4.8 Article

Insight into Ion Diffusion Dynamics/Mechanisms and Electronic Structure of Highly Conductive Sodium-Rich Na3+xLaxZr2-xSi2PO12 (0 ≤ x ≤ 0.5) Solid-State Electrolytes

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 13, Issue 11, Pages 13132-13138

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.0c21882

Keywords

NASICON; solid-state electrolyte; NMR; XAS; La doping; high ionic conductivity; diffusion mechanism

Funding

  1. Natural Science Foundation of China (NSFC) [U1432249]
  2. National Key R&D Program of China [2017YFA0205002]
  3. Priority Academic Program Development (PAPD) of Jiangsu Higher Education Institutions
  4. Jiangsu Key Laboratory for Carbon-Based Functional Materials and Devices
  5. Collaborative Innovation Center of Suzhou Nano Science Technology
  6. Natural Science and Engineering Research Council of Canada (NSERC)
  7. Canada Research Chair Program (CRC)
  8. Canada Foundation for Innovation (CFI)
  9. University of Western Ontario (UWO)
  10. National High Magnetic Field Laboratory by NSF Cooperative Agreement [DMR-1644779]
  11. State of Florida

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Solid-state electrolytes (SSEs) have been explored as a safer and more durable alternative to liquid electrolytes, with NASICON-type SSEs showing promise due to their high ionic conductivity and low thermal expansivity. Doping La into the NASICON structure significantly enhances the ionic conductivity, with La3+ ions existing as phosphate impurities instead of occupying Zr4+ sites. Increasing Si/P ratio and sodium ion occupancy contribute to the enhanced ionic conductivity in the altered NASICON phase, suggesting Si/P composition modifications as a promising strategy for further improvement.
Solid-state electrolytes (SSEs) have attracted considerable attention as an alternative for liquid electrolytes to improve safety and durability. Sodium Super Ionic CONductor (NASICON)-type SSEs, typically Na3Zr2Si2PO12, have shown great promise because of their high ionic conductivity and low thermal expansivity. Doping La into the NASICON structure can further elevate the ionic conductivity by an order of magnitude to several mS/cm. However, the underlying mechanism of ionic transportation enhancement has not yet been fully disclosed. Herein, we fabricate a series of Na(3+)xLaxZr(2-x)Si(2)PO(12) (0 <= x <= 0.5) SSEs. The electronic and local structures of constituent elements are studied via synchrotron-based X-ray absorption spectroscopy, and the ionic dynamics and Na-ion conduction mechanism are investigated by solid-state nuclear magnetic resonance spectroscopy. The results prove that La3+ ions exist in the form of phosphate impurities such as Na3La(PO4)(2) instead of occupying the Zr4+ site. As a result, the increased Si/P ratio in the NASICON phase, accompanied by an increase in the sodium ion occupancy, makes a major contribution to the enhancement of ionic conductivity. The spin-lattice relaxation time study confirms the accelerated Na+ motions in the altered NASICON phase. Modifications on the Si/P composition can be a promising strategy to enhance the ionic conductivity of NASICON.

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