Abstract

Doping of heteroatom into well-structured mesoporous carbon architecture can significantly augment the capacitive performance. In this work, we report P-doped graphitic hollow carbon spheres (P-GHCS) grown over Fe-KIT-6 through the in situ approach using the catalytic CVD technique. The obtained P-GHCS possesses a relatively high surface area with uniform mesoporous structure, good graphitization with tunable P-doping contents. The highly favorable structure and desirable heteroatom doping were taken into account to evaluate the P-GHCS as a modified electrode material towards high-performance supercapacitor. The optimized P-GHCS-800 sample exhibits superior specific capacitance (Csp) 321 F g−1 at 0.2 A g−1 with outstanding cycling stability with 2.9% loss of its initial capacitance after 2000 cycles in 6 M KOH electrolyte background in the three-electrode computerized system. More importantly, the fabricated P-GHCS-800 symmetric supercapacitor device can withstand at a wide potential width of 2.0 V, together with remarkable cyclic stability (89.09%) after 2000 cycles at a current density of 1 A g−1 in aqueous 1 M Na2SO4 as electrolyte providing a relatively high energy density of 10.83 Wh kg−1 with a power density of 222.78 W kg−1. Additionally, we demonstrated the single symmetric supercapacitor cell which provided sufficient energy to turn on a red LED of 20 mW and emit light over a certain period of time opens up possible realistic applications.

Highlights

  • With the limited obtainability of fossil fuel, continually growing energy consumption, and rising demand for environmental protection, it is essential and urgent to find a green, highly efficient, and sustainable energy-storage system [1]

  • The electrochemical performance of the prepared PGHCS electrodes was conducted on an electrochemical workstation (Autolab PGSTAT 302 N) using cyclic voltammetry (CV), galvanostatic charge/discharge (GCD) and electrochemical impedance spectroscopy (EIS) in three-electrode and two-electrode cell configuration

  • The P-doped graphitic hollow carbon spheres (P-GHCS) were grown over Fe-KIT-6 catalytic support at various temperature ranges such as 750, 800, and 850 °C through CVD technique

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Summary

Introduction

With the limited obtainability of fossil fuel, continually growing energy consumption, and rising demand for environmental protection, it is essential and urgent to find a green, highly efficient, and sustainable energy-storage system [1]. According to the equation E = (1/2)CV2 [1], the energy density (E) of the supercapacitor is straightforwardly relative to capacitance (C) of the electrode materials and square of the electrolytes operating voltage window (V). It was evident that there are two approaches to enhancing the energy density of a supercapacitor, one is developing the electrode materials specific capacitance (Csp) and the other is increasing the cell voltage of the assembled device. The phosphorus-doped carbon can expand the cell voltage because of enhancing electro-oxidation prevention of carbon-based electrode provoked by phosphorus-containing functional groups, which significantly improves the energy density of supercapacitors [31]. It is essential to hunt a kind of novel carbon based electrode materials with high oxygen and hydrogen evaluation overpotential to expand the operating voltage, and it can further enhance the energy density of supercapacitor. The assembled symmetric supercapacitor device can drive a larger potential window (2.0 V) with high cycling stability (89.09%)

Synthesis of Fe-KIT-6 catalytic support
Growth and purification of P-GHCS
Materials characterization
Electrode preparation and electrochemical characterization
Results and discussion
M Na2SO4
Conclusion
Full Text
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