Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/106799
DC FieldValueLanguage
dc.contributorDepartment of Applied Physics-
dc.creatorZhang, D-
dc.creatorCheng, H-
dc.creatorHao, X-
dc.creatorSun, Q-
dc.creatorZhang, T-
dc.creatorXu, X-
dc.creatorMa, Z-
dc.creatorYang, T-
dc.creatorDing, J-
dc.creatorLiu, X-
dc.creatorYang, M-
dc.creatorHuang, X-
dc.date.accessioned2024-06-04T07:39:50Z-
dc.date.available2024-06-04T07:39:50Z-
dc.identifier.urihttp://hdl.handle.net/10397/106799-
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjecthigh-salinity conditionen_US
dc.subjecthydrogen productionen_US
dc.subjectnon-noble-metal electrocatalystsen_US
dc.subjectoxygen evolution reactionen_US
dc.subjectseawater splittingen_US
dc.titleStable Seawater Oxidation at High-Salinity Conditions Promoted by Low Iron-Doped Non-Noble-Metal Electrocatalystsen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage15581-
dc.identifier.epage15590-
dc.identifier.volume13-
dc.identifier.issue23-
dc.identifier.doi10.1021/acscatal.3c03528-
dcterms.abstractElectrocatalytic seawater splitting offers a promising avenue for cost-effective and environmentally friendly hydrogen production. However, the activity of catalysts has significantly degraded at high-salinity conditions, preventing commercial-scale practical applications. Here, we demonstrate that iron-doped nickel-based electrocatalysts with low doping concentration exhibit an outstanding performance for the oxygen evolution reaction (OER) in seawater, particularly at high-salinity conditions. Notably, the OER catalysts present only a marginal increase in overpotential of ∼5 mV as the sodium chloride concentration in the electrolyte increases from 0 M to saturation. Furthermore, the low iron-doped electrocatalysts sustain consistent oxygen generation over 100 h of operation in a saturated seawater electrolyte. Supported by first-principles calculations, we unravel that low-concentration iron doping in Ni-based catalysts can mitigate chloride ion adsorption, thereby amplifying the OER activity in saturated seawater electrolytes, which is in contrast with high iron-doped electrocatalysts. Our work provides a useful perspective on designing catalysts for electrolytic seawater OER, potentially paving the way for large-scale implementation of seawater splitting technologies.-
dcterms.accessRightsembargoed accessen_US
dcterms.bibliographicCitationACS catalysis, 1 Dec. 2023, v. 13, no. 23, p. 15581-15590-
dcterms.isPartOfACS catalysis-
dcterms.issued2023-12-
dc.identifier.scopus2-s2.0-85179151623-
dc.identifier.eissn2155-5435-
dc.description.validate202406 bcch-
dc.identifier.FolderNumbera2746en_US
dc.identifier.SubFormID48199en_US
dc.description.fundingSourceSelf-fundeden_US
dc.description.pubStatusPublisheden_US
dc.date.embargo2024-12-01en_US
dc.description.oaCategoryGreen (AAM)en_US
Appears in Collections:Journal/Magazine Article
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Embargo End Date 2024-12-01
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