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Ni- and Cu-co-Intercalated Layered Manganese Oxide for Highly Efficient Electro-Oxidation of Ammonia Selective to Nitrogen.

Authors :
Nagita K
Yuhara Y
Fujii K
Katayama Y
Nakayama M
Source :
ACS applied materials & interfaces [ACS Appl Mater Interfaces] 2021 Jun 23; Vol. 13 (24), pp. 28098-28107. Date of Electronic Publication: 2021 May 27.
Publication Year :
2021

Abstract

We fabricated a thin film of layered MnO <subscript>2</subscript> whose interlayer space was occupied by hydrated Ni <superscript>2+</superscript> and Cu <superscript>2+</superscript> ions. The process consisted of electrodeposition of layered MnO <subscript>2</subscript> intercalated with tetrabutylammonium cations (TBA <superscript>+</superscript> ) by anodic oxidation of aqueous Mn <superscript>2+</superscript> ions in the presence of TBA <superscript>+</superscript> , followed by ion exchange of the initially incorporated bulkier TBA <superscript>+</superscript> with the denser transition metals in solution. The resulting layered MnO <subscript>2</subscript> co-intercalated with Ni <superscript>2+</superscript> and Cu <superscript>2+</superscript> ions (NiCu/MnO <subscript>2</subscript> ) catalyzed the ammonia oxidation reaction (AOR) in an alkaline electrolyte with a much lower overpotential than its Ni <superscript>2+</superscript> - and Cu <superscript>2+</superscript> -intercalated single-cation counterparts. Surprisingly, the NiCu/MnO <subscript>2</subscript> electrode achieved a faradic efficiency as high as nearly 100% (97.4%) for nitrogen evolution at a constant potential of +0.6 V vs Hg/HgO. This can be ascribed to the occurrence of the AOR in the potential region where water is stable and dimerization of the partially dehydrogenated ammonia species is preferred, thereby forming an N-N bond, rather than to be further oxidized into NO <subscript>x</subscript> species.

Details

Language :
English
ISSN :
1944-8252
Volume :
13
Issue :
24
Database :
MEDLINE
Journal :
ACS applied materials & interfaces
Publication Type :
Academic Journal
Accession number :
34043316
Full Text :
https://doi.org/10.1021/acsami.1c04422