Preparation of intergrown P/O-type biphasic layered oxides as high-performance cathodes for sodium ion batteries
This study reports on the solid-state synthesis and characterization of novel quaternary P/O intergrown biphasic Na 0.8 Mn y Ni 0.8− y Fe 0.1 Ti 0.1 O 2 ( y = 0.6, 0.55, 0.5, 0.45) cathode materials. Electrochemical tests reveal superior performance of the P/O biphasic materials in a sodium ion batt...
Saved in:
Published in | Journal of materials chemistry. A, Materials for energy and sustainability Vol. 9; no. 22; pp. 13151 - 1316 |
---|---|
Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Cambridge
Royal Society of Chemistry
14.06.2021
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | This study reports on the solid-state synthesis and characterization of novel quaternary P/O intergrown biphasic Na
0.8
Mn
y
Ni
0.8−
y
Fe
0.1
Ti
0.1
O
2
(
y
= 0.6, 0.55, 0.5, 0.45) cathode materials. Electrochemical tests reveal superior performance of the P/O biphasic materials in a sodium ion battery compared to the single P2 or O3 phases, proving the beneficial effect of the intergrowth of P2 and O3 materials. The nature of the P/O interface was studied by transmission electron microscopy. The analysis shows a semi-coherent interface grown along the
a
/
b
and
c
axes with local differences in the transition metal concentration along the interface between the two phases. EDX and EELS characterization revealed a charge compensation mechanism across the phase boundary based on variation of the transition element distribution, balancing the different sodium contents in the P and O phases. The results reported in this study provide a better understanding of P/O biphasic materials.
P/O intergrown biphasic sodium cathode materials with improved electrochem. properties were prepared. TEM revealed a semi-coherent interface with uniform oxidation state but different metal concentrations balancing sodium concentration differences. |
---|---|
Bibliography: | 10.1039/d1ta00627d Electronic supplementary information (ESI) available. See DOI |
ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/d1ta00627d |