ABSTRACT
With the mounting need for clean and renewable energy, catalysts for hydrogen production based on earth abundant elements are of great interest. Herein, we describe the synthesis, characterization, and catalytic activity of two nickel complexes based on the pyridinediimine ligand that possess basic nitrogen moieties of pyridine and imidazole that could potentially serve as pendent bases to enhance catalysis. Although these ligands have previously been reported to be complexed to some metal ions, they have not been applied to nickel. The nickel complex with the pendent pyridines was found to be the most active of the two, catalyzing proton reduction electrochemically with an overpotential of 490 mV. The appearance of a wave that preceded the Ni(I/0) redox couple in the presence of protons suggests that protonation of a dissociated pyridine was likely. Further evidence of this was provided with density functional theory calculations, and a mechanism of hydrogen production is proposed. Furthermore, in a light-driven system containing Ru(bpy)32+ and ascorbic acid, TON of 1400 were obtained.
