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PostDoc
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NMR Spectroscopy
Since many of the materials of interest in our catalysis studies are metal oxide and mixed metal oxides, and many of the catalytic reactions of interest are redox reactions, it follows that a key element present at the reaction interface is oxygen. We have chosen to develop the use of this element, in particular the 17O isotope, a spin 5/2 quadrupolar nucleus, to probe the structure at reaction sites. The common isotopes of oxygen 16O, 18O, have no magnetic moment and are invisible in the NMR experiment. 17O is just 0.037% naturally abundant, so experiments incorporate a synthetic step to introduce the 17O label. While labor intensive, this chemical dimension provides a very important site-selectivity advantage, depending on the 17O component that are introduced at high abundance.
Indeed, the historic driving force for the implementation of µcoils is the gain in sensitivity achieved by this technique. Our interest in µcoils is in optimizing quadrupole NMR. We have generated large excitation fields by employing coils with ca 100 um diameters. The nutation plots to the right demonstrate rf field strengths of 6.2, 12.4 and 24.8 MHz in (a), (b), and (c) respectively. Future developments will combine high rf excitation and MAS NMR, with the goal of making solid state quadrupolar NMR more efficient.
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