Vacancy Engineering of Nickel Single-Atom Catalysts to Enable Low-Triggering-Potential Electrochemiluminescence of Carbon Nitride

The electrochemiluminescence (ECL) instability of graphitic carbon nitride (CN) caused by electrode passivation at a triggering potential exceeding −0.9 V has been widely recognized. Although doping, heterostructure, and vacancy engineering have been attempted to mitigate the electrode passivation of CN, achieving a strong ECL of CN at a potential of no more than −0.9 V remains a formidable challenge. This work innovatively developed nitrogen vacancy (Nv) engineering of nickel single-atom catalysts (Ni SACs) to enable ECL emission of CN at −0.9 V without any exogenous coreactants. The introduction of rich Nv on CN not only promoted the electrochemical reduction of CN but also adjusted the coordination environment of Ni single atoms (Ni SA ) to form a Ni–N 6 coordination structure. Theoretical calculation revealed that the Ni–N 6 structure effectively reduced the energy barrier of the oxygen reduction pathway and activated dissolved oxygen to produce a large number of reactive oxygen species (ROS), thus significantly promoting ECL emission and reducing the ECL potential of CN. As a proof of concept, Ni SA -Nv-CN was applied for sensitive ECL detection of the cancer biomarker flap endonuclease 1 (FEN1) with the aid of a multipath-activated CRISPR/Cas12a amplification strategy. Nv engineering of SACs provides a new thought to solve the electrode passivation of CN.