W Single-Atom Catalyst for CH 4 Photooxidation in Water Vapor.
Ye WangJiangwei ZhangWen-Xiong ShiGui-Lin ZhuangQiu-Ping ZhaoJing RenPeng ZhangHua-Qing YinTong-Bu LuZhi-Ming ZhangPublished in: Advanced materials (Deerfield Beach, Fla.) (2022)
Solar-driven high-efficiency and direct conversion of methane into high-value-added liquid oxygenates against overoxidation remains a great challenge. Herein, facile and mass fabrication of low-cost tungsten single-atom photocatalysts is achieved by directly calcining urea and sodium tungstate under atmosphere (W-SA-PCN-m, urea amount m = 7.5, 15, 30, and 150 g). The single-atom photocatalysts can manage H 2 O 2 in situ generation and decomposition into ·OH, thus achieving highly efficient CH 4 photooxidation in water vapor under mild conditions. Systematic investigations demonstrate that integration of multifunctions of methane activation, H 2 O 2 generation, and decomposition into one photocatalyst can dramatically promote methane conversion to C1 oxygenates with a yield as high as 4956 µmol g cat -1 , superior to that of the most reported non-precious photocatalysts. Liquid-solid phase transition can induce the products to facilely switch in from HCOOH to CH 3 OH by pulling the catalyst above water with CH 3 OH/HCOOH ratio from 10% (in H 2 O) to 80% (above H 2 O).