Tuning ORR selectivity of π-conjugated cobalt corroles from 2e- to 4e-

Abstract

Efficient oxygen reduction reaction (ORR) is crucial for the performance of fuel cells and other electrochemical devices. Seeking for stable and electrochemically selective 2e- and 4e- ORR electrocatalyst is yet a challenge, making the design extremely important and outmost of interest. In this study, we demonstrate a method to tune ORR selectivity by adjusting the local cobalt density through oligo-/polymerization of π-conjugated cobalt(III) A2B and A3-corroles to linear and two-dimensional matrix structures. These heterogeneous catalysts exhibit remarkable physicochemical properties, fast charge transfer kinetics, electrochemical reversibility, and high durability. Unselective three-electron transfer kinetics with n = 2.5–2.9 in between −0.20 V and +0.40 V vs. RHE are detected with the π-conjugated cobalt(III) A2B- corrole polymers. Highly selective four-electron kinetics with n = 3.7 in between −0.20 V and +0.40 V vs. RHE are detected by employing the cobalt A3-corrole oligomers during the ORR catalysis.

Keywords

• Cobalt
• Corrole
• Polymer
• H2O2 and H2O electrosynthesis
• Catalyst
• Oxygen reduction reactions