Topology-Driven Sodium Storage and Conversion in Covalent Fullerene Networks

Abstract Fullerene network is an emergent two-dimensional (2D) carbon allotrope in which C60 molecules are covalently bonded to form a quasi-hexagonal pattern (qHP). The intermolecular covalent bonding significantly reshapes the intrinsic electronic structure of the C60 units, leading to enhanced structural stability and electrochemical activity. Herein, we report unconventional high-density Na-ion storage and electrocatalytic conversion properties of fullerene networks (qHP-C60) driven by their covalent quasi-hexagonal topology. As an anode material for sodium-ion batteries, the covalent framework facilitates intermolecular charge transfer and creates favorable sites for Na+ adsorption, delivering a maximum reversible capacity of 279 mAh g–1 at 25 mA g–1. In addition, the interconnected and curved C60 subunits induce inhomogeneous electron distribution, accelerating the reaction kinetics of NaCl/Cl2 conversion in sodium-chlorine batteries. This enables a high current density (15,000 mA g–1 versus 1,000–1,500 mA g–1) at a significantly reduced catalyst loading amount (5 wt % versus 60–80 wt %) compared to benchmark catalysts. Our study provides insights into the covalent structural engineering of carbon materials for high-performance energy applications.

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Publication Details

Journal
ACS Nano
Published
2026-08-19
DOI
https://doi.org/10.1021/acsnano.6c09620
Primary Topic
Advancements in Battery Materials
Type
article
Field-Weighted Citation Impact
0.00

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article

Topology-Driven Sodium Storage and Conversion in Covalent Fullerene Networks

Shitao Geng, Hao Mei, Huisheng Peng, Wentao Fan et al.
ACS Nano
Advancements in Battery Materials
article

Topology-Driven Sodium Storage and Conversion in Covalent Fullerene Networks

Shitao Geng, Hao Mei, Huisheng Peng, Wentao Fan, Hao Sun, Antonio Gaetano Ricciardulli, Hui Yu, Paolo Samorı́, Shitao Wu, Qiuchen Xu, Yiyong Mai, Yuxuan Zhang, Sheng Yang, Shuo Wang, Yan Wang, Chengxiao Zhang, Shanshan Tang
article en

Abstract

Abstract Fullerene network is an emergent two-dimensional (2D) carbon allotrope in which C60 molecules are covalently bonded to form a quasi-hexagonal pattern (qHP). The intermolecular covalent bonding significantly reshapes the intrinsic electronic structure of the C60 units, leading to enhanced structural stability and electrochemical activity. Herein, we report unconventional high-density Na-ion storage and electrocatalytic conversion properties of fullerene networks (qHP-C60) driven by their covalent quasi-hexagonal topology. As an anode material for sodium-ion batteries, the covalent framework facilitates intermolecular charge transfer and creates favorable sites for Na+ adsorption, delivering a maximum reversible capacity of 279 mAh g–1 at 25 mA g–1. In addition, the interconnected and curved C60 subunits induce inhomogeneous electron distribution, accelerating the reaction kinetics of NaCl/Cl2 conversion in sodium-chlorine batteries. This enables a high current density (15,000 mA g–1 versus 1,000–1,500 mA g–1) at a significantly reduced catalyst loading amount (5 wt % versus 60–80 wt %) compared to benchmark catalysts. Our study provides insights into the covalent structural engineering of carbon materials for high-performance energy applications.

ACS Nano
Shanghai Jiao Tong University (CN), Fudan University (CN), ShanghaiTech University (CN), Institut de Science et d'Ingénierie Supramoléculaires (FR)
National Natural Science Foundation of China, Ministry of Education of the People's Republic of China, Science and Technology Commission of Shanghai Municipality, Shanghai Jiao Tong University, Fundamental Research Funds for the Central Universities, HORIZON EUROPE Digital, Industry and Space
Affordable and clean energy
Openalex Percentile: Top 19%
Advancements in Battery Materials
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