Supramolecular confinement pyrolysis to carbon-supported Mo nanostructures spanning four scales for hydroquinone determination

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. Mo 2 C nanoparticles, Mo 2 C 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＞Mo 2 C nanodots＞Mo nanoclusters＞Mo 2 C 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. • Mo nanostructures spanning four scales are fabricated. • The electrochemical behavior of HQ on the above Mo nanostructures is studied. • Performance sequence is Mo SAs＞Mo 2 C NDs＞Mo NCs＞Mo 2 C NPs. • Mo SAs/NPO-C shows a wide detection range and a low detection limit for HQ.