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Stabilization of ?-iron carbide as high-temperature catalyst under realistic Fischer-Tropsch synthesis conditions.


ABSTRACT: The development of efficient catalysts for Fischer-Tropsch (FT) synthesis, a core reaction in the utilization of non-petroleum carbon resources to supply energy and chemicals, has attracted much recent attention. ?-Iron carbide (?-Fe2C) was proposed as the most active iron phase for FT synthesis, but this phase is generally unstable under realistic FT reaction conditions (> 523?K). Here, we succeed in stabilizing pure-phase ?-Fe2C nanocrystals by confining them into graphene layers and obtain an iron-time yield of 1258??molCO gFe-1s-1 under realistic FT synthesis conditions, one order of magnitude higher than that of the conventional carbon-supported Fe catalyst. The ?-Fe2C@graphene catalyst is stable at least for 400?h under high-temperature conditions. Density functional theory (DFT) calculations reveal the feasible formation of ?-Fe2C by carburization of ?-Fe precursor through interfacial interactions of ?-Fe2C@graphene. This work provides a promising strategy to design highly active and stable Fe-based FT catalysts.

SUBMITTER: Lyu S 

PROVIDER: S-EPMC7719174 | biostudies-literature | 2020 Dec

REPOSITORIES: biostudies-literature

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Stabilization of ε-iron carbide as high-temperature catalyst under realistic Fischer-Tropsch synthesis conditions.

Lyu Shuai S   Wang Li L   Li Zhe Z   Yin Shukun S   Chen Jie J   Zhang Yuhua Y   Li Jinlin J   Wang Ye Y  

Nature communications 20201204 1


The development of efficient catalysts for Fischer-Tropsch (FT) synthesis, a core reaction in the utilization of non-petroleum carbon resources to supply energy and chemicals, has attracted much recent attention. ε-Iron carbide (ε-Fe<sub>2</sub>C) was proposed as the most active iron phase for FT synthesis, but this phase is generally unstable under realistic FT reaction conditions (> 523 K). Here, we succeed in stabilizing pure-phase ε-Fe<sub>2</sub>C nanocrystals by confining them into graphen  ...[more]

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