Construction of an efficient molecular enrichment and magnetic separation flow with Fe3O4@Ag@COF for ratiometric SERS detection of methamidophos

• Fe 3 O 4 @Ag@COF based detection flow exhibits an excellent SERS performance. • COF endows Fe 3 O 4 @Ag@COF with a platform for enriching MTD molecules. • Fe 3 O 4 @Ag@COF with MTD molecules can be separated from complex matrix by magnetism. • The Raman peaks of COF can be employed as an internal standard for ratiometric SERS sensing. • The detection flow exhibited an ultra-low MTD detection of 8.3 × 10 -5 mg/kg. As a typical organophosphorus pesticide widely utilized in agricultural production with its residue as enormous threat to human health and environment, methamidophos (MTD) has gained increasing attention in recent years, so, it is necessary to develop an effective strategy to detect MTD from complex matrix. Here, an efficient molecular enrichment and magnetic separation flow was constructed through Fe 3 O 4 @Ag@COF (covalent organic framework) for ratiometric SERS detection of MTD. Specifically, Fe 3 O 4 @Ag@COF is shown to have a high-density hot-spot region and optimal SERS performance by adjusting the particle size and addition volume of Fe 3 O 4 @Ag. COF endows Fe 3 O 4 @Ag@COF with a platform for enriching MTD molecules and isolating impurities, allowing the separation of Fe 3 O 4 @Ag@COF with MTD molecules from complex matrix by magnetism. More importantly, due to its natural core–shell structure, the Raman peaks of COF can be employed as an internal standard for ratiometric SERS sensing, thereby increasing its analysis accuracy and reliability. Under the optimal extraction method and solvent conditions, the developed detection flow exhibited a wide linear range from 10 -4 M to 10 -9 M and a low MTD detection limit of 8.3 × 10 -5 mg/kg. Furthermore, the SERS sensor had excellent reproducibility and long-term stability with a low relative standard deviation (RSD). In practical application, this detection flow was tested for quantifying trace MTD in green tea samples, with recoveries of 89.54 % to 101.89 % and RSDs below 5 % (n = 5), comparable to the performance of gas chromatography mass spectrometry (GC–MS).