This title appears in the Scientific Report :
2023
Please use the identifier:
http://hdl.handle.net/2128/34040 in citations.
Please use the identifier: http://dx.doi.org/10.1002/aenm.202202712 in citations.
Kinetics and Pore Formation of the Sodium Metal Anode on NASICON‐Type Na 3.4 Zr 2 Si 2.4 P 0.6 O 12 for Sodium Solid‐State Batteries
Kinetics and Pore Formation of the Sodium Metal Anode on NASICON‐Type Na 3.4 Zr 2 Si 2.4 P 0.6 O 12 for Sodium Solid‐State Batteries
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...
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Personal Name(s): | Ortmann, Till (Corresponding author) |
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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 (Corresponding author) | |
Contributing Institute: |
Werkstoffsynthese und Herstellungsverfahren; IEK-1 |
Published in: | Advanced energy materials, 13 (2023) 5, S. 2202712 |
Imprint: |
Weinheim
Wiley-VCH
2023
|
DOI: |
10.1002/aenm.202202712 |
Document Type: |
Journal Article |
Research Program: |
Batteries in Application |
Link: |
OpenAccess OpenAccess |
Publikationsportal JuSER |
Please use the identifier: http://dx.doi.org/10.1002/aenm.202202712 in citations.
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 conduc-tivity 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 transmis-sion electron microscopy. Based on pressure- and temperature-dependent impedance analyses, it is concluded that the Na|Na3.4Zr2Si2.4P0.6O12 interface 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 equilibra-tion is faster and mainly caused by creep at increased external load. The pre-sented information provides useful insights into a more profound evaluation of the sodium metal anode in solid-state batteries. |