Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/113283
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dc.contributorDepartment of Applied Physicsen_US
dc.contributorPhotonics Research Instituteen_US
dc.contributorResearch Institute for Advanced Manufacturingen_US
dc.creatorShe, Sen_US
dc.creatorChen, HCen_US
dc.creatorChen, Cen_US
dc.creatorZhu, Yen_US
dc.creatorChen, Gen_US
dc.creatorSong, Yen_US
dc.creatorXiao, Yen_US
dc.creatorLin, Zen_US
dc.creatorZu, Den_US
dc.creatorPeng, Len_US
dc.creatorLi, Hen_US
dc.creatorZhu, Yen_US
dc.creatorTsang, YHen_US
dc.creatorHuang, Hen_US
dc.date.accessioned2025-06-02T06:57:22Z-
dc.date.available2025-06-02T06:57:22Z-
dc.identifier.issn1936-0851en_US
dc.identifier.urihttp://hdl.handle.net/10397/113283-
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.rightsCopyright © 2025 The Authors. Published by American Chemical Society. This publication is licensed under CC-BY 4.0 (https://creativecommons.org/licenses/by/4.0/).en_US
dc.rightsThe following publication She, S., Chen, H. C., Chen, C., Zhu, Y., Chen, G., Song, Y., ... & Huang, H. (2025). Regulating Ru–Ru Distance in RuO2 Catalyst by Lattice Hydroxyl for Efficient Water Oxidation. ACS nano, 19(19), 18513-18521 is available at https://doi.org/10.1021/acsnano.5c01937.en_US
dc.subjectLattice hydroxylen_US
dc.subjectOxygen evolution reactionen_US
dc.subjectProton exchange membrane water electrocatalysisen_US
dc.subjectRuthenium oxideen_US
dc.subjectRu−Ru distanceen_US
dc.titleRegulating Ru-Ru distance in RuO2 catalyst by lattice hydroxyl for efficient water oxidationen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage18513en_US
dc.identifier.epage18521en_US
dc.identifier.volume19en_US
dc.identifier.issue19en_US
dc.identifier.doi10.1021/acsnano.5c01937en_US
dcterms.abstractHighly active and durable electrocatalysts for the oxygen evolution reaction (OER) are crucial for proton exchange membrane water electrolysis (PEMWE). While doped RuO2 catalysts demonstrate good activity and stability, the presence of dopants limits the number of exposed active sites and complicates Ru recovery. Here, we present a monometallic RuO2 (d-RuO2) with lattice hydroxyl in the periodic structure as a high-performance OER electrocatalyst. The obtained d-RuO2 catalyst exhibits a low overpotential of 150 mV and long-term operational stability of 500 h at 10 mA cm-2, outperforming many Ru/Ir-based oxides ever reported. A PEMWE device using d-RuO2 sustains operation for 348 h at 200 mA cm-2. In-situ characterization reveals that the incorporation of lattice hydroxyl increases the Ru-Ru distance, which facilitates the turnover of the Ru oxidation state and promotes the formation of stable edge-sharing [RuO6] octahedra during the OER, thereby accelerating the formation of O-O bonds and suppressing the overoxidation of Ru sites. Additionally, the small particle size of the catalyst decreases the three-phase contact line and promotes bubble release. This study will provide insights into the design and optimization of catalysts for various electrochemical reactions.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationACS nano, 20 May 2025, v. 19, no. 19, p. 18513-18521en_US
dcterms.isPartOfACS nanoen_US
dcterms.issued2025-05-20-
dc.identifier.scopus2-s2.0-105004437889-
dc.identifier.pmid40329443-
dc.identifier.eissn1936-086Xen_US
dc.description.validate202505 bchyen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_TA-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextHong Kong Polytechnic University; Natural Science Foundation of Jiangsu Provinceen_US
dc.description.pubStatusPublisheden_US
dc.description.TAACS (2025)en_US
dc.description.oaCategoryTAen_US
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