4.6 Article

Na1+xMnx/2Zr2-x/2(PO4)3 as a Li+ and Na+ Super Ion Conductor for Solid-State Batteries

Journal

ACS ENERGY LETTERS
Volume 6, Issue 2, Pages 429-436

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsenergylett.0c02513

Keywords

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Funding

  1. U.S. Department of Energy (DOE) [DE-AC05-00OR22725]
  2. Laboratory Directed Research and Development (LDRD) Program at Oak Ridge National Laboratory
  3. Office of Energy Efficiency and Renewable Energy (EERE) Vehicle Technologies Office (VTO)
  4. Scientific User Facilities Division, Office of Basic Sciences, U.S. Department of Energy

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This study reports the dual ion conduction capability of Na-based NASICON type super iron conductor materials using Na1+xMnx/2Zr2-x/2(PO4)(3) (NMZP) as a candidate system. The NMZPs exhibit high room-temperature conductivities and good cycling stability against both Na and Li metals, showcasing dual ion conduction. Mechanistic investigations confirm the Na-Li ion-exchange in these materials during electrochemical cycling.
Here we report dual ion conduction capability of Na-based NASICON type super iron conductor materials using Na1+xMnx/2Zr2-x/2(PO4)(3) (NMZP) as a candidate system. This method enables the use of Na-based NASICON material family in both Na as well as Li all solid-state batteries (SSBs). NZMPs with x = 1.5 and x = 2 showed the highest room-temperature conductivities of 2.86 x 10(-5) and 2.82 x 10(-5) S cm(-1), respectively. Crystallographic analysis using neutron diffraction revealed that conductivities observed in these materials are related to the variations in the Na-O bond length and the concentration of mobile sodium content. Using galvanostatic plating and stripping tests, we show that these NMZPs boast good cycling stability against both Na and Li metals, which also reveals dual ion conduction. Mechanistic investigations through postmortem SEM/EDS and XPS characterizations of the alkali metal and the cycled NMZPs confirm that the Na-Li ion-exchange occurs readily in these materials when electrochemically cycled.

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