Nonporous, conducting bimetallic coordination polymers with an advantageous electronic structure for boosted faradaic capacitance.

Conductive coordination polymers (c-CPs) are promising electrode materials for supercapacitors (SCs) owing to their excellent conductivity, designable structures and dense redox sites. However, despite their high intrinsic density and outstanding electrical properties, nonporous c-CPs have largely been overlooked in SCs because of their low specific surface areas and deficient ion-diffusion channels. Herein, we demonstrate that the nonporous c-CPs AgBHT (BHT = benzenehexathiolate) and CuAgBHT are both battery-type capacitor materials with high specific capacitances and a large potential window. Notably, nonporous CuAgBHT with bimetallic bis(dithiolene) units exhibits superior specific capacitance (372 F g at 0.5 A g) and better rate capability than isostructural AgBHT. Structural and electrochemical studies showed that the enhanced charge transfer between different metal sites is responsible for its outstanding capacitive performance. Additionally, the assembled CuAgBHT//AC SC device displays a favorable energy density of 17.1 W h kg at a power density of 446.1 W kg and an excellent cycling stability (90% capacitance retention after 5000 cycles). This work demonstrates the potential applications of such nonporous redox-active c-CPs in SCs and highlights the roles of bimetallic redox sites in capacitive performance, which hold promise for the future development of c-CP-based energy storage technologies.