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Improvement of Electrochemical Water Oxidation by Fine-Tuning the Structure of Tetradentate N4 Ligands of Molecular Copper Catalysts
Vise andre og tillknytning
2017 (engelsk)Inngår i: ChemSusChem, ISSN 1864-5631, E-ISSN 1864-564X, Vol. 10, nr 22, s. 4581-4588Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Two copper complexes, [(L1)Cu(OH2)](BF4)2 [1; L1=N,N′-dimethyl-N,N′-bis(pyridin-2-ylmethyl)-1,2-diaminoethane] and [(L2)Cu(OH2)](BF4)2 [2, L2=2,7-bis(2-pyridyl)-3,6-diaza-2,6-octadiene], were prepared as molecular water oxidation catalysts. Complex 1 displayed an overpotential (η) of 1.07 V at 1 mA cm−2 and an observed rate constant (kobs) of 13.5 s−1 at η 1.0 V in pH 9.0 phosphate buffer solution, whereas 2 exhibited a significantly smaller η (0.70 V) to reach 1 mA cm−2 and a higher kobs (50.4 s−1) than 1 under identical test conditions. Additionally, 2 displayed better stability than 1 in controlled potential electrolysis experiments with a faradaic efficiency of 94 % for O2 evolution at 1.58 V, when a casing tube was used for the Pt cathode. A possible mechanism for 1- and 2-catalyzed O2 evolution reactions is discussed based on the experimental evidence. These comparative results indicate that fine-tuning the structures of tetradentate N4 ligands can bring about significant change in the performance of copper complexes for electrochemical water oxidation.

sted, utgiver, år, opplag, sider
Wiley-VCH Verlagsgesellschaft, 2017. Vol. 10, nr 22, s. 4581-4588
Emneord [en]
copper, electrocatalysis, homogeneous catalysis, N ligands, water oxidation, Catalysis, Catalysts, Ligands, Oxidation, Rate constants, Controlled potential electrolysis, Experimental evidence, Faradaic efficiencies, Phosphate buffer solutions, Possible mechanisms, Tuning, coordination compound, ligand, oxygen, water, chemical structure, chemistry, electrochemical analysis, electrolysis, oxidation reduction reaction, procedures, Coordination Complexes, Electrochemical Techniques, Molecular Structure, Oxidation-Reduction
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Identifikatorer
URN: urn:nbn:se:kth:diva-227141DOI: 10.1002/cssc.201701458ISI: 000416158500035PubMedID: 28868648Scopus ID: 2-s2.0-85035058311OAI: oai:DiVA.org:kth-227141DiVA, id: diva2:1202992
Forskningsfinansiär
Swedish Energy AgencySwedish Research CouncilKnut and Alice Wallenberg Foundation
Merknad

QC 20180502

Tilgjengelig fra: 2018-05-02 Laget: 2018-05-02 Sist oppdatert: 2019-02-07bibliografisk kontrollert

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