Abstract
The cost- and material-efficient development of nextgeneration
catalysts would benefit greatly from a molecular-level understanding
of the interaction between reagents and catalysts in chemical
conversion processes. Here, we trace the conversion of alkene and glycol in
single zeolite catalyst particles with unprecedented chemical and spatial
resolution. Combined nonlinear Raman and two-photon fluorescence
spectromicroscopies reveal that alkene activation constitutes the first
reaction step toward glycol etherification and allow us to determine the
activation enthalpy of the resulting carbocation formation. Considerable
inhomogeneities in local reactivity are observed for micrometer-sized
catalyst particles. Product ether yields observed on the catalyst are ca. 5
times higher than those determined off-line. Our findings are relevant for
other heterogeneous catalytic processes and demonstrate the immense
potential of novel nonlinear spectromicroscopies for catalysis research.
Original language | English |
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Pages (from-to) | 1124-1129 |
Number of pages | 6 |
Journal | Journal of the American Chemical Society |
Volume | 134 |
Issue number | 2 |
DOIs | |
Publication status | Published - 2012 |