The inorganic cation-tailored “trapdoor” effect of silicoaluminophosphate zeolite for highly selective CO₂ separation

Abstract

Functional nanoporous materials are widely explored for CO₂ separation, in particular, small-pore aluminosilicate zeolites having a "trapdoor" effect. Such an effect allows the specific adsorbate to push away the sited cations inside the window followed by exclusive admission to the zeolite pores, which is more advantageous for highly selective CO₂ separation. Herein, we demonstrated that the protonated organic structure-directing agent in the small-pore silicoaluminophosphate (SAPO) <b>RHO</b> zeolite can be directly exchanged with Na⁺, K⁺, or Cs⁺ and that the Na⁺ form of SAPO-<b>RHO</b> exhibited unprecedented separation for CO₂/CH₄, superior to all of the nanoporous materials reported to date. Rietveld refinement revealed that Na⁺ is sited in the center of the single eight-membered ring (<i>s</i>8<i>r</i>), while K⁺ and Cs⁺ are sited in the center of the double 8-rings (<i>d</i>8<i>r</i>s). Theoretical calculations showed that the interaction between Na⁺ and the <i>s</i>8<i>r</i> in SAPO-<b>RHO</b> was stronger than that in aluminosilicate <b>RHO</b>, giving an enhanced "trapdoor" effect and record high selectivity for CO₂ with the separation factor of 2196 for CO₂/CH₄ (0.02/0.98 bar). The separation factor of Na-SAPO-<b>RHO</b> for CO₂/N₂ was 196, which was the top level among zeolitic materials. This work opens a new avenue for gas separation by using diverse silicoaluminophosphate zeolites in terms of the cation-tailored "trapdoor" effect.