摘要
Aluminum fluoride layers (AlFx) were prepared by the in situ etching of Ti 3 AlC 2 with 1,1-difluoroethane at elevated temperatures. During etching, Ti layers were fluorinated to stable TiF 3 interacting with C to confine the Al species and sublimable TiF 4 . Al layers were fluorinated to unsaturated AlFx with relatively weak Lewis acidity. Due to the sublimation of TiF 4 , more AlFx acting as the main active centers were exposed to the reactants, and the surface areas of the confined-AlFx were increased, which contributed to the enhanced activity of the catalyst. The evaluation of the dehydrofluorination reaction showed that confined-AlFx layers presented higher reaction rate than F-γ-Al 2 O 3 and AlF 3 . Besides, it was unexpected that TiF 3 also exhibited activity for the reaction, even though the activity was much lower than confined-AlFx. Finally, the experimental results were confirmed by DFT calculations.
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