Synergistic oxygen vacancy-rich CuO/visible light activation of peroxymonosulfate for degradation of rhodamine B: fast catalyst synthesis and degradation mechanism

This work outlines the synthesis of copper oxide nanoparticles (CuO-SC) loaded with a number of oxygen vacancies by a fast sodium citrate assisted precipitation method with no need of calcination. X-ray diffraction, scanning electron microscopy, UV-Vis diffuse reflectance spectroscopy, time-resolved fluorescence lifetime and electrochemical impedance spectra were used to characterize the as-synthesized nanocomposites. The results indicated that the CuO-SC nanoparticles had regular fusiform shape with high surface area, wide light harvesting window, fast charge transport and high carrier concentration. As a result, the catalytic activity of the CuO-SC/peroxymonosulfate (PMS)/visible light (Vis) system for the degradation of rhodamine B (RhB) was much higher than that of as-prepared CuO nano powder in the absence of sodium citrate. Almost 98.0% of the initial RhB dyes was decomposed in 20 min with 0.12 g L(−1) PMS and 0.3 g L(−1) catalyst. Meantime, it exhibited high catalytic stability with little deactivation after four runs and a wide application range of pH. Moreover, RhB can be readily degraded with backgrounds of Cl(−), NO(3)(−), SO(4)(2−), HCO(3)(−) and low concentration of humic acid in a CuO-SC/PMS/Vis system. Combined with the results of electron spin resonance paramagnetic spectroscopy, X-ray photoelectron spectroscopy and radical quenching experiments, holes, superoxide radicals and a small amount of sulfate radicals, hydroxyl radicals and singlet oxygen were involved in the CuO-SC/PMS/Vis system. Furthermore, a possible degradation mechanism based on the synergistic effect of radical reaction and non-radical reaction was proposed based on the above results.