“…In the FT-IR spectra (Figure b), the vibrational peaks at ∼1467, 1342, 1280, and 1243 cm –1 are attributed to CH 2 scissoring, CH 2 wagging, asymmetric stretching, and CH 2 symmetric twisting of the PEO matrix, respectively. The strong characteristic peak at 1075 cm –1 is assigned to the C–O–C symmetric/asymmetric stretching modes of PEO chains. , The LiClO 4 salt exhibits the FT-IR peaks of a free ClO 4 – anion (dissociated part) at ∼947 cm –1 , as well as the undissociated LiClO 4 at ∼1645 cm –1 . , Notably, the addition of the Co 3 O 4 @PDA filler results in a blue shift of the ClO 4 – peak to ∼949 cm –1 , implying the formation of Lewis acid–base pairs between the catechol of PDA and ClO 4 – . , The dissociation degree of Li salt can be speculated from the relative intensity of ClO 4 – with respect to LiClO 4 . It is clear that the Co 3 O 4 @PDA CPE displays the highest ClO 4 – intensity compared to the Co 3 O 4 CPE and PEO SPE, suggesting the enhanced dissociation degree of LiClO 4 salt after filling the Co 3 O 4 @PDA additive.…”