Reactive Carbide-Based Synthesis and Microstructure of NASICON Sodium Metal All Solid-State Electrolyte

  • Callum J. Campbell
  • , Scott Monismith
  • , Vikalp Raj
  • , Yixian Wang
  • , Qianqian Yan
  • , Cole D. Fincher
  • , Rohit Raj
  • , Yet Ming Chiang
  • , John Watt
  • , Josefine D. McBrayer
  • , David Mitlin

Research output: Contribution to journalArticlepeer-review

Abstract

Reactive carbide precursor-based synthesis of NASICON-type NZSP (Na1+xZr2SixP3-xO12) solid-state electrolyte (SSE) is demonstrated, in contrast to the established oxide-based approach. Exothermic decomposition of ZrC and SiC in air homogenizes microstructure, yielding 98% compact density after conventional sintering at 1200 °C. Quantitative stereology demonstrates that significant microstructural differences are present. Compacts of carbide-derived Carb-NZSP are 98% dense with a secondary zirconium oxide (ZrO2) volume fraction of 0.2% ± 0.3%, versus 93% dense and 3% ± 1% for oxide-derived baseline. For Carb-NZSP, the secondary glassy phosphate phase is agglomerated, while for baseline, it is dispersed and percolated. Electrochemical testing combined with post-mortem analysis demonstrates how microstructural control of secondary phases is critical for dendrite suppression: Carb-NZSP critical current density (CCD) is 3.1 ± 0.8 mA cm2 at 0.1 mAh cm2, versus 1.0 ± 0.7 mA cm−2 at 0.1 mAh cm−2. Cryogenic focused ion beam (cryo-FIB) analysis demonstrates that in both materials, the porous 2D sheet-like sodium metal dendrites propagate around and subsume NZSP grains, likely following a path enriched with glassy phase and with porosity. Dendrites also flow around isolated zirconia particles. Phase field simulation reveals deflection of dendrites by mechanically tough zirconia, while brittle glassy phase accelerates dendrite growth, especially when finely distributed.

Original languageEnglish
JournalAdvanced Materials
DOIs
StateAccepted/In press - 2025
Externally publishedYes

Funding

This work was supported by the Mechano‐Chemical Understanding of Solid Ion Conductors, an Energy Frontier Research Center funded by the US DOE, Office of Science, Office of Basic Energy Science, contract number DE‐SC0023438. This work was supported by The University of Texas at Austin Energy Institute, Strategic Energy Seed Grant Program. This work was supported and performed, in part, at the Center for Integrated Nanotechnologies, an Office of Science User Facility operated for the U.S. Department of Energy (DOE) Office of Science. Los Alamos National Laboratory, an affirmative action equal opportunity employer, is managed by Triad National Security, LLC for the U.S. Department of Energy's NNSA, under contract 89233218CNA000001. Sandia National Laboratories is a multi‐mission laboratory managed and operated by National Technology & Engineering Solutions of Sandia, LLC (NTESS), a wholly owned subsidiary of Honeywell International Inc., for the U.S. Department of Energy's National Nuclear Security Administration (DOE/NNSA) under contract DE‐NA0003525. This work was supported by The Welch Foundation (F‐2206). The authors are thankful to Dr. Rémi Dingreville and Dr. Sergei A. Ivanov for much helpful discussion.

Keywords

  • NASICON
  • dendrite growth
  • microstructure
  • sodium-metal batteries
  • solid-state batteries

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