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Abstract Metallic silver (Ag) sites exhibit a robust ability to suppress undesired C−C coupling in the electrocatalytic semihydrogenation of acetylene (C 2 H 2) into ethylene (ESAE), leading to satisfactory selectivity and stability. However, the relatively low reaction kinetics still hinder its practical value. Here, the facet‐dependent ESAE performance is first evaluated to increase the sluggish hydrogenation kinetics and provide mechanistic insight for subsequent catalyst design. As a result, the Ag nanocubes with 100 surfaces demonstrate a partial current density of 337 mA cm −2 at −1. 5 V vs. RHE, greatly outperforming their counterparts with 111 surfaces exposed. Further comparisons of H 2 O splitting and C 2 H 2 hydrogenation reveal that the activation of C 2 H 2 is a crucial factor in promoting the kinetics of ethylene electrosynthesis. Additionally, experimental and theoretical mechanistic characterizations demonstrate that stronger C 2 H 2 adsorption over the 100 surface strengthens the π conjugation of C 2 H 2, leading to the delocalization of π electrons to promote the activation of C 2 H 2 for enhanced hydrogenation kinetics.
Miao et al. (Wed,) studied this question.