Issue 32, 2022, Issue in Progress

Preparation of N/O co-doped porous carbon by a one-step activation method for supercapacitor electrode materials

Abstract

Heteroatom-doped carbon materials used in supercapacitors are low in cost and demonstrate extraordinary performance. Here, ethylenediamine tetraacetic acid (EDTA) with intrinsic N and O elements is selected as a raw material for the preparation of heteroatom self-doped porous carbon. Furthermore, N/O self-doped porous carbon with a large surface area has been successfully prepared using K2CO3 as the activator. The derived sample with a 1 : 2 molar ratio of EDTA to K2CO3 (EK-2) demonstrates a porous structure, rich defects, a large surface area of 2057 m2 g−1 and a micropore volume of 0.25 cm3 g−1. Benefiting from high N content (2.89 at%) and O content (10.75 at%), EK-2 exhibits superior performance, including high capacitance of 325 F g−1 at 1 A g−1 and outstanding cycling stability with 96.8% retention after 8000 cycles at 10 A g−1, which strongly confirms its immense potential toward many applications. Additionally, the maximum energy density of EK-2 reaches was 17.01 W h kg−1 at a power density of 350 W kg−1 in a two-electrode system. This facile and versatile strategy provides a scalable approach for the batch synthesis of N/O co-doped carbonaceous electrode materials for energy storage.

Graphical abstract: Preparation of N/O co-doped porous carbon by a one-step activation method for supercapacitor electrode materials

Article information

Article type
Paper
Submitted
29 Apr 2022
Accepted
06 Jul 2022
First published
21 Jul 2022
This article is Open Access
Creative Commons BY license

RSC Adv., 2022,12, 20866-20875

Preparation of N/O co-doped porous carbon by a one-step activation method for supercapacitor electrode materials

D. Liu, Y. Liu, Y. Ding and B. Fan, RSC Adv., 2022, 12, 20866 DOI: 10.1039/D2RA02732A

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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