Lead-cooled fast reactor (LFR) is one of the most promising reactor types among the six reactor concepts outlined in the Technology Roadmap for Generation IV Nuclear Energy Systems. Lead-bismuth eutectics (LBEs) are often used as coolants for LFRs because of their excellent economy and safety. However, structural materials are eroded by high-density LBEs at high temperatures. The compatibility between LBE and structural materials is a key problem that must be urgently solved for the development and application of LFRs. Due to the pinning of dislocations and grain boundaries as well as capture of displaced atoms and helium bubbles by oxide nanoparticles, oxide dispersion strengthened (ODS) alloys exhibit outstanding high-temperature mechanical properties and swelling resistance under irradiation. Fe-based ODS alloys have emerged as candidates for cladding tubes and structural materials in advanced reactors. A protective alumina scale can be formed on the alloy surface by adding Al to ODS alloys, which prevents the further penetration of LBEs into the alloy substrate. However, Y-Al-O complex-oxide nanoparticles with a slightly larger size compared to Y-Ti-O complex nanoparticles (in ODS FeCr alloy) are also formed in the alloy, leading to a slight decrease in the high-temperature strength of ODS FeCrAl alloys. It is known that adding a small amount of Zr to ODS FeCrAl alloys is an effective strategy to compensate for the decrease of mechanical properties caused by the coarseness of oxide nanoparticles, as numerous small-sized Y-Zr-O complex nanoparticles would preferentially precipitate instead of Y-Al-O complex nanoparticles. Thus far, studies on the corrosion behavior and corresponding mechanism of ODS FeCrAl alloys containing Zr in LBEs have been scarce. In this work, ODS FeCrAl alloys containing Zr were prepared via powder metallurgy. After the alloys were corroded by an oxygen-saturated static liquid LBE at 550 ^oC for 10000 h, its corrosion products were characterized by SEM, XRD, and EPMA. The effects of Zr, Ti, Al, and O contents on the corrosion resistance of ODS FeCrAl alloys were studied. Due to the combination of Zr and O and its interference with the outward diffusion of Al at the initial stage of oxidation, no continuous, protective aluminum oxide scale was formed on the surface of the ODS FeCrAl alloys. The corrosion products were mainly composed of thin alumina scale and multilayer oxide nodules, and no peeling of oxidation products was observed on any of the specimens. Further, it was revealed that the outer layer of these oxide nodules was composed of Fe₃O₄ with a magnetite phase, the inner layer was composed of spinel FeCr₂O₄ and Fe(Cr, Al)₂O₄, and the internal oxidation zone (IOZ) contained the oxide of Al and Cr. In addition, the distribution and morphology of oxide nodules were also affected by the contents of Ti, Al, and O in the alloys. With an increase in O content, high-density Y-Zr-O complex nanoparticles precipitated in the ODS FeCrAl alloys containing Zr, which led to a reduction in the content of residual Zr in the substrate. Consequently, the Zr content, which adversely affected the formation of alumina scale, was reduced, and the quantity, thickness, and surface transverse dimension of oxide nodules decreased. Introducing Ti into the ODS FeCrAl alloys containing Zr was also found to be unfavorable to the formation of the alumina scale as its impact on corrosion behavior was similar to that of Zr. With the addition of Ti, an increased number of oxide nodules were formed on the surface of Zr-containing ODS FeCrAl alloys. Because the addition of (4.0%-5.5%)Al does not prevent the formation of Fe-rich oxide nodules on the ODS FeCrAl alloys containing approximately 0.3%Zr, it is necessary to further increase the Al content in the matrix to obtain a continuous alumina scale.