Decoupling the roles of carbon and metal oxides on the electrocatalytic reduction of oxygen on La1−xSrxCoO3−δ perovskite composite electrodes. Issue 6 (28th January 2019)
- Record Type:
- Journal Article
- Title:
- Decoupling the roles of carbon and metal oxides on the electrocatalytic reduction of oxygen on La1−xSrxCoO3−δ perovskite composite electrodes. Issue 6 (28th January 2019)
- Main Title:
- Decoupling the roles of carbon and metal oxides on the electrocatalytic reduction of oxygen on La1−xSrxCoO3−δ perovskite composite electrodes
- Authors:
- Mefford, J. Tyler
Kurilovich, Aleksandr A.
Saunders, Jennette
Hardin, William G.
Abakumov, Artem M.
Forslund, Robin P.
Bonnefont, Antoine
Dai, Sheng
Johnston, Keith P.
Stevenson, Keith J. - Abstract:
- Abstract : Experiment and microkinetic modeling decouple the synergistic roles of La1− x Sr x CoO3− δ perovskite oxides and carbon additives during the oxygen reduction reaction. Abstract : Perovskite oxides are active room-temperature bifunctional oxygen electrocatalysts in alkaline media, capable of performing the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) with lower combined overpotentials relative to their precious metal counterparts. However, their semiconducting nature necessitates the use of activated carbons as conductive supports to generate applicably relevant current densities. In efforts to advance the performance and theory of oxide electrocatalysts, the chemical and physical properties of the oxide material often take precedence over contributions from the conductive additive. In this work, we find that carbon plays an important synergistic role in improving the performance of La1− x Sr x CoO3− δ (0 ≤ x ≤ 1) electrocatalysts through the activation of O2 and spillover of radical oxygen intermediates, HO2 − and O2 −, which is further reduced through chemical decomposition of HO2 − on the perovskite surface. Through a combination of thin-film rotating disk electrochemical characterization of the hydrogen peroxide intermediate reactions (hydrogen peroxide reduction reaction (HPRR), hydrogen peroxide oxidation reaction (HPOR)) and oxygen reduction reaction (ORR), surface chemical analysis, HR-TEM, and microkinetic modeling on La1− x Sr xAbstract : Experiment and microkinetic modeling decouple the synergistic roles of La1− x Sr x CoO3− δ perovskite oxides and carbon additives during the oxygen reduction reaction. Abstract : Perovskite oxides are active room-temperature bifunctional oxygen electrocatalysts in alkaline media, capable of performing the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) with lower combined overpotentials relative to their precious metal counterparts. However, their semiconducting nature necessitates the use of activated carbons as conductive supports to generate applicably relevant current densities. In efforts to advance the performance and theory of oxide electrocatalysts, the chemical and physical properties of the oxide material often take precedence over contributions from the conductive additive. In this work, we find that carbon plays an important synergistic role in improving the performance of La1− x Sr x CoO3− δ (0 ≤ x ≤ 1) electrocatalysts through the activation of O2 and spillover of radical oxygen intermediates, HO2 − and O2 −, which is further reduced through chemical decomposition of HO2 − on the perovskite surface. Through a combination of thin-film rotating disk electrochemical characterization of the hydrogen peroxide intermediate reactions (hydrogen peroxide reduction reaction (HPRR), hydrogen peroxide oxidation reaction (HPOR)) and oxygen reduction reaction (ORR), surface chemical analysis, HR-TEM, and microkinetic modeling on La1− x Sr x CoO3− δ (0 ≤ x ≤ 1)/carbon (with nitrogen and non-nitrogen doped carbons) composite electrocatalysts, we deconvolute the mechanistic aspects and contributions to reactivity of the oxide and carbon support. … (more)
- Is Part Of:
- Physical chemistry chemical physics. Volume 21:Issue 6(2019)
- Journal:
- Physical chemistry chemical physics
- Issue:
- Volume 21:Issue 6(2019)
- Issue Display:
- Volume 21, Issue 6 (2019)
- Year:
- 2019
- Volume:
- 21
- Issue:
- 6
- Issue Sort Value:
- 2019-0021-0006-0000
- Page Start:
- 3327
- Page End:
- 3338
- Publication Date:
- 2019-01-28
- Subjects:
- Chemistry, Physical and theoretical -- Periodicals
541.3 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/cp#!issueid=cp016040&type=current&issnprint=1463-9076 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c8cp06268d ↗
- Languages:
- English
- ISSNs:
- 1463-9076
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6475.306000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 9507.xml