Tailoring OER/ORR Activity in TM1N4 Catalysts through First-/Second-Shell Nitrogen Doping: A Density Functional Theory Investigation

Abstract

Proposing an effective modification strategy to optimize catalyst reaction potentials is crucial for enhancing catalytic performance. In this study, we employed a combined approach by adjusting nitrogen dopants in the first- and second-shell environments to tailor the OER/ORR reaction potentials of Fe1N4, Co1N4, and Ni1N4 active centers. Using density functional theory simulations, we systematically compared the effects of first- and second-shell nitrogen dopants on the local atomic/electronic structures and catalytic activities. The results showed that first-shell nitrogen dopants had a dominant influence on the reaction potentials, while second-shell dopants provided fine-tuning adjustments. This combined regulation of nitrogen dopants in both shells significantly lowered the overpotentials for OER and ORR, enhancing the overall catalytic performance. Specifically, N2-doped Fe1-pyrrole N4 and N2-doped Fe1-pyridine N4 active centers demonstrated the lowest overpotentials of 205 mV for OER and 208 mV for ORR, respectively. This strategy offers a promising pathway for designing more efficient catalysts.