Interface-Induced Phase Evolution and Spatial Distribution of Fe-Based Catalysts for Fischer–Tropsch Synthesis
Xiaoxue Han, Qiao Zhao, Huiyong Gong, Chongyang Wei, Jing Lv, Yue Wang, Mei‐Yan Wang, Shouying Huang, Xinbin Ma
Abstract
Fe-based catalysts undergo complex reduction, carburization, and phase interconversion as well as oxidation during Fischer–Tropsch synthesis (FTS). Unraveling the evolution of carbides and establishing the dominant factors are essential for rational design and modulation of Fe-based catalysts. In this work, Fe–oxide interfaces were constructed to investigate the effect on phase transformation and FTS performance. By correlating performance to the composition of iron species, the crucial role of Fe 2.2 C in high CO conversion and C 5+ productivity has been confirmed. More importantly, a heterogeneous spatial distribution of iron carbides and oxides induced by Fe–oxide interfaces was observed. Fe 3 O 4 preferentially forms at interfaces with the coexistence of carbon-rich Fe 2.2 C at subadjacent interfaces, while Fe 5 C 2 locates at the region away from oxides or in the bare Fe catalyst. Further ex / in situ characterizations, including XPS, TPO, in situ XRD, and in situ IR, were conducted for revealing the mechanism. This study provides insights for iron carbides formation and stability by modulating interfaces, which guides the further development of Fe-based FTS catalysts.