Quantifiable Regulation of Chemical Kinetics Barriers for Creation of Single-Atom Metal Sites on Photocatalytic Atomic Layers.

Cation exchange (CE) under mild conditions promises a facile strategy to anchor single metal sites on colloidal chalcogenides toward catalytic applications, which however has seldom been demonstrated. The dilemma behind this is the rapid kinetics and high efficiency of the reaction disfavoring atomic dispersion of the metal species. Here we report that a fine-tuning of the affinity between the incoming metal cations and the deliberately introduced ligands can be exploited to manipulate the kinetics of the CE reaction, in a quantitative and systematic manner defined by the Tolman electronic parameter of the ligands used. Moreover, the steric effect of metal-ligand complexes offers thermodynamic preference for spatial isolation of the metal atoms. These thereby allow the rational construction of single atom catalysts (SACs) via simple one-step CE reactions, as exemplified by the CE-derived incorporation of single metal atoms (M = Cu, Ag, Au, Pd) on SnS 2 two-unit-cell layers through M-S coordination.