Transport Mediating Core–Shell Photocatalyst Architecture for Selective Alkane Oxidation
Chenlu Xie, Eddie Sun, Gang Wan, Jian Zheng, Raghubir Gupta, Arun Majumdar
Abstract
The high activation barrier of the C–H bond in methane, combined with the high propensity of methanol and other liquid oxygenates toward overoxidation to CO 2, have historically posed significant scientific and industrial challenges to the selective and direct conversion of methane to energy-dense fuels and chemical feedstocks. Here, we report a unique core–shell nanostructured photocatalyst, silica encapsulated TiO 2 decorated with AuPd nanoparticles (TiO 2 @SiO 2 -AuPd), that prevents methanol overoxidation on its surface and possesses high selectivity and yield of oxygenates even at high UV intensity. This room-temperature approach achieves high selectivity for oxygenates (94.5%) with a total oxygenate yield of 15.4 mmol/g cat ·h at 9.65 bar total pressure of CH 4 and O 2 . The working principles of this core–shell photocatalyst were also systematically investigated. This design concept was further demonstrated to be generalizable for the selective oxidation of other alkanes.