<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Liao F</submitter><funding>Ministry of Science and Technology of the People&amp;apos;s Republic of China (Chinese Ministry of Science and Technology)</funding><funding>Ministry of Science and Technology of the People&amp;amp;apos;s Republic of China</funding><pagination>1248</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9985653</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(1)</volume><pubmed_abstract>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&lt;sub>0.25&lt;/sub>IrO&lt;sub>2&lt;/sub> (I2/m (12)) precursor. The formation mechanism of IrO&lt;sub>2&lt;/sub> nanoribbon is clearly revealed, with its further conversion to IrO&lt;sub>2&lt;/sub> nanosheet with a trigonal phase. When applied as an electrocatalyst for the oxygen evolution reaction in acidic condition, the intrinsic catalytic activity of IrO&lt;sub>2&lt;/sub> nanoribbon is higher than that of tetragonal phase IrO&lt;sub>2&lt;/sub> due to the low d band centre of Ir in this special monoclinic phase structure, as confirmed by density functional theory calculations.</pubmed_abstract><journal>Nature communications</journal><pubmed_title>Iridium oxide nanoribbons with metastable monoclinic phase for highly efficient electrocatalytic oxygen evolution.</pubmed_title><pmcid>PMC9985653</pmcid><funding_grant_id>2017YFA0204800</funding_grant_id><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Liao F</pubmed_authors><pubmed_authors>Fan Z</pubmed_authors><pubmed_authors>Shao M</pubmed_authors><pubmed_authors>Ji Y</pubmed_authors><pubmed_authors>Zhu W</pubmed_authors><pubmed_authors>Zhong J</pubmed_authors><pubmed_authors>Kang Z</pubmed_authors><pubmed_authors>Shao Q</pubmed_authors><pubmed_authors>Yin K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Iridium oxide nanoribbons with metastable monoclinic phase for highly efficient electrocatalytic oxygen evolution.</name><description>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&lt;sub>0.25&lt;/sub>IrO&lt;sub>2&lt;/sub> (I2/m (12)) precursor. The formation mechanism of IrO&lt;sub>2&lt;/sub> nanoribbon is clearly revealed, with its further conversion to IrO&lt;sub>2&lt;/sub> nanosheet with a trigonal phase. When applied as an electrocatalyst for the oxygen evolution reaction in acidic condition, the intrinsic catalytic activity of IrO&lt;sub>2&lt;/sub> nanoribbon is higher than that of tetragonal phase IrO&lt;sub>2&lt;/sub> due to the low d band centre of Ir in this special monoclinic phase structure, as confirmed by density functional theory calculations.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Mar</publication><modification>2026-03-17T15:23:46.402Z</modification><creation>2025-02-18T23:35:21.689Z</creation></dates><accession>S-EPMC9985653</accession><cross_references><pubmed>36871002</pubmed><doi>10.1038/s41467-023-36833-1</doi></cross_references></HashMap>