H<sup>+</sup>−H<sup>−</sup> Pairs in Partially Oxidized MAX Phases for Bifunctional Catalytic Conversion of Furfurals into Linear Ketones
Qiang Deng, Rong Zhou, Yongchao Zhang, Xiang Li, Jiahui Li, Shaobo Tu, Guan Sheng, Jun Wang, Zheling Zeng, Tatchamapan Yoskamtorn, Shik Chi Edman Tsang
Abstract
Abstract Currently, less favorable C=O hydrogenation and weak concerted acid catalysis cause unsatisfactory catalytic performance in the upgrading of biomass‐derived furfurals (i.e., furfural, 5‐methyl furfural, and 5‐hydroxymethyl furfural) to ketones (i.e., cyclopentanone, 2,5‐hexanedione, and 1‐hydroxyl‐2,5‐hexanedione). A series of partially oxidized MAX phase (i.e., Ti 3 AlC 2 , Ti 2 AlC, Ti 3 SiC 2 ) supporting Pd catalysts were fabricated, which showed high catalytic activity; Pd/Ti 3 AlC 2 in particular displayed high performance for conversion of furfurals into targeted ketones. Detailed studies of the catalytic mechanism confirm that in situ hydrogen spillover generates Frustrated Lewis H + −H − pairs, which not only act as the hydrogenation sites for selective C=O hydrogenation but also provide acid sites for ring opening. The close intimate hydrogenation and acid sites promote bifunctional catalytic reactions, substantially reducing the reported minimum reaction temperature of various furfurals by at least 30–60 °C.