BNPd single-atom catalysts for selective hydrogenation of acetylene to ethylene: a density functional theory study

摘要

The mechanisms of selective hydrogenation of acetylene to ethylene on B₁₁N₁₂Pd single-atom catalyst were investigated through the density functional theory by using the 6-31++G** basis set. We studied the adsorption characteristics of H₂ and C₂H₂, and simulated the reaction mechanism. We discovered that H₂ underwent absolute dissociative chemisorption on single-atom Pd, forming the B₁₁N₁₂Pd(2H) dihydride complex, and then the hydrogenation reaction with C₂H₂ proceeded. The hydrogenation reaction of acetylene on the B₁₁N₁₂Pd complex complies with the Horiuti–Polanyi mechanism, and the energy barrier was as low as 26.55?kcal?mol?1. Meanwhile, it also has a higher selectivity than many bimetallic alloy single-atom catalysts.