The decisive role of adsorbed OH* in low‐potential CO electro‐oxidation on single‐atom catalytic sites

Abstract CO impurity‐induced catalyst deactivation has long been one of the biggest challenges in proton‐exchange membrane fuel cells, with the poisoning phenomenon mainly attributed to the overly strong adsorption on the catalytic site. Here, we present a mechanistic study that overturns this understanding by using Rh‐based single‐atom catalysis centers as model catalysts. We precisely modulated the chelation structure of the Rh catalyst by coordinating Rh with C or N atoms, and probed the reaction mechanism by surface‐enhanced Raman spectroscopy. Direct spectroscopic evidence for intermediates indicates that the reactivity of adsorbed OH*, rather than the adsorption strength of CO*, dictates the CO electrocatalytic oxidation behavior. The RhN₄ sites, which adsorb the OH* intermediate more weakly than RhC₄ sites, showed prominent CO oxidation activity that not only far exceeded the traditional Pt/C but also the RhC₄ sites with similar CO adsorption strength. From this study, it is clear that a paradigm shift in future research should be considered to rationally design high‐performance CO electro‐oxidation reaction catalysts by sufficiently considering the water‐related reaction intermediate during catalysis.