Boosting sodium storage in needle coke-derived hard carbon anode via mild ammonium persulfate activation

Abstract

Needle coke features low cost, high carbon yield, and good electrical conductivity. It is considered a promising precursor for the carbon anode for sodium-ion batteries, but poor structural tunability and inferior performance limit further development. Herein, we report a facile strategy to achieve needle coke-derived hard carbon (NCAPS) with multiscale structures via activation with ammonium persulfate (APS). Systematic characterization revealed that ammonium persulfate activation introduced appropriate oxygen-containing functional groups on the surface of needle coke, while creating a turbostratic microstructure with balanced defect density and mesopores, thereby supplying abundant adsorption sites of Na+ and improving electrochemical performance. Benefiting from its appropriate structure and chemical composition, NCAPS exhibited a reversible capacity of 212.6 mAh g−1 after 200 cycles at 0.2C, which was 37% higher than non-activated needle coke-derived hard carbon, and an excellent rate capability of 195.0 mAh g−1 at 5C. We utilized APS-assisted activation to enable multiscale structural optimization, thereby significantly enhancing Na+ storage kinetics and electrochemical performance. Herein, we provide a mild activation approach for designing a high-performance sodium-ion battery hard carbon anode from a low-cost and highly aromatic precursor.

Graphical abstract: Boosting sodium storage in needle coke-derived hard carbon anode via mild ammonium persulfate activation

Supplementary files

Article information

Article type
Communication
Submitted
22 Dec 2025
Accepted
06 Mar 2026
First published
20 Mar 2026

Nanoscale Horiz., 2026, Advance Article

Boosting sodium storage in needle coke-derived hard carbon anode via mild ammonium persulfate activation

L. Yang, L. Yue, C. Shi, T. Zhao, Z. Wang, X. Zheng, J. Zhao, J. Zhao and J. Tang, Nanoscale Horiz., 2026, Advance Article , DOI: 10.1039/D5NH00831J

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