Oxide Solid-State Sodium Batteries Sintered at 400 °C Using an NaBO2·4H2O Sintering Aid
Source abstract
Abstract
In this study, a Na 3.1 Zr 1.95 Mg 0.05 (SiO 4 ) 2 (PO 4 ) (NZMSP) solid electrolyte is successfully densified at 400 °C by employing NaBO 2 ·4H 2 O (NBO2) as a sintering aid. The NZMSP solid electrolyte containing 20 wt % NBO2 shows a total ionic conductivity of 3.3 × 10 –4 S cm –1 at 25 °C and demonstrates more stable Na deposition/stripping cycles compared with samples without NBO2. Although the Na 3 V 2 (PO 4 ) 3 (NVP) active material sintered with NZMSP containing 20 wt % NBO2 decomposes after sintering, NVP with 1 or 5 wt % NBO2 remains mostly intact. An Na/NZMSP/NVP battery containing 5 wt % NBO2 exhibits an initial discharge capacity of 171 mAh g –1 at 1.0–4.0 V vs Na + /Na, which is comparable to the theoretical capacity, 176.4 mAh g –1 . Additionally, a symmetric NVP/NZMSP/NVP battery containing 5 wt % NBO2 is operated with an initial discharge capacity of 70.4 mAh g –1 . This study demonstrates that the NBO2 sintering aid enables cost-effective, low-temperature fabrication of oxide solid-state sodium batteries.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Battery Materials and Technologies · Advancements in Battery Materials · Thermal Expansion and Ionic Conductivity
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Central Research Institute of Electric Power Industry, 2-6-1 Nagasaka, Yokosuka, Kanagawa 240-0196, Japan
Funding
Japan Society for the Promotion of Science
References (25)
Show source-provided references
1. 10.1038/s41560-023-01208-910.1038/s41560-023-01208-9 ↗
2. 10.1038/natrevmats.2016.10310.1038/natrevmats.2016.103 ↗
3. 10.1002/aenm.20170301210.1002/aenm.201703012 ↗
4. 10.1021/cr500192f10.1021/cr500192f ↗
5. 10.1063/5.015155910.1063/5.0151559 ↗
6. 10.1038/srep3233010.1038/srep32330 ↗
7. 10.1039/C9TA00048H10.1039/C9TA00048H ↗
8. 10.1016/j.jpowsour.2021.23076510.1016/j.jpowsour.2021.230765 ↗
9. 10.1002/advs.20160027510.1002/advs.201600275 ↗
10. 10.1038/s41560-020-00759-510.1038/s41560-020-00759-5 ↗
11. 10.1016/j.electacta.2012.11.03810.1016/j.electacta.2012.11.038 ↗
12. 10.1111/jace.1528810.1111/jace.15288 ↗
13. 10.1016/j.scriptamat.2017.10.01010.1016/j.scriptamat.2017.10.010 ↗
14. 10.1021/acsaem.0c0004710.1021/acsaem.0c00047 ↗
15. 10.1021/acsami.1c1391310.1021/acsami.1c13913 ↗
16. 10.1016/j.jpowsour.2018.04.06710.1016/j.jpowsour.2018.04.067 ↗
17. 10.1021/acsaem.2c0036510.1021/acsaem.2c00365 ↗
18. 10.1016/j.jpowsour.2013.09.05110.1016/j.jpowsour.2013.09.051 ↗
19. 10.1002/batt.20230007510.1002/batt.202300075 ↗
20. 10.1016/j.ijhydene.2011.12.10610.1016/j.ijhydene.2011.12.106 ↗
21. 10.1017/CBO978051152479010.1017/CBO9780511524790 ↗
22. 10.1002/aenm.20120080310.1002/aenm.201200803 ↗
23. 10.1016/j.solidstatesciences.2017.08.01710.1016/j.solidstatesciences.2017.08.017 ↗
24. 10.1021/acsaem.0c0082010.1021/acsaem.0c00820 ↗
25. 10.1002/aenm.20190288110.1002/aenm.201902881 ↗