Molecular Precursor Routes for Ag-Based Metallic, Intermetallic, and Metal Sulfide Nanoparticles: Their Comparative ORR Activity Trend at Solid|Liquid and Liquid|Liquid Interfaces

[Image: see text] The electrochemical conversion of oxygen to water is a crucial process required for renewable energy production, whereas its first two-electron step produces a versatile chemical and oxidant—hydrogen peroxide. Improving performance and widening the limited selection of the potential catalysts for this reaction is a step toward the implementation of clean-energy technologies. As silver is known as one of the most effective catalysts of oxygen reduction reaction (ORR), we have designed a suitable molecular precursor pathway for the selective synthesis of metallic (Ag), intermetallic (Ag(3)Sb), and binary or ternary metal sulfide (Ag(2)S and AgSbS(2)) nanomaterials by judicious control of reaction conditions. The decomposition of xanthate precursors under different reaction conditions in colloidal synthesis indicates that carbon–sulfur bond cleavage yields the respective metal sulfide nanomaterials. This is not the case in the presence of trioctylphosphine when the metal–sulfur bond is broken. The synthesized nanomaterials were applied as catalysts of oxygen reduction at the liquid–liquid and solid–liquid interfaces. Ag exhibits the best performance for electrochemical oxygen reduction, whereas the electrocatalytic performance of Ag and Ag(3)Sb is comparable for peroxide reduction in an alkaline medium. Scanning electrochemical microscopy (SECM) analysis indicates that a flexible 2-electron to 4-electron ORR pathway has been achieved by transforming metallic Ag into intermetallic Ag(3)Sb.