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Substrate-Enabled Room-Temperature Electrochemical Deposition of Crystalline ZnMnO3.
Rettenmaier, Karin; Zickler, Gregor A; Redhammer, Günther J; Berger, Thomas.
Affiliation
  • Rettenmaier K; Department of Chemistry and Physics of Materials, University of Salzburg, Jakob-Haringer-Straße 2a, A-5020, Salzburg, Austria.
  • Zickler GA; Department of Chemistry and Physics of Materials, University of Salzburg, Jakob-Haringer-Straße 2a, A-5020, Salzburg, Austria.
  • Redhammer GJ; Department of Chemistry and Physics of Materials, University of Salzburg, Jakob-Haringer-Straße 2a, A-5020, Salzburg, Austria.
  • Berger T; Department of Chemistry and Physics of Materials, University of Salzburg, Jakob-Haringer-Straße 2a, A-5020, Salzburg, Austria.
Chemphyschem ; 24(1): e202200586, 2023 Jan 03.
Article in En | MEDLINE | ID: mdl-36070988
ABSTRACT
Mixed transition metal oxides have emerged as promising electrode materials for electrochemical energy storage and conversion. To optimize the functional electrode properties, synthesis approaches allowing for a systematic tailoring of the materials' composition, crystal structure and morphology are urgently needed. Here we report on the room-temperature electrodeposition of a ternary oxide based on earth-abundant metals, specifically, the defective cubic spinel ZnMnO3 . In this unprecedented approach, ZnO surfaces act as (i) electron source for the interfacial reduction of MnO4 - in aqueous solution, (ii) as substrate for epitaxial growth of the deposit and (iii) as Zn precursor for the formation of ZnMnO3 . Epitaxial growth of ZnMnO3 on the lateral facets of ZnO nanowires assures effective electronic communication between the electroactive material and the conducting scaffold and gives rise to a pronounced 2-dimensional morphology of the electrodeposit forming - after partial delamination from the substrate - twisted nanosheets. The synthesis strategy shows promise for the direct growth of different mixed transition metal oxides as electroactive phase onto conductive substrates and thus for the fabrication of binder-free nanocomposite electrodes.
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