open access publication

Article, 2024

Surface ZnO x on zirconia is highly active for high temperature methanol synthesis

Journal of Catalysis, ISSN 1090-2694, 0021-9517, Volume 431, Page 115389, 10.1016/j.jcat.2024.115389

Contributors

Nikolajsen, M.T. [1] Grivel, Jean-Claude Roger 0000-0001-7835-9054 [1] Gaur, Abhijeet 0000-0001-5328-9280 [2] Hansen, L.P. [3] Baumgarten, Lorena 0000-0002-4510-0676 [2] Schjødt, Niels Christian 0009-0001-0358-8503 [3] Mentzel, U.V. [3] Grunwaldt, Jan-Dierk 0000-0003-3606-0956 [2] Sehested, J. [3] Christensen, Jakob Munkholt 0000-0002-2495-8905 [1] Høj, Martin 0000-0002-8482-3359 (Corresponding author) [1]

Affiliations

  1. [1] Technical University of Denmark
  2. [NORA names: DTU Technical University of Denmark; University; Denmark; Europe, EU; Nordic; OECD];
  3. [2] Karlsruhe Institute of Technology
  4. [NORA names: Germany; Europe, EU; OECD];
  5. [3] Topsoe A/S, Kgs. Lyngby 2800, Denmark
  6. [NORA names: Denmark; Europe, EU; Nordic; OECD]

Abstract

Zinc containing mixed metal oxides and supported zinc oxide are stable and selective methanol synthesis catalysts at temperatures where a subsequent methanol to hydrocarbons reaction can occur directly. This work provides fundamental insights into ZnO-based high temperature methanol synthesis catalysts. A pronounced support effect was observed, where ZrO2 provided a beneficial effect while SiO2 exerted a detrimental effect compared to bulk ZnO. Preparing co-precipitated ZnO-ZrO2 catalysts showed that the initial activity correlated with the amount of amorphous ZnO on the surface of the support and that the catalytic activity increased with time on stream as zinc oxide migrated out of a solid solution with ZrO2 and onto the support surface. Hence the active phase appeared to be ZnO surface species and not zinc oxide in a solid solution with ZrO2. Operando XAS coupled with modulation excitation spectroscopy unravelled that the surface ZnO was partly reduced under operating conditions, as surface ZnO x , with x approximately equal to 0.98. In-situ DRIFTS further uncovered that the surface ZnO x activated CO2 and formed methanol via carbonate, formate and methoxide species. XPS finally showed that ZrO2 withdrew electrons from ZnO, facilitating oxygen abstraction to form the partly reduced ZnO x , which in turn facilitated the activation of CO2.

Keywords

Abstract, CO2, SiO2, XAS, XPS, ZnO, ZnO x, ZnO., ZnO–ZrO2 catalyst, ZrO2, activate CO2, activation of CO2, active phase, activity, amorphous ZnO, amount, carbon, catalyst, catalytic activity, conditions, detrimental effects, drift, effect, electron, excitation spectroscopy, formation, high-temperature methanol synthesis, hydrocarbon reactions, in situ DRIFTS, metal, metal oxides, methanol, methanol synthesis, methanol synthesis catalyst, methanol-to-hydrocarbons reaction, methoxide, methoxide species, modulation, modulation excitation spectroscopy, operando, operando XAS, operating conditions, operation, oxidation, oxygen, oxygen abstraction, phase, reaction, solid solution, solution, species, spectroscopy, support, surface, surface ZnO, surface species, synthesis, synthesis catalyst, temperature, zinc, zinc oxide, zirconia

Funders

  • Danish Ministry of Higher Education and Science
  • Deutsche Forschungsgemeinschaft

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