Redox Targeting-Based Vanadium Redox-Flow Battery
Source abstract
Abstract
The low energy density and narrow operating temperature window besides the relatively high cost of the vanadium redox-flow battery (VRB) severely hinder its commercial deployment. Herein, in conjunction with low-concentration VO2+/VO2+ catholyte, we introduce a redox targeting-based VRB (RT-VRB) system in which a Prussian blue analogue (PBA), (VO)6[Fe(CN)6]3, is employed as a capacity booster to address the above issues. The charges are reversibly stored in the PBA loaded in the cathodic tank via a redox-targeting reaction with the VO2+/VO2+. Therefore, the concentration of catholyte has been reduced to 0.6 M without sacrificing the capacity. This provides ample room to broaden the operating temperature window of a RT-VRB relative to a conventional VRB. The theoretical volumetric capacity of the PBA could reach 135 Ah/L, which is more than 3 times that of VRB. We anticipate that the RT-VRB system demonstrated here would give credible impetus for VRB chemistry for robust and high-density energy storage applications.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced battery technologies research · Advancements in Battery Materials · Supercapacitor Materials and Fabrication
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials Science and Engineering, Faculty of Engineering, National University of Singapore, 117576 Singapore
School of Chemical, Biological, and Environmental Engineering, Oregon State University, Corvallis, Oregon 97331, United States
Institute of Chemical and Engineering Sciences, 1 Pesek Road, Jurong Island 627833, Singapore
Funding
Energy Market Authority of Singapore · U.S. Department of Energy · National Science Foundation
References (27)
Show source-provided references
1. 10.1126/science.121274110.1126/science.1212741 ↗
2. 10.1021/cr100290v10.1021/cr100290v ↗
3. 10.1002/admi.20150030910.1002/admi.201500309 ↗
4. 10.1039/c0ee00770f10.1039/c0ee00770f ↗
5. 10.1016/j.jpowsour.2008.12.11310.1016/j.jpowsour.2008.12.113 ↗
6. 10.1016/j.memsci.2018.11.00910.1016/j.memsci.2018.11.009 ↗
7. 10.1007/s10800-011-0312-110.1007/s10800-011-0312-1 ↗
8. 10.1149/2.006306jes10.1149/2.006306jes ↗
9. 10.1016/j.jpowsour.2016.11.07110.1016/j.jpowsour.2016.11.071 ↗
10. 10.1016/j.electacta.2011.03.04810.1016/j.electacta.2011.03.048 ↗
11. 10.1002/aenm.20110000810.1002/aenm.201100008 ↗
12. 10.1039/C5EE03764F10.1039/C5EE03764F ↗
13. 10.1126/sciadv.150088610.1126/sciadv.1500886 ↗
14. 10.1016/j.electacta.2019.13470410.1016/j.electacta.2019.134704 ↗
15. 10.1002/aenm.20160149110.1002/aenm.201601491 ↗
16. 10.1039/C7TA02660A10.1039/C7TA02660A ↗
17. 10.1016/j.nanoen.2019.10394110.1016/j.nanoen.2019.103941 ↗
18. 10.3891/acta.chem.scand.27-348210.3891/acta.chem.scand.27-3482 ↗
19. 10.1039/C6RA26731A10.1039/C6RA26731A ↗
20. 10.1039/c3cp54428a10.1039/c3cp54428a ↗
21. 10.1039/c0jm00174k10.1039/c0jm00174k ↗
22. 10.1021/ac950380k10.1021/ac950380k ↗
23. 10.1021/acsami.6b0159210.1021/acsami.6b01592 ↗
24. 10.1039/C6RA13385A10.1039/C6RA13385A ↗
25. 10.1002/chem.20140306110.1002/chem.201403061 ↗
26. 10.1016/j.nanoen.2018.07.05810.1016/j.nanoen.2018.07.058 ↗
27. 10.1021/jp410499210.1021/jp4104992 ↗