Insight into the Role of Closed‐Pore Size on Rate Capability of Hard Carbon for Fast‐Charging Sodium‐Ion Batteries

S Shuhao Xiao (CAS Key Laboratory of Molecular Nanostructure and Nanotechnology Beijing National Laboratory For Molecular Sciences (BNLMS) Institute of Chemistry Chinese Academy of Sciences (CAS) Beijing P. R. China) Y Yu‐Jie Guo (CAS Key Laboratory of Molecular Nanostructure and Nanotechnology Beijing National Laboratory For Molecular Sciences (BNLMS) Institute of Chemistry Chinese Academy of Sciences (CAS) Beijing P. R. China) H Han‐Xian Chen (CAS Key Laboratory of Molecular Nanostructure and Nanotechnology Beijing National Laboratory for Molecular Sciences (BNLMS) Institute of Chemistry Chinese Academy of Sciences (CAS) Beijing 100190 P. R. China) H Haizhou Liu Z Zhou‐Quan Lei (Institute of Chemistry Chinese Academy of Sciences (CAS) Beijing 100190 China) L Lin‐Bo Huang (CAS Key Laboratory of Molecular Nanostructure and Nanotechnology Beijing National Laboratory For Molecular Sciences (BNLMS) Institute of Chemistry Chinese Academy of Sciences (CAS) Beijing P. R. China) R Ruo‐Xi Jin (CAS Key Laboratory of Molecular Nanostructure and Nanotechnology Beijing National Laboratory for Molecular Sciences (BNLMS) Institute of Chemistry Chinese Academy of Sciences (CAS) Beijing 100190 P. R. China) X Xiao‐Chuan Su (Institute of Chemistry Chinese Academy of Sciences (CAS) Beijing 100190 China) Q Qianyu Zhang (College of Materials Science and Engineering) Y Yu‐Guo Guo (CAS Key Laboratory of Molecular Nanostructure and Nanotechnology Beijing National Laboratory For Molecular Sciences (BNLMS) Institute of Chemistry Chinese Academy of Sciences (CAS) Beijing P. R. China)

Abstract

Abstract The sluggish Na ion diffusion kinetics and Na metal plating in hard carbon negative electrodes restrict the fast‐charging of sodium‐ion batteries, which is intricately entwined with the crystal structure and pore structure. Here, the pore structures of hard carbon materials are focused on and reveal that the pore size significantly affects the Na‐filling potentials during the sodiation process. Specifically, the micro closed pores exhibit higher Na‐filling potentials, which reduces risks of Na metal plating at high current densities, thus enabling improved rate performance. As a result, the optimized hard carbon with closed micropores (1.6 nm) achieves an initial capacity exceeding 400 mAh g −1 at 20 mA g −1 and a plateau retention rate of 73.3% at a current density of 500 mA g −1 . Paired with P2‐type layered oxide positive electrodes, the 2.2 Ah pouch cell shows 10 min charging for ≈90% of the capacity and ≈90% capacity retention after 1500 cycles at a 6C rate. This work establishes a bridge between pore size and rate performance, offering guidance for the design of fast‐charging sodium‐ion batteries.

Article Details

Volume / Issue Vol. 37, Issue 28
Published July 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (10)

S

Shuhao Xiao

CAS Key Laboratory of Molecular Nanostructure and Nanotechnology Beijing National Laboratory For Molecular Sciences (BNLMS) Institute of Chemistry Chinese Academy of Sciences (CAS) Beijing P. R. China

Y

Yu‐Jie Guo

CAS Key Laboratory of Molecular Nanostructure and Nanotechnology Beijing National Laboratory For Molecular Sciences (BNLMS) Institute of Chemistry Chinese Academy of Sciences (CAS) Beijing P. R. China

H

Han‐Xian Chen

CAS Key Laboratory of Molecular Nanostructure and Nanotechnology Beijing National Laboratory for Molecular Sciences (BNLMS) Institute of Chemistry Chinese Academy of Sciences (CAS) Beijing 100190 P. R. China

H

Haizhou Liu

Z

Zhou‐Quan Lei

Institute of Chemistry Chinese Academy of Sciences (CAS) Beijing 100190 China

L

Lin‐Bo Huang

CAS Key Laboratory of Molecular Nanostructure and Nanotechnology Beijing National Laboratory For Molecular Sciences (BNLMS) Institute of Chemistry Chinese Academy of Sciences (CAS) Beijing P. R. China

R

Ruo‐Xi Jin

CAS Key Laboratory of Molecular Nanostructure and Nanotechnology Beijing National Laboratory for Molecular Sciences (BNLMS) Institute of Chemistry Chinese Academy of Sciences (CAS) Beijing 100190 P. R. China

X

Xiao‐Chuan Su

Institute of Chemistry Chinese Academy of Sciences (CAS) Beijing 100190 China

Q

Qianyu Zhang

College of Materials Science and Engineering

Y

Yu‐Guo Guo

CAS Key Laboratory of Molecular Nanostructure and Nanotechnology Beijing National Laboratory For Molecular Sciences (BNLMS) Institute of Chemistry Chinese Academy of Sciences (CAS) Beijing P. R. China