Aerogel Architectures Boost Oxygen‐Evolution Performance of NiFe2Ox Spinels to Activity Levels Commensurate with Nickel‐Rich Oxides. Issue 9 (29th June 2016)
- Record Type:
- Journal Article
- Title:
- Aerogel Architectures Boost Oxygen‐Evolution Performance of NiFe2Ox Spinels to Activity Levels Commensurate with Nickel‐Rich Oxides. Issue 9 (29th June 2016)
- Main Title:
- Aerogel Architectures Boost Oxygen‐Evolution Performance of NiFe2Ox Spinels to Activity Levels Commensurate with Nickel‐Rich Oxides
- Authors:
- Chervin, Christopher N.
DeSario, Paul A.
Parker, Joseph F.
Nelson, Eric S.
Miller, Bryan W.
Rolison, Debra R.
Long, Jeffrey W. - Abstract:
- Abstract: Nickel–iron oxides and oxyhydroxides are among the most active oxygen‐evolution reaction (OER) catalysts in alkaline electrolytes. Compositions rich in Ni are reported to show superior activity, but the establishment of competitive OER activity with lower cost, Fe‐rich analogues is more desirable for metal–air batteries and other devices that will see large‐scale production. Herein, we demonstrate that by controlling pore–solid architecture and the degree of crystallinity, we achieve a single‐phase, Fe‐rich NiFe2 O x catalyst that matches the OER performance metrics previously demonstrated for compositions with higher Ni‐to‐Fe ratios. We also show that OER activity linearly tracks increases in the catalyst surface area, whereas the degree of ex situ surface hydroxylation does not play a significant role. To prepare the pore–solid structured forms, NiFe2 O x gels were synthesized by using an epoxide‐initiated sol–gel method and subsequently processed to aerogels or xerogels. The activities of these two sol–gel‐derived nanostructures were compared with a nanoparticulate analogue with lower specific surface area, prepared by using conventional precipitation methods. The higher surface area and larger pore volume expressed by the NiFe2 O x formed as an aerogel result in a performance‐competitive OER overpotential of 356 mV at a current density of 10 mA cm −2, with an approximately 140 mV improvement relative to the low‐surface‐area, precipitated analogue. Abstract :Abstract: Nickel–iron oxides and oxyhydroxides are among the most active oxygen‐evolution reaction (OER) catalysts in alkaline electrolytes. Compositions rich in Ni are reported to show superior activity, but the establishment of competitive OER activity with lower cost, Fe‐rich analogues is more desirable for metal–air batteries and other devices that will see large‐scale production. Herein, we demonstrate that by controlling pore–solid architecture and the degree of crystallinity, we achieve a single‐phase, Fe‐rich NiFe2 O x catalyst that matches the OER performance metrics previously demonstrated for compositions with higher Ni‐to‐Fe ratios. We also show that OER activity linearly tracks increases in the catalyst surface area, whereas the degree of ex situ surface hydroxylation does not play a significant role. To prepare the pore–solid structured forms, NiFe2 O x gels were synthesized by using an epoxide‐initiated sol–gel method and subsequently processed to aerogels or xerogels. The activities of these two sol–gel‐derived nanostructures were compared with a nanoparticulate analogue with lower specific surface area, prepared by using conventional precipitation methods. The higher surface area and larger pore volume expressed by the NiFe2 O x formed as an aerogel result in a performance‐competitive OER overpotential of 356 mV at a current density of 10 mA cm −2, with an approximately 140 mV improvement relative to the low‐surface‐area, precipitated analogue. Abstract : Aerogels excel : NiFe2 O x aerogel catalysts provide superior O2 ‐evolution activity relative to other nanostructured analogues. The higher surface area and larger pore volume expressed by the aerogel form provide an OER overpotential of 356 mV at 10 mA cm −2, with an approximately 140 mV improvement relative to a precipitated analogue. A linear relationship is observed between the surface area of NiFe2 Ox and OER activity. … (more)
- Is Part Of:
- ChemElectroChem. Volume 3:Issue 9(2016)
- Journal:
- ChemElectroChem
- Issue:
- Volume 3:Issue 9(2016)
- Issue Display:
- Volume 3, Issue 9 (2016)
- Year:
- 2016
- Volume:
- 3
- Issue:
- 9
- Issue Sort Value:
- 2016-0003-0009-0000
- Page Start:
- 1369
- Page End:
- 1375
- Publication Date:
- 2016-06-29
- Subjects:
- gels -- battery technology -- ferrite -- spinel phases -- water splitting
Electrochemistry -- Periodicals
541.37 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/%28ISSN%292196-0216 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/celc.201600206 ↗
- Languages:
- English
- ISSNs:
- 2196-0216
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3133.496200
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 644.xml