Department of Chemical Engineering and Materials Science, Stevens Institute of Technology, Hoboken, NJ 07030, USA.
Operando Molecular Spectroscopy and Catalysis Laboratory, Department of Chemical Engineering, Lehigh University, Bethlehem, PA 18015, USA. Department of Chemical Engineering, National Chung Hsing University, Taichung, Taiwan, Republic of China.
Science. 2015 May 8;348(6235):686-90. doi: 10.1126/science.aaa7048. Epub 2015 Apr 9.
Direct methane conversion into aromatic hydrocarbons over catalysts with molybdenum (Mo) nanostructures supported on shape-selective zeolites is a promising technology for natural gas liquefaction. We determined the identity and anchoring sites of the initial Mo structures in such catalysts as isolated oxide species with a single Mo atom on aluminum sites in the zeolite framework and on silicon sites on the zeolite external surface. During the reaction, the initial isolated Mo oxide species agglomerate and convert into carbided Mo nanoparticles. This process is reversible, and the initial isolated Mo oxide species can be restored by a treatment with gas-phase oxygen. Furthermore, the distribution of the Mo nanostructures can be controlled and catalytic performance can be fully restored, even enhanced, by adjusting the oxygen treatment.
在具有钼(Mo)纳米结构的择形沸石负载的催化剂上将甲烷直接转化为芳烃是一种很有前途的天然气液化技术。我们确定了此类催化剂中初始 Mo 结构的身份和锚定位置,这些结构包括沸石骨架中铝位上的单 Mo 原子和沸石外表面上的硅位上的单 Mo 原子的孤立氧化物物种。在反应过程中,初始的孤立 Mo 氧化物物种团聚并转化为碳化 Mo 纳米颗粒。这一过程是可逆的,初始的孤立 Mo 氧化物物种可以通过气相氧处理来恢复。此外,通过调整氧处理,可以控制 Mo 纳米结构的分布,并完全恢复甚至增强催化性能。