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Updated: Jul 16, 2025

Preparation of Graphene Liquid Cells for the Observation of Lithium-ion Battery Material
Published on: February 5, 2019
Bimetal Oxide Reduction-Induced Perforation Strategy for Preparing a Multi-Microchannel Graphene-Based Anode Material
Tao Liu1, Yu Yang2, Xuejie Wang1
1Laboratory of Solar Fuel, Faculty of Materials Science and Chemistry, China University of Geosciences, 68 Jincheng Street, Wuhan 430078, P. R. China.
Abstract:
A sodium-ion battery, with a wide operating range, is much cheaper and safer than a lithium battery. Graphene is regarded as a promising carbon material in the preparation of anode materials. However, the large two-dimensional (2D) graphene sheets restrain the cross-plane diffusion of electrolyte ions, limiting the further improvement of rate performance. Herein, a nanohybrid of FeCo2Se4 and holey graphene (FeCo2Se4/HG) has been successfully prepared by the synchronism of pore creation and active material growth. Specifically, FeCo-oxide nanoparticles serve as the etching agents, generating in-plane nanoholes and subsequently converted into FeCo2Se4. The nanoholes provide a high density of cross-plane diffusion channels for sodium ions, serving as ionic diffusion shortcuts between different graphene layers to accelerate ion transport across the entire electrode. The unique architecture endows FeCo2Se4/HG with superior rate capability (411.2 mA h g-1 at 20 A g-1) and a specific capacity of 432.4 mA h g-1 at 2.0 A g-1 after 2000 cycles with a capacity retention rate of 92.4%. Therefore, pore engineering makes it possible for holey graphene-based electrodes to achieve outstanding rate performance and superb cycling durability.
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