Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/113034
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dc.contributorDepartment of Applied Biology and Chemical Technology-
dc.creatorLu, L-
dc.creatorSun, M-
dc.creatorWu, T-
dc.creatorLu, Q-
dc.creatorChen, B-
dc.creatorChan, CH-
dc.creatorWong, HH-
dc.creatorLi, Z-
dc.creatorHuang, B-
dc.date.accessioned2025-05-19T00:51:58Z-
dc.date.available2025-05-19T00:51:58Z-
dc.identifier.urihttp://hdl.handle.net/10397/113034-
dc.language.isoenen_US
dc.publisherWiley-VCH Verlag GmbH & Co. KGaAen_US
dc.rights© 2025 The Authors. ChemElectroChem published by Wiley-VCH GmbH. This is an open access article under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits use, distribution and reproduction in any medium, provided the original work is properly cited.en_US
dc.rightsThe following publication L. Lu, M. Sun, T. Wu, Q. Lu, B. Chen, C. Hei Chan, H. Ho Wong, Z. Li, B. Huang, Perovskite Oxides for Electrocatalytic Hydrogen/Oxygen Evolution Reaction. ChemElectroChem 2025, 12, e202400648 is available at https://doi.org/10.1002/celc.202400648.en_US
dc.subjectElectrocatalysisen_US
dc.subjectHERen_US
dc.subjectMechanismsen_US
dc.subjectOERen_US
dc.subjectPerovskite oxidesen_US
dc.titlePerovskite oxides for electrocatalytic hydrogen/oxygen evolution reactionen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume12-
dc.identifier.issue4-
dc.identifier.doi10.1002/celc.202400648-
dcterms.abstractSince the excessive exploitation of fossil fuels will cause wars for oil, developing sustainable and eco-friendly energy resources to solve the energy crisis and realize the carbon-neutrality goal has been a hot issue. Water electrolysis has been acknowledged as a promising technology for hydrogen (H2)/oxygen (O2) evolution reaction (HER/OER) since the overall water splitting reaction rates can be well controlled by applying appropriate electrode voltage. Whereas the sluggish electrochemical reactions kinetics on both the cathode and anode have greatly restricted the energy conversion efficiency. Thus, developing highly active electrocatalysts to reduce the overpotentials required for electrolytic HER/OER is of great significance in increasing the utilization rates of electrical power and lowering production costs. ABO3-structured perovskite-oxides based electrocatalysts possess the merits of low cost, high structural stability, and lattice compatibility, and thus they have attracted intense research attention in recent decays. To inspire both theoretical and experimental researchers to design novel perovskite-oxide electrocatalysts for efficient HER/OER, the fundamental electrode reaction mechanisms, the effects of synthetic methods on material morphologies, recently reported perovskite-oxide electrocatalysts and effective tuning strategies on enhancing the electrocatalytic activities of existing perovskite-oxides have been fully discussed in this review.-
dcterms.abstractGraphical abstract: [Figure not available: see fulltext.]-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationChemElectroChem, 16 Feb. 2025, v. 12, no. 4, e202400648-
dcterms.isPartOfChemElectroChem-
dcterms.issued2025-02-16-
dc.identifier.scopus2-s2.0-85216872309-
dc.identifier.eissn2196-0216-
dc.identifier.artne202400648-
dc.description.validate202505 bcch-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOSen_US
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThe National Key R&D Program of China (2021YFA1501101); National Natural Science Foundation of China/Research Grant Council of Hong Kong Joint Research Scheme (N_PolyU502/21); National Natural Science Foundation of China/Research Grants Council of Hong Kong Collaborative Research Scheme (CRS_PolyU504/22); Projectsof Strategic Importance of The Hong Kong Polytechnic University (Project Code: 1-ZE2 V); Shenzhen Fundamental Research Scheme-General Program (JCYJ20220531090807017); Natural Science Foundation of Guangdong Province (2023 A1515012219)en_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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