“…The Raman spectra in Figure i exhibit characteristic peaks at approximately 199.1, 279.8, 389.1, and 580 cm –1 , , which correspond to the vibrations of the C, O, F, and OH functional groups (T X ) and the Ti–C vibration of Ti 3 C 2 T X MXene and are indicated by the red bars. The Raman peaks of PVPh were exhibited at 641.7, 843.7, and 1087.5 cm –1 , which correspond to the vibrations of the aromatic ring deformation, out-of-plane CH deformation, and in-plane CH deformation and are indicated by the blue bars. − Therefore, the Raman spectra of the PL-MXene displayed the typical strong peaks of MXene and the weak peaks of PVPh. The HR-XRD results of the PL-MXene electrode are nearly identical to those of an MXene layer before depositing a PVPh layer, as shown in Figure j.…”