The Role of Sintering Temperature and Dual Metal Substitutions (Al 3+ , Ti 4+ ) in the Development of NASICON-Structured Electrolyte

The aim of this study is to synthesize Li Al Ti Sn (PO ) sodium super ion conductor (NASICON) -based ceramic solid electrolyte and to study the effect of dual metal substitution on the electrical and structural properties of the electrolyte. The performance of the electrolyte is analyzed based on th...

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Published inMaterials Vol. 14; no. 23; p. 7342
Main Authors Rusdi, Hashlina, Rusdi, Roshidah, Aziz, Shujahadeen B, Alsubaie, Abdullah Saad, Mahmoud, Khaled H, Kadir, Mohd F Z
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 30.11.2021
MDPI
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Summary:The aim of this study is to synthesize Li Al Ti Sn (PO ) sodium super ion conductor (NASICON) -based ceramic solid electrolyte and to study the effect of dual metal substitution on the electrical and structural properties of the electrolyte. The performance of the electrolyte is analyzed based on the sintering temperature (550 to 950 °C) as well as the composition. The trend of XRD results reveals the presence of impurities in the sample, and from Rietveld Refinement, the purest sample is achieved at a sintering temperature of 950 °C and when x = 0.6. The electrolytes obey Vegard's Law as the addition of Al and Ti provide linear relation with cell volume, which signifies a random distribution. The different composition has a different optimum sintering temperature at which the highest conductivity is achieved when the sample is sintered at 650 °C and x = 0.4. Field emission scanning electron microscope (FESEM) analysis showed that higher sintering temperature promotes the increment of grain boundaries and size. Based on energy dispersive X-ray spectroscopy (EDX) analysis, x = 0.4 produced the closest atomic percentage ratio to the theoretical value. Electrode polarization is found to be at maximum when x = 0.4, which is determined from dielectric analysis. The electrolytes follow non-Debye behavior as it shows a variety of relaxation times.
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ISSN:1996-1944
1996-1944
DOI:10.3390/ma14237342