Electrodeposited MnOx/PEDOT Composite Thin Films for the Oxygen Reduction Reaction
Source abstract
Abstract
Manganese oxide (MnOx) was anodically coelectrodeposited with poly(3,4-ethylenedioxythiophene) (PEDOT) from an aqueous solution of Mn(OAc)2, 3,4-ethylenedioxythiophene, LiClO4 and sodium dodecyl sulfate to yield a MnOx/PEDOT composite thin film. The MnOx/PEDOT film showed significant improvement over the MnOx only and PEDOT only films for the oxygen reduction reaction, with a >0.2 V decrease in onset and half-wave overpotential and >1.5 times increase in current density. Furthermore, the MnOx/PEDOT films were competitive with commercial benchmark 20% Pt/C, outperforming it in the half-wave ORR region and exhibiting better electrocatalytic selectivity for the oxygen reduction reaction upon methanol exposure. The high activity of the MnOx/PEDOT composite is attributed to synergistic charge transfer capabilities, attained by coelectrodepositing MnOx with a conductive polymer while simultaneously achieving intimate substrate contact.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Conducting polymers and applications · Electrocatalysts for Energy Conversion · Advanced battery technologies research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials, Devices & Energy Technologies, Sandia National Laboratories, Albuquerque, New Mexico 87185, United States
Funding
Laboratory Directed Research and Development
References (35)
Show source-provided references
1. 10.1016/j.nanoen.2014.09.00910.1016/j.nanoen.2014.09.009 ↗
2. 10.1039/C5CC02262B10.1039/C5CC02262B ↗
3. 10.1039/c2cc32971a10.1039/c2cc32971a ↗
4. 10.1039/c2cp40841d10.1039/c2cp40841d ↗
5. 10.1021/ja104587v10.1021/ja104587v ↗
6. 10.1016/S0926-860X(98)00430-X10.1016/S0926-860X(98)00430-X ↗
7. 10.1149/1.154167510.1149/1.1541675 ↗
8. 10.1016/j.micromeso.2009.04.00810.1016/j.micromeso.2009.04.008 ↗
9. 10.1039/c1ee01942b10.1039/c1ee01942b ↗
10. 10.1016/j.powtec.2012.01.02410.1016/j.powtec.2012.01.024 ↗
11. 10.1002/elan.20130025410.1002/elan.201300254 ↗
12. 10.1002/anie.20110925710.1002/anie.201109257 ↗
13. Elschner A. · 201010.1201/b10318 ↗
14. 10.1039/cc996000272310.1039/cc9960002723 ↗
15. 10.1149/1.211983810.1149/1.2119838 ↗
16. 10.1016/j.electacta.2010.02.03010.1016/j.electacta.2010.02.030 ↗
17. 10.1021/ja711238210.1021/ja7112382 ↗
18. 10.1016/j.electacta.2012.11.03410.1016/j.electacta.2012.11.034 ↗
19. 10.1186/s11671-015-0859-610.1186/s11671-015-0859-6 ↗
20. Wu Z. Y. · Int. J. Electrochem. Sci. · 2012 · 7 · 123010.1016/S1452-3981(23)13410-9 ↗
21. 10.1021/jp503986510.1021/jp5039865 ↗
22. 10.1039/c3ra46167j10.1039/c3ra46167j ↗
23. Ma J. · Int. J. Electrochem. Sci. · 2015 · 10 · 456210.1016/S1452-3981(23)06645-2 ↗
24. 10.1039/c2jm32106h10.1039/c2jm32106h ↗
25. 10.1021/am405771y10.1021/am405771y ↗
26. 10.1021/am506459f10.1021/am506459f ↗
27. 10.1002/smll.20130364210.1002/smll.201303642 ↗
28. 10.1126/science.115926710.1126/science.1159267 ↗
29. 10.1016/j.electacta.2013.11.16510.1016/j.electacta.2013.11.165 ↗
30. 10.1016/j.electacta.2008.07.08210.1016/j.electacta.2008.07.082 ↗
31. 10.1021/la980909j10.1021/la980909j ↗
32. 10.1021/jp205544310.1021/jp2055443 ↗
33. 10.1016/S0013-4686(02)00815-010.1016/S0013-4686(02)00815-0 ↗
34. 10.1021/ef100034x10.1021/ef100034x ↗
35. 10.1149/1.356800410.1149/1.3568004 ↗