4.6 Article

Solid-State Electrochemical Synthesis of Silicon Clathrates Using a Sodium-Sulfur Battery Inspired Approach

Journal

JOURNAL OF THE ELECTROCHEMICAL SOCIETY
Volume 168, Issue 2, Pages -

Publisher

ELECTROCHEMICAL SOC INC
DOI: 10.1149/1945-7111/abdfe5

Keywords

Batteries Li-ion; Bulk crystal growth; Solid-State Ionics

Funding

  1. NSF DMR [1710017, 1709813, 2004514, 2004579]
  2. ASU Fulton Schools of Engineering Dean's Fellowships [NNCI-ECCS-1542160]
  3. Direct For Mathematical & Physical Scien
  4. Division Of Materials Research [1710017, 2004579] Funding Source: National Science Foundation
  5. Direct For Mathematical & Physical Scien
  6. Division Of Materials Research [1709813, 2004514] Funding Source: National Science Foundation

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The paper presents a method for the selective formation of Na8Si46 clathrates through electrochemical oxidation at high temperatures, showing that product morphology and selection can be altered by adjusting reaction conditions. The electrochemical performance of the synthesized product at room temperature is evaluated for the first time, indicating potential for controlled crystal growth and a better understanding of the formation processes of intermetallic clathrates through solid-state electrochemical oxidation of Zintl phases at high temperatures.
Clathrates of Tetrel elements (Si, Ge, Sn) have attracted interest for their potential use in batteries and other applications. Sodium-filled silicon clathrates are conventionally synthesized through thermal decomposition of the Zintl precursor Na4Si4, but phase selectivity of the product is often difficult to achieve. Herein, we report the selective formation of the type I clathrate Na8Si46 using electrochemical oxidation at 450 degrees C and 550 degrees C. A two-electrode cell design inspired by high-temperature sodium-sulfur batteries is employed, using Na4Si4 as working electrode, Na beta ''-alumina solid electrolyte, and counter electrode consisting of molten Na or Sn. Galvanostatic intermittent titration is implemented to observe the oxidation characteristics and reveals a relatively constant cell potential under quasi-equilibrium conditions, indicating a two-phase reaction between Na4Si4 and Na8Si46. We further demonstrate that the product selection and morphology can be altered by tuning the reaction temperature and Na vapor pressure. Room temperature lithiation of the synthesized Na8Si46 is evaluated for the first time, showing similar electrochemical characteristics to those in the type II clathrate Na24Si136. The results show that solid-state electrochemical oxidation of Zintl phases at high temperatures can lead to opportunities for more controlled crystal growth and a deeper understanding of the formation processes of intermetallic clathrates.

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