SBA-16 silica with intact surface hydroxyl groups was quickly obtained (5 min) via a fast-microwaveassisted method, and further adopted as an efficient template for the synthesis of three-dimensional (3D) ordered mesoporous CuO x -CeO 2 catalysts (htpCCx) through a simple and reproducible host-guest interaction. XRD, XPS, H 2 -TPR, and Raman results reveal that many of the Cu 2+ ions in htpCCx are incorporated into the CeO 2 lattice, leading to the formation of a Cu x Ce 12x O 22d solid solution, which produces a large number of oxygen vacancies and enhances the reducibility of the metal. The interaction of Cu and Ce is essential to the reaction as it maintains the Cu 2+ /Cu 1+ and Ce 4+ /Ce 3+ redox couples. The catalyst has a 3D mesostructure and possesses remarkably enhanced low-temperature activity for the combustion of epichlorohydrin. HtpCC20 has been identified as the most powerful catalyst for this reaction, with the reaction rate at 165 uC being about 6.3 and 33.3 times higher than those of catalysts synthesized using conventional incipient impregnation and thermal combustion methods, respectively. Furthermore, htpCC20 shows superior CO 2 selectivity (.99%) and stability (no deactivation occurs after 50 h reaction). It is believed that the dispersion of the active phase, density of surface active oxygen, and lowtemperature reducibility are the dominant factors governing the catalytic performance.