Facile generation of unsaturated-coordinated and atomically-dispersed hafnium active sites for the highly efficient catalytic transfer hydrogenation of levulinic acid

The sluggish kinetic of the hydrogen transfer reaction pose a significant challenge in developing efficient catalytic transfer hydrogenation (CTH) system for upgrading biomass-derived platform molecules. In this contribution, for the first time, hafnium (Hf) species have been found to coordinate with the hydroxyl groups on halloysite nanotubes surface to construct a single-atom Hf catalyst (Hf@HNTs) with unsaturated-coordinated structure at room temperature. Especially, the Hf(1.7)@HNTs delivered an impressive catalytic performance for the CTH of levulinic acid (LvA) to gamma-valerolactone (GVL) with high turn-over frequency (TOF) of 43.1 h −1 at 160 °C, considerably exceeding that of coordination-saturated HfO 2 and state-of-art Hf-based catalysts. Experimental and density functional theory (DFT) studies revealed that Hf(1.7)@HNTs possessed unsaturated-coordinated and atomically-dispersed Hf-O Lewis acid-base pairs, which favored the adsorption and activation of LvA. Moreover, DFT calculations explicitly demonstrated that the energy barriers for the hydrogen transfer between the LvA and hydrogen donor were significantly reduced on the Hf(1.7)@HNTs than that of HfO 2 .