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Defective and “c-Disordered” Hortensia-like Layered MnOx as an Efficient Electrocatalyst for Water Oxidation at Neutral pH
Uppsala University, Disciplinary Domain of Science and Technology, Physics, Department of Physics and Astronomy, Molecular and Condensed Matter Physics.ORCID iD: 0000-0003-2412-8503
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2017 (English)In: ACS Catalysis, ISSN 2155-5435, E-ISSN 2155-5435, Vol. 7, no 9, 6311-6322 p.Article in journal, Editorial material (Refereed) Published
Abstract [en]

The development of a highly active manganese-based water oxidation catalyst in the design of an ideal artificial photosynthetic device operating under neutral pH conditions remains a great challenge, due to the instability of pivotal Mn3+ intermediates. We report here defective and “c-disordered” layered manganese oxides (MnOx-300) formed on a fluorine-doped tin oxide electrode by constant anodic potential deposition and subsequent annealing, with a catalytic onset (0.25 mA/cm2) at an overpotential (η) of 280 mV and a benchmark catalytic current density of 1.0 mA/cm2 at an overpotential (η) of 330 mV under neutral pH (1 M potassium phosphate). Steady current density above 8.2 mA/cm2 was obtained during the electrolysis at 1.4 V versus the normal hydrogen electrode for 20 h. Insightful studies showed that the main contributing factors for the observed high activity of MnOx-300 are (i) a defective and randomly stacked layered structure, (ii) an increased degree of Jahn–Teller distorted Mn3+ in the MnO6 octahedral sheets, (iii) effective stabilization of Mn3+, (iv) a high surface area, and (v) improved electrical conductivity. These results demonstrate that manganese oxides as structural and functional models of an oxygen-evolving complex (OEC) in photosystem II are promising catalysts for water oxidation in addition to Ni/Co-based oxides/hydroxides.

Place, publisher, year, edition, pages
2017. Vol. 7, no 9, 6311-6322 p.
National Category
Energy Systems
Identifiers
URN: urn:nbn:se:uu:diva-329320DOI: 10.1021/acscatal.7b00420ISI: 000410005700085OAI: oai:DiVA.org:uu-329320DiVA: diva2:1140642
Funder
Swedish Energy AgencyKnut and Alice Wallenberg FoundationSwedish Research Council
Available from: 2017-09-12 Created: 2017-09-12 Last updated: 2017-12-07Bibliographically approved

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Philippe, BertrandValvo, MarioRensmo, Håkan

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