4.7 Article

Investigation of K modified P2 Na0.7Mn0.8Mg0.2O2 as a cathode material for sodium-ion batteries

期刊

CRYSTENGCOMM
卷 21, 期 1, 页码 172-181

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c8ce01532e

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资金

  1. Australian Research Council [DE160100237, DP170100269]
  2. AMMRF at the Electron Microscope Unit at UNSW
  3. Australian Research Council [DE160100237] Funding Source: Australian Research Council

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Sodium-ion batteries (NIBs) are emerging as a potentially cheaper alternative to lithium-ion batteries (LIBs) due to the larger abundance of sodium and in some cases the similar intercalation chemistry to LIBs. Here we report the solid state synthesized K-modified P2 Na0.7Mn0.8Mg0.2O2 which adopts hexagonal P6(3)/mmc symmetry. The second charge/discharge capacity for the as-prepared material is 115/111 mA h g(-1) between 1.5-4.2 V at a current density of 15 mA g(-1), which reduces to 61/60 mA h g(-1) after 100 cycles. Scanning transmission electron microscopy coupled with energy-dispersive X-ray spectroscopy (STEM-EDS) analysis shows a heterogeneous distribution of K and solid state Na-23 NMR illustrates that the presence of K perturbs the local environment of Na within the P2 Na0.7Mn0.8Mg0.2O2 crystal structure. Larger scale X-ray absorption near-edge structure (XANES) data on the K L-edge also illustrate that K is present on the surface of electrodes in preference to the bulk. In situ synchrotron X-ray diffraction (XRD) data illustrates that the P2 structural motif is preserved, featuring a solid solution reaction for most of charge-discharge except at the charged and discharged states where multiple phases are present. The K-modified sample of P2 Na0.7Mn0.8Mg0.2O2 is compared with the K-free samples in terms of both structural evolution and electrochemical performance.

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