Phase Engineering of Zirconia Support Promotes the Catalytic Dehydrogenation of Formic Acid by Pd Active Sites

The development of Pd-based catalysts with outstanding activity and stability can further promote the hydrogen storage application of formic acid (FA). Regulating the support structure is an effective strategy for enhancing active sites in heterogeneous catalytic systems. This study prepared three types of nanosized ZrO₂ through phase engineering to support Pd metal and investigated the implications of support structure on the microenvironment of active sites, thus revealing the structure-activity relationship of the catalysts. The hollow nanoframes like Pd/ZrO₂-F with a moderate t-ZrO₂ content exhibit remarkable stability and catalytic performance with a TOF of 1348 h^-1 at an ambient temperature. Density functional theory (DFT) calculations verify that the crystal phase of ZrO₂ can dramatically affect the metal-support interaction and change the Pd electronic state. Moreover, the dehydrogenation energy profiles reveal the synergy effect between ZrO₂ phases on Pd active sites in the reaction. Pd/m-ZrO₂ is more conducive to the dissociation of FA, and Pd/t-ZrO₂ has energy advantages in hydrogen recombination. This work provides a new perspective for understanding the synergistic effect of the zirconia crystal phase on formic acid dehydrogenation by Pd active sites.