journal article·2024-02-12Open access

Branched Diamine Electrolytes for Na+-Solvent Cointercalation into Graphite

Zachary Tyson Gossage, Tomooki Hosaka, Ryoichi Tatara, Shinichi Komaba

ACS Applied Energy Materials· Volume 7· Issue 3

Abstract

High Resolution Image Download MS PowerPoint Slide Recently, graphite has been recognized as a potential negative electrode for sodium (Na)-ion batteries via the use of a solvent cointercalation mechanism. However, nearly all works exploring this mechanism have focused on glymes, which are stable for reversible cointercalation. Herein, we demonstrate branched diamines, such as 1,3-diaminopentane, as alternative cointercalating solvents showing initial capacities up to 130 mAh/g for graphite in Na cells. X-ray diffraction indicated a reversible and smaller expansion of the lattice compared to glymes, which nearly doubles the volumetric capacity. In all, our work indicates some appealing characteristics when amine electrolytes are cointercalated into graphite.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Graphene research and applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Applied Chemistry, Tokyo University of Science, Tokyo 162-8601, Japan

Funding

Ministry of Education, Culture, Sports, Science and Technology · Core Research for Evolutional Science and Technology · Japan Society for the Promotion of Science · TEPCO Memorial Foundation

References (28)

Show source-provided references
1. https://iupac.org/iupac-2022-top-ten/ (accessed December 2022).
2. 10.1246/cl.20056810.1246/cl.200568 ↗
3. 10.1016/j.jpowsour.2020.22887210.1016/j.jpowsour.2020.228872 ↗
4. 10.1038/s41467-019-10551-z10.1038/s41467-019-10551-z ↗
5. 10.1038/nchem.208510.1038/nchem.2085 ↗
6. 10.1039/D2SC00946C10.1039/D2SC00946C ↗
7. 10.1039/D0CS00187B10.1039/D0CS00187B ↗
8. 10.1016/j.elecom.2015.09.00210.1016/j.elecom.2015.09.002 ↗
9. 10.1080/0001873810010136710.1080/00018738100101367 ↗
10. 10.1002/anie.20140373410.1002/anie.201403734 ↗
11. 10.1021/acsami.9b0676010.1021/acsami.9b06760 ↗
12. 10.1038/ncomms503310.1038/ncomms5033 ↗
13. 10.1149/1945-7111/ac9c3310.1149/1945-7111/ac9c33 ↗
14. 10.1002/aenm.20170272410.1002/aenm.201702724 ↗
15. 10.1002/adfm.20140298410.1002/adfm.201402984 ↗
16. 10.1021/acsenergylett.2c0229510.1021/acsenergylett.2c02295 ↗
17. 10.1149/1.204418810.1149/1.2044188 ↗
18. 10.1039/D0TA12607A10.1039/D0TA12607A ↗
19. 10.1149/1.275298510.1149/1.2752985 ↗
20. 10.1002/aenm.20160151910.1002/aenm.201601519 ↗
21. 10.1021/ic201661y10.1021/ic201661y ↗
22. 10.1021/acs.jpcc.5b0301610.1021/acs.jpcc.5b03016 ↗
23. 10.1002/ente.20200088010.1002/ente.202000880 ↗
24. 10.1088/1361-6528/aac69a10.1088/1361-6528/aac69a ↗
25. 10.1016/j.elecom.2014.04.01410.1016/j.elecom.2014.04.014 ↗
26. 10.1002/anie.20200196610.1002/anie.202001966 ↗
27. 10.1002/batt.20230022810.1002/batt.202300228 ↗
28. 10.1126/science.aab159510.1126/science.aab1595 ↗