High-Voltage Symmetric Nonaqueous Redox Flow Battery Based on Modularly Tunable [Ru2M(μ3-O)(CH3CO2)6(py)3] (M = Ru, Mn, Co, Ni, Zn) Cluster Compounds with Multielectron Storage Capability
Source abstract
Abstract
Redox flow batteries (RFBs) provide an attractive solution for large-scale energy buffering and storage. This report describes the development of nonaqueous RFBs based on trimetallic coordination cluster compounds: [Ru2M(μ3-O)(CH3CO2)6(py)3] (M = Ru, Mn, Co, Ni, Zn). The all-ruthenium complex exhibited stable battery cycles in anolyte–catholyte symmetric operation, with rarely observed multielectron storage in a single molecule. Moreover, the complex holds modularly tunable synthetic handles for systematic improvements in solubility and redox potentials. An optimized battery stack containing [Ru3(μ3-O)(CH3CO2)6(py)3]+ anolyte and [Ru2Co(μ3-O)(CH3CO2)6(py)3] catholyte yielded stable cycles with a discharge voltage of 2.4 V, comparable to the state-of-the-art nonaqueous RFBs. Explanation for the exceptional stability of the charged states and prediction of systematic tunability of the redox potentials of the cluster compounds were assisted by DFT calculations.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced battery technologies research · Electrocatalysts for Energy Conversion · Advancements in Battery Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, Yonsei University, 50 Yonsei-ro, Seodaemun-gu, Seoul 03722, Republic of Korea
Department of Chemistry, Sookmyung Women’s University, 100 Cheongpa-ro 47 gil, Yongsan-gu, Seoul 04310, Republic of Korea
Funding
National Research Foundation of Korea
References (34)
Show source-provided references
1. 10.1109/TEC.2003.82230510.1109/TEC.2003.822305 ↗
2. 10.1126/science.121274110.1126/science.1212741 ↗
3. 10.1039/C8EE01419A10.1039/C8EE01419A ↗
4. 10.1021/cr500720t10.1021/cr500720t ↗
5. 10.1002/adfm.20120069410.1002/adfm.201200694 ↗
6. 10.1002/anie.20160492510.1002/anie.201604925 ↗
7. 10.1016/j.est.2019.10084410.1016/j.est.2019.100844 ↗
8. 10.1002/adma.20190202510.1002/adma.201902025 ↗
9. 10.1038/natrevmats.2016.8010.1038/natrevmats.2016.80 ↗
10. 10.1039/C6EE02057G10.1039/C6EE02057G ↗
11. 10.1021/jacs.7b0875110.1021/jacs.7b08751 ↗
12. 10.1002/anie.20171342310.1002/anie.201713423 ↗
13. 10.1002/anie.20211193910.1002/anie.202111939 ↗
14. 10.1016/j.coelec.2019.08.00610.1016/j.coelec.2019.08.006 ↗
15. 10.1002/cssc.20200235410.1002/cssc.202002354 ↗
16. 10.1039/D0TA07891C10.1039/D0TA07891C ↗
17. 10.1021/acsaem.0c0235010.1021/acsaem.0c02350 ↗
18. 10.1021/acssuschemeng.1c0719010.1021/acssuschemeng.1c07190 ↗
19. 10.1021/ic50190a00710.1021/ic50190a007 ↗
20. 10.1039/DT974000078610.1039/DT9740000786 ↗
21. 10.1039/C7DT01152K10.1039/C7DT01152K ↗
22. 10.1246/bcsj.65.158510.1246/bcsj.65.1585 ↗
23. 10.1016/S0020-1693(00)85165-810.1016/S0020-1693(00)85165-8 ↗
24. 10.1021/acs.jpcc.1c0154410.1021/acs.jpcc.1c01544 ↗
25. 10.1021/acsanm.0c0117010.1021/acsanm.0c01170 ↗
26. 10.1021/acs.inorgchem.8b0278010.1021/acs.inorgchem.8b02780 ↗
27. 10.1021/ic00085a00310.1021/ic00085a003 ↗
28. 10.1039/C5EE02341F10.1039/C5EE02341F ↗
29. 10.1039/C7TA01285C10.1039/C7TA01285C ↗
30. 10.1021/jacs.9b0734510.1021/jacs.9b07345 ↗
31. 10.1038/s41467-020-17662-y10.1038/s41467-020-17662-y ↗
32. 10.1016/j.jpowsour.2015.02.08310.1016/j.jpowsour.2015.02.083 ↗
33. 10.1021/acssuschemeng.9b0724410.1021/acssuschemeng.9b07244 ↗
34. 10.1021/acsaem.0c0273310.1021/acsaem.0c02733 ↗