Unraveling the Dominance of Structural Vacancies in Sodium Ion Conductivity in NaSOF.

J Phys Chem Lett

Department of Chemistry, College of Sciences, Shanghai University, 99 Shangda Road, Shanghai 200444, People's Republic of China.

Published: August 2023

AI Article Synopsis

  • Solid electrolytes, crucial for energy storage and conversion, often show both paddle-wheel effects and vacancy diffusion mechanisms, but their exact contributions are unclear.
  • Our study focuses on the phase stability and ionic conductivity of NaSOF (NSOF) and magnesium-doped NaSOF (NaMgSOF, NMSOF), revealing that Na vacancies in NMSOF boost ionic conductivity by two orders of magnitude compared to NSOF.
  • Additionally, NMSOF has a lower phase transition temperature than NSOF, and Raman spectroscopy indicates that SO rotation has little impact on sodium conductivity, enhancing our understanding of sodium conduction in these materials.

Article Abstract

Solid electrolytes are important materials for energy storage and conversion applications, and the coexistence of the paddle-wheel effect and vacancy diffusion mechanism is commonly observed in many solid electrolytes. However, the mechanism that significantly contributes to this remains unknown. To address this issue, we assess the phase stability and conduction properties of NaSOF (NSOF) and magnesium-doped NSOF (NaMgSOF, NMSOF). Our results reveal that incorporating Na vacancies in NSOF (i.e., NMSOF) leads to a significant increase in ionic conductivity, with a 2 order of magnitude difference compared to NSOF. The phase transition temperature of NMSOF is also significantly lower than that of NSOF, demonstrating the role of vacancies in enhancing the mobility of Na cations. Furthermore, Raman spectroscopy confirms that the polyanion SO rotation has a minor effect on the sodium conduction mechanism. Our study provides a fundamental understanding of the sodium conduction mechanism of polyanion-based sodium superionic conductors, including the impact of vacancies on Na conductivity.

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Source
http://dx.doi.org/10.1021/acs.jpclett.3c01220DOI Listing

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