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Scott R. Docherty

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4 records found

Journal article (2026) - N. Phongprueksathat, Gina Noh, Scott R. Docherty, D. Vico Van Berkel, Yannik Stiefel, Christophe Copéret, A. Urakawa
The synergistic Cu–metal oxide (Cu–MOx) interface is critical for selective CO2 hydrogenation to methanol, yet its mechanistic function, the central, long-debated feature of industrial Cu/ZnO/Al2O3, remains ambiguous. Using operando transient DRIFTS-SSITKA, we elucidate the roles of M+ sites (Zn2+, Ga3+, and In3+) on model Cu─M/SiO2 catalysts prepared by surface organometallic chemistry (SOMC). X-ray absorption spectroscopy reveals that these promoters restructure from alloys after reduction to cationic species at the interface under reaction conditions. We find the promoter's electronic effect on formate bond strengths provides quantitative descriptors for both activity and selectivity. All catalysts follow a common formate spillover mechanism, with methoxy hydrogenation/desorption as the rate-limiting step. The intrinsic CH3OH formation rate follows a Sabatier-type volcano with C─O bond strength, while selectivity correlates linearly with C─H bond strength (a proxy for the formate decomposition barrier). Cu─Ga/SiO2 shows the fastest spillover, suppressing CO formation and yielding the highest selectivity; Cu─Zn/SiO2 has optimal binding for the highest activity; In3+ binds formate too strongly, creating a kinetic trap on the strong-binding side of the volcano. These findings bring mechanistic clarity to the debated Cu─Zn(O) synergy, showing selectivity is governed by a balance of electronic stabilization and spillover dynamics. ...
Journal article (2023) - Hui Zhou, Scott R. Docherty, Alexey Fedorov, Nat Phongprueksathat, Zixuan Chen, Andrey V. Bukhtiyarov, Igor P. Prosvirin, Olga V. Safonova, Atsushi Urakawa, Christophe Copéret, Christoph R. Müller
The direct synthesis of methanol via the hydrogenation of CO2, if performed efficiently and selectively, is potentially a powerful technology for CO2 mitigation. Here, we develop an active and selective Cu-Zn/SiO2 catalyst for the hydrogenation of CO2 by introducing copper and zinc onto dehydroxylated silica via surface organometallic chemistry and atomic layer deposition, respectively. At 230 °C and 25 bar, the optimized catalyst shows an intrinsic methanol formation rate of 4.3 g h-1 gCu-1 and selectivity to methanol of 83%, with a space-time yield of 0.073 g h-1 gcat-1 at a contact time of 0.06 s g mL-1. X-ray absorption spectroscopy at the Cu and Zn K-edges and X-ray photoelectron spectroscopy studies reveal that the CuZn alloy displays reactive metal support interactions; that is, it is stable under H2 atmosphere and unstable under conditions of CO2 hydrogenation, indicating that the dealloyed structure contains the sites promoting methanol synthesis. While solid-state nuclear magnetic resonance studies identify methoxy species as the main stable surface adsorbate, transient operando diffuse reflectance infrared Fourier transform spectroscopy indicates that μ-HCOO*(ZnOx) species that form on the Cu-Zn/SiO2 catalyst are hydrogenated to methanol faster than the μ-HCOO*(Cu) species that are found in the Zn-free Cu/SiO2 catalyst, supporting the role of Zn in providing a higher activity in the Cu-Zn system. ...
Journal article (2022) - Scott R. Docherty, Nat Phongprueksathat, Erwin Lam, Gina Noh, Olga V. Safonova, Atsushi Urakawa, Christophe Coperet
On page 452, column 1 (lines 12?23) reads: H2 and CO chemisorption show an uptake of 0.91 molH2 molPd?1 and 0.61 molCO molPd ?1, respectively (Table 1, Supporting Information S6). Considering a 1:1 CO/Pd stoichiometry,32 the dispersion from CO chemisorption (D?CO) equals 61%, in a reasonable agreement with the dispersion from TEM (D?TEM 70%; Supporting Information S9).32 While H2 chemisorption is not effective for a determination of the metal dispersion of Pd nanoparticles due to the formation of a stable bulk hydride with larger particles (2.6 nm),32 a comparison of the H2 uptake and D?CO would correspond to approximately three hydrogen atoms per surface Pd. ...