtain composites characterized by significantly improved thermal, mechanical, and dielectric properties. Nevertheless, as can be observed before the planned application, the type and amount of filler needs to be determined, bearing in mind the requirements and the purpose of the resulting material.