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104 reviewsMoisture contained in vehicle exhaust gas normally degrades the capacity and efficiency of Pd ion-exchanged
zeolites as NOx adsorbents by competitive adsorption on active sites. Here, we report a counterexample to
this general proposition, in which moisture facilitates the storage of NO as a nitrosyl complex on hydrated Pd
ions in high temperature calcined FER-type zeolites. Divalent Pd2+ cations upon elevated temperature (>800 ◦C)
calcination occupy sterically constrained cationic position in the zeolite framework, and become inactive for the
adsorption of probe molecules such as NO. These ‘hidden’ Pd ions, however, are accessible by NO when the
zeolite is hydrated, but readily release NO as dehydration proceeds. Combined systematic in situ infra-red data
with X-ray diffraction Rietveld analyses reveal that the high temperature-induced relocation of Pd ions to more
stable cationic positions located near 6-membered ring of the ferrierite cage is responsible for this behavior.