Revealing the origin of single‐atom W activity in H2O2 electrocatalytic production: Charge symmetry‐breaking

The low‐energy electrochemical production of hydrogen peroxide (H2O2) has garnered significant attention as a viable alternative to traditional industrial routes, with the goal of achieving carbon neutrality. For their H2O2 selectivity in the two‐electron oxygen reduction reaction (ORR), the coordination environment of tungsten (W)‐based materials is critical. In this study, atomically dispersed W single atoms were immobilized on N‐doped carbon substrates by a facile pyrolysis method to obtain a W single‐atom catalyst (W‐SAC). The coordination environment of an isolated W single atom with a tetra‐coordinated porphyrin‐like structure in W‐SAC was determined by X‐ray photoelectron spectroscopy and X‐ray absorption spectroscopy analysis. Notably, the as‐prepared W‐SAC showed superior two‐electron ORR activity in 0.1 M KOH solution, including high onset potential (0.89 V), high H2O2 selectivity (82.5%), and excellent stability. By using differential phase contrast‐scanning transmission electron microscopy and density functional theory calculations, it is revealed that the charge symmetry‐breaking of W atoms changes the adsorption behavior of the intermediates, leading to enhanced reactivity and selectivity for two‐electron ORR. This work broadens the avenue for understanding the charge transfer of W‐based electrocatalytic materials and the in‐depth reaction mechanism of SACs in two‐electron ORR.