Turning Adversity into Advantage: Investigating the Capacity Decay Mode of Carboxylate Functionalized-Anthraquinone in Organic Redox Flow Batteries
Source abstract
Abstract
Organic redox-molecule-based flow batteries (ORFB) are considered a potential alternative to the inorganic counterparts in flow battery systems as, technically speaking, organic materials are ubiquitous and can be synthesized anywhere. Nevertheless, they were also known to degrade in a multitude of ways in flow battery ambience. In this study, 4,4′-((9,10-dioxo-9,10-dihydroanthracene-1,5-diyl)bis(oxy))dibutyric acid (1,5-DCAQ) is used as an anolyte in alkaline media. As carboxylate interacts intramolecularly with the carbonyl group of 1,5-DCAQ, the aromatic portion of the molecule exhibits an association with the Nafion membrane separator through lipophilic interaction, causing capacity decay of the cell. We have modified this curse into a boon by functionalizing the thermally activated graphite felt anode with the Nafion ionomer, thereby retaining the redox molecule around the electrode instead of the membrane, achieving 99.9% of theoretical capacity and 95% Coulombic efficiency at 15 mA cm –2 current density. As this molecule exhibits a solubility of 0.5 M, the system with suitable optimization is expected to deliver a solubility of up to 26.8 Ah L –1 .
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced battery technologies research · Advanced Battery Technologies Research · Electrochemical Analysis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Clean Energy Laboratory, Department of Chemistry, Indian Institute of Technology Madras, Chennai, Tamil Nadu 600036, India
Funding
Indian Institute of Technology Madras · Department of Science and Technology, Ministry of Science and Technology, India · Ministry of Education, India
References (26)
Show source-provided references
1. Kittner N. · 2020 · 11910.1016/B978-0-12-818762-3.00008-X ↗
2. 10.1016/j.enconman.2014.07.06310.1016/j.enconman.2014.07.063 ↗
3. 10.1016/j.jpowsour.2012.10.06010.1016/j.jpowsour.2012.10.060 ↗
4. 10.1016/j.ensm.2021.02.03210.1016/j.ensm.2021.02.032 ↗
5. 10.1021/acsaem.3c0079910.1021/acsaem.3c00799 ↗
6. 10.1007/s12039-023-02244-410.1007/s12039-023-02244-4 ↗
7. 10.1016/j.est.2019.10084410.1016/j.est.2019.100844 ↗
8. 10.1149/1945-7111/ac311410.1149/1945-7111/ac3114 ↗
9. 10.1007/s40820-023-01174-710.1007/s40820-023-01174-7 ↗
10. 10.1002/9783527832767.ch3610.1002/9783527832767.ch36 ↗
11. 10.1016/j.jpowsour.2020.22944510.1016/j.jpowsour.2020.229445 ↗
12. 10.3390/molecules2702056010.3390/molecules27020560 ↗
13. 10.1038/srep3910110.1038/srep39101 ↗
14. 10.1149/2.1001409jes10.1149/2.1001409jes ↗
15. 10.1021/acsami.3c0808910.1021/acsami.3c08089 ↗
16. 10.1016/j.jechem.2022.11.05310.1016/j.jechem.2022.11.053 ↗
17. 10.1021/acsaem.2c0283310.1021/acsaem.2c02833 ↗
18. 10.1016/j.chempr.2019.04.02110.1016/j.chempr.2019.04.021 ↗
19. 10.1021/acs.inorgchem.1c0147310.1021/acs.inorgchem.1c01473 ↗
20. 10.1126/science.aab303310.1126/science.aab3033 ↗
21. 10.1021/acsaem.2c0139210.1021/acsaem.2c01392 ↗
22. 10.1016/j.cattod.2020.12.01210.1016/j.cattod.2020.12.012 ↗
23. 10.1134/S003602361106016710.1134/S0036023611060167 ↗
24. 10.1139/v84-15810.1139/v84-158 ↗
25. 10.1021/ja807961s10.1021/ja807961s ↗
26. 10.1016/j.drudis.2009.07.01410.1016/j.drudis.2009.07.014 ↗