A facile method to
produce zeolitic imidazolate frameworks (ZIF-8,
ZIF-67, and solid–solution ZIFs (mixed Co and Zn)) is reported.
ZIF crystals are produced via a reaction–diffusion framework
(RDF) by diffusing an outer solution at a relatively high concentration
of the 2-methyl imidazole linker (HmIm) into an agar gel matrix containing
the metal ions (zinc(II) and/or cobalt(II)) at room temperature.
Accordingly, a propagating supersaturation wave, initiated at the
interface between the outer solution and the gel matrix, leads to
a precipitation front with a gradient of crystal sizes ranging between
100 nm and 55 μm along the reaction tube. While the precipitation
fronts of ZIF-8 and ZIF-67 travel the same distance for the same initial
conditions, ZIF-8 crystals therein are consistently smaller than the
ZIF-67 crystals due to the disparity of their rate of nucleation and
growth. The effects of the temperature, the concentration of the reagents,
and the thickness of the gel matrix on the growth of the ZIF crystals
are investigated. We also show that by using RDF we can envisage the
formation mechanism of the ZIF crystals, which consists of the aggregation
of ZIF nanospheres to form the ZIF-8 dodecahedrons. Moreover, using
RDF, the formation of a solid–solution ZIF via the incorporation
of Co(II) and Zn(II) cations within the same framework is achieved
in a controlled manner. Finally, we demonstrate that doping ZIF-8
by Co(II) enhances the photodegradation of methylene blue dye under
visible light irradiation in the absence of hydrogen peroxide.