Lithium Ion Battery Materials as Tunable, Redox Non-Innocent Catalyst Supports
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 (Li<sub>x</sub>Mn<sub>2</sub>O<sub>4</sub>) to yield single-sites of Ni<sup>2</sup><sub></sub><sup>+</sup> (Ni/Li<sub>x</sub>Mn<sub>2</sub>O<sub>4</sub>). 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 Li<sub>x</sub>Mn<sub>2</sub>O<sub>4</sub>. Catalyst control through support redox non-innocence was extended to an organotantalum complex on lithium titanium oxide (Li<sub>x</sub>TiO<sub>2</sub>), demonstrating the generality of this phenomenon.