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. 2021 May 24;3:669763. doi: 10.3389/fmedt.2021.669763

Figure 1.

Figure 1

(A) Chemical structures of the common OCPs polypyrrole, poly(3,4-ethylenedioxythiophene) and polyaniline. (B) Schematic illustrating the incorporation of a dopant anion during oxidation of monomeric species to form the OCP conjugated backbone (PPy). (B) Reproduced with permission from Gilmore et al. (27).