ZIF 67 Based Highly Active Electrocatalysts as Oxygen Electrodes in Water Electrolyzer
Source abstract
Abstract
Mitigating high overpotential losses originating from the sluggish oxygen evolution reaction (OER) during water electrolysis is key to establishing a sustainable hydrogen generation technique. In this article, we report a Co-imidazolate framework (ZIF 67) as an OER catalyst that exhibits high activity in both a three electrode cell and an electrolyzer. Additionally, Fe, Ni, and Zn have been incorporated into ZIF 67 to evaluate their effects on the OER activity of ZIF 67. Due to the high charge conductivity of ZIF 67, none of the reported catalyst was carbonized at high temperature, a process that is generally accompanied by significant mass loss. Finally, in addition to being highly active, these catalysts are scalable which makes them promising candidates for application in commercial power markets.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Fuel Cells and Related Materials · Advanced battery technologies research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Chemistry and Nanoscience Center, National Renewable Energy Laboratory, 15013 Denver West Parkway, Golden, Colorado 80401, United States
Department of Chemistry, Colorado School of Mines, 164 Coolbaugh Hall, Golden, Colorado 80401, United States
Funding
National Renewable Energy Laboratory
References (45)
Show source-provided references
1. 10.1039/C8EE01157E10.1039/C8EE01157E ↗
2. 10.1149/2.F04181if10.1149/2.F04181if ↗
3. 10.1149/08511.0003ecst10.1149/08511.0003ecst ↗
4. 10.1126/science.121285810.1126/science.1212858 ↗
5. 10.1021/acscatal.7b0378710.1021/acscatal.7b03787 ↗
6. 10.1021/ja104587v10.1021/ja104587v ↗
7. 10.1039/C4EE00370E10.1039/C4EE00370E ↗
8. 10.1039/C8TA08149B10.1039/C8TA08149B ↗
9. 10.1021/cs300264410.1021/cs3002644 ↗
10. 10.1021/acs.chemmater.5b0314810.1021/acs.chemmater.5b03148 ↗
11. 10.1021/acscatal.5b0148110.1021/acscatal.5b01481 ↗
12. 10.1038/ncomms494910.1038/ncomms4949 ↗
13. 10.1039/c3ta12118f10.1039/c3ta12118f ↗
14. 10.1038/nchem.93110.1038/nchem.931 ↗
15. 10.1002/anie.20160068710.1002/anie.201600687 ↗
16. 10.1002/adfm.20180088610.1002/adfm.201800886 ↗
17. 10.1021/ja506254g10.1021/ja506254g ↗
18. 10.1021/j100238a04810.1021/j100238a048 ↗
19. 10.1021/ja508255310.1021/ja5082553 ↗
20. 10.1021/ja508412810.1021/ja5084128 ↗
21. 10.1126/science.123044410.1126/science.1230444 ↗
22. 10.1002/aenm.20160273310.1002/aenm.201602733 ↗
23. 10.1039/C5SC04425A10.1039/C5SC04425A ↗
24. 10.1039/C6EE01160H10.1039/C6EE01160H ↗
25. 10.1002/anie.20161263510.1002/anie.201612635 ↗
26. 10.1039/C6TA00223D10.1039/C6TA00223D ↗
27. 10.1021/jp057135h10.1021/jp057135h ↗
28. 10.1126/science.120083210.1126/science.1200832 ↗
29. 10.1039/C6TA07860E10.1039/C6TA07860E ↗
30. 10.1039/C7TC03150E10.1039/C7TC03150E ↗
31. 10.1149/2.0361807jes10.1149/2.0361807jes ↗
32. 10.1002/ange.20150424210.1002/ange.201504242 ↗
33. 10.1016/j.matlet.2012.05.07710.1016/j.matlet.2012.05.077 ↗
34. 10.1039/c2dt30174a10.1039/c2dt30174a ↗
35. 10.1039/b910606e10.1039/b910606e ↗
36. 10.30919/es8d71010.30919/es8d710 ↗
37. 10.1039/C9EE00950G10.1039/C9EE00950G ↗
38. 10.1016/j.joule.2017.11.01410.1016/j.joule.2017.11.014 ↗
39. 10.1021/cr100232610.1021/cr1002326 ↗
40. 10.1016/j.cattod.2015.08.01410.1016/j.cattod.2015.08.014 ↗
41. 10.1021/cm404090310.1021/cm4040903 ↗
42. 10.1038/srep4615410.1038/srep46154 ↗
43. 10.1103/PhysRevLett.65.114810.1103/PhysRevLett.65.1148 ↗
44. 10.1149/2.0151611jes10.1149/2.0151611jes ↗
45. 10.1039/C4TA06527A10.1039/C4TA06527A ↗