The influence of ionic radii and valence of dopants in Ce_0.9La_xYb_yZr_0.1−x−yO_2−δ (x = 0, 0.05, 0.1, y = 0, 0.05, 0.1) on the oxidation kinetics were investigated by thermogravimetric analysis in synthetic air and were compared to undoped ceria. Samples co-doped with Zr–La and Zr–Yb exhibited moderate oxidation kinetics that were slower than undoped ceria, but much faster than 10mol% Zr-doped ceria. The extrinsic oxygen vacancy induced by the trivalent dopants improves the kinetics at oxidation temperatures below 700 °C, where the diffusion, and not the surface exchange reaction is the limiting factor. A smaller ionic radius of the substituent (i.e. r(Yb³⁺) < r(La³⁺)) in the co-doped ceria tends to facilitate lower activation energy resulting in slightly faster oxidation kinetics at temperatures below 700 °C. In contrast, additional extrinsic vacancies are rather obstructive at high temperatures (i.e. T > 700 °C) due to a change of rate limiting mechanism from bulk oxygen diffusion to surface exchange reaction. Overall, the valence of the dopant rather than the ionic radius seems to determine the oxidation kinetics primarily, and additional La or Yb doping on Zr-doped ceria is appealing especially when the applications are focused on low temperature reactions.