Issue 48, 2024

Hierarchically porous Zn0.76Co0.24S/CoS heterostructures confined in N,S-co-doped carbon as high-performance anodes for sodium-ion batteries

Abstract

Owing to the favorable merits of substantial capacity, low price, and eco-friendliness, metal sulfides have been widely desired as prospective anodes for sodium-ion batteries. However, the huge volumetric variation, inferior electrical conductivity, and sluggish Na+-storage kinetics seriously impede their large-scale practical applications. Herein, hierarchically porous Zn0.76Co0.24S/CoS heterostructures confined in N,S-co-doped carbon architectures (ZCS@NSC) have been rationally designed and engineered through a MOF-engaged sulfurization approach. In this delicate architecture, hierarchically porous nanostructures effectively alleviate the huge volumetric variation and also provide a mass of fast diffusion paths for Na+ ions in the Na+-storage reactions. The Zn0.76Co0.24S/CoS heterostructures contribute plentiful active Na+-storage sites and accelerate the Na+ ion diffusion kinetics. The NSC layer effectively mitigates the volumetric variation by the confinement effect and also establishes a highly conductive framework for rapid charge transfer during the cycling process. Profiting from the favorable synergistic effects, the resulting ZCS@NSC anode yields high capacity (568.2 mA h g−1 at 0.1 A g−1) and good rate properties (224.1 mA h g−1 at 10.0 A g−1) together with satisfied cyclic performance (68.3% capacity retention at 1.0 A g−1 after 300 cycles).

Graphical abstract: Hierarchically porous Zn0.76Co0.24S/CoS heterostructures confined in N,S-co-doped carbon as high-performance anodes for sodium-ion batteries

Supplementary files

Article information

Article type
Paper
Submitted
08 Aug 2024
Accepted
16 Nov 2024
First published
18 Nov 2024

New J. Chem., 2024,48, 20258-20267

Hierarchically porous Zn0.76Co0.24S/CoS heterostructures confined in N,S-co-doped carbon as high-performance anodes for sodium-ion batteries

C. Li, Q. Li, Y. Zhang and K. Cao, New J. Chem., 2024, 48, 20258 DOI: 10.1039/D4NJ03543G

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