Sulfonate-Based Triazine Multiple-Electron Anolyte for Aqueous Organic Flow Batteries
Source abstract
Abstract
High Resolution Image Download MS PowerPoint Slide A new highly soluble triazine derivative (SPr) 3 4TpyTz showing three reversible redox processes with fast kinetics and high diffusion coefficients has been synthesized using an efficient, low-cost, and straightforward synthetic route. Concentrated single cell tests and DFT studies reveal a tendency of the reduced triazine species to form aggregates which could be avoided by tuning the supporting electrolyte concentration. Under the right conditions, (SPr) 3 4TpyTz shows no capacity decay and good Coulombic, voltage, and energy efficiencies for the storage of two electrons. The storage of further electrons leads to a higher capacity decay and an increase of the electrolyte pH, suggesting the irreversible protonation of the generated species. So, a plausible mechanism has been proposed. A higher concentration of (SPr) 3 4TpyTz shows slightly higher capacity decay and lower efficiencies due to the aggregate formation.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced battery technologies research · Membrane-based Ion Separation Techniques · Advanced Battery Materials and Technologies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Applied Physical Chemistry, Universidad Autónoma de Madrid, c/Fco. Tomás y Valiente 7, Cantoblanco, Madrid 28049, Spain
Department of Organic Chemistry, Universidad Autónoma de Madrid, Madrid 28049, Spain
Research Group of Battery Materials and Technologies, Department of Mechanical and Materials Engineering, Faculty of Technology, University of Turku, Turku 20014, Finland
Funding
Luonnontieteiden ja Tekniikan Tutkimuksen Toimikunta · H2020 European Research Council
References (29)
Show source-provided references
1. 10.1126/science.121274110.1126/science.1212741 ↗
2. 10.1021/cr100290v10.1021/cr100290v ↗
3. 10.1021/cr500720t10.1021/cr500720t ↗
4. 10.1002/aenm.20110000810.1002/aenm.201100008 ↗
5. 10.1039/c4ee02158d10.1039/c4ee02158d ↗
6. 10.1002/adma.20200213210.1002/adma.202002132 ↗
7. 10.1021/acs.energyfuels.0c0285510.1021/acs.energyfuels.0c02855 ↗
8. 10.1016/j.mtener.2020.10063410.1016/j.mtener.2020.100634 ↗
9. 10.1149/1945-7111/aba33810.1149/1945-7111/aba338 ↗
10. 10.3390/molecules2613382310.3390/molecules26133823 ↗
11. 10.1016/j.chempr.2019.04.02110.1016/j.chempr.2019.04.021 ↗
12. 10.1021/acsenergylett.7b0130210.1021/acsenergylett.7b01302 ↗
13. 10.1002/cssc.20200246710.1002/cssc.202002467 ↗
14. 10.1038/s41586-021-03399-110.1038/s41586-021-03399-1 ↗
15. 10.1039/d0se00687d10.1039/d0se00687d ↗
16. 10.3390/molecules2702056010.3390/molecules27020560 ↗
17. 10.1038/srep3910110.1038/srep39101 ↗
18. 10.1038/nature1290910.1038/nature12909 ↗
19. 10.1126/science.aab303310.1126/science.aab3033 ↗
20. 10.1038/nenergy.2016.10210.1038/nenergy.2016.102 ↗
21. 10.1038/ncomms1323010.1038/ncomms13230 ↗
22. 10.1016/j.chempr.2017.11.00110.1016/j.chempr.2017.11.001 ↗
23. 10.1002/anie.20171051710.1002/anie.201710517 ↗
24. 10.1021/acsmaterialslett.1c0066810.1021/acsmaterialslett.1c00668 ↗
25. 10.1002/anie.20210721610.1002/anie.202107216 ↗
26. 10.1002/wene.43910.1002/wene.439 ↗
27. 10.1002/anie.20211001010.1002/anie.202110010 ↗
28. 10.1002/anie.20221460110.1002/anie.202214601 ↗
29. 10.1039/c8cs00508g10.1039/c8cs00508g ↗