Electrocatalytic Hydrogen Evolution of Bent Bis(dipyrrin) Ni(II) Complexes

Abstract

Planar Ni(II) porphyrinoid complexes have been widely used in electrochemical carbon dioxide reduction reaction and oxygen reduction reaction as well as hydrogen evolution reaction (HER). However, nonplanar Ni(II) tetra-pyrrolic complexes have not been thoroughly investigated thus far. In this study, three highly bent bis(dipyrrin) Ni(II) complexes have been synthesized to investigate their structure, electronic property, and electrocatalytic HER activities. Cyclic voltammetry and thin-layer UV-visible spectroelectrochemistry studies revealed four redox processes, yielding two reduced species as the final products. The <i>i</i>_c/<i>i</i>_p values of phenyl- and pentafluorophenyl-bearing bis(dipyrrin) Ni(II) complexes were >30 when trifluoroacetic acid was used as the proton source, and their Faradaic efficiencies for H₂ generation were >93%. Density functional theory calculations of the HERs revealed low endothermic energies of bent bis(dipyrrin) Ni(II) complexes.