Fanhui Liao, Weibin Liang, Meixian Li, Donghai Xu, Le Yang
Selective hydrogenation of carboxylic acids to alcohols remains a challenge due to the requirement of synergistic multiple active sites for H 2 activation, reactant adsorption, and selective C–O bond scission. Here, we construct a series of Co–Al metal–metal oxide (MMO) catalysts via the hydrogen-induced reduction of layered double hydroxide (LDH) precursors with tunable Co/Al ratios. The optimal Co 4 Al 1 -MMO catalyst exhibits highly dispersed Co 0 nanoparticles alongside abundant oxygen vacancies (O v -Co). The Co 0 /O v -Co dual sites synergistically promote H 2 dissociation and carbonyl oxygen C=O bond activation, while moderate lattice oxygen stabilizes the metastable structure. Under mild conditions (180 °C, 2 MPa of H 2, 3 h), the catalyst achieves 100% conversion of octanoic acid with 99% alcohol selectivity, outperforming state-of-the-art noble-metal systems. This work provides a general strategy for engineering cooperative metallic/defective sites in nonprecious MMO catalysts for selective hydrogenation reactions.