“…Compared with the spectra of the pure MWCNT, the appearance of C]O stretching vibration peak of the carboxylic group at 1705 cm À1 confirms the carboxylic functionalization of the MWCNTs in the MWCNTseCOOH spectrum [30]. For the PEDOT/Cl spectrum, the vibrations around 1350 and 1520 cm À1 originate from the quinoid structure and stretching modes of CeC and C]C in the thiophene ring, respectively [31]. Vibrations at 1206, 1144, 1089, and 1053 cm À1 are attributed to stretching of the CeOeC bond in the ethylenedioxy group, peak at 926 cm À1 is ascribed to the ethylenedioxy ring deformation mode, and the vibration modes of the CeS bond in the thiophene ring are observed at 692, 843 and 980 cm À1 [32e34].…”