Investigation of K modified P2 Na0.7Mn0.8Mg0.2O2 as a cathode material for sodium-ion batteries
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 h...
Gespeichert in:
Veröffentlicht in: | CrystEngComm 2019-01, Vol.21 (1), p.172-181 |
---|---|
Hauptverfasser: | , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | 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 P63/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 23Na 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. |
---|---|
ISSN: | 1466-8033 |
DOI: | 10.1039/c8ce01532e |