Abstract

Sodium ion capacitors (SICs) have attracted considerable attentions since it is integrating the complementary features of both high energy and power densities. One of the most crucial tasks for develop highly efficient SICs is to increase the faradaic Na+ redox kinetics from the battery-type anode to match the electrical double-layer capacitance-type cathode. In this work, Mo2C nanoparticles uniformly anchored into cross-linked hierarchical porous carbon (HPC-Mo2C) have been produced by a water-soluble NaCl template strategy. The as-obtained HPC-Mo2C composite shows a large specific surface area of 385.6 m2 g−1 with well distributed micro–meso–macropores structure, delivering a superior rate capability (108.2 mAh g−1 at 5 A g−1) and robust long-term cycling of 190.6 mAh g−1 at 1 A g−1 after 2500 cycles. Electrochemical measurements illustrate that the Mo2C nanoparticles uniformly anchored into cross-linked hierarchical porous structure can accelerate fast Na+ diffusion kinetics toward excellent rate capacity and increase the pseudocapacitive behavior for the redox reaction. The SIC composed of HPC-Mo2C as anode and activated carbon (AC) as cathode delivers an impressive energy density of 130.2 Wh kg−1 and ultra-high power density of 30,000.0 W kg−1, as well as an unprecedented cycling stability of 88.9% retention after 10,000 cycles with a potential range of 0–4.0 V. This work may cater to the requirements for rationale kinetic matching electrode for the advanced SICs.

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