A single-atom Cu–N(2) catalyst eliminates oxygen interference for electrochemical sensing of hydrogen peroxide in a living animal brain

Hydrogen peroxide (H(2)O(2)) plays essential roles in various physiological and pathological processes. The electrochemical hydrogen peroxide reduction reaction (HPRR) has been recognized as an efficient approach to H(2)O(2) 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 (Cu(1)/C(3)N(4)) 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 Cu(1)/C(3)N(4) single-atom catalyst (SAC). With the Cu(1)/C(3)N(4) SAC as the electrocatalyst, we fabricated microsensors that have a good response to H(2)O(2), but not to O(2) 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 H(2)O(2) production induced by mercaptosuccinate and glutathione monoethyl ester in a living animal brain.