Abstract

Two novel carbons (MCs) derived from moxa floss of different storage years have been prepared by two low-cost and facile approaches, which are hydrothermal carbonization at a low temperature (200 °C) and direct pyrolysis at a moderate temperature (500 °C) followed by potassium hydroxide (KOH) activation strategy at a high temperature (800 °C), respectively. The physicochemical properties of MCs are investigated by Raman spectra, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), field-emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), and nitrogen adsorption–desorption isotherms. Results show that MCs derived from moxa floss of different storage years by two facile approaches possess different morphologies: MCs by hydrothermal carbonization (denoted as MC-1, MC-2 and MC-3) exhibit porous nanosheet structures, the highest specific surface area is about 1788.6 m2 g−1, and the largest total pore volumes is around 0.8170 cm3 g−1, while MCs by direct pyrolysis (denoted as MC-4, MC-5 and MC-6) have basically blocky and rod-like morphologies, the highest specific surface area is about 1628.0 m2 g−1, and the largest total pore volume is around 0.7058 cm3 g−1. However, despite the different morphologies, all MCs possess a similar hierarchical porous structure, numerous heteroatom groups and good electrical conductivity. Therefore, these low-cost, biomass-derived porous carbons with promising capacitive performance are used for supercapacitors application with high performance, for example, the as-assembled supercapacitor based on MC-5 exhibits a high specific capacitance of 288.3 F g−1 at 0.25 A g−1, an excellent rate performance of 243.5 F g−1 even at 30 A g−1 with 84.5% capacitance retention of its initial specific capacitance, and an outstanding long-term cycling stability with 98.7% capacitance retention after 10 000 cycles at 5 A g−1. Furthermore, the maximum energy density for these supercapacitors with an aqueous electrolyte in a two-electrode system is about 10.0 W h kg−1 at a power density of 70.3 W kg−1. Therefore, this work opens up a whole new field for the applications of moxa floss and this novel concept of moxa floss use is an extremely promising strategy for developing high-performance carbons with porous structures and heteroatom-doping from renewable sources.

Highlights

  • The moxa oss of different storage years was directly subjected to hydrothermal carbonization at a low temperature (200 C) (or pyrolysis at a moderate temperature (500 C)) followed by potassium hydroxide (KOH) activation at a high temperature (800 C), giving moxa oss-derived porous carbons (MCs). These resulting carbons possess different morphologies but exhibit high speci c surface area up to 1788.6 m2 gÀ1, hierarchical porous structure coexisting of micro, meso, and macro-pores, numerous heteroatom (O and N) functional groups, long-term cycling stability as well as excellent capacitive performance, for example, the as-assembled supercapacitor based on moxa oss-derived porous carbons (MCs)-5 exhibits a high speci c capacitance of 288.3 F gÀ1 at 0.25 A gÀ1, an excellent rate performance of 243.5 F gÀ1 even at 30 A gÀ1 with 84.5% capacitance retention of its initial speci c capacitance, and an outstanding long-term cycling stability with 98.7% capacitance retention a er 10 000 cycles at 5 A gÀ1

  • The morphologies of MC were characterized by field-emission scanning electron microscopy (FESEM) observations (Fig. 1)

  • Regardless of moxa oss of different storage years as carbon precursors, three samples of MC (MC-1, MC-2 and MC3) fabricated by hydrothermal carbonization exhibit the porous nanosheet structures, but three samples of MC (MC-4, MC-5 and MC-6) fabricated by direct pyrolysis have the basically blocky and rod-like morphology, which can imply that the method of precarbonization is closely related with the morphology change of MC

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Summary

Introduction

Paper supercapacitors.[25,26,27] there is in dire need to fabricate carbon materials with enhanced features. The moxa oss of different storage years was directly subjected to hydrothermal carbonization at a low temperature (200 C) (or pyrolysis at a moderate temperature (500 C)) followed by potassium hydroxide (KOH) activation at a high temperature (800 C), giving moxa oss-derived porous carbons (MCs) These resulting carbons possess different morphologies but exhibit high speci c surface area up to 1788.6 m2 gÀ1, hierarchical porous structure coexisting of micro-, meso-, and macro-pores, numerous heteroatom (O and N) functional groups, long-term cycling stability as well as excellent capacitive performance, for example, the as-assembled supercapacitor based on MC-5 exhibits a high speci c capacitance of 288.3 F gÀ1 at 0.25 A gÀ1, an excellent rate performance of 243.5 F gÀ1 even at 30 A gÀ1 with 84.5% capacitance retention of its initial speci c capacitance, and an outstanding long-term cycling stability with 98.7% capacitance retention a er 10 000 cycles at 5 A gÀ1. Using moax oss as carbon source to prepare biomass-derived carbons for high-power supercapacitors is an extremely promising strategy for developing low-cost and high performance electrode materials and pursuing new application of Artemisia argyi

Materials
Structural characterization
Supercapacitors preparation and electrochemical measurements
Morphologies and structures of MC
Chemical composition analysis of MC
Electrochemical characterization of MC
Conclusions
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