Iridium oxide nanoribbons with metastable monoclinic phase for highly efficient electrocatalytic oxygen evolution
Metastable metal oxides with ribbon morphologies have promising applications for energy conversion catalysis, however they are largely restricted by their limited synthesis methods. In this study, a monoclinic phase iridium oxide nanoribbon with a space group of C2/m is successfully obtained, which...
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Published in | Nature communications Vol. 14; no. 1; pp. 1248 - 11 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
04.03.2023
Nature Publishing Group Nature Portfolio |
Subjects | |
Online Access | Get full text |
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Summary: | Metastable metal oxides with ribbon morphologies have promising applications for energy conversion catalysis, however they are largely restricted by their limited synthesis methods. In this study, a monoclinic phase iridium oxide nanoribbon with a space group of C2/m is successfully obtained, which is distinct from rutile iridium oxide with a stable tetragonal phase (P42/mnm). A molten-alkali mechanochemical method provides a unique strategy for achieving this layered nanoribbon structure via a conversion from a monoclinic phase K
0.25
IrO
2
(I2/m (12)) precursor. The formation mechanism of IrO
2
nanoribbon is clearly revealed, with its further conversion to IrO
2
nanosheet with a trigonal phase. When applied as an electrocatalyst for the oxygen evolution reaction in acidic condition, the intrinsic catalytic activity of IrO
2
nanoribbon is higher than that of tetragonal phase IrO
2
due to the low
d
band centre of Ir in this special monoclinic phase structure, as confirmed by density functional theory calculations.
Well-defined metastable phase nanostructures are a core issue for catalyst design. Here, the authors report metastable monoclinic phase IrO2 nanoribbons obtained via a molten-alkali mechanochemical method, which exhibit intrinsic high performance towards the acidic oxygen evolution reaction. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 2041-1723 2041-1723 |
DOI: | 10.1038/s41467-023-36833-1 |