Ortmann, Till ; Burkhardt, Simon ; Eckhardt, Janis Kevin ; Fuchs, Till ; Ding, Ziming ; Sann, Joachim ; Rohnke, Marcus ; Ma, Qianli ; Tietz, Frank ; Fattakhova‐Rohlfing, Dina ; Kübel, Christian ; Guillon, Olivier ; Heiliger, Christian ; Janek, Jürgen (2022)
Kinetics and Pore Formation of the Sodium Metal Anode on NASICON‐Type Na₃.₄Zr₂Si₂.₄P₀.₆O₁₂ for Sodium Solid‐State Batteries.
In: Advanced Energy Materials, 13 (5)
doi: 10.1002/aenm.202202712
Artikel, Bibliographie
Dies ist die neueste Version dieses Eintrags.
Kurzbeschreibung (Abstract)
In recent years, many efforts have been made to introduce reversible alkali metal anodes using solid electrolytes in order to increase the energy density of next‐generation batteries. In this respect, Na₃.₄Zr₂Si₂.₄P₀.₆O₁₂ is a promising solid electrolyte for solid‐state sodium batteries, due to its high ionic conductivity and apparent stability versus sodium metal. The formation of a kinetically stable interphase in contact with sodium metal is revealed by time‐resolved impedance analysis, in situ X‐ray photoelectron spectroscopy, and transmission electron microscopy. Based on pressure‐ and temperature‐dependent impedance analyses, it is concluded that the Na|Na₃.₄Zr₂Si₂.₄P₀.₆O₁₂interface kinetics is dominated by current constriction rather than by charge transfer. Cross‐sections of the interface after anodic dissolution at various mechanical loads visualize the formed pore structure due to the accumulation of vacancies near the interface. The temporal evolution of the pore morphology after anodic dissolution is monitored by time‐resolved impedance analysis. Equilibration of the interface is observed even under extremely low external mechanical load, which is attributed to fast vacancy diffusion in sodium metal, while equilibration is faster and mainly caused by creep at increased external load. The presented information provides useful insights into a more profound evaluation of the sodium metal anode in solid‐state batteries.
| Typ des Eintrags: | Artikel |
|---|---|
| Erschienen: | 2022 |
| Autor(en): | Ortmann, Till ; Burkhardt, Simon ; Eckhardt, Janis Kevin ; Fuchs, Till ; Ding, Ziming ; Sann, Joachim ; Rohnke, Marcus ; Ma, Qianli ; Tietz, Frank ; Fattakhova‐Rohlfing, Dina ; Kübel, Christian ; Guillon, Olivier ; Heiliger, Christian ; Janek, Jürgen |
| Art des Eintrags: | Bibliographie |
| Titel: | Kinetics and Pore Formation of the Sodium Metal Anode on NASICON‐Type Na₃.₄Zr₂Si₂.₄P₀.₆O₁₂ for Sodium Solid‐State Batteries |
| Sprache: | Englisch |
| Publikationsjahr: | 2022 |
| Ort: | Darmstadt |
| Verlag: | Wiley-VCH |
| Titel der Zeitschrift, Zeitung oder Schriftenreihe: | Advanced Energy Materials |
| Jahrgang/Volume einer Zeitschrift: | 13 |
| (Heft-)Nummer: | 5 |
| Kollation: | 17 Seiten |
| DOI: | 10.1002/aenm.202202712 |
| Zugehörige Links: | |
| Kurzbeschreibung (Abstract): | In recent years, many efforts have been made to introduce reversible alkali metal anodes using solid electrolytes in order to increase the energy density of next‐generation batteries. In this respect, Na₃.₄Zr₂Si₂.₄P₀.₆O₁₂ is a promising solid electrolyte for solid‐state sodium batteries, due to its high ionic conductivity and apparent stability versus sodium metal. The formation of a kinetically stable interphase in contact with sodium metal is revealed by time‐resolved impedance analysis, in situ X‐ray photoelectron spectroscopy, and transmission electron microscopy. Based on pressure‐ and temperature‐dependent impedance analyses, it is concluded that the Na|Na₃.₄Zr₂Si₂.₄P₀.₆O₁₂interface kinetics is dominated by current constriction rather than by charge transfer. Cross‐sections of the interface after anodic dissolution at various mechanical loads visualize the formed pore structure due to the accumulation of vacancies near the interface. The temporal evolution of the pore morphology after anodic dissolution is monitored by time‐resolved impedance analysis. Equilibration of the interface is observed even under extremely low external mechanical load, which is attributed to fast vacancy diffusion in sodium metal, while equilibration is faster and mainly caused by creep at increased external load. The presented information provides useful insights into a more profound evaluation of the sodium metal anode in solid‐state batteries. |
| Freie Schlagworte: | current constriction, impedance spectroscopy, interphase growth, NASICON electrolytes, SEI formation, sodium metal anodes |
| Sachgruppe der Dewey Dezimalklassifikatin (DDC): | 500 Naturwissenschaften und Mathematik > 530 Physik 600 Technik, Medizin, angewandte Wissenschaften > 660 Technische Chemie |
| Fachbereich(e)/-gebiet(e): | 11 Fachbereich Material- und Geowissenschaften 11 Fachbereich Material- und Geowissenschaften > Materialwissenschaft 11 Fachbereich Material- und Geowissenschaften > Materialwissenschaft > In-Situ Elektronenmikroskopie |
| Hinterlegungsdatum: | 02 Aug 2024 12:52 |
| Letzte Änderung: | 02 Aug 2024 12:52 |
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Verfügbare Versionen dieses Eintrags
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Kinetics and Pore Formation of the Sodium Metal Anode on NASICON‐Type Na₃.₄Zr₂Si₂.₄P₀.₆O₁₂ for Sodium Solid‐State Batteries. (deposited 12 Mai 2023 08:57)
- Kinetics and Pore Formation of the Sodium Metal Anode on NASICON‐Type Na₃.₄Zr₂Si₂.₄P₀.₆O₁₂ for Sodium Solid‐State Batteries. (deposited 02 Aug 2024 12:52) [Gegenwärtig angezeigt]
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