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Träfflista för sökning "WFRF:(Amann Markus) "

Sökning: WFRF:(Amann Markus)

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  • Amann, Peter, et al. (författare)
  • The state of zinc in methanol synthesis over a Zn/ZnO/Cu(211) model catalyst
  • 2022
  • Ingår i: Science. - : American Association for the Advancement of Science (AAAS). - 0036-8075 .- 1095-9203. ; 376:6593, s. 603-608
  • Tidskriftsartikel (refereegranskat)abstract
    • The active chemical state of zinc (Zn) in a zinc-copper (Zn-Cu) catalyst during carbon dioxide/carbon monoxide (CO2/CO) hydrogenation has been debated to be Zn oxide (ZnO) nanoparticles, metallic Zn, or a Zn-Cu surface alloy. We used x-ray photoelectron spectroscopy at 180 to 500 millibar to probe the nature of Zn and reaction intermediates during CO2/CO hydrogenation over Zn/ZnO/Cu(211), where the temperature is sufficiently high for the reaction to rapidly turn over, thus creating an almost adsorbate-free surface. Tuning of the grazing incidence angle makes it possible to achieve either surface or bulk sensitivity. Hydrogenation of CO2 gives preference to ZnO in the form of clusters or nanoparticles, whereas in pure CO a surface Zn-Cu alloy becomes more prominent. The results reveal a specific role of CO in the formation of the Zn-Cu surface alloy as an active phase that facilitates efficient CO2 methanol synthesis.  
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  • Degerman, David, 1989-, et al. (författare)
  • Effect of CO2-Rich Syngas on the Chemical State of Fe(110) during Fischer-Tropsch Synthesis
  • 2024
  • Ingår i: The Journal of Physical Chemistry C. - 1932-7447 .- 1932-7455.
  • Tidskriftsartikel (refereegranskat)abstract
    • We have used in situ X-ray photoelectron spectroscopy to obtain information about the chemical state of a Fe single-crystal catalyst upon addition of CO2 in the syngas feed during Fischer–Tropsch synthesis (FTS) between 85 and 550 mbar. We found that at certain temperatures, the ternary mixture of CO, CO2, and H2 yields a chemical state which is resemblant of neither the CO hydrogenation nor the CO2 hydrogenation reaction mixtures in isolation. The addition of CO2 to a CO + H2 reaction mixture mostly affects the chemical state at low-temperature FTS conditions (i.e., below 254 °C). In this temperature span, the ternary reaction mixture resulted in a carburized surface, whereas the CO + H2 reaction led to surface oxidation. We propose a hypothesis, where a carbonate intermediate produced by CO2 interaction with Fe oxide aids the reduction of the Fe oxide, paving the way for the carburization of the Fe by dissociated CO. Very small differences in the spectra of the CO + H2 and the CO + CO2 + H2 reaction mixtures were observed above 254 °C, suggesting that the CO2 is a spectator in these conditions. Changing the total pressure of both the CO hydrogenation and ternary reaction mixture causes quantitative changes in the spectra at both low- and high-temperature FTS conditions, the degree of oxidation/carburization was affected in the low-temperature-FTS regime, and the degree of hydrocarbon build-up was affected in the high-temperature-FTS.
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  • Gleißner, Robert, et al. (författare)
  • Role of Oxidation–Reduction Dynamics in the Application of Cu/ZnO-Based Catalysts
  • 2023
  • Ingår i: ACS Applied Nano Materials. - 2574-0970. ; 6:9, s. 8004-8016
  • Tidskriftsartikel (refereegranskat)abstract
    • We investigated Cu nanoparticles (NPs) on vicinal and basal ZnO supports to obtain an atomistic picture of the catalyst’s structure under in situ oxidizing and reducing conditions. The Cu/ZnO model catalysts were investigated at elevated gas pressures by high energy grazing incidence X-ray diffraction and ambient pressure X-ray photoelectron spectroscopy (AP-XPS). We find that the Cu nanoparticles are fully oxidized to Cu2O under atmospheric conditions at room temperature. As the nanoparticles swell during oxidation, they maintain their epitaxy on basal ZnO (000 ± 1) surfaces, whereas on the vicinal ZnO (101̅4) surface, the nanoparticles undergo a coherent tilt. We find that the oxidation process is fully reversible under H2 flow at 500 K, resulting in predominantly well-aligned nanoparticles on the basal surfaces, whereas the orientation of Cu NPs on vicinal ZnO was only partially restored. The analysis of the substrate crystal truncation rods evidences the stability of basal ZnO surfaces under all gas conditions. No Cu–Zn bulk alloy formation is observed. Under CO2 flow, no diffraction signal from the nanoparticles is detected, pointing to their completely disordered state. The AP-XPS results are in line with the formation of CuO. Scanning electron microscopy images show that massive mass transport has set in, leading to the formation of larger agglomerates. 
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7.
  • Johansson, Matti, et al. (författare)
  • Integrated Assessment Modeling of Air Pollution in Four European Countries.
  • 2001
  • Ingår i: Water, Air and Soil Pollution. - 1573-2932. ; 130:1-4, s. 175-186
  • Tidskriftsartikel (refereegranskat)abstract
    • The integrated assessment modeling on acid rain has incorporated several related effects and pollutants into a multi-pollutant/multi-effect approach, resulting in complex integrated models and policy assessments. The development and implementation of effects-oriented cost-effective emission reduction strategies in Europe are based on integrated assessment models. The project on national integrated assessment modeling in Finland, Denmark, Spain and Sweden aimed to support the national evaluation of European emission reduction strategies. The tasks covered the comparison of inventories and projections for emissions of sulfur, nitrogen oxides, ammonia and volatile organic compounds, assessment of control techniques and related costs, concentration and deposition scenarios to estimate environmental effects of acidification, eutrophication and ground-level ozone and their temporal aspects, uncertainty analyses on both individual modules and whole integrated models, and dissemination of results to stakeholders. The integrated assessment modeling provided a consistent framework for the harmonization of input data and in-depth scientific research tasks on emissions, pollutant loading and impacts including comprehensive uncertainty analyses, and facilitated the dissemination of knowledge to policy-makers.
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8.
  • Kerrebrouck, Joris Van, et al. (författare)
  • 726.7-Gb/s 1.5-μm single-mode VCSEL discrete multi-tone transmission over 2.5-km multicore fiber
  • 2018
  • Ingår i: 2018 Optical Fiber Communications Conference and Exposition, OFC 2018 - Proceedings. - : Institute of Electrical and Electronics Engineers Inc.. - 9781943580385 ; , s. 1-3
  • Konferensbidrag (refereegranskat)abstract
    • A 107Gb/s net-rate DMT optical signal was generated using a single-mode long-wavelength VCSEL with a modulation bandwidth of 23 GHz. We experimentally demonstrated a total net-rate up to 726.7Gb/s at 1.5μm over 2.5km 7-core dispersion-uncompensated MCF.
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  • Knudsen, Jan, et al. (författare)
  • Stroboscopic operando spectroscopy of the dynamics in heterogeneous catalysis by event-averaging
  • 2021
  • Ingår i: Nature Communications. - : Springer Science and Business Media LLC. - 2041-1723. ; 12:1
  • Tidskriftsartikel (refereegranskat)abstract
    • Heterogeneous catalyst surfaces are dynamic entities that respond rapidly to changes in their local gas environment, and the dynamics of the response is a decisive factor for the catalysts’ action and activity. Few probes are able to map catalyst structure and local gas environment simultaneously under reaction conditions at the timescales of the dynamic changes. Here we use the CO oxidation reaction and a Pd(100) model catalyst to demonstrate how such studies can be performed by time-resolved ambient pressure photoelectron spectroscopy. Central elements of the method are cyclic gas pulsing and software-based event-averaging by image recognition of spectral features. A key finding is that at 3.2 mbar total pressure a metallic, predominantly CO-covered metallic surface turns highly active for a few seconds once the O2:CO ratio becomes high enough to lift the CO poisoning effect before mass transport limitations triggers formation of a √5 oxide.
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