Rare-Earth Element Substitution of Na1+xZr2SixP3–xO12 (x = 2) Solid Electrolyte: Implications for All-Solid-State Na Ion Batteries
Source abstract
Abstract
Along with the widening application and growing market size of energy storage devices, the development of cost-effective rechargeable batteries with a high level of operational safety has become a major challenge. To this end, an all-solid-state battery (ASSB), which is composed of a thin film instead of a liquid, is an attractive candidate. In this study, we investigated a facile method for preparing sodium superionic conductor structured Na1+xZr2SixP3–xO12 (0 ≤ x ≤ 3, NZSP). Various attempts were made to improve the sinterability of NZSP, but the results are still unsatisfactory. We employed the reaction sintering method so that the phase formation and densification proceeded simultaneously, resulting in the densification of NZSP with minimal impurities. Furthermore, we successfully substituted rare-earth elements (REs) into the Zr site of the NZSP to tune its structural properties in the nanoscale and improve its ionic conductivity. Electrochemical impedance spectroscopy results confirmed the improvement of the ionic conductivity of both the pristine NZSP and the RE-doped variant, indicating the effectiveness of reaction sintering. When reaction sintering and RE substitution were employed together, La-doped NZSP was an attractive solid electrolyte for application in ASSBs. Our results highlight the effectiveness of reaction sintering for obtaining an impurity-free and highly dense multicomponent compound.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Thermal Expansion and Ionic Conductivity
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials Science and Engineering, Korea Advanced Institute of Science and Technology, Daejeon 34141, Republic of Korea
School of Chemistry, The University of New South Wales, Sydney 2052, NSW, Australia
Department of Engineering Ceramics, Korea Institute of Materials Science, Changwon 51508, Gyeongnam, Republic of Korea
Funding
National Research Foundation of Korea · Ministry of Trade, Industry and Energy · Australian Research Council
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