The adjustment of the electrochemiluminescence (ECL) of polymeric carbon nitride (C3N4) is essential for its application in sensitive immunoassays. However, such modification through aggregation-induced emission (AIE) has not yet been reported. Herein, aggregation-induced ECL in C3N4 oligomer (CNO) was induced through the introduction of a rotatable imine moiety, with the resulting material exhibiting excellent performance in the targeted immunodetection of neuron-specific enolase. Phenyl-modified CNO was synthesized through one-step pyrolysis at a reduced temperature. The rotatable benzene ring and triazine group formed a dynamic structure, which exhibited strong aggregation in water-doped solvents. compared to unmodified graphitic C3N4, CNO demonstrated higher intrinsic ECL efficiency and more readily accessible ECL signals. AIE inducing polymerization was conducted via nanoprecipitation, and the resulting CNO micro-flowers were employed as a sensing platform. A CNO-based sensor was prepared by combining CNO micro-flowers with copper-based bimetallic phenolic network nanoparticles as a quencher. Sensitive signal quenching was achieved owing to the electron transfer of Cu2+ and antioxidation properties of polyphenolic structures. The prepared sandwich-type immunosensor for neuron-specific enolase showed a limit of detection of 0.12 pg/mL in the detection range of 0.001-100 ng/mL. This study presents an effective strategy for the ECL signal amplification of C3N4, which is conducive to fundamental research in ECL and the application of the proposed sensor in the early diagnosis of diseases.
Keywords: Aggregation-induced electrochemiluminescence; Carbon nitride oligomer; Dual quenching; Immunoassay of NSE; Metal-phenolic network.
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