A single-atom Cu–N2 catalyst eliminates oxygen interference for electrochemical sensing of hydrogen peroxide in a living animal brain

Hydrogen peroxide (H₂O₂) plays essential roles in various physiological and pathological processes. The electrochemical hydrogen peroxide reduction reaction (HPRR) has been recognized as an efficient approach to H₂O₂ sensing; however, the HPRR has always suffered from low tolerance against the oxygen reduction reaction (ORR), resulting in poor selectivity of the HPRR-based sensing platform. In this study, we find that the electrochemical HPRR occurs preferentially compared to the ORR when isolated Cu atoms anchored on carbon nitride (Cu₁/C₃N₄) are used as a single-atom electrocatalyst, which is theoretically attributed to the lower energy barrier of the HPRR than that of the ORR on a Cu₁/C₃N₄ single-atom catalyst (SAC). With the Cu₁/C₃N₄ SAC as the electrocatalyst, we fabricated microsensors that have a good response to H₂O₂, but not to O₂ or other electroactive neurochemicals. When implanted into a living rat brain, the microsensor shows excellent in vivo sensing performance, enabling its application in real-time quantitative investigation of the dynamics of H₂O₂ production induced by mercaptosuccinate and glutathione monoethyl ester in a living animal brain.

We have achieved the selective monitoring of H₂O₂ fluctuation in vivo free from O₂ interference by a single-atom Cu–N₂ electrocatalyst.