Metal nanostructures with high atom utilization, abundant active sites, and special electron structures should be beneficial to the electrochemical monitoring of hydroquinone (HQ), a highly toxic environmental pollutant. However, traditional nanostructures, especially non-noble metals generally suffer from severe aggregation, or consist of a mixture of nanoparticles and nanoclusters, resulting in low detection sensitivity. Herein, we precisely control the size of Mo-based nanostructures spanning four scales (viz. Mo2C nanoparticles, Mo2C nanodots, Mo nanoclusters and Mo single atoms) anchored on N, P, O co-doped carbon support. The detection sensitivity of four samples toward the HQ follows the orders of Mo single atoms＞Mo2C nanodots＞Mo nanoclusters＞Mo2C nanoparticles. The catalytic ability of four catalysts is investigated, also showing the same order. The supported Mo single atoms show superior electro-sensing performance for HQ with wide linear range (0.02-200 μM) and low detection limit (0.005 μM), surpassing most previously reported catalysts. Moreover, the coexistence of dihydroxybenzene isomers of catechol (CC) and resorcinol (RC) does not interfere with the detection of HQ on the Mo single-atom sensor. This work opens up a polyoxometalate-based confinement pyrolysis approach to constructing ultrafine metal-based nanostructures spanning multiple-scales for efficient electrochemical applications.
Keywords: Hydroquinone determination; Mo single atoms; Mo-based nanostructures; Multiscale levels.
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