Abstract
The development of general strategies
for the electronic tuning of a catalyst’s active site is an ongoing challenge
in heterogeneous catalysis. To this end we report the application of cathode and
anode materials as redox non-innocent catalyst supports that can be continuously
modulated as a function of lithium intercalation. A zero valent nickel complex
was oxidatively grafted onto the surface of lithium manganese oxide (LixMn2O4)
to yield single-sites of Ni2+ (Ni/LixMn2O4).
Its activity for olefin hydrogenation was found to be a function of the redox state
of the support material, with the most lithiated variant showing the most
activity. X-ray absorption, X-ray photoelectron, solid-state nuclear magnetic resonance
and electron paramagnetic resonance spectroscopies, and electron microscopy
techniques established
the nature of the nickel species on LixMn2O4. Catalyst control through support redox non-innocence
was extended to an organotantalum complex on lithium titanium oxide (LixTiO2),
demonstrating the generality of this phenomenon.
Supplementary materials
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FINAL CathodeSupportManuscript SI 20210209
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