Abstract
Core-shell ZIF-8@ZIF-67- and ZIF-67@ZIF8-based zeolitic imidazolate frameworks (ZIFs) were synthesized solvothermally using a seed-mediated methodology. Transmission electron microscopy-energy-dispersive X-ray spectrometry, line scan, elemental mapping, X-ray photoelectron spectroscopy, and inductively coupled plasma-atomic emission spectroscopy analyses were performed to confirm the formation of a core-shell structure with the controlled Co/Zn elemental composition of similar to 0.50 for both the core-shell ZIFs. The synthesized core-shell ZIF-8@ZIF-67 and ZIF-67@ZIF8 frameworks conferred enhanced H-2 (2.03 and 1.69 wt %) storage properties at 77 K and 1 bar, which are ca. 41 and 18%, respectively, higher than that of the parent ZIF-8. Notably, the distinctly remarkable H-2 storage properties shown by both the core-shell ZIFs over the bimetallic Co/Zn-ZIF and the physical mixture of ZIF-8 and ZIF-67 clearly evidenced their unique structural properties (confinement of porosity) and elemental heterogeneity due to the core-shell morphology of the outperforming core-shell ZIFs. Moreover, H-2 adsorption isotherm data of these frameworks are best fitted with the Langmuir model (R-2 >= 0.9999). Along with the remarkably enhanced H-2 storage capacities, the core-shell ZIFs also displayed an improved CO2 capture behavior. Hence, we demonstrated here that the controlled structural features endorsed by the rationally designed porous materials may find high potential in H-2 storage applications.