“…The peaks at 1306, 1242, 1162, and 829 cm À 1 were assigned to the CÀ N stretching of the aromatic secondary amine, CÀ N + stretching of the polarized structure, and in-plane and out-of-plane of CÀ H bending vibration, respectively, which were consistent with previous FTIR spectra of PANI. [25][26][27][28] After adding Nafion, the new peak at 1042 cm À 1 can be assigned to the symmetric stretching of the SO 3 2À group in Nafion (Figure 2a and S5), and the intensity of the CÀ N + peak increases with increasing Nafion content (Figure 2a), indicating that the Nafion was doped into PANI. The inplane CÀ H stretching vibration of PANI at 1162 cm À 1 showed a low wavenumber shift (or red shift) with increasing Nafion content (Table S1), which can be attributed to the electrostatic interactions between the sulfonate group of Nafion and the amino group of PANI.…”