Synthesis of Pyrochlore-type Li 1.25 La 0.58 Nb 2 O 6 F Solid Electrolyte via Spark Plasma Sintering
Source abstract
Abstract
Oxide-based lithium-ion conductors are attractive due to their chemical stability. Among these, pyrochlore-type oxyfluorides have emerged as a solid electrolyte family with high ionic conductivity and strong water tolerance. However, their ionic conductivity remains lower than those of previously reported sulfide- and oxychloride-based solid electrolytes. In addition, sintered pellets exhibit poor densification, limiting lithium-ion transport. In this study, spark plasma sintering (SPS) was employed to prepare and densify pyrochlore-type Li 1.25 La 0.58 Nb 2 O 6 F solid electrolytes. SPS enables rapid synthesis within minutes compared to conventional solid-state synthesis and yields dense pellets with a relative density of 98%. Owing to the reduction of grain boundary resistance, the SPS-processed samples exhibited the highest bulk conductivity (15 mS cm –1 at 300 K) reported to date for oxide-based lithium-ion conductors. This study is significant in the development of oxide-based solid electrolytes, opening opportunities in a field long dominated by sulfide-, chloride-, and oxychloride-based systems.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Nuclear materials and radiation effects · Molten salt chemistry and electrochemical processes · Chemical Synthesis and Characterization
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
National Institute of Advanced Industrial Science and Technology (AIST), Midorigaoka 1-8-31, Ikeda, Osaka 56308577, Japan
Funding
Japan Society for the Promotion of Science
References (27)
Show source-provided references
1. 10.1016/j.jpowsour.2015.02.05410.1016/j.jpowsour.2015.02.054 ↗
2. 10.1016/j.nanoen.2017.01.02810.1016/j.nanoen.2017.01.028 ↗
3. 10.1038/nenergy.2016.14110.1038/nenergy.2016.141 ↗
4. 10.1039/C8EE01053F10.1039/C8EE01053F ↗
5. 10.1016/j.jpowsour.2018.04.02210.1016/j.jpowsour.2018.04.022 ↗
6. 10.1021/acs.chemrev.4c0089410.1021/acs.chemrev.4c00894 ↗
7. 10.1021/acsenergylett.4c0246010.1021/acsenergylett.4c02460 ↗
8. 10.1038/nmat306610.1038/nmat3066 ↗
9. 10.1126/science.add713810.1126/science.add7138 ↗
10. 10.1002/adma.20180307510.1002/adma.201803075 ↗
11. 10.1038/s41570-023-00541-710.1038/s41570-023-00541-7 ↗
12. 10.1007/s41918-023-00179-510.1007/s41918-023-00179-5 ↗
13. 10.1002/anie.20221758110.1002/anie.202217581 ↗
14. 10.1016/j.ensm.2024.10335910.1016/j.ensm.2024.103359 ↗
15. 10.1021/acs.chemmater.5c0062710.1021/acs.chemmater.5c00627 ↗
16. 10.1021/jacs.4c0314210.1021/jacs.4c03142 ↗
17. 10.1021/acs.chemrev.9b0042710.1021/acs.chemrev.9b00427 ↗
18. 10.1016/j.ensm.2018.10.01210.1016/j.ensm.2018.10.012 ↗
19. 10.1111/j.1151-2916.2003.tb03318.x10.1111/j.1151-2916.2003.tb03318.x ↗
20. 10.1149/1.209669310.1149/1.2096693 ↗
21. 10.1016/0038-1098(93)90841-A10.1016/0038-1098(93)90841-A ↗
22. 10.1021/acs.chemmater.3c0328810.1021/acs.chemmater.3c03288 ↗
23. 10.1016/j.ssi.2025.11692410.1016/j.ssi.2025.116924 ↗
24. 10.1016/j.mser.2008.09.00310.1016/j.mser.2008.09.003 ↗
25. 10.1002/adem.20130040910.1002/adem.201300409 ↗
26. 10.1002/adem.20200005110.1002/adem.202000051 ↗
27. 10.1002/ejic.20100059910.1002/ejic.201000599 ↗