In Situ Encapsulated CuCo@M-SiO2 for Higher Alcohol Synthesis from Biomass-Derived Syngas

Higher alcohol synthesis (HAS) from biomass-derived syngas (CO/H 2 ) is of considerable interest but has a challenge to achieve a satisfying yield, as it is a competitive reaction between C–C coupling and CO insertion. Herein, we employed a solvent (dihydric alcohol) coordination-assisted impregnation strategy to synthesize a series of catalysts with Cu and Co encapsulated in ordered mesoporous SiO 2 (denoted as CuCo@M-SiO 2 ). This synthesis strategy could effectively anchor Cu and Co cations at a close distance owing to the solvent coordination effect. Additionally, the carbon derived from the thermal decomposition (inert atmosphere) of the solvent ligand portrayed a critical role in in situ reduction of Cu and Co species and synchronous confinement. It also helped structural dispersant (“spacer”) and inhibited the aggregation of Cu nanoparticles (NPs). The as-prepared CuCo@M-SiO 2 catalyst contained multiple types of synergistic active sites (Cu 0, Co 0, and Co n + ) that collaborated with each other to enhance the higher alcohol yield. It is confirmed that the CO conversion and higher alcohol selectivity were closely related to solvent-assisted ligands. Among the selected solvent ligands (ethylene glycol, 1,2-propanediol, and 1,4-butanediol), the CuCo@M-SiO 2 catalyst derived from 1,2-propanediol-assisted impregnation exhibited a remarkably catalytic performance because of the appropriate confinement effect with smaller CuCo NPs. Notably, the CO conversion was as high as 82.2% with space–time yield toward 16.1 mmol g cat –1 h –1 of ethanol. A narrow alcohol distribution of C 1 –C 3 -mixed alcohols was over 97.2%. These synthetic strategies may provide new avenues for designing effective and stable catalysts for HAS.