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Type II germanium clathrates have recently been investigated for potential applications as anodes in batteries due to their cage-like structures that can accommodate electrochemical insertion of guest ions. To synthesize type II Ge clathrates (Ge136), several experimental routes use thermal or electrochemical desodiation of the Zintl phase compound Na4Ge4. However, the mechanism by which Na atoms are removed from the precursor to form clathrates is not well understood. Herein, we use first-principles density functional theory and nudged elastic band calculations to understand the reaction mechanism and formation energies of the products typically observed in the synthesis, namely, NaδGe136 (0 < δ < 24) type II clathrates and hexagonal phase Na1–xGe3+z. Specifically, we confirm the energetic feasibility of Na vacancy formation in Na4Ge4 and find that the barrier for Na vacancy migration is only 0.37 eV. This relatively low energy barrier is consistent with the ease with which Na4Ge4 can be desodiated to form the products. We also discuss the energetics, sodium migration pathways, and potential electrochemical performance of Ge136 as anode material for Na-ion batteries. Overall, this study highlights how first-principles calculations can be used to understand the synthesis mechanism and desodiation processes in clathrate materials and will help guide researchers in the design and evaluation of new open framework compounds as viable materials for energy storage applications.
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Solid-State Electrochemical Synthesis of Silicon Clathrates Using a Sodium-Sulfur Battery Inspired Approach
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 Na8Si46using electrochemical oxidation at 450 °C and 550 °C. A two-electrode cell design inspired by high-temperature sodium-sulfur batteries is employed, using Na4Si4as working electrode, Naβ″-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 Na4Si4and 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 Na8Si46is 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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- PAR ID:
- 10303793
- Publisher / Repository:
- The Electrochemical Society
- Date Published:
- Journal Name:
- Journal of The Electrochemical Society
- Volume:
- 168
- Issue:
- 2
- ISSN:
- 0013-4651
- Page Range / eLocation ID:
- Article No. 020516
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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