Electronic properties of double-atom catalysts for electrocatalytic oxygen evolution reaction in alkaline solution: a DFT study

Abstract

In alkaline solution, the electrocatalytic oxygen evolution reaction (OER) of dual transition metal atom (2TM) nitrogen-decorated graphene as a double-atom catalyst (DAC) has received special attention. Here, using density functional theory (DFT) calculations, the OER electrocatalysis of 2TM-pyridine/amino-nitrogen-decorated graphene (2TM-N_PAG and 2TM-N_PG. 2TM represents FeCo, FeNi, Conti) is studied. The electrocatalytic OER mechanism is that 2TM-N_PG acts as the pre-catalyst, while the real catalysts are 2TM-N_PAG and 2TM-N_PG-O. In particular, CoNi-N_PAG and CoNi-N_PG-O exhibit higher OER activity compared to state-of-the-art RuO₂ at pH = 14. It is confirmed that the potential-determining step is also the rate-determining step. Amino-nitrogen is the main accepter of electrons from CoNi atoms and pyridine-nitrogen is the main acceptor of electrons from nearby C atoms. The role of different N coordination continues to influence the entire electrocatalytic OER process of CoNi-NG. Simultaneously, the overpotential of CoNi-NG is in a volcano-shaped relationship with the electronic properties (oxidation state or d-band center) of the catalytic site of Co. Moreover, CoNi-N_PAG and CoNi-N_PG-O are the closest to the center of the OER overpotential (a function of the d-band center and oxidation state) contour plot, implying that they exhibit the best catalytic activity among all the CoNi-NG materials. The optimal electronic properties of CoNi-N_PAG and CoNi-N_PG-O contribute towards their excellent OER performance, and provide a new breakthrough in developing high-performance DACs.