Zeolites with appropriately narrow pore apertures can kinetically enhance the selective adsorption of CO₂ over N₂. Here, we showed that the exchangeable cations (e.g., Na⁺ or K⁺) on zeolite ZK-4 play an important role in the CO₂ selectivity. Zeolites NaK ZK-4 with Si/Al = 1.8–2.8 had very high CO₂ selectivity when an intermediate number of the exchangeable cations were K⁺ (the rest being Na⁺). Zeolites NaK ZK-4 with Si/Al = 1.8 had high CO₂ uptake capacity and very high CO₂-over-N₂ selectivity (1190). Zeolite NaK ZK-4 with Si/Al = 2.3 and 2.8 also had enhanced CO₂ selectivity with an intermediate number of K⁺ cations. The high CO₂ selectivity was related to the K⁺ cation in the 8-rings of the α-cage, together with Na⁺ cations in the 6-ring, obstructing the diffusion of N₂ throughout the zeolite. The positions of the K⁺ cation in the 8-ring moved slightly (max 0.2 Å) toward the center of the α-cage upon the adsorption of CO₂, as revealed by in situ X-ray diffraction. The CO₂-over-N₂ selectivity was somewhat reduced when the number of K⁺ cations approached 100%. This was possibly due to the shift in the K⁺ cation positions in the 8-ring when the number of Na⁺ was going toward 0%, allowing N₂ diffusion through the 8-ring. According to in situ infrared spectroscopy, the amount of chemisorbed CO₂ was reduced on zeolite ZK-4s with increasing Si/Al ratio. In the context of potential applications, a kinetically enhanced selection of CO₂ could be relevant for applications in carbon capture and bio- and natural gas upgrading.