An spectroscopy revealed identification overlapping peaks of PPy. A powerful peak at 805 cm-1 for PPyPT and in decrease intensity for of compounds in PPy composites such as PTA and CDC at the same time the PPy composites made PPyCDC belong to tungsten trioxide (WO3) [33], confirming that PTA was successfully in EG possessing lower conductivities soon after formation shown in shifts of peaks in Raman incorporated. From the Raman spectrum of CDC only two peaks may be identified, disorspectroscopy. FTIR spectroscopy could determine PTA inclusion at the same time as-1 PPy signals all der-induced D peak at 1353 cm-1 and the graphite G-peak at 1595 cm [34]. Figure S1 shown with further EG peaks revealed.Materials 2021, 14,identified as CH2 rocking vibration. In summary, the characterization offered by Raman spectroscopy revealed identification of compounds in PPy composites which include PTA and CDC at the same time the PPy composites produced in EG getting lower conductivities right after formation shown in shifts of peaks in Raman spectroscopy. FTIR spectroscopy could determine PTA inclusion together with all PPy sig8 of 18 nals shown with further EG peaks revealed. To investigate the ion-contents of oxidized and reduced PPy samples EDX spectroscopy of cross-section images was performed and also the outcomes are shown in Figure 3a . To investigate the PPy composites such as PPy/DBS straight just after polymerization EDX spectra of pristineion-contents of oxidized and reduced PPy samples EDX spectroscopy of cross-section photos was performed plus the benefits are shownincluded carbon (in oxidized state, 0.6 V) are presented in Figure S2a,b. The spectra with in Figure 3a . EDX spectra of pristine PPy S3a . peaks are shown in Figure composites such as PPy/DBS directly following polymerization (in oxidized state, 0.six V) are presented in Figure S2a,b. The spectra with incorporated carbon peaks are shown in Figure S3a .Components 2021, 14, x FOR PEER REVIEW9 ofFigure three.3. (a), EDX Thromboxane B2 supplier spectroscopyof cross-section images of PPy samples polymerized in EG:Milli-Q at oxidation for example Figure (a), EDX spectroscopy of cross-section images of PPy samples polymerized in EG:Milli-Q at oxidation such asPPyPToxox and PPyCDCox (black line) and at reduction PPyPTred and PPyCDCred (green line) well these PPy films polPPyPT and PPyCDCox (black line) and at reduction PPyPTred and PPyCDCred (green line) as also those PPy films polymerized in EG oxidation with Tianeptine sodium salt In Vivo PPyPT-EGox and PPyCDC-EGox (blue line) and at and at reduction PPyPT-EGred and ymerized in EG at at oxidation with PPyPT-EGox and PPyCDC-EGox (blue line) reduction PPyPT-EGred and PPyCDCPPyCDC-EGred (red line), and in samples samples in-PC and4 in (c,d), those in NaClO4-aq electrolytes. EGred (red line), and in (b) PPy (b) PPy in NaClO4 NaClO -PC and in (c,d), these in NaClO4 -aq electrolytes.From Figure S3a the carbon peak (C) isis shown at 0.26 keV and located slightly inFrom Figure S3a the carbon peak (C) shown at 0.26 keV and discovered slightly improved together with the addition of CDC materials (Figure S3b,d). In Figure 3a the oxygen peak creased with all the addition of CDC materials (Figure S3b,d). In Figure 3a the oxygen peak 3- – (O) shown atat 0.52 keV refers to PTA (PWOO403-) at the same time DBS- molecules immobilized in (O) shown 0.52 keV refers to PTA (PW12 12 40 ) as well DBS molecules immobilized in PPy and partly fromthe applied electrolyte NaClO4.four . The sodium peak (Na) isshown at PPy and partly from the applied electrolyte NaClO The sodium peak (Na) is shown at 1.04 keV, referring to.