4.8 Article

Low-temperature synthesis of Fe2(MoO4)3 nanosheets: A cathode for sodium ion batteries with kinetics enhancement

期刊

NANO RESEARCH
卷 14, 期 11, 页码 3977-3987

出版社

TSINGHUA UNIV PRESS
DOI: 10.1007/s12274-021-3323-1

关键词

low-temperature synthesis; cathode; sodium ion batteries; kinetics; Na+ super ionic conductor (NASICON)

资金

  1. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Science, ICT and Future Planning [NRF-2017R1A2B3011967]
  2. Engineering Research Center through National Research Foundation of Korea (NRF) - Korean Government (MSIT) [NRF-2018R1A5A1025224]

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In this study, an orthorhombic Na super ionic conductor structural Fe-2(MoO4)(3) nanosheet was synthesized and applied as a cathode material for SIBs, showing a high specific capacity and improved cycling performance. The unique morphology and improved kinetics of electrochemical reaction contribute to the enhanced performance under high- and low-temperature conditions.
Sodium ion batteries (SIBs) are alternatives to lithium ion batteries (LIBs), and offer some significant benefits such as cost reduction and a lower environmental impact; however, to compete with LIBs, further research is required to improve the performance of SIBs. In this study, an orthorhombic Na super ionic conductor structural Fe-2(MoO4)(3) nanosheet with amorphous-crystalline core-shell alignment was synthesized using a facile low-temperature water-vapor-assisted solid-state reaction and applied as a cathode material for SIBs. The obtained material has a well-defined three-dimensional stacking structure, and exhibits a high specific capacity of 87.8 mAh center dot g(-1) at a current density of 1 C = 91 mA center dot g(-1) after 1,000 cycles, which is due to the considerable contribution of extra surface-related reaction such as the pseudo-capacitive process. This material shows significantly improved cycling and rated behavior as well as enhanced performance under high- and low-temperature conditions, as compared to the same materials prepared by the conventional high-temperature solid-state reaction. This enhancement is explained by the unique morphology in combination with the improved kinetics of the electrochemical reaction due to its lower charge transfer resistance and higher sodium ion conductivity.

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