▎ 摘　　要

Organic toxins are persistent chemicals of global concern capable of accumulating in environment and food. Surface enhanced Raman spectroscopy (SERS) is a promising technique that facilitates onsite detection of organic toxins. However, the fabrication of a SERS substrate is complicated and difficult to provide flexibility, fastness and cost-effectiveness. This study aims to develop a paper-based SERS method using grape skin-gold nanoparticles/graphene oxide (GE-AuNPs/GO) as SERS substrate and evaluate its efficiency with rhodamine 6G (Rh6G) as a model organic toxin and a real water and food contaminant. GE-AuNPs synthesized by green method using grape skin waste extract and GE-AuNPs/GO showed a surface plasmon resonance at 536 and 539 nm, particle size 18.6 and 19.5 nm, and zeta potential-44.6 and-59.7 mV, respectively. Paper-based SERS substrates were prepared by coating a hydrophobic thin-film of 30% polydimethylsiloxane solution in hexane on Whatman no. 1 filter paper, followed by drop-casting GE-AuNPs or GE-AuNPs/GO and drying. The SERS signals of Rh6G showed an enhancement factor of 5.8 x 10(4) for GE-AuNPs and 1.92 x 10(9) for GE-AuNPs/GO, implying that a combination of electromagnetic surface plasmon, charge transfer and molecular resonances may be responsible for a higher enhancement of signal by the latter. A low detection limit of 7.33 x 10(-11) M in the linear range of 10(-11)-10(-5) M was obtained for GE-AuNPs/GO, while the relative standard deviation of repeatability and reproducibility was 9.6 and 12.6%, respectively. Paper-based GE-AuNPs/GO SERS substrate was highly stable as < 20% loss in efficiency was shown over a 60-day storage period. Application to real samples showed a high recovery of Rh6G from tap water (93.9-100.8%) as well as food samples such as red chilli powder (91.0-95.4%), red glutinous rice ball (96.6-98.3%) and tomato ketchup (98.9-102.3%) after QuEChERS extraction. Collectively, the developed paper-based GE-AuNPs/GO can be a potential substrate for sensitive onsite detection of rhodamine 6G by SERS method.