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International journal of hydrogen energy, 2023-04, Vol.48 (29), p.10891-10902
2023
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Autor(en) / Beteiligte
Titel
Electrocatalytic hydrogen evolution by Co(II) complexes of bistriazolylpyridines
Ist Teil von
  • International journal of hydrogen energy, 2023-04, Vol.48 (29), p.10891-10902
Ort / Verlag
Elsevier Ltd
Erscheinungsjahr
2023
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • Two cobalt complexes [Co(L1)2](ClO4)2⋅4CH3CN (1) and [Co(L2)2](ClO4)2⋅2CH3CN⋅0.5H2O (2) of the new click-derived bistriazolylpyridines 2,6-bis(1-(pyridin-2-yl)-1H-1,2,3-triazol-4-yl)isonicotinate methyl ester (L1) and 2,6-bis-(1-methoxycarbonylmethyl-1H-1,2,3-triazol-4-yl)isonicotinate methyl ester (L2) were synthesized and characterized. The electrocatalytic hydrogen evolution reaction (HER) mediated by complexes 1 and 2 was studied in CH3CN in the presence of acetic acid. Both complexes catalyzed HER with low overpotentials and high Faradaic efficiencies (370 mV and 93% for 1, 300 mV and 95% for 2). The distal substituents on the triazolyl moiety of the bistriazolylpyridines have apparent impacts on the redox and catalytic properties of 1 and 2. The catalytic behaviors were further studied using spectroelectrochemistry and the reductant cobaltocene. It was found that the reduction of the bistriazolylpyridines was necessary for the catalytic activity. Plausible pathways were proposed for the HER mediated by 1 and 2. This work provided some hints for the preparation of HER catalysts based on the redox-active triazolylpyridine ligands. Hydrogen evolution was boosted by Co(II) complexes of click-derived bistriazolylpyridines and the distal groups on the bistriazolylpyridines had apparent impacts on the catalytic activities. [Display omitted] •Synthesis and characterization of cobalt complexes of click-derived bistriazolylpyridines.•Redox properties of cobalt complexes of bistriazolylpyridines.•Electrocatalytic hydrogen evolution by cobalt complexes of bistriazolylpyridines.
Sprache
Englisch
Identifikatoren
ISSN: 0360-3199
eISSN: 1879-3487
DOI: 10.1016/j.ijhydene.2022.11.242
Titel-ID: cdi_crossref_primary_10_1016_j_ijhydene_2022_11_242

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