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Water splitting is a promising approach for storing intermittent renewable energies, such as sunlight in the clean chemical bonds as a hydrogen fuel. Two water-soluble octahedral cobalt (III) complexes, [Co(bpb)(OAc)(H2O)], 1, (bpb(2-) = N,N' -bis[(2-pyridine carboxamide)-1,2-benzene] dianion) and [Co(cbpb)(OAc)(H2O)], 2, (cbpb(2-) = N,N'-bis[(2-pyridine carboxamide)-4-chloro-1,2-benzene] dianion) were synthesised and characterised by CHN elemental analysis, UV-Vis, FT-IR and single-crystal X-ray diffraction techniques. The two carboxamide ligands had been prepared in the ionic liquid TBAB as an environmentally benign reaction medium. The electrocatalytic water splitting activity of 1 and 2 showed that both complexes are highly active for the water splitting in aqueous solutions. Turn Over Frequency (TOF) values were, for 1 and 2 respectively, 527 and 490 mol of hydrogen in each mole of catalyst per hour at an overpotential of 738 mV (pH = 7.0). Such a performance can be ascribed to the flat ligands, the electroactivity of the metal centre and carboxamide ligands and the ability of losing the axial ligands around the metal-ion centre during the reduction process which provide different reduction pathways for an HER process. (C) 2022 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
Michael Graetzel, Shaik Mohammed Zakeeruddin