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Abstract Single-atom catalysts show excellent catalytic performance because of their coordination environments and electronic configurations. However, controllable regulation of single-atom permutations still faces challenges. Herein, we demonstrate that a polarization electric field regulates single atom permutations and forms periodic one-dimensional Au single-atom arrays on ferroelectric Bi 4 Ti 3 O 12 nanosheets. The Au single-atom arrays greatly lower the Gibbs free energy for CO 2 conversion via Au-O=C=O-Au dual-site adsorption compared to that for Au-O=C=O single-site adsorption on Au isolated single atoms. Additionally, the Au single-atom arrays suppress the depolarization of Bi 4 Ti 3 O 12 , so it maintains a stronger driving force for separation and transfer of photogenerated charges. Thus, Bi 4 Ti 3 O 12 with Au single-atom arrays exhibit an efficient CO production rate of 34.15 µmol·g −1 ·h −1 , ∼18 times higher than that of pristine Bi 4 Ti 3 O 12 . More importantly, the polarization electric field proves to be a general tactic for the syntheses of one-dimensional Pt, Ag, Fe, Co and Ni single-atom arrays on the Bi 4 Ti 3 O 12 surface.
Liu et al. (Fri,) studied this question.