Extended Conjugation Acceptors Increase Specific Energy Densities in sr-Conjugated Redox Polymers

Organic materials are a sustainable alternative to replace inorganic transition metal-based cathodes in rechargeable intercalation batteries. Among the possible redox active organic materials, conjugated polymers with multiple redox sites per repeat unit are expected to afford high energy and power densities while being resistant to dissolution when in contact with battery electrolytes. However, accessing the full capacity of polymeric electrodes while ensuring electrochemical reversibility has been challenging. Using diketopyrrolopyrrole (DPP)-based donor- acceptor (D-A) polymers as model systems and complementary electrochemical experiments and first-principles calculations, we show that conjugated backbone moieties that minimize charge localization on the electron accepting repeat units lead to near theoretical discharge capacities. Further, the capacity enhancement is associated with better rate performance and improved electrochemical stability of the polymer over prolonged cycling. Our work suggests that charge density on the electron accepting moiety is a potential descriptor for rationally designing redox-active polymer electrodes that afford high discharge capacities along with a long cycle life.

Automated summary

Organic materials are a sustainable alternative to replace inorganic transition metal-based cathodes in rechargeable intercalation batteries. Among them, conjugated polymers with multiple redox sites per repeat unit show high energy and power densities with resistance to dissolution. In this study, using diketopyrrolopyrrole (DPP)-based donor-acceptor (D-A) polymers, it is found that minimizing charge localization on the electron accepting repeat units leads to near theoretical discharge capacities. Furthermore, this capacity enhancement improves the rate performance and electrochemical stability of the polymer during prolonged cycling.