Can polyoxometalates enhance the capacitance and energy density of activated carbon in organic electrolyte supercapacitors?

• A hybrid electrode made of (TEAPW12) and activated carbon (AC) outperforms AC in a high-V organic electrolyte supercapacitor • The inorganic cluster undergoes multi-electron reactions in the hybrid material, even in an aprotic organic electrolyte. • Volumetric capacitance increases by ~36% with polyoxometalates hybridization without sacrificing voltage window. • We are demonstrating for the first time the effective use of polyoxometalates in aprotic electrolyte supercapacitors. Polyoxometalates (POMs) have been shown to work as faradaic additives to activated carbon (AC) in acidic aqueous electrolytes. Yet, their use in organic media allows not only for added capacity but also higher voltage. Here we show that the tetraethylammonium derivative of phosphotungstate [PW 12 O 40 ]3− (PW12) can be homogeneously distributed throughout the pores of activated carbon (AC) in organic solvents such as N,N'-dimethylformamide (DMF) and demonstrate the use of this hybrid electrode material in an organic electrolyte (1 M TEABF4 in acetonitrile) supercapacitor. Our results show the efficient electroactivity of the PW12 cluster even in the absence of protons, providing a higher voltage than aqueous electrolytes and fast and reversible redox activity. The hybrid material shows a combination of double-layer (AC) and redox (PW12) capacities leading to an increase (36%) in volumetric capacitance with respect to pristine AC in the same organic electrolyte (1 M TEABF4 in acetonitrile). Remarkably, we were able to quantify this increase as coming predominantly from non-diffusion-limited processes thanks to the utterly dispersed nature of POMs. Moreover, the hybrid material delivers a good rate capability and excellent cycle stability (93% retention of the initial capacitance after 10,000 cycles). This study has a profound significance on improving capacitance of carbon-based materials in organic electrolytes. Image, graphical abstract [ABSTRACT FROM AUTHOR]