A series of Ce 1-x Zr x O 2 (x = 0, 0.1, 0.2, 0.3) solid solution supported lean-burn NO x trap (LNT) catalysts K/LaCoO 3 /Ce 1-x Zr x O 2 were prepared by successive impregnation. After sulfation the supported perovsikte LaCoO 3 was well maintained; reducing treatment partly destroyed the perovsikte, but it can be well recovered by re-oxidation treatment. Based on NO x storage and sulfurresisting performance of the catalysts, the optimal atomic ratio of Zr in Ce 1-x Zr x O 2 support is x = 0.2. The catalyst K/LaCoO 3 /Ce 0.8 Zr 0.2 O 2 exhibits much better NO x storage capacity than the Pt-based catalyst Pt/K/Ce 0.8 Zr 0.2 O 2 , which is highly related to its stronger capability for NO to NO 2 oxidation. During NO x storage much larger amounts of nitrate and nitrite species were identified by in situ DRIFTS over perovskite-based catalysts than over Pt-based one. The H 2 -TPR results reveal that after deep sulfation little sulfur species were deposited on the catalyst K/LaCoO 3 /Ce 1-x Zr x O 2 , showing strong sulfur-resisting ability. As a result, it is thought that the full replacement of Pt by perovskite LaCoO 3 in the corresponding LNT catalysts is feasible.