Year: 2026
Type: article
Abstract: ABSTRACT Manipulating the spillover of reactants represents a pivotal strategy to govern reaction pathways and boost the efficiency of heterogeneous catalysis, enabling reactive species to spontaneously navigate the path of least kinetic resistance. Herein, we establish a “catalytic shunt” by integrating discrete Ag/SiO 2 and Ag/CeO 2 nanounits into a unique Ag/CeO 2 ||SiO 2 architecture that decouples competing reaction steps in dimethyl oxalate (DMO) hydrogenation to methyl glycolate (MG). Notably, Ag/CeO 2 with well‐defined polyhedral Ag nanoparticles is catalytically inert, due to overwhelming C═O adsorption on positively charged Ag δ+ sites. However, mechanically integrating with Ag/SiO 2 (featuring spherical Ag NPs) unlocks unprecedented activity for C═O hydrogenation. In this featured configuration (Ag/CeO 2 ||SiO 2 ), in‐depth characterizations and theoretical calculations reveal that H 2 is activated on metallic Ag 0 (Ag/SiO 2 moieties) and efficiently spills over to activate DMO pre‐polarized on Ag δ+ (Ag/CeO 2 subunits). Remarkably, even with only 5% of Ag nanoparticles on CeO 2 , the Ag/CeO 2 ||SiO 2 system delivers a turnover frequency (TOF) 6‐fold higher than benchmark Ag/SiO 2 . The engineered configuration ensures ultra‐high H 2 utilization and enhanced thermal stability, maintaining robust stability over 1000 h. This spatial shunting strategy thus provides a powerful paradigm for the rational design of cooperative catalytic interfaces that circumvent competitive adsorption limits.
DOI: 10.1002/anie.3975660
Institutions: Xiamen University, North University of China
Language: English
Subfield: Organic Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: bronze
Awards: G1338417440, G3653223971, G8726661846
OpenAlex ID: W7204477773