Metal-organic-framework derived Zn-V-based oxide with charge storage mechanism as high-performance anode material to enhance lithium and sodium storage.

J Colloid Interface Sci

Guangzhou Key Laboratory of Materials for Energy Conversion and Storage, Key Laboratory of Theoretical Chemistry of Environment, Ministry of Education, School of Chemistry, South China Normal University, Guangzhou 510006, PR China. Electronic address:

Published: December 2023

AI Article Synopsis

  • Transition metal oxides are promising for battery applications but struggle with low electrical conductivity and significant volume changes during use.
  • Researchers developed ZnVO material from a Zn-V-MOF template to enhance performance in lithium-ion and sodium-ion batteries.
  • The ZnVO structure showed impressive discharge capacities in both types of batteries and benefited from theoretical calculations that support its efficiency.

Article Abstract

Transition metal oxides have been extensively studied due to their large theoretical capacities, but their practical application has been hampered by low electrical conductivity and dramatic volume fluctuation during cycling. In this work, we synthesized ZnVO material using Zn-V-MOF (metal-organic framework) as a sacrificial template to improve the electrochemical characteristics of lithium-ion batteries (LIBs) and sodium-ion batteries (SIBs). Unique dodecahedral structure, larger specific surface area and higher ability to mitigate volume changes, improve the electrochemical reaction active site while accelerating ion transport. ZnVO with 2-methylimidazole as a ligand demonstrated a discharge capacity of 1225.9 mAh/g in LIBs and 761.6 mAh/g in SIBs after 300 cycles at 0.2 C. Density functional theory (DFT) calculation illustrates the smaller diffusion barrier energy and higher specific capacity in LIBs that is ascribed to the fact that Li has a smaller size and hence its diffusion is easier. This study may lead to a path for the manufacturing of high-performance LIBs and SIBs.

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http://dx.doi.org/10.1016/j.jcis.2023.08.139DOI Listing

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