Boosting CO hydrogenation towards C 2+ hydrocarbons over interfacial TiO 2-x /Ni catalysts.
Ming XuXuetao QinYao XuXiaochen ZhangLirong ZhengJin-Xun LiuMeng WangXi LiuDing MaPublished in: Nature communications (2022)
Considerable attention has been drawn to tune the geometric and electronic structure of interfacial catalysts via modulating strong metal-support interactions (SMSI). Herein, we report the construction of a series of TiO 2-x /Ni catalysts, where disordered TiO 2-x overlayers immobilized onto the surface of Ni nanoparticles (~20 nm) are successfully engineered with SMSI effect. The optimal TiO 2-x /Ni catalyst shows a CO conversion of ~19.8% in Fischer-Tropsch synthesis (FTS) process under atmospheric pressure at 220 °C. More importantly, ~64.6% of the product is C 2+ paraffins, which is in sharp contrast to the result of the conventional Ni catalyst with the main product being methane. A combination study of advanced electron microscopy, multiple in-situ spectroscopic characterizations, and density functional theory calculations indicates the presence of Ni δ- /TiO 2-x interfacial sites, which could bind carbon atom strongly, inhibit methane formation and facilitate the C-C chain propagation, lead to the production of C 2+ hydrocarbon on Ni surface.
Keyphrases
- metal organic framework
- transition metal
- density functional theory
- ionic liquid
- visible light
- highly efficient
- quantum dots
- molecular dynamics simulations
- molecular dynamics
- electron microscopy
- magnetic resonance
- room temperature
- signaling pathway
- electron transfer
- magnetic resonance imaging
- working memory
- particulate matter
- contrast enhanced