Substitution Index‐Prediction Rules for Low‐Potential Plateau of Hard Carbon Anodes in Sodium‐Ion Batteries

Y Yunfei Xue Y Yaxin Chen Y Yazhan Liang L Liluo Shi (School of Materials Science and Physics China University of Mining and Technology Xuzhou 221116 China) R Rui Ma (College of Materials, State Key Laboratory of Physical Chemistry of Solid Surfaces, iChEM, College of Chemistry and Chemical Engineering, College of Energy, School of Life Sciences, College of Physical Science and Technology, and Discipline of Intelligent Instrument and Equipment) X Xia Qiu (School of Materials Science and Physics China University of Mining and Technology Xuzhou 221116 China) Y Ying Li N Nannan Guo (State Key Laboratory of Chemistry and Utilization of Carbon Based Energy Resources College of Chemistry Xinjiang University Urumqi China) Q Quanchao Zhuang (School of Materials and Physics & Center of Mineral Resource Waste Recycling China University of Mining and Technology Xuzhou Jiangsu 221116 China) B Baojuan Xi Z Zhicheng Ju (School of Materials and Physics & Center of Mineral Resource Waste Recycling China University of Mining and Technology Xuzhou Jiangsu 221116 China) S Shenglin Xiong

Abstract

Abstract Establishing prediction rules for the low‐potential plateau (LPP) of hard carbon (HC) anodes is crucial for constructing high‐energy‐density sodium‐ion batteries (SIBs). While current studies suggest that the closed pores of HC can enhance the LPP performance, the rules for directly predicting the LPP from precursors have yet to be established. Here, prediction rules for the LPP of HC anodes in SIBs—the substitution index ( Δ ) of precursor are introduced. Three carbon models (disordered carbon, closed‐pore‐dominated carbon, and turbostratic carbon) are constructed to verify the accuracy of Δ and to explore the closed‐pore formation and LPP mechanism. In detail, as the Δ increases from 0.06 to 0.22, the LPP capacity rises from 25 to 278 mAh g⁻¹, revealing a strong linear correlation between Δ of precursor and LPP capacity. In situ XRD, Raman, and ex situ SAXS, EPR further confirm that sodium storage in HC can be categorized into adsorption (>0.4 V), interlayer storage (0.4 to 0.15 V), and pore‐filling (below 0.15 V). This work not only elucidates the sodium storage mechanisms, but also provides one efficient design guideline for advanced carbon anodes in SIBs.

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 (12)

Y

Yunfei Xue

Y

Yaxin Chen

Y

Yazhan Liang

L

Liluo Shi

School of Materials Science and Physics China University of Mining and Technology Xuzhou 221116 China

R

Rui Ma

College of Materials, State Key Laboratory of Physical Chemistry of Solid Surfaces, iChEM, College of Chemistry and Chemical Engineering, College of Energy, School of Life Sciences, College of Physical Science and Technology, and Discipline of Intelligent Instrument and Equipment

X

Xia Qiu

School of Materials Science and Physics China University of Mining and Technology Xuzhou 221116 China

Y

Ying Li

N

Nannan Guo

State Key Laboratory of Chemistry and Utilization of Carbon Based Energy Resources College of Chemistry Xinjiang University Urumqi China

Q

Quanchao Zhuang

School of Materials and Physics & Center of Mineral Resource Waste Recycling China University of Mining and Technology Xuzhou Jiangsu 221116 China

B

Baojuan Xi

Z

Zhicheng Ju

School of Materials and Physics & Center of Mineral Resource Waste Recycling China University of Mining and Technology Xuzhou Jiangsu 221116 China

S

Shenglin Xiong