journal article·2019-08-26

Symmetric Phthalocyanine Charge Carrier for Dual Redox Flow Battery/Capacitor Applications

Camden Hunt, Maxwell Mattejat, Cassidy Anderson, Lior Sepunaru, Gabriel Ménard

ACS Applied Energy Materials· Volume 2· Issue 8
Publisher page

Abstract

Utilizing a slurry-based symmetric charge carrier coupled with a conductive carbon additive is a promising method for developing simple, low-cost, and stable hybrid electrochemical flow systems for energy storage. Here, we used a manganese nitride 1,4,8,11,15,18,22,25-octaethoxyphthalocyanine (EtOPcMnN; 1) as a five-redox-state symmetric charge carrier for slurry-based dual redox flow battery/capacitor applications. Electrochemical analyses of 1 revealed a wide voltage gap, fast heterogeneous electron-transfer rates, and excellent stability toward galvanostatic cycling. Slurry-state static cell measurements utilizing 1 with a conductive carbon additive, Ketjenblack, were performed and showed high faradaic efficiency and minimal capacity fade using a glass frit porous separator.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advanced battery technologies research · Supercapacitor Materials and Fabrication · Electrocatalysts for Energy Conversion

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

Affiliations

Department of Chemistry and Biochemistry, University of California, Santa Barbara, California 93106, United States

Funding

University of California, Santa Barbara · California Nanosystems Institute

References (30)

Show source-provided references
1. 10.1126/science.121274110.1126/science.1212741 ↗
2. 10.1021/cr100290v10.1021/cr100290v ↗
3. 10.1007/s10800-011-0348-210.1007/s10800-011-0348-2 ↗
4. IEA Energy Storage: Tracking Clean Energy Progress. https://www.iea.org/tcep/energyintegration/energystorage/ (accessed May 2019).
5. 10.1021/acsaem.8b0187410.1021/acsaem.8b01874 ↗
6. 10.1039/C8EE00686E10.1039/C8EE00686E ↗
7. 10.1126/science.aab303310.1126/science.aab3033 ↗
8. 10.1039/C8TA03312A10.1039/C8TA03312A ↗
9. 10.1021/cr500720t10.1021/cr500720t ↗
10. 10.1039/c3cp53428f10.1039/c3cp53428f ↗
11. 10.1002/aenm.20110015210.1002/aenm.201100152 ↗
12. 10.1039/C6TA08733G10.1039/C6TA08733G ↗
13. 10.1002/aenm.20110076810.1002/aenm.201100768 ↗
14. 10.1149/2.0011505jes10.1149/2.0011505jes ↗
15. 10.1002/anie.20171342310.1002/anie.201713423 ↗
16. 10.1021/jacs.8b1289910.1021/jacs.8b12899 ↗
17. Leznoff C. C. · 1989
18. USITC. Industry & Trade Summary: Synthetic Organic Pigments. https://www.usitc.gov/publications/docs/pubs/industry_trade_summaries/pub3021.pdf (accessed May 1, 2019).
19. 10.1021/acsenergylett.7b0026110.1021/acsenergylett.7b00261 ↗
20. 10.1039/C5EE02341F10.1039/C5EE02341F ↗
21. 10.1016/j.elecom.2009.10.00610.1016/j.elecom.2009.10.006 ↗
22. Zanello P. · 200310.1039/9781847551146 ↗
23. BASi. DigiSim Simulation Software for Cyclic Voltammetry. http://www.basinc.com/products/ec/digisim/ (accessed May 2019).
24. 10.1021/acscentsci.7b0054410.1021/acscentsci.7b00544 ↗
25. 10.1021/ac60230a01610.1021/ac60230a016 ↗
26. 10.1002/elan.20030285110.1002/elan.200302851 ↗
27. 10.1149/2.0971602jes10.1149/2.0971602jes ↗
28. 10.1039/c3ra00115f10.1039/c3ra00115f ↗
29. 10.1149/2.0891807jes10.1149/2.0891807jes ↗
30. 10.1039/C2CP44466F10.1039/C2CP44466F ↗