Abstract

The kinetics incompatibility between battery-type anode and capacitive-type cathode for sodium ion hybrid capacitors (SIHCs) seriously hinders their overall performance output. Herein, we construct a SIHCs device by coupling with quantum grade vanadium nitride (VN) nanodots anchored in one-dimensional N/F co-doped carbon nanofiber cages hybrids (VNQDs@PCNFs-N/F) as the freestanding anode and the corresponding activated N/F co-doped carbon nanofiber cages (APCNFs-N/F) as cathode. The strong coupling of VN quantum dots with N/F co-doped 1D conductive carbon cages effectively facilitates the ion/electron transport and intercalation-conversion-deintercalation reactions, ensuring fast sodium storage to surmount aforesaid kinetics incompatibility. Additionally, density functional theory calculations cogently manifest that the abundant active sites in the VNQDs@PCNFs-N/F configuration boost the Na+ adsorption/reaction activity well which will promote both "intrinsic" and "extrinsic" pseudocapacitance and further improve anode kinetics. Consequently, the assembled SIHCs device can achieve high energy densities of 157.1 and 95.0 Wh kg-1 at power densities of 198.8 and 9100.5 W kg-1, respectively, with an ultralong cycling life over 8000 cycles. This work further verified the feasibility of kinetics-compatible electrode design strategy toward metal ion hybrid capacitors.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call