Gold nanoparticles (AuNPs) are widely used as optical probes in colorimetric detection, thanks to their high molar extinction coefficient. However, sample matrixes of high salinity or strong acidity/alkalinity often break the electrostatic repulsion of AuNPs suspension, or/and the surface functionality of AuNPs, causing strong and unfavorable interferences. Photochemical vapor generation (PVG) is an efficient technique for the sample matrix separation. Besides, it possesses distinct features of green reducing reagent, reduced interferences from concomitant elements, and direct speciation by the assistance of photocatalyst. Herein, we developed a photochemical vapor generation (PVG) method for the green and direct speciation analysis of inorganic selenium (i.e., Se(IV) and Se(VI)), by colorimetric or visual monitoring of unmodified AuNPs. The generated Se species from PVG were directed into the AuNPs solution for a reaction to take place, which produced a specific new absorption band at 600 nm for detection. The experimental parameters, including the concentration of organic acid, the sample flow rate, the concentration of AuNPs, and the flow rate of carries gas, were optimized in detail. Under optimized conditions, the limits of detection (LOD) for Se(IV) and Se(VI) were 0.007 and 0.006 μg mL −1 by UV−vis detection, respectively. It is worth mentioning that 0.08 μg mL −1 Se can induce an obvious color change, which can be directly observed with the naked eye. Relative standard deviations (RSDs) of 4.5% and 4.3% were obtained from seven replicate measurements of 0.15 μg mL −1 Se(IV) and Se(VI) standard solution, respectively. The developed assay has been successfully applied for the speciation of Se in a dietary supplement sample and environmental water samples including lake water, seawater, simulated water reference materials, and tap water.

The metal stable isotope detection strategy demonstrates a wide linear range and a low detection limit, showing promising potential in clinical diagnosis.