Ceiba flower-derived hard carbon with multi-dimensional self-supported structures and its ZnIn2S4-based composites: long-term stable anode materials for sodium-ion batteries

Abstract

Biomass-derived functional carbon materials have attracted increasing research attention due to their cost-effectiveness, environmental friendliness, and easy adjustability of compositions and structures. Especially, for sodium-ion batteries (SIBs), which are widely recognized as a promising alternative to lithium-ion batteries, biomass-derived hard carbon holds the greatest potential as an anode material for commercialization in the near future. In this paper, through a facile carbonization process, a multi-dimensional structured N-doped hard carbon with rational pores and defects has been successfully synthesized from an abundant and easy-accessible biomass precursor of ceiba flower, which delivers a remarkable initial coulombic efficiency of 83.2%. When incorporated with ZnIn2S4 nanoarchitectures, the fabricated composites maintain the multi-dimensional structures with further-optimized pores, defects and electronic structures, achieving a high reversible capacity of 510.2 mA h g−1 after 1000 cycles at 1 A g−1. Considering the low-cost raw materials, environment-friendly and facile synthetic process, high initial coulombic efficiency and high reversible capacity, these ceiba-derived materials hold great application potential as anode materials for high-performance SIBs.

Graphical abstract: Ceiba flower-derived hard carbon with multi-dimensional self-supported structures and its ZnIn2S4-based composites: long-term stable anode materials for sodium-ion batteries

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Article information

Article type
Paper
Submitted
08 May 2025
Accepted
21 Jun 2025
First published
23 Jun 2025

Phys. Chem. Chem. Phys., 2025, Advance Article

Ceiba flower-derived hard carbon with multi-dimensional self-supported structures and its ZnIn2S4-based composites: long-term stable anode materials for sodium-ion batteries

X. Wu, W. Liu, Z. Wu and F. Lin, Phys. Chem. Chem. Phys., 2025, Advance Article , DOI: 10.1039/D5CP01724F

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