4.6 Article

Controlled synthesis of hierarchical porous carbons with different morphologies and their application for potassium and lithium ion batteries

Journal

NEW JOURNAL OF CHEMISTRY
Volume 45, Issue 22, Pages 9882-9891

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1nj01622a

Keywords

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Funding

  1. Jiangsu University of Science and Technology Research Start-Up Fund [1062921905]

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In this study, nitrogen-doped hierarchical porous activated carbons were successfully synthesized from bio wastes, showing different morphologies and pore structures that can be controlled by KOH etching time. The synthesized carbons exhibited excellent performance in potassium and lithium-ion storage, with different morphologies displaying varying specific capacities and cycling performances. The superior electrochemical properties of the carbons were attributed to their hierarchical porous structure and modified chemical structures due to nitrogen doping, showing potential for further exploration in porous carbons from bio wastes by chemical scientists.
Activated carbon is an ideal candidate as an anode material for rechargeable metal-ion batteries. However, the synthesis of highly porous and heteroatom-doped carbons with high yields and controlled morphologies is a grand challenge. Herein, heteroatom nitrogen-doped (in situ) hierarchical porous activated carbons with interconnected macro/meso/micropores and controlled morphologies were prepared from bio wastes using a facile synthesis technique. The surface morphology, pore distribution and crystal structure of the synthesized carbons were thoroughly investigated for various KOH etching times. Experimental results revealed that different morphologies i.e. 3-dimensional interconnected structures, nanosheets, and nanospheres, were achieved with significant pores and specific surface areas. Synthesized carbons were tested for potassium and lithium-ion storage. PIBs exhibited a maximum reversible capacity of 526 mA h g(-1) at 20 mA g(-1) and an excellent cycling performance (retaining 212 mA h g(-1) after 150 cycles at 20 mA g(-1)) with N-doped active carbon nanospheres. Whereas, the reversible capacity of 1394 mA h g(-1) at 50 mA g(-1) with an excellent cycling performance (retaining 536 mA h g(-1) after 500 cycles at 500 mA g(-1)) was delivered by N-doped active carbon nanospheres against Li+/Li. Furthermore, cyclic voltammetry and electrochemical impedance spectroscopy were employed to quantify the guest ion storage mechanisms and diffusion coefficients. The excellent electrochemistries of the synthesized carbons are attributed to their hierarchical porous structure, which provides micro reaction chambers, and modified chemical structures owing to heteroatom (nitrogen) doping. We hope that these findings will encourage chemical scientists to explore porous carbons from bio wastes.

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