摘要
The amplification of detection signals is an important method for improving the sensitivity of electrochemical detection. This study presents an efficient strategy for preparing electrochemical catalytic materials using a simple self-assembly technique to encapsulate Fe single atoms (Fe–SAs) and Ni single atoms (Ni–SAs) in the Cu-benzene-1,3,5-tricarboxylic acid (Cu-BTC) metal–organic framework to form a Cu-BTC@FeNi–SAs catalytic system. Subsequently, Cu-BTC@FeNi–SAs was modified on the surface of a gold electrode, and sulfadiazine was used as a template to prepare a molecularly imprinted polymer (MIP) on the modified electrode. After eluting sulfadiazine, an MIP was obtained for specifically recognising sulfadiazine. When sulfadiazine was adsorbed by the MIP, a differential pulse voltammetry (DPV) signal occurred in response, thus detecting sulfadiazine. The adoption of Cu-BTC-fixed FeNi–SAs significantly facilitated mass transfer during the reaction, thus improving the DPV response signal. When used to detect sulfadiazine, the sensor had a linear range from 5 × 10−12 to 6000 × 10−12 mol L−1 and a detection limit of 1.14 × 10−12 mol L−1. It also successfully detected sulfadiazine residue in seawater and fish samples with recovery rates between 91.02% and 99.20%.
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