The adsorption of CO 2 on zeolite Li-Rho (unit cell composition Li 9.8 Al 9.8 Si 38.2 O 96 ) has been investigated by the measurement of adsorption isotherms (273 -300 K), breakthrough curves with a CO 2 /CH 4 /He mixture (308 K) and in situ synchrotron X-ray powder diffraction in CO 2 (298 K). The Rho framework distorts when in the Li-form to give a shape selective adsorbent for CO 2 over CH 4 , although breakthrough curves reveal diffusional limitations. In situ synchrotron powder XRD follows the expansion of the Li-Rho unit cell upon adsorption, which remains single phase to a CO 2 pressure of ca. 0.6 bar. Partial cation exchange of Li-2 Rho by Na + or Cs + gives two series of M,Li-Rho zeolites (M = Na, Cs). Where the occupancy of window sites (8R, D8R) between lta cages is less than 50%, hysteresis is not observed in CO 2 isotherms at 298 K. For Cs 1.8 Li 8 -Rho, which has a larger unit cell and a wider window than zeolite Li-Rho due to the presence of large Cs + cations in double 8-ring sites, breakthrough curves indicate faster CO 2 diffusion without significant loss of selectivity. We propose this control of adsorption kinetics of the flexible zeolite Rho via modification of cation content as a mechanism for cation controlled molecular sieving.