The rational synthesis of catalysts with controllable
structures
and the study of their structure–activity relationships to
break the limitations of traditional catalysts remain challenging.
Herein, tetrakis(dimethylamido)tin (TDMASn) exposures were used to
modify silicalite-1 (S-1) lacking suitable chemisorption sites on
their surfaces to provide Pt nucleation sites, obtaining a Pt/20TDMASn/S-1
sample. For comparison, Pt species supported on bare S-1 (Pt/S-1)
and Pt species supported on the S-1 of pre-deposited SnO2 (Pt/20SnO2/S-1) were also prepared. Catalysts were characterized
extensively by X-ray diffraction, temperature-programmed reduction,
transmission electron microscopy, X-ray photoelectron spectroscopy,
and diffuse-reflectance infrared Fourier transform spectroscopy of
adsorbed CO. The results showed that this surface modification (TDMASn
or SnO2) yielded up to about a 40-times increase in Pt
content after 20 cycles of Pt atomic layer deposition (ALD). Compared
with Pt/20SnO2/S-1, Pt/20TDMASn/S-1 had a smaller particle
size, stronger interactions between the metal species and the support,
and a lower Sn0 content, thus resulting in a remarkably
higher initial propane conversion in the propane dehydrogenation (PDH)
reaction. The catalytic activity could also be optimized based on
the number of ALD-TDMASn exposures. As a consequence, Sn not only
provided nucleation sites for Pt but also acted as a promoter to enhance
the catalyst performance. This fundamental understanding will help
researchers obtain suitable catalysts for PDH processes.