Promoting oxygen evolution of IrO2 in acid electrolyte by Mn. (10th January 2021)
- Record Type:
- Journal Article
- Title:
- Promoting oxygen evolution of IrO2 in acid electrolyte by Mn. (10th January 2021)
- Main Title:
- Promoting oxygen evolution of IrO2 in acid electrolyte by Mn
- Authors:
- Etzi Coller Pascuzzi, Marco
Hofmann, Jan P.
Hensen, Emiel J.M. - Abstract:
- Highlights: Mn addition improves the activity of IrO2 in the oxygen evolution reaction (OER). Mn substituting for Ir in crystalline rutile IrO2 . Increased OER activity linked to surface Ir 3+ species. Lower Tafel slopes and higher surface-normalized OER activity upon Mn addition. A too high Mn content leads to segregated Mn3 O4, largely removed during OER. Abstract: IrO2 is considered one of the most active electrocatalysts for the oxygen evolution reaction (OER) relevant to electrochemical water splitting in, for instance, proton-exchange membrane electrolyzers. Scaling up of such catalysts is hampered by the high price of Ir. We demonstrate in this work that IrO2 can be promoted by Mn in terms of electrochemical performance at nearly similar stability. The enhancement in electrochemical performance can be attributed to a higher electrochemically active surface and a higher intrinsic activity of the Ir-Mn oxide surface. Mn promotion led to lower Tafel slopes and higher surface-normalized current densities and can be related to the introduction of Mn in the crystalline structure of IrO2 . Specifically, the introduction of Mn led to an increased amount of Ir 3+ species at the surface, which are thought to be involved in the OER. Extensive characterization showed that the fresh anodes consisted of Mn-doped IrO2 with Mn3 O4 at higher Mn content. The latter spinel oxides were easily removed during initial anodic polarization. The synergy between Ir and Mn is maintained duringHighlights: Mn addition improves the activity of IrO2 in the oxygen evolution reaction (OER). Mn substituting for Ir in crystalline rutile IrO2 . Increased OER activity linked to surface Ir 3+ species. Lower Tafel slopes and higher surface-normalized OER activity upon Mn addition. A too high Mn content leads to segregated Mn3 O4, largely removed during OER. Abstract: IrO2 is considered one of the most active electrocatalysts for the oxygen evolution reaction (OER) relevant to electrochemical water splitting in, for instance, proton-exchange membrane electrolyzers. Scaling up of such catalysts is hampered by the high price of Ir. We demonstrate in this work that IrO2 can be promoted by Mn in terms of electrochemical performance at nearly similar stability. The enhancement in electrochemical performance can be attributed to a higher electrochemically active surface and a higher intrinsic activity of the Ir-Mn oxide surface. Mn promotion led to lower Tafel slopes and higher surface-normalized current densities and can be related to the introduction of Mn in the crystalline structure of IrO2 . Specifically, the introduction of Mn led to an increased amount of Ir 3+ species at the surface, which are thought to be involved in the OER. Extensive characterization showed that the fresh anodes consisted of Mn-doped IrO2 with Mn3 O4 at higher Mn content. The latter spinel oxides were easily removed during initial anodic polarization. The synergy between Ir and Mn is maintained during chronopotentiometric stability test. Graphical abstract: Image, graphical abstract … (more)
- Is Part Of:
- Electrochimica acta. Volume 366(2021)
- Journal:
- Electrochimica acta
- Issue:
- Volume 366(2021)
- Issue Display:
- Volume 366, Issue 2021 (2021)
- Year:
- 2021
- Volume:
- 366
- Issue:
- 2021
- Issue Sort Value:
- 2021-0366-2021-0000
- Page Start:
- Page End:
- Publication Date:
- 2021-01-10
- Subjects:
- oxygen evolution reaction -- IrO2 -- Manganese -- overpotential -- stability
Electrochemistry -- Periodicals
Electrochemistry, Industrial -- Periodicals
541.37 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00134686 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.electacta.2020.137448 ↗
- Languages:
- English
- ISSNs:
- 0013-4686
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3698.950000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 14990.xml