Journal
JOURNAL OF PHYSICAL CHEMISTRY C
Volume 121, Issue 15, Pages 8490-8497Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.7b01744
Keywords
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Funding
- Aston University for a Ph.D. studentship
- EPSRC [EP/K014676/1, EP/ K014749/1, EP/M005186/2]
- China Scholarship Council (CSC)
- European Research Council Advanced Grant MolArt [247299]
- Leverhulme Trust's Early Career Fellowship scheme
- Royal Society
- EPSRC [EP/M005186/2, EP/K014749/1, EP/M005186/1, EP/K014676/1] Funding Source: UKRI
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Furfural is a key bioderived platform chemical whose reactivity under hydrogen atmospheres affords diverse chemical intermediates. Here, temperature-programmed reaction spectrometry and complementary scanning tunneling microscopy (STM) are employed to investigate furfural adsorption and reactivity over a Pt(111) model catalyst. Furfural decarbonylation to furan is highly sensitive to reaction conditions, in particular, surface crowding and associated changes in the adsorption geometry: furfural adopts a planar geometry on clean Pt(111) at low coverage, tilting at higher coverage to form a densely packed furfural adlayer. This switch in adsorption geometry strongly influences product selectivity. STM reveals the formation of hydrogen-bonded networks for planar furfural, which favor decarbonylation on clean Pt(111) and hydrogenolysis in the presence of coadsorbed hydrogen. Preadsorbed hydrogen promotes furfural hydrogenation to furfuryl alcohol and its subsequent hydrogenolysis to methyl furan, while suppressing residual surface carbon. Furfural chemistry over Pt is markedly different from that over Pd, with weaker adsorption over the former affording a simpler product distribution than the latter; Pd catalyzes a wider range of chemistry, including ring-opening to form propene. Insight into the role of molecular orientation in controlling product selectivity will guide the design and operation of more selective and stable Pt catalysts for furfural hydrogenation.
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