Catalyst Screening and Mechanism Elucidation of Two-Dimensional Transition Metal Coordinated Porphyrin-Analogue Materials for Nitrogen Fixation
Wenfeng Hu, Bingyi Song, Li‐Ming Yang
Abstract
This paper reports the construction of a series of two-dimensional (2D) transition metal coordinated porphyrin-analogue catalytic materials and employs a combined strategy of the first-principles calculations and high-throughput screening to systematically investigate their catalytic activity and reaction mechanisms of electrocatalytic nitrogen reduction reaction (NRR). Ninety metal porphyrin-analogue catalysts are obtained by embedding 30 transition metals (3–5d series) into three classes of two-dimensional porphyrin-analogue substrates. High-throughput screening and full reaction pathway search reveal that MoP p -β- H - meso -Diyne, MoP p - meso - H -β-Ph and MoP p - meso - H -β-Py are the optimal catalysts via the distal pathway with onset potentials of −0.21, −0.26 and −0.28 V, respectively. WP p - meso - H -β-Py and ReP p -β- H - meso -Diyne also exhibit good catalytic performance with onset potentials of −0.46 and −0.46 V, respectively. All five catalytic materials demonstrate good electronic conductivity and high stability. A volcano-shaped relationship is unveiled between the free energy change of the first protonation step (Δ G *N 2 → *N 2 H ) and the onset potential ( U onset ), which can be utilized to describe the catalytic activity of NRR and guide the design and selection of efficient catalysts.