A nanodispersed
intermetallic GaPd2/SiO2 catalyst
is prepared by simple impregnation of industrially relevant high-surface-area
SiO2 with Pd and Ga nitrates, followed by drying, calcination,
and reduction in hydrogen. The catalyst is tested for CO2 hydrogenation to methanol at ambient pressure, revealing that the
intrinsic activity of the GaPd2/SiO2 is higher
than that of the conventional Cu/ZnO/Al2O3,
while the production of the undesired CO is lower. A combination of
complementary in situ and ex situ techniques are used to investigate
the GaPd2/SiO2 catalyst. In situ X-ray diffraction
and in situ extended X-ray absorption fine structure spectroscopy
show that the GaPd2 intermetallic phase is formed upon
activation of the catalyst via reduction and remains stable during
CO2 hydrogenation. Identical location–transmission
electron microscopy images acquired ex situ (i.e., micrographs of
exactly the same catalyst area recorded at the different steps of
activation and reaction procedure) show that nanoparticle size and
dispersion are defined upon calcination with no significant changes
observed after reduction and methanol synthesis. Similar conclusions
can be drawn from electron diffraction patterns and images acquired
using environmental TEM (ETEM), indicating that ETEM results are representative
for the catalyst treated at ambient pressure. The chemical composition
and the crystalline structure of the nanoparticles are identified
by scanning TEM energy dispersive X-ray spectroscopy, selected area
electron diffraction, and atomically resolved TEM images.