Reveals that MXene supports influence dehydrogenation activity and stability in catalysts, suggesting new designs for efficient reactions.
Herein, a series of few layer MXene (Ti 3 C 2 T x, Ti 3 CNT x, Ti 2 NT x, Ti 2 CT x, Cr 2 CT x, Nb 2 CT x, and V 2 CT x ) are synthesized via a LiF/HCl etching-exfoliation method and employed as supports for Pt catalysts in fixed-bed methylcyclohexane (MCH) dehydrogenation reactions. The Pt/MXene catalysts exhibit strong support-dependent dehydrogenation activity and stability. Notably, Pt/Ti 3 C 2 T x shows the highest and most stable hydrogen evolution performance over the studied temperature range, while Pt/Nb 2 CT x deactivates due to carbon deposition at moderate to high temperatures. X-ray photoelectron spectroscopy analysis reveals that MXene supports effectively modulate the Pt 0 /Pt 2+ /Pt 4+ distribution, indicating unique metal–support electronic interactions. Further analysis using gas chromatography–mass spectrometry identifies olefin intermediates generated in the reaction, showing that interfacial chemical differences among MXene supports influence the reactant adsorption configuration, initial dehydrogenation sites, and intermediate isomerization behavior. Overall, this study elucidates how MXene supports regulate Pt sites and MCH dehydrogenation pathways, providing valuable insights for the design of efficient LOHC catalysts.
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Zhang et al. (2026) studied this question.
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