Abstract

AbstractAn improved hematite α‐Fe2O3catalysts composed of uniform nanodisks closed with (0001) basal facets and {11‐20} side facets are prepared via a simple hydrothermal route. Moreover, by simply tuning the mass of the reaction precursors of Fe(NO3)3⋅9H2O, the size of the obtained hematite α‐Fe2O3nanodisks is controlled in the range of 600–100 nm in diameter and 43–230 nm in thickness, respectively. Due to the exposed (0001) basal facets and {11‐20} facets, in which more amount of Fe3+ion involved, the obtained α‐Fe2O3nanodisks exhibit enhanced reducibility. The maximum H2consumption occurs at relative lower temperature, ca. 490 °C for the smallest α‐Fe2O3nanodisks of 43 nm in thickness and 100 nm in diameter, respectively. Relatively, the Fe3+ions situated at (0001) planes facilitate the Fischer‐Tropsch synthesis (FTS) compared to that situated at {11‐20} planes. Due to the well dispersion and high fraction of (0001) basal facets, the α‐Fe2O3nanodisks with middle size of 190 nm in thickness and 400 nm in diameter propose the high CO2conversion and high hydrocarbon selectivity. Since more amount of (0001) basal facets are masked by the orientation aggregation along [0001] induced by the self‐magnetization, the least α‐Fe2O3nanodisks provide a declined catalytic performance for CO2hydrogenation.

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