Electrocatalytic reduction of protons to dihydrogen by the cobalt tetraazamacrocyclic complex [Co(N4H)Cl2]+: mechanism and benchmarking of performances

The cobalt tetraazamacrocyclic [Co(N4H)Cl-2](+) complex is becoming a popular and versatile catalyst for the electrocatalytic evolution of hydrogen, because of its stability and superior activity in aqueous conditions. We present here a benchmarking of its performances based on the thorough analysis of cyclic voltammograms recorded under various catalytic regimes in non-aqueous conditions allowing control of the proton concentration. This allowed a detailed mechanism to be proposed with quantitative determination of the rate-constants for the various protonation steps, as well as identification of the amine function of the tetraazamacrocyclic ligand to act as a proton relay during H-2 evolution.

Automated summary

The cobalt tetraazamacrocyclic [Co(N4H)Cl-2](+) complex is a popular and versatile catalyst for electrocatalytic hydrogen evolution due to its stability and superior activity in aqueous conditions. By analyzing cyclic voltammograms under non-aqueous conditions, a detailed mechanism and quantitative determination of rate-constants for protonation steps were proposed, with the identification of the amine function as a proton relay during H-2 evolution.