A Comparative Study of Polypyrrole and Ag/Polypyrrole Hybrid Nanocomposites as Sensitive Material Used for New Dry Polarizable Bioimpedance Sensors

: Three types of dry polarizable electric bioimpedance sensor for skin bioimpedance monitoring without skin preparation have been developed. The sensitive materials as a component of these sensors are the conductive polypyrrole and hybrid nanocomposite polypyrrole-Ag, with 10% and 20% Ag incorporated in the polypyrrole matrix. The hybrid nanocomposites Ag nanoparticles (NPs)/polypyrrole were obtained by introducing the colloid solution of Ag NPs in pyrrole solution, followed by polymerisation, and calculated for 10% and 20% of monomer’s mass. The structural characterisation and morphological analysis of these sensitive materials were carried-out by Raman spectrometry, Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy, and energy-dispersive X-ray spectroscopy. In making the electrodes, the technique of pressing powders of polypyrrole and hybrid composites Ag NPs/polypyrrole in a hydraulic press was used in the form of a disk. The electric bioimpedance performance of sensors was investigated using a two-point method in the frequency range of 1–300 kHz, at a voltage of 2 V peak-peak , on six human subjects, three men and three women. For these three bioimpedance sensors, it was found that the electric bioimpedance of the skin decreases across the frequency range and shows good linearity of the impedance-frequency curve on the range frequency of interest in bioimpedance measurements. on with incorporated in the PPY matrix as sensitive materials, developed for bioimpedance


Introduction
Electrical impedance of biological tissue, named electric bioimpedance, is used for medical diagnosis due to properties such as the possibility of monitoring organs and tissues' state, both in vivo and in vitro modes. Moreover, it can offer the relatively simple possibility of technological achievement for bioimpedance sensors [1]. Bioimpedance presents an advantage because it is a technique that provides health information in a non-invasive way. This medical technique involves an injection of alternating electric current in human tissues at very low intensity. In the technique of bioimpedance measurements, performed under the influence of the injected electric current, the biologic tissues, organs, cells medium behave like conductors, dielectrics, or insulators, each depending on their composition. Because of this phenomenon, bioimpedance dependence on frequency produces much information about the biological medium's psychological state under investigation [2]. This investigation refers to the changes taking place in organs, muscle, nerves, brain, heart, skin, eye retina in establishing a diagnosis, can be made by clinical methods, like ECG (PPY), are used in various fields like flexible electronic devices, sensors, catalysis, batteries, supercapacitors, microactuators, anti-electrostatic coatings, low-cost solar cells, and biomedical, due to their excellent electrical conductivity, thermal stability, environmental stability and relative ease of synthesis. These good properties come from their chemical structure, e.g., conjugated electrons or alternating the single bond with a double bond system [22][23][24][25][26]. A conductive polymer used as a bioimpedance electrode can be the composite PEDOT/PSS, poly (3,4-ethylenedioxythiophene):(styrenesulfonic acid), where PSS is used as a doping agent. Karimullaha, A.S. et al. developed a bioimpedance sensor based on PEDOT/PSS, with low impedance, over conventional material such as gold, which is due to the low charge transfer resistance of PEDOT/PSS [27]. Takamatsu, S. et al. developed a bioimpedance sensor based on PEDOT/PSS coated on a fabric characterised by low impedance and long-term stability. However, making the sensor is complex and expensive and presents a poor linearity of the impedance-frequency curve [28]. This polymer was used to achieve the electrode patterns on textiles because it presents a low impedance contact with human skin. From the conductive polymers, the polypyrrole was the most studied, experimented and used in various applications because of its good electrical and electronic properties, good stability derived from its aromatic ring chemical structure, and π-conjugated bonds, which can be modified by oxidation and protonation [29,30]. Conductive polymers are present in a variety of biomedical applications like implants for neural prosthetics [31], biomaterials for biosensors application [32], evaluation of their biocompatibility in nerve tissue in vitro and in vivo [33], as a biomaterial for implants [34], and in studies on the interaction of cells and tissues of polypyrrole [35]. For ECG measurements, Jimenez, O.T. et al. developed a bioimpedance disk sensor with polypyrrole, without no conductive agglutinant, to increase the electrical conductivity of the sensitive material [36].
This paper presents a new dry polarizable bioimpedance sensor based on polypyrrole and silver (Ag) nanoparticles (NPs)/polypyrrole hybrid nanocomposites. Ag NPs were chosen for the functionalisation of polypyrrole for two main reasons: the increase in the sensitive materials' electrical conductivity and its antimicrobial properties [37], respectively.
The advantages of the presented sensors consist of low impedance values in the frequency range of interest for skin bioimpedance monitoring, good linearity of the impedance vs. frequency curve in the same frequency range, and simple realisation without using complex equipment and inexpensive construction. In addition, the paper presents a comparative study of these new sensing materials.

Materials and Methods
Pyrrole monomer for synthesis (97% purity and density of 0.967-0.971 g/cm 3 ) was purchased from Merck; FeCl 3 × 6H 2 O (99.8%) and AgNO 3 salts, of analytical grade, were purchased from REACTIVUL SA Romania. Deionised water was used as a solvent. The polypyrrole and Ag Np/polypyrrole composites synthesis follow the path described in reference [17].

Polypyrrole Synthesis
PPY was synthesised using a chemical oxidative polymerisation method using pyrrole monomer and FeCl 3 × 6H 2 O as an oxidative agent ( Figure 1). Briefly, a solution of 0.05 M pyrrole monomer was added, over 45 min, dropwise, in a solution of 0.115 M FeCl 3 × 6H 2 O, under stirring at room temperature (the ratio of monomer/ FeCl 3 × 6H 2 O was 1/2.33). The mixture was slowly stirred for another 4 h. After that, the solution was left at room temperature for 24 h without mixing. Monomer pyrrole's polymerisation reaction with an aqueous solution of FeCl 3 × 6H 2 O is a fast reaction to obtain a black precipitate [38]. The black precipitate formed was filtered and washed with deionised water and dried for 24 h at room temperature, followed by drying at 80 • C for 10 h. The oxidative polymerisation reaction of pyrrole in the presence of oxidative agent FeCl 3 × 6H 2 O is described by the following reaction [30,36,38] (1).
The flow of the synthesis stages of the sensitive material polypyrrole is present Figure 1.

Ag NP/PPY Hybrid Nanocomposite Synthesis
The Ag NPs were obtained following a chemical synthesis route by reducing a tion of AgNO3 with hydrazine (the ratio of AgNO3/Hydrazine was 1/3) at a temper of 80 °C. The pale-yellow colloidal silver solution was mixed with a fresh solution of The flow of the synthesis stages of the sensitive material polypyrrole is presented in Figure 1.
The flow of the synthesis stages of the sensitive material polypyrrole is presented in Figure 1.

Ag NP/PPY Hybrid Nanocomposite Synthesis
The Ag NPs were obtained following a chemical synthesis route by reducing a solution of AgNO 3 with hydrazine (the ratio of AgNO 3 /Hydrazine was 1/3) at a temperature of 80 • C. The pale-yellow colloidal silver solution was mixed with a fresh solution of pyrrole monomer/FeCl 3 × 6H 2 O, following the same steps as the polypyrrole synthesis described  role monomer/FeCl3 × 6H2O, following the same steps as the polypyrrole synthesis described above ( Figure 2). Thus, two composites of 10% and 20% (w/w) of Ag Np in polypyrrole were obtained.

Obtaining the Dry Polarizable Electric Bioimpedance Sensors
In making the bioimpedance electrodes, the polypyrrole and Ag/polypyrrole hybrid nanocomposite powders were pressed in disk format, with 6 tons force/cm 2 pressure, by using a hydraulic press: Ø 12 mm ± 0.2 mm, h = 1.6 ± 0.3 mm for PPY and Ø 12 mm ± 0.2 mm, h = 2.5 ± 0.3 mm for Ag NPs/PPY nanocomposite. A layer of conductive silver paste was deposited on one side of the obtained disks. Each of the disks thus obtained are arranged on another silver disk of the same diameter. The dry polarizable electric bioimpedance sensor (Figure 3) was obtained by using two electrodes arranged at 6 cm from each other.

Obtaining the Dry Polarizable Electric Bioimpedance Sensors
In making the bioimpedance electrodes, the polypyrrole and Ag/polypyrrole hybrid nanocomposite powders were pressed in disk format, with 6 tons force/cm 2 pressure, by using a hydraulic press: Ø 12 mm ± 0.2 mm, h = 1.6 ± 0.3 mm for PPY and Ø 12 mm ± 0.2 mm, h = 2.5 ± 0.3 mm for Ag NPs/PPY nanocomposite. A layer of conductive silver paste was deposited on one side of the obtained disks. Each of the disks thus obtained are arranged on another silver disk of the same diameter. The dry polarizable electric bioimpedance sensor ( Figure 3) was obtained by using two electrodes arranged at 6 cm from each other. using a hydraulic press: Ø 12 mm ± 0.2 mm, h = 1.6 ± 0.3 mm for PPY and Ø mm, h = 2.5 ± 0.3 mm for Ag NPs/PPY nanocomposite. A layer of conductive was deposited on one side of the obtained disks. Each of the disks thus obta ranged on another silver disk of the same diameter. The dry polarizable ele pedance sensor (Figure 3) was obtained by using two electrodes arranged a each other.  The electrical connection is made from the opposite side of the silver disk.

Equipment
The structures of PPY and Ag NPs/PPY hybrid nanocomposites were studied by attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscoy using a spectrometer Jasco 4200 coupled with an ATR JASCO PRO 470-H accessory. The samples were measured directly by placing them on the ATR device's crystal and pressing with a controlled force, in the following conditions: the spectral range of 4000-500 cm −1 , resolution 4 cm −1 , scans number/spectrum: 50 accumulations. Raman spectroscopy measurements were performed with a Raman-dispersive spectrometer-LabRam HR Evolution, Horiba Jobin Yvone, France, equipped with laser extinction of 633 nm, acquisition time 15 s, and 100 accumulation/spectrum. The Raman spectra were used to characterise the disorder degree in the synthesised nanocomposite. The morphology of the samples PPY and Ag NPs/PPY nanocomposite was studied by scanning electron microscopy (SEM) using a Carl Zeiss SMT FESEM-FIB (Scanning Microscope Tunnelling Field Emission Scanning Electron Microscope-Focused Ion Beam) Auriga type scanner in the following conditions: the tension of acceleration 10 kV and magnitude of 20 and 50 k. The elemental analysis (energy-dispersive X-ray spectroscopy (EDX)) was performed with a dispersive energy probe of Inca Energy 250 type Oxford Instruments Ltd. England coupled to SEM. The electric bioimpedance measurements were carried-out with a precision LCR (Inductance Capacitance Resistance) meter, AGILENT E4980 A type, in the frequency range of 1-300 kHz. The configuration was in two points measurement, the simplest set-up method for electric bioimpedance measurements [4], by using a bioimpedance sensor made of the two obtained electrodes (Figure 3). Figure 4 shows the Raman spectra recorded on the three sensitive materials. The most important band in the Raman spectra for pyrrole is the one present around 1605 cm −1 , representing the vibration mode characteristic of the C=C bonds, which form the skeleton of the polypyrrole [39]. The Raman spectrum shows an increase of the band intensity, positioned at around 1605 cm −1 , with the amount of silver, which concludes that the increase of the percentage of silver causes modifications of the crystalline structure of the polypyrrole. The second important group of bands appears at 1321 cm −1 and 1331 cm −1 , attributed to the pyrrolic ring's stretching mode. The third important group of bands appears at 1040-1054 cm −1 , determined by the C-H bond's plane deforma-tion. Also, it can be observed that the intensity of the bands at 1321-1331 cm −1 and 1040-1054 cm −1 increases with the amount of silver (Ag). The introduction of silver (Ag) determines the polypyrrole's amorphisation, deformation of the pyrrole ring, and the C-H bond [39]. The introduction of a large quantity, respectively of 20% Ag, leads to the disruption of the polypyrrole's internal structure, reducing its crystallinity.

EER REVIEW
7 of 20 3228 cm −1 is attributed to the stretching of N-H and C-H bonds [43,44]. The Ag NPs' introduction into the PPY structure leads to some PPY FTIR characteristic bands' displacements, indicating specific interactions between Ag NPs and the PPY functional groups, especially those in the N-H group region [43,45].

Fourier Transform Infrared (FTIR) Spectroscopy
The molecular structures of synthesised polypyrrole and nanocomposites with 10% and 20% silver (Ag) embedded into polymer matrix were analysed using FTIR spectroscopy ( Figure 5). The allure of the obtained FTIR spectra confirms the structural configuration of the PPY indicated from the literature data: the peak at 780 cm −1 attributed to C-H out of plane of the polypyrrole ring, the peak at 1040 cm −1 represents N-H in plane deformation [40], the peak located at 1186 cm −1 is assigned to C-N stretching vibration [41]. The peaks at 1288 cm −1 and 1040 cm −1 are assigned to C-N in plane vibration; the peak at 1557 cm −1 is attributed to the polypyrrole ring's vibration [41,42]. The broad peak at 3228 cm −1 is attributed to the stretching of N-H and C-H bonds [43,44]. The Ag NPs' introduction into the PPY structure leads to some PPY FTIR characteristic bands' displacements, indicating specific interactions between Ag NPs and the PPY functional groups, especially those in the N-H group region [43,45].

The Morphological Analysis
The morphological structure of the three sensor materials was undertaken by SEM microscopy ( Figure 6). The SEM images show a classic polypyrrole structure consisting o globular units with average dimensions around 400 nm formed by the collision of smaller globular formations with average dimensions around 200 nm. In the case of the 10%Ag/PPY hybrid nanocomposite (Figure 6b), a classical structure is observed, mainly globular but with smaller dimensions than in the case of simple PPY. In addition, an in homogeneous dispersion of Ag NPs clusters can be observed on the PPY surface. These non-homogeneous silver clusters have submicron sizes, formed of particles with wurtzite

The Morphological Analysis
The morphological structure of the three sensor materials was undertaken by SEM microscopy ( Figure 6). The SEM images show a classic polypyrrole structure consisting of globular units with average dimensions around 400 nm formed by the collision of smaller globular formations with average dimensions around 200 nm. In the case of the 10%Ag/PPY hybrid nanocomposite (Figure 6b), a classical structure is observed, mainly globular but with smaller dimensions than in the case of simple PPY. In addition, an inhomogeneous dispersion of Ag NPs clusters can be observed on the PPY surface. These non-homogeneous silver clusters have submicron sizes, formed of particles with wurtzite crystalline structure (parallelepiped with a height of 200-300 nm and widths of 100 nm (Figure 6c)). In the case of the 20%Ag/PPY hybrid nanocomposite, the structure is similar to the one previously presented. In both cases, the PPY covers the silver nanoparticles, as in the core-shell structure.

Elemental Analysis
The backscattered electron images, the spectra and elemental mapping for the samples PPY, 10%Ag/PPY and 20%Ag/PPY (Figures 7-9) confirms the presence of C, N, Cl and O for all analysed materials and of Ag for 10%Ag/PPY and 20%Ag/PPY hybrid nanocomposites, which confirms the incorporation of Ag into the polymer PPY phase. For all samples, EDX mapping shows a relative homogeneous distribution of C, N, Cl, and O, but for Ag, some aggregates distribution in composites, much more distinguished in the sample with 20%Ag/PPY, is observed. crystalline structure (parallelepiped with a height of 200-300 nm and widths of 100 nm (Figure 6c)). In the case of the 20%Ag/PPY hybrid nanocomposite, the structure is similar to the one previously presented. In both cases, the PPY covers the silver nanoparticles, as in the core-shell structure. (c)

Elemental Analysis
The backscattered electron images, the spectra and elemental mapping for the samples PPY, 10%Ag/PPY and 20%Ag/PPY (Figures 7-9) confirms the presence of C, N, Cl and O for all analysed materials and of Ag for 10%Ag/PPY and 20%Ag/PPY hybrid nanocomposites, which confirms the incorporation of Ag into the polymer PPY phase. For all samples, EDX mapping shows a relative homogeneous distribution of C, N, Cl, and O, but for Ag, some aggregates distribution in composites, much more distinguished in the sample with 20%Ag/PPY, is observed.

Measurements of Magnitude Level of Skin Bioimpedance
The dry polarizable electric bioimpedance sensors is realized by using two electrodes. These two electrodes were glued on an adhesive strip for bioimpedance measurements and spaced at 6 cm apart from each other (Figures 3 and 4). The equivalent parallel scheme Rpe-Cpe (Resistance-Capacity) corresponding for electrodes is shown in Figure 10.
Appl. Sci. 2021, 11, x FOR PEER REVIEW 1 The dry polarizable electric bioimpedance sensors is realized by using two trodes. These two electrodes were glued on an adhesive strip for bioimpedance me ments and spaced at 6 cm apart from each other (Figures 3 and 4). The equivalent p scheme Rpe-Cpe (Resistance-Capacity) corresponding for electrodes is shown in F 10. For electrical impedance measurements of electrode with frequency, disk-s electrodes were silvered with silver paste on both sides, as shown in Figure 11. For electrical impedance measurements of electrode with frequency, disk-shaped electrodes were silvered with silver paste on both sides, as shown in Figure 11. For electrical impedance measurements of electrode with frequenc electrodes were silvered with silver paste on both sides, as shown in Figur   Figure 11. Disk-shaped electrode made with sensitive materials PPY or hybrid nan 10%Ag/PPY or hybrid nanocomposite 20%Ag/PPY, silvered with silver paste on bo Table 1 shows electrical impedance Ze, in therms of magnitude leve capacity and Rpe resistance respectively of the electrode. The values of obtained is corresponding to the equivalent parallel Rpe-Cpe scheme for e ure 10). The obtained data is corresponding for three electrodes made with terials PPY and hybrid nanocomposites 10%Ag/PPY and 20%Ag/PPY, res measurements of electric impedance of electrode were performed at an app voltage of 2 Vpeak-peak, for the frequency range of 10-300 kHz and at a 25 °C, by using a precision LCR meter, AGILENT E4980 A type. It can b electrodes made with hybrid nanocomposites 10%Ag/PPY and 20%Ag/PP materials have a good linearity of the impedance vs. frequency in the freq 10-300 kHz ( Figure 12). In addition, the value of electric impedance of el with hybrid nanocomposites 10%Ag/PPY and 20%Ag/PPY is quasi-con quency ( Figure 12). U Figure 11. Disk-shaped electrode made with sensitive materials PPY or hybrid nanocomposite 10%Ag/PPY or hybrid nanocomposite 20%Ag/PPY, silvered with silver paste on both sides. Table 1 shows electrical impedance Ze, in therms of magnitude level and the Cpe capacity and Rpe resistance respectively of the electrode. The values of measurements obtained is corresponding to the equivalent parallel Rpe-Cpe scheme for electrodes ( Figure 10). The obtained data is corresponding for three electrodes made with sensitive materials PPY and hybrid nanocomposites 10%Ag/PPY and 20%Ag/PPY, respectively. The measurements of electric impedance of electrode were performed at an applied sinusoidal voltage of 2 Vpeak-peak, for the frequency range of 10-300 kHz and at a temperature of 25 • C, by using a precision LCR meter, AGILENT E4980 A type. It can be seen that the electrodes made with hybrid nanocomposites 10%Ag/PPY and 20%Ag/PPY as sensitive materials have a good linearity of the impedance vs. frequency in the frequency range of 10-300 kHz ( Figure 12). In addition, the value of electric impedance of electrodes made with hybrid nanocomposites 10%Ag/PPY and 20%Ag/PPY is quasi-constant with frequency ( Figure 12). The measurement of magnitude of the level of skin bioimpedance in series wit two electrodes' impedance can be performed at two points, by using the dry polariz electric bioimpedance sensor.
For the magnitude level of total bioimpedance measurements, i.e., skin bioimpeda in series with two electrodes' impedance, six subjects participated, three men with initials, LPD, RC, CO with ages between 32 and 59 years old, and three women with initials FB, CB, II, with ages between 43 and 52 years old. The dry bioimpedance sen was attached distally on the left wrist along with the radial artery ( Figure 13). The measurement of magnitude of the level of skin bioimpedance in series with of two electrodes' impedance can be performed at two points, by using the dry polarizable electric bioimpedance sensor.
For the magnitude level of total bioimpedance measurements, i.e., skin bioimpedance in series with two electrodes' impedance, six subjects participated, three men with the initials, LPD, RC, CO with ages between 32 and 59 years old, and three women with the initials FB, CB, II, with ages between 43 and 52 years old. The dry bioimpedance sensor was attached distally on the left wrist along with the radial artery ( Figure 13).
Appl. Sci. 2021, 11, x FOR PEER REVIEW 12 Figure 13. The used test bench image for total bioimpedance measurements and dry polariza bioimpedance sensor location on the arm of the subject.
The magnitude level of total bioimpedance measurements, i.e., for skin bioim ance in series with two electrodes' impedance were achieved with the subjects in th ting position on the same day for each subject. In a first stage, for all the six subjec The magnitude level of total bioimpedance measurements, i.e., for skin bioimpedance in series with two electrodes' impedance were achieved with the subjects in the sitting position on the same day for each subject. In a first stage, for all the six subjects selected, the impedance was measured only with PPY and 20%Ag/PPY composite bioimpedance sensors, in the frequency range of 1-300 kHz. In Table 2 the experimental data are presented. In the case of the PPY bioimpedance sensor, the total bioimpedance decreases with frequency ( Figure 14), and this decrease is more significant in the case of male subjects than female subjects. Thus, at the low frequency of 1 kHz, the total bioimpedance values in the case of the male subjects were between 16-65.70 kΩ much lower values compared to 58.7-155 kΩ in the case of the female subjects; it is possible that the skin of the male is more conductive than the skin conductivity of females. In the case of the 20%Ag/PPY hybrid nanocomposite sensor, the same tendency of decreasing the total bioimpedance with frequency is observed, but compared to neat PPY, the total bioimpedance values are increased due to Ag NPs incorporated in the polymer chain and obstruction of polymer electron gaps. In addition, the total bioimpedance values obtained at a low frequency of 1 kHz are increased in the case of female subjects, with values between of 220-380 kΩ compared to those of the male subjects between of 41-100 kΩ, except for a single male whose total bioimpedance value is 450 kΩ (Figure 15). The same tendency was observed for measurements performed at 300 kHz.  Moreover, the measurements performed to obtain variation of electric impedance of electrodes with frequency ( Figure 12) shows the influence of Ag NPs incorporated in the polymer. On that account for electrodes realised with the sensitive material PPY, the impedance of electrode was in the range of 236.59-488.8 Ω while for electrodes that realised with hybrid nanocomposites 10%Ag/PPY was in the range of 124-143.2 Ω and in the range of 92. 15-102.84 Ω for hybrid nanocomposites 20%Ag/PPY.
In addition, the total bioimpedance values obtained at a low frequency of 1 kHz are increased in the case of female subjects, with values between of 220-380 kΩ compared to those of the male subjects between of 41-100 kΩ, except for a single male whose total bioimpedance value is 450 kΩ (Figure 15). The same tendency was observed for measurements performed at 300 kHz. . Figure 15. The magnitude of total electric bioimpedance versus frequency measurements of 20%Ag/PPY nanocomposite bioimpedance sensor for all subjects.  Table 3 presents the experimental data regarding the total electric bioimpedance variation with frequency for three of the subjects, a man (LPD) and two women (CB and FB). For comparison, the measurements were taken by using three bioimpedance sensors made with sensitive materials: PPY and 10%Ag/PPY and 20%Ag/PPY hybrid nanocomposites.
In this case, a decrease of the total bioimpedance with frequency for all the three human subjects tested (Table 3) was observed. On the frequency domain tested of 1-300 kHz, a more pronounced decrease is found at high frequencies (250-300 kHz), especially for the bioimpedance sensor made with sensitive material 10%Ag/PPY nanocomposite, compared to bioimpedance sensors made with PPY and 20%Ag/PPY nanocomposite. Values of 16-220 kΩ for 1 kHz to 1.80-0.512 kΩ for 300 kHz were observed. At the frequency of 300 kHz, the lowest bioimpedance values were obtained, respectively 0.512 kΩ for men LPD, 1.44 kΩ and 1.33 kΩ for women CB and FB. These trends are also illustrated in Figures 16-18. In this case, a decrease of the total bioimpedance with frequency for all the thre man subjects tested (Table 3) was observed. On the frequency domain tested of 1-300 a more pronounced decrease is found at high frequencies (250-300 kHz), especial the bioimpedance sensor made with sensitive material 10%Ag/PPY nanocomposite, pared to bioimpedance sensors made with PPY and 20%Ag/PPY nanocomposite. V of 16-220 kΩ for 1 kHz to 1.80-0.512 kΩ for 300 kHz were observed. At the frequen 300 kHz, the lowest bioimpedance values were obtained, respectively 0.512 kΩ for LPD, 1.44 kΩ and 1.33 kΩ for women CB and FB. These trends are also illustrated in ures 16-18. . Figure 16. The magnitude of total electric bioimpedance versus frequency for all bioimpedan sensors for subject LPD. Appl. Sci. 2021, 11, x FOR PEER REVIEW 15 . Figure 17. The magnitude of total electric bioimpedance versus frequency for all bioimpedan sensors, for subject CB. In addition, it is worth mentioning that on the analysed frequency range, wer served lower bioimpedance values for the male subjects compared to the bioimped values obtained for the female subjects, resulting in a different behaviour between th sexes in terms of bioimpedance. Appl. Sci. 2021, 11, x FOR PEER REVIEW 15 . Figure 17. The magnitude of total electric bioimpedance versus frequency for all bioimpedan sensors, for subject CB. In addition, it is worth mentioning that on the analysed frequency range, wer served lower bioimpedance values for the male subjects compared to the bioimped values obtained for the female subjects, resulting in a different behaviour between th sexes in terms of bioimpedance. In addition, it is worth mentioning that on the analysed frequency range, were observed lower bioimpedance values for the male subjects compared to the bioimpedance values obtained for the female subjects, resulting in a different behaviour between the two sexes in terms of bioimpedance.
A comparative evaluation of results with the literature considered another polymeric material, namely PDMS [46]. A flexible dry electrode for long-term EEG measurement based on PDMS material was realised and tested. The magnitude of total electric bioimpedance was measured by using two electrodes were placed on skin separately (about 3 cm), and then current is applied to measure impedance ( Figure 19). The signal of LCR meter is set to 2 V and the frequency range of 20 Hz-10 kHz. In this study, 10 tests on five different participants are performed [46].

FOR PEER REVIEW
16 of 20 cm), and then current is applied to measure impedance ( Figure 19). The signal of LCR meter is set to 2 V and the frequency range of 20 Hz-10 kHz. In this study, 10 tests on five different participants are performed [46]. Figure 19. Schematic diagram of measurement circuit for magnitude of total electric bioimpedance versus frequency (adapted from [46]).
The results of these measurements are shown in Figure 20.  Figure 19. Schematic diagram of measurement circuit for magnitude of total electric bioimpedance versus frequency (adapted from [46]).
The results of these measurements are shown in Figure 20. Both AgNPs/PPY hybrid nanocomposites as well as PDMS presented a tendency to decrease with frequency of the measured skin bioimpedance. Due to the obstruction of the polymer electron gaps by Ag NPs, the bioimpedance values in the frequency range of 1-300 kHz were higher compared to the behaviour of PDMS in the frequency range of 20 Hz-10 kHz. For both hybrid nanocomposites 10%Ag/PPY and 20%Ag/PPY as well as for PDMS the results obtained indicated a good tendency of quasi-linear decreasing of the electric skin bioimpedance with frequency. Figure 19. Schematic diagram of measurement circuit for magnitude of total electri versus frequency (adapted from [46]).
The results of these measurements are shown in Figure 20.

Conclusions
This paper presents three types of dry polarizable bioimpedance sensors, based on conductive polymer, PPY and hybrid nanocomposite PPY-Ag, with 10 and 20% Ag incorporated in the PPY matrix as sensitive materials, developed for electric bioimpedance measurements.
The conductive polymer PPY was synthesized by chemical oxidative polymerization using FeCl 3 × 6H 2 O like oxidizing agent in molar ratio polymer/oxidizing agent 1:2.33. For hybrid composites synthesis Ag/PPY, the colloid solution of Ag NPs was introduced in the pyrrole solution, followed by polymerization.
The structure and morphology of the sensitive materials were assessed through a series of investigative methods, and it was found that the introduction of Ag NPs in the PPY leads to the formation of silver clusters covered by PPY, similar to a core-shell structure. In addition, an amorphization of the polypyrrole should be considered in the presence of Ag NPs. From Raman spectra are resulted that a first important band appears at 1605 cm −1 , representing the vibration mode of the C=C bonds. The second band appears at 1321 and 1331 cm −1 attributed to the stretching mode of the pyrrolic ring and the third important band appears at 1040-1054 cm −1 , determined by the plane deformation of the C-H bond.
For PPY, ATR FTIR spectra identified the functions: the peak at 780 cm −1 is attributed to C-H out of plane of polypyrrole ring, the peak to 1040 cm −1 represents N-H in plane deformation, the peak located at 1186 cm −1 is assigned to C-N stretching vibration. Ag NP's introduction into the PPY structure leads to some PPY FTIR characteristic bands' displacements, indicating specific interactions between Ag NPs and the PPY functional groups, especially those in the N-H group region.
The SEM images show a classic polypyrrole structure consisting of globular units with average dimensions around 400 nm formed by the collision of smaller globular formations with average dimensions around 200 nm. In the cases of 10%Ag/PPY and 20%Ag/PPY hybrid nanocomposites the PPY covers the silver nanoparticles, as in the core-shell structure.
In making the bioimpedance electrodes, the polypyrrole and Ag/polypyrrole hybrid nanocomposite powders were pressed in disk format. A layer of conductive silver paste on one side of the obtained disks was deposited. Each of the disks thus obtained are arranged on another silver disk of the same diameter. For obtaining the dry polarizable electric bioimpedance sensor, two electrodes arranged at 6 cm from each other were used. The electrical connection is making from the opposite side of each silver disk.
The values obtained for the impedance of the electrode, for all the polymeric materials used, were much lower and almost constant in relation to the total bioimpedance (impedance measured for skin bioimpedance in series with two electrodes impedance), for the whole spectrum of frequencies. For this reason, the conclusions regarding the total bioimpedance can be considered true also for the skin bioimpedance in the first approximation.
The skin electric bioimpedance measurements were performed at two points, by using the dry polarizable electric bioimpedance sensor made of two bioimpedance electrodes, glued on an adhesive strip, and applying a sinusoidal voltage of 2 V peak-peak , in the frequency range of 1-300 kHz, at room temperature. The electric bioimpedance measurements were performed on six human subjects, both men and women, between 32 and 59 years old. For all cases, the bioimpedance decreased with frequency, more pronounced in the case of males. At the low frequency of 1 kHz, the bioimpedance values ranged between 16-65.7 kΩ for male subjects and 58.7-155 kΩ for female subjects.
The measurement of the useful signal can be influenced by noise. In the case of measurements of the useful signal in order to obtain total electric bioimpedance by using a precision LCR meter, AGILENT E4980 A type, the measuring probe TL09A ensured an accuracy of 1%. However, to develop ECG equipment that uses the dry polarizable electric bioimpedance sensors made with sensitive materials 10%Ag/PPY or 20%Ag/PPY hybrid nanocomposite it was necessary for the useful signal to be taken in differential mode and the input impedance to be of MΩ values. The problem of shielding and filtering the signal by using bandpass filters must also be solved.
Both AgNPs/PPY hybrid nanocomposites presented a tendency to decrease the measured skin bioimpedance with frequency, but compared to the behaviour of PPY, the bioimpedance values were higher due to the obstruction of the polymer electron gaps by Ag NPs. For hybrid nanocomposites 10%Ag/PPY and 20%Ag/PPY the results obtained indicate the best tendency of quasi-linear decrease of the electric skin bioimpedance with frequency compared to the PPY material.
For the nanocomposite 20%Ag/PPY, the tendency of decreasing the electric skin bioimpedance with frequency was observed but compared to the behaviour of PPY and 10%Ag/PPY the electric skin bioimpedance values were higher, because a higher quantity of Ag NPs inserted in polymer obstructs the hopping of electrons in polymer.
The importance of measurements for skin bioimpedance is given by the possibility of performing studies related to monitoring wound healing in post-operative phases.
The results obtained indicate that both sensitive materials the hybrid nanocomposite 10%Ag/PPY and 20%Ag/PPY can be considered for obtaining the bioimpedance sensors.
Future developments will study the possibility of using the dry polarizable electric bioimpedance sensors at frequencies lower than 100 Hz as well as higher than 300 kHz, in order to take over the signals of the ECG (electrocardiogram), EMG (electromyogram) and EEG (electroencephalography) types. These studies and further developments will be performed for a larger number of subjects and will involve statistical data processing.