Wen Wang, Jinsong Sun, Jiajun Liu, Zihao Zheng, Yaxu Sun, Yongzhuang Liu, Qinqin Xia, Zhihan Tong, Haipeng Yu
Glucose and 5-hydroxymethylfurfural (5-HMF) are attractive platforms for sustainable biomass valorization, yet cellulose conversion remains limited by substrate concentration, reaction conditions, and complex catalyst designs. Here, we report an acidic bifunctional solvent system (ZnCl2-H3PO4) that can both disrupt cellulose structure and promote rapid in situ cascade hydrolysis to glucose and 5-HMF. In this system, ZnCl2 (a Lewis acid) facilitates protonation of the β-1,4-glycosidic oxygen, while H3PO4 (a Brønsted acid) accelerates Zn2+ desolvation, together reducing cellulose crystallinity, activating C-O-C bonds, and lowering the energy barrier for carbocation formation. Under mild conditions (65°C), the process reaches completion within 10 min, achieving 94.8 mol% glucose (with a high concentration ∼ 130 mg/mL). Furthermore, this bifunctional solvent shows promise for converting the released glucose into 5-HMF by leveraging ZnCl2 for isomerization and H3PO4 for dehydration. This approach avoids the high temperatures and elaborates catalyst architectures typical of conventional acid hydrolysis, offering a streamlined route to efficient cellulose conversion.