DC Field | Value | Language |
---|---|---|
dc.contributor | Department of Applied Biology and Chemical Technology | en_US |
dc.creator | Tsang, CS | en_US |
dc.creator | Lee, LYS | en_US |
dc.creator | Cheung, KC | en_US |
dc.creator | Chan, PH | en_US |
dc.creator | Wong, WL | en_US |
dc.creator | Wong, KY | en_US |
dc.date.accessioned | 2021-09-23T03:33:23Z | - |
dc.date.available | 2021-09-23T03:33:23Z | - |
dc.identifier.issn | 2196-0216 | en_US |
dc.identifier.uri | http://hdl.handle.net/10397/91198 | - |
dc.language.iso | en | en_US |
dc.publisher | Wiley-VCH | en_US |
dc.subject | Coordination chemistry | en_US |
dc.subject | Electrocatalysis | en_US |
dc.subject | Pyridyl ligand | en_US |
dc.subject | Ruthenium(IV)-oxo complexes | en_US |
dc.subject | Water oxidation | en_US |
dc.title | Unexpected promotional effects of alkyl-tailed ligands and anions on the electrochemical generation of ruthenium(IV)-oxo complexes | en_US |
dc.type | Journal/Magazine Article | en_US |
dc.description.otherinformation | Title on author’s file: Electrochemical generation of ruthenium (IV)–oxo complexes : an unexpected promotion effects from the alkyl-tailed ligand and anions | en_US |
dc.identifier.spage | 2221 | en_US |
dc.identifier.epage | 2230 | en_US |
dc.identifier.volume | 8 | en_US |
dc.identifier.issue | 12 | en_US |
dc.identifier.doi | 10.1002/celc.202100364 | en_US |
dcterms.abstract | Electro-generation of RuIV=O species from the RuII-aqua complex is a crucial step to excel the electrocatalytic water oxidation performance of ruthenium oxo complexes. We report herein the synthesis and X-ray crystal structural characterizations of new RuII-aqua complexes containing N-substituted 2,2′-dipyridylamine ligands (L) tagged with an alkyl chain of various lengths, [Ru(tpy)(L)(OH2)]2+. Cyclic voltammetric analyses show that the length of the alkyl chain exerts great influence on the electro-generation of RuIV=O species. The L with a longer alkyl chain in an acidic aqueous medium promotes the conversion of RuIII−OH to RuIV=O efficiently. Surprisingly, this conversion can be further enhanced by the presence of perchlorate anions. Chronocoulometric data reveal that the alkyl chain on L promotes the adsorption of the ruthenium complex on the electrode surface. Bulk electrolysis results indicate that the [Ru(tpy)(dppa)(OH2)]2+ (dppa=(2,2′-dipyridyl)-n-propylamine) gives the most active electrocatalytic water oxidation activity among the ruthenium-aqua complexes investigated in this study. | en_US |
dcterms.accessRights | embargoed access | en_US |
dcterms.bibliographicCitation | ChemElectroChem, 14 June 2021, v. 8, no. 12, p. 2221-2230 | en_US |
dcterms.isPartOf | ChemElectroChem | en_US |
dcterms.issued | 2021-06-14 | - |
dc.identifier.scopus | 2-s2.0-85105963089 | - |
dc.description.validate | 202109 bchy | en_US |
dc.description.oa | Not applicable | en_US |
dc.identifier.FolderNumber | a1032-n01 | - |
dc.identifier.SubFormID | 2454 | - |
dc.description.fundingSource | Others | en_US |
dc.description.fundingText | The Innovation and Technology Commission and The Hong Kong Polytechnic University | en_US |
dc.description.pubStatus | Published | en_US |
dc.date.embargo | 2022.06.13 | en_US |
Appears in Collections: | Journal/Magazine Article |
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