Carbon-Supported Iron Phosphides: Highest Intrinsic Oxygen Evolution Activity of the Iron Triad
Source abstract
Abstract
We compared the oxygen evolution reaction (OER) activity of carbon-supported iron triad metal phosphide nanoparticles using Fe-purified KOH electrolyte. We prepared these catalysts with nearly identical structural properties using an ammonia-assisted ambient hydrolysis deposition (AHD) method allowing us to explore how their compositions affect their OER activities. We discovered that iron phosphide is far superior to its counterparts with an onset potential lower by 150 mV. Furthermore, we found that the anodic voltammetric scan with associated oxidation of Fe(II) in the phosphide generates OER active sites; however, ambient oxidation of iron phosphide prior to that anodic scan deactivates the catalyst.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Advanced battery technologies research · Fuel Cells and Related Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, Oregon State University, Corvallis, Oregon 97331-4003, United States
Hewlett-Packard, Inc., Corvallis, Oregon 97330, United States
Funding
Oregon State University
References (29)
Show source-provided references
1. Denholm P. · 201510.2172/1226167 ↗
2. 10.1126/science.285.5428.68710.1126/science.285.5428.687 ↗
3. 10.1126/science.110319710.1126/science.1103197 ↗
4. 10.1073/pnas.060339510310.1073/pnas.0603395103 ↗
5. 10.1016/j.solener.2006.10.00510.1016/j.solener.2006.10.005 ↗
6. Randolph, K.; Miller, E.; Peterson, D.; Lyubovsky, M.; Cierpik-Gold, K.; Sink, C.; Li, D.; Holladay, J.; Chapman, B.; Soto, H.; Rafael, T. U.S. Driving Research and Innovation for Vehicle Efficiency and Energy Sustainability Partnership. Hydrogen Production Tech Team Roadmap; November 2017.
7. 10.1149/2.F04181if10.1149/2.F04181if ↗
8. 10.1039/C5EE01155H10.1039/C5EE01155H ↗
9. 10.1021/acs.inorgchem.6b0292910.1021/acs.inorgchem.6b02929 ↗
10. 10.1021/acs.chemmater.7b0005510.1021/acs.chemmater.7b00055 ↗
11. 10.1016/j.elecom.2017.04.01410.1016/j.elecom.2017.04.014 ↗
12. 10.1021/acsanm.7b0012210.1021/acsanm.7b00122 ↗
13. 10.1039/C6TA04025J10.1039/C6TA04025J ↗
14. 10.1021/ja403440e10.1021/ja403440e ↗
15. 10.1021/nn504855310.1021/nn5048553 ↗
16. 10.1039/C4TA06642A10.1039/C4TA06642A ↗
17. 10.1021/acs.chemmater.6b0214810.1021/acs.chemmater.6b02148 ↗
18. 10.1021/ja502379c10.1021/ja502379c ↗
19. 10.1039/c3ta14278g10.1039/c3ta14278g ↗
20. 10.1002/chem.20140228010.1002/chem.201402280 ↗
21. 10.1002/adma.20039002010.1002/adma.200390020 ↗
22. 10.1021/acs.chemmater.6b0279610.1021/acs.chemmater.6b02796 ↗
23. 10.1021/acscatal.5b0155110.1021/acscatal.5b01551 ↗
24. 10.1021/jacs.5b0028110.1021/jacs.5b00281 ↗
25. 10.1021/acs.jpclett.5b0165010.1021/acs.jpclett.5b01650 ↗
26. 10.1021/ja307507a10.1021/ja307507a ↗
27. 10.1038/srep1216710.1038/srep12167 ↗
28. 10.1039/c1cp22470k10.1039/c1cp22470k ↗
29. 10.1021/jacs.7b0321110.1021/jacs.7b03211 ↗