Source abstract
Abstract
Sodium all-solid-state batteries may become a novel storage technology overcoming the safety and energy density issues of (liquid-based) sodium ion batteries at low cost and good resource availability. However, compared to liquid electrolyte cells, contact issues and capacity losses due to interface reactions leading to high cell resistance are still a problem in solid-state batteries. In particular, sulfide-based electrolytes, which show very high ionic conductivity and good malleability, exhibit degradation reactions at the interface with electrode materials and carbon additives. A new group of solid electrolytes, i.e., sodium halides, shows wider potential windows and better stability at typical cathode potentials. A detailed investigation of the interface reactions of Na 3 SbS 4 and Na 2.4 Er 0.4 Zr 0.6 Cl 6 as catholytes in cathodes and their cycling performance in full cells is performed. X-ray spectroscopy, time-of-flight spectrometry, and impedance spectroscopy are used to study the interface of each catholyte with a transition metal oxide cathode active material. In addition, impedance measurements were used to study the separator electrolyte Na 3 SbS 4 with the catholyte Na 2.4 Er 0.4 Zr 0.6 Cl 6 . In conclusion, cathodes with Na 2.4 Er 0.4 Zr 0.6 Cl 6 show a higher stability at low C-rates, resulting in lower interfacial resistance and improved cycling performance.
Source: openalex_inverted_index · Quality: baseline
Affiliations
Institute for Physical Chemistry, Justus Liebig University Giessen, Giessen 35392, Germany
Center for Materials Research (ZfM), Justus Liebig University Giessen, Giessen 35392, Germany
Institute for Inorganic and Analytical Chemistry, University of Münster, Münster 48149, Germany
Institute of Chemistry, Humboldt University Berlin, Berlin 12489, Germany
Institut für Energie-und Klimaforschung (IEK), IEK-12: Helmholtz-Institut Münster, Forschungszentrum Jülich, Münster 48149, Germany
Funding
Bundesministerium f?r Bildung und Forschung · Deutsche Forschungsgemeinschaft