Journal
TOPICS IN CATALYSIS
Volume 63, Issue 15-18, Pages 1412-1423Publisher
SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s11244-020-01306-y
Keywords
Fischer-Tropsch synthesis; Chain growth mechanism; Cobalt catalysts; Synchrotron XPS; Near-ambient pressure XPS; Elementary surface reactions
Categories
Funding
- Netherlands Organization for Scientific Research (NWO)
- Syngaschem BV
- Synfuels China Technology Co. Ltd.
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The identity of the surface intermediates involved in chain growth during Fischer-Tropsch synthesis remains a topic of ongoing debate. In the present work we use a combination of temperature programmed reaction spectroscopy and high resolution X-ray photoemission spectroscopy to study the reactivity of C(3)H(x)adsorbates on a Co(0001) single crystal surface in order to explore the stabilities of the different C(3)H(x)surface intermediates and to study elementary reaction steps relevant to chain growth and chain termination. Propene (H3C-CH=CH2) and propyl (H3C-CH2-CH2-) adsorbates react below 200 K already, either by desorption of propene or by dehydrogenation to adsorbed propyne (H3C-C equivalent to CH). Co-adsorbed H(ad)and CO(ad)do not affect the temperature at which propyl and propene react, but they do suppress the dehydrogenation pathway in favour of propene desorption. Their high reactivity under simulated FTS conditions disqualifies them as feasible intermediates for FTS, which requires long-lived intermediates to match the low monomer formation rate. Propyne, the most stable C(3)H(x)adsorbate in the absence of COad, is hydrogenated to propylidyne (H3C-CH2-C equivalent to) > 230 K when both CO(ad)and H(ad)are present. Propylidyne dimerization occurs around 313 K and produces a 3-hexyne (H5C2-C equivalent to C-C2H5) surface intermediate which is hydrogenated to 3-hexene (H5C2-CH=CH-C2H5) above 350 K. These findings are of direct relevance to FTS: they show that the high coverage of CO(ad)and H(ad)present during the reaction influence the reactivity of C(x)H(y)adsorbates involved in chain growth and ultimately steer product selectivity. The findings provide further experimental support for the previously proposed alkylidyne chain growth mechanism on close-packed cobalt terraces: CO stabilizes C(x)H(y)growth intermediates in the alkylidyne form and growth proceeds via coupling of a long chain alkylidyne and methylidyne (CH).
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