Oxygen Vacancy-Enriched Alumina Stabilized Pd Nanocatalysts for Selective Hydrogenation of Phenols
Qingyuan Wu1,2, Yuanyuan Zhong1, Lu Zhou1
1New Cornerstone Science Laboratory, State Key Laboratory for Physical Chemistry of Solid Surfaces, Collaborative Innovation Center of Chemistry for Energy Materials, and National & Local Joint Engineering Research Center of Preparation Technology of Nanomaterials, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China.
Abstract:
The prevalence of electronic defects has not been successfully demonstrated in nonreducible oxides. This work presents a straightforward approach to the preparation of a yellow alumina rich in F-centers (oxygen vacancies containing free electrons), which is well characterized by systematic spectral methods. The surface electron density of the as-prepared F-center enriched alumina sample was estimated to be approximately 0.35 mmol·g-1. Free electrons on the surface can reduce palladium precursors in situ, leading to the deposition of fine Pd nanoparticles on alumina. The produced Pd nanocatalysts are highly effective in the selective hydrogenation of phenol to cyclohexanone, achieving a high catalytic performance under mild conditions (30 °C and 0.1 MPa of H2). Systematic mechanism investigations reveal that hydroxyl radicals generated at the catalyst interfaces facilitate the activation of phenol. The activated phenol is then sequentially hydrogenated to give the intermediate 2-cyclohexenone and then the desired cyclohexanone. The catalyst system demonstrates efficacy in selectively hydrogenating substituted phenols into a wide array of functional ketones.
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