Ying Yang,Dongcheng Ren,ChunLi Shang,Zhongzhen Ding,Xinruo Luo
Direct conversion of cellulose to high yield 1,2-propylene glycol (1,2-PG) is amazing in the biomass valorization to diols, since this process is atom-economic, carbon neutral, and the produced 1,2-PG has a large market demand. However, it is very challenging to control cellulose hydrogenolysis owing to high reactivity of intermediates (like glucose) and metal-acid repelling, leading to decreased selectivity of metal-acid multi-functional catalysts. Aimed at this, we herein developed a highly selective metal-acid catalyst (Ru/NC@void@MC-SO 3 H) with site isolated Ru clusters (1.4 nm) on the core and sulfoacids on the shell in a yolk-shell nanoreactor by a layer-by-layer assembly before chemical transformation. The spatial isolation of metal and acid sites integrated in a mesoporous yolk-shell nanoreactor not only facilitates the metal-acid synergism in hydrolysis, isomerization/hydrogenolysis and hydrogenation cascade reactions, but also provides a designated diffusion pathway that is favorable for reaction species. As expected, the elaborately fabricated Ru/NC@void@MC-SO 3 H proves to be highly selective to 1,2- PG (38 % yield), delivering a productivity of 342.86 mol h −1 g Ru –1 and an extremely high turnover number of 173264, outperforming the state-of-art metal-acid catalysts for cellulose hydrogenolysis to 1,2-PG. Our characterization and performance test suggest that sulfoacids are mainly responsible for cellulose hydrolysis, while N -stabilized Ru centers contribute to the glucose isomerization to fructose and its further hydrogenolysis to dihydroxyacetone, followed by hydrogenation to 1,2-PG on metallic Ru species. The acidity and basicity optimized for site isolated Ru/NC@void@MC-SO 3 H is beneficial to balance intermediate reactions, rendering a higher selectivity to target 1,2-PG. The concept illustrated in this study will provide a guide for the development of other site isolated multi- functional catalysts towards cellulosic biomass conversion and other cascade reactions.
The electrochemical oxidation of 5-hydroxymethylfurfural (HMFOR) in alkaline electrolyte is a promising strategy for producing high-value chemicals from biomass derivatives. However, the disproportionation of aldehyde groups under strong alkaline conditions and the polymerization of HMF to form humic substances can impact the purity of 2,5-furandicarboxylic acid (FDCA) products. The use of neutral electrolytes offers an alternative environment for electrolysis, but the lack of OH − ions in the electrolyte often leads to low current density and low yields of FDCA. In this study, a sandwich-structured catalyst, consisting of Ru clusters confined between unilamellar MnO 2 nanosheets (S-Ru/MnO 2 ), was used in conjunction with an electrochemical pulse method to realize the electrochemical conversion of 5-hydroxymethylfurfural into FDCA in neutral electrolytes. Pulse electrolysis and the strong electron transfer between Ru clusters and MnO 2 nanosheets help maintain Ru in a low oxidation state, ensuring high activity. The increased *OH generation led to a groundbreaking current density of 47 mA/cm 2 at 1.55 V vs. reversible hydrogen electrode (RHE) and an outstanding yield rate of 98.7 % for FDCA in a neutral electrolyte. This work provides a strategy that combines electrocatalyst design with an electrolysis technique to achieve remarkable performance in neutral HMFOR.