Issue 19, 2020

Rational design of high nitrogen-doped and core–shell/mesoporous carbon nanospheres with high rate capability and cycling longevity for pseudocapacitive sodium storage

Abstract

Carbonaceous materials are extensively used as sodium-ion battery (SIB) anodes for their cost-effectiveness, high conductivity and reasonably high capacity. Unfortunately, these anodes suffer from poor rate performances and unsatisfactory lifespan. Herein, the design and construction of high nitrogen-doped, core–shell and intra-core mesoporous structured carbon nanospheres (designated as HN-CSMCNs) for high-rate and stable SIBs is reported. HN-CSMCNs are facilely synthesized by the self-assembly of block copolymer polystyrene-b-poly(acrylic acid), cetyltrimethylammonium bromide and dopamine hydrochloride, and subsequent pyrolysis under an NH3 atmosphere. As an anode for SIBs, HN-CSMCNs exhibit outstanding specific capacity (ca. 251 mA h g−1 at 0.1 A g−1), rate capability (ca. 104 mA h g−1 at 15 A g−1), and more importantly, especially stable cycling properties with a capacity of ca. 153 mA h g−1 being retained after 20 000 cycles at 10 A g−1. Electrochemical analysis demonstrates that the core–shell and intra-core mesoporous structures, expanded inter-planar distance and high pyrrolic/pyridinic-N doping of HN-CSMCNs together contribute to the superior sodium storage capability via a pseudocapacitive-dominated electrochemical kinetics, thus leading to superior electrochemical performances for SIBs.

Graphical abstract: Rational design of high nitrogen-doped and core–shell/mesoporous carbon nanospheres with high rate capability and cycling longevity for pseudocapacitive sodium storage

Supplementary files

Article information

Article type
Paper
Submitted
21 Mar 2020
Accepted
27 Apr 2020
First published
28 Apr 2020

J. Mater. Chem. A, 2020,8, 9768-9775

Rational design of high nitrogen-doped and core–shell/mesoporous carbon nanospheres with high rate capability and cycling longevity for pseudocapacitive sodium storage

J. Mao, D. Niu, N. Jiang, G. Jiang, M. Chen, Y. Li and J. Shi, J. Mater. Chem. A, 2020, 8, 9768 DOI: 10.1039/D0TA03229H

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