Surface structure and reactivity of
multi-component oxides at the atomic scale
Subproject P02
Multi-component metal oxides exhibit a plethora of stoichiometry-dependent structural phases at the surface, even if the composition of the bulk is kept the same. The long-term objective of P02 is to unravel the relationship between surface electronic and geometric structure and reactivity, to ultimately tune these materials for energy-related reactions such as the ORR. The project applies the surface science approach. We will grow well-defined, epitaxial perovskite thin films of LSFO and LSMO in a UHV-based PLD/surface science apparatus under tight control of the surface stoichiometry in the first project period. We will determine the coordinates of surface atoms quantitatively using LEED-IV in close collaboration with theoretical groups.
Theoretical models will also help with interpreting atomically-resolved ncAFM/STM images. These images give direct insights into the behavior of polarons in these complex materials and show how adsorbates such as O2, H2O, CO, and CO2 interact with electronic and structural defects. XPS, TPD, and FTIR of these well-defined systems will deliver desorption energies, vibrational frequencies, and spectral fingerprints. These experimental data on well-defined systems will build a bridge when tested under ‘realistic’ environments at high pressure/temperature and in aqueous solutions. They will also serve to validate ML-based theory approaches.
Expertise
Our expertise is experimental surface science. We operate a total of seven ultrahigh-vacuum (UHV) chambers, which contain virtually all main experimental surface science techniques, as well as an (electro-)chemistry lab.
All chambers are equipped with facilities for sample preparation (sputtering/annealing/gas dosing), as well as various growth techniques (e-beam evaporators, Knudsen cells, UHV-compatible sputter deposition, pulsed laser deposition (PLD)).
Analysis techniques used in our research include:
- Scanning Tunneling Microscopy (STM) (in UHV 4K – 300 K, electrochemical STM)
- Atomic Force Microscopy (AFM): UHV-based (q+ sensor) and in the ambient (cantilever-based)
- Low-Energy Electron Diffraction (LEED)
- Reflection High Energy Diffraction (RHEED)
- X-ray Photoelectron Spectroscopy (XPS)
- Ultraviolet Photoelectron Spectroscopy (UPS)
- Auger Electron Spectroscopy (AES)
- Low-energy He+ ion scattering (LEIS)
- Thermal Programmed Desorption Spectroscopy (TPD)
Team
Former Members
Publications
2016
Lukashuk, Liliana; Föttinger, Karin; Kolar, Elisabeth; Rameshan, Christoph; Teschner, Detre; Hävecker, Michael; Knop-Gericke, Axel; Yigit, Nevzat; Li, Hao; McDermott, Eamon; Stöger-Pollach, Michael; Rupprechter, Günther
Operando XAS and NAP-XPS studies of preferential CO oxidation on Co3O4 and CeO2-Co3O4 catalysts
Journal ArticleOpen AccessIn: Journal of Catalysis, vol. 344, pp. 1–15, 2016.
Abstract | Links | BibTeX | Tags: P08, P10, pre-TACO
@article{Lukashuk2016,
title = {Operando XAS and NAP-XPS studies of preferential CO oxidation on Co_{3}O_{4} and CeO_{2}-Co_{3}O_{4 }catalysts},
author = {Liliana Lukashuk and Karin Föttinger and Elisabeth Kolar and Christoph Rameshan and Detre Teschner and Michael Hävecker and Axel Knop-Gericke and Nevzat Yigit and Hao Li and Eamon McDermott and Michael Stöger-Pollach and Günther Rupprechter},
doi = {10.1016/j.jcat.2016.09.002},
year = {2016},
date = {2016-12-01},
urldate = {2016-12-01},
journal = {Journal of Catalysis},
volume = {344},
pages = {1--15},
publisher = {Elsevier BV},
abstract = {Co_{3}O_{4} is a promising catalyst for removing CO from H_{2} streams via the preferential CO oxidation (PROX). A Mars-van-Krevelen redox mechanism is often suggested but a detailed knowledge especially of the oxidation state of the catalytically active surface under reaction conditions is typically missing. We have thus utilized operando X-ray absorption spectroscopy to examine structure and oxidation state during PROX, and near atmospheric pressure-XPS at low photoelectron kinetic energies and thus high surface sensitivity to monitor surface composition changes. The rather easy surface reduction in pure CO (starting already at ∼100 °C) and the easy reoxidation by O_{2} suggest that molecularly adsorbed CO reacts with lattice oxygen, which is replenished by gas phase O_{2}. Nevertheless, the steady state concentration of oxygen vacancies under reaction conditions is too low even for XPS detection so that both the bulk and surface of Co_{3}O_{4} appear fully oxidized during PROX. Furthermore, the effect of adding CeO_{2} (a less active material) to Co_{3}O_{4} was studied. Promotion of Co_{3}O_{4} with 10 wt% CeO_{2} increases the reduction temperatures in CO and H_{2} and enhances the PROX activity. Since CeO_{2} is a less active material, this can only be explained by a higher activity of the Co-O-Ce interface.},
keywords = {P08, P10, pre-TACO},
pubstate = {published},
tppubtype = {article}
}
Wolfbeisser, Astrid; Sophiphun, Onsulang; Bernardi, Johannes; Wittayakun, Jatuporn; Föttinger, Karin; Rupprechter, Günther
Methane dry reforming over ceria-zirconia supported Ni catalysts
Journal ArticleOpen AccessIn: Catalysis Today, vol. 277, pp. 234–245, 2016.
Abstract | Links | BibTeX | Tags: P08, P10, pre-TACO
@article{Wolfbeisser2016,
title = {Methane dry reforming over ceria-zirconia supported Ni catalysts},
author = {Astrid Wolfbeisser and Onsulang Sophiphun and Johannes Bernardi and Jatuporn Wittayakun and Karin Föttinger and Günther Rupprechter},
doi = {10.1016/j.cattod.2016.04.025},
year = {2016},
date = {2016-11-15},
urldate = {2016-11-15},
journal = {Catalysis Today},
volume = {277},
pages = {234--245},
publisher = {Elsevier BV},
abstract = {Nickel nanoparticles supported on Ce_{1-x}Zr_{x}O_{2} mixed oxides prepared by different synthesis methods, as well as Ni-ZrO_{2} and Ni-CeO_{2}, were evaluated for their catalytic performance in methane dry reforming (MDR). MDR is an interesting model reaction to evaluate the reactivity and surface chemistry of mixed oxides. Textural and structural properties were studied by N_{2} adsorption and XRD. Mixed oxide preparation by co-precipitation resulted in catalysts with higher surface area than that of pure ZrO_{2} or CeO_{2}. XRD analysis showed the formation of different Ce_{1-x}Zr_{x}O_{2} solid solutions depending on using a surfactant or not. The catalyst prepared by surfactant assisted co-precipitation was not active for methane dry reforming most likely because of the encapsulation of Ni particles by ceria-zirconia particles, as revealed by TEM and H_{2} chemisorption. The catalytic activity of the catalyst prepared by co-precipitation without surfactant was comparable to Ni-ZrO_{2}. Clearly, catalyst activity strongly depends on preparation and on the resulting phase composition rather than on nominal composition. Compared to Ni-ZrO_{2} the ceria-zirconia supported Ni catalyst did not achieve higher activity or stability for methane dry reforming but, nevertheless, the formation of filamentous carbon was strongly reduced (100 times less carbonaceous species). Consequently, using ceria-zirconia as a support material decreases the risk of reactor tube blocking.},
keywords = {P08, P10, pre-TACO},
pubstate = {published},
tppubtype = {article}
}
2014
Föttinger, Karin; Rupprechter, Günther
Journal ArticleIn: Accounts of Chemical Research, vol. 47, no. 10, pp. 3071–3079, 2014.
Abstract | Links | BibTeX | Tags: P08, P10, pre-TACO
@article{Foettinger2014,
title = {In Situ Spectroscopy of Complex Surface Reactions on Supported Pd–Zn, Pd–Ga, and Pd(Pt)–Cu Nanoparticles},
author = {Karin Föttinger and Günther Rupprechter},
doi = {10.1021/ar500220v},
year = {2014},
date = {2014-09-23},
journal = {Accounts of Chemical Research},
volume = {47},
number = {10},
pages = {3071--3079},
publisher = {American Chemical Society (ACS)},
abstract = {It is well accepted that catalytically active surfaces frequently adapt to the reaction environment (gas composition, temperature) and that relevant “active phases” may only be created and observed during the ongoing reaction. Clearly, this requires the application of in situ spectroscopy to monitor catalysts at work. While changes in structure and composition may already occur for monometallic single crystal surfaces, such changes are typically more severe for oxide supported nanoparticles, in particular when they are composed of two metals. The metals may form ordered intermetallic compounds (e.g. PdZn on ZnO, Pd_{2}Ga on Ga_{2}O_{3}) or disordered substitutional alloys (e.g. PdCu, PtCu on hydrotalcite). We discuss the formation and stability of bimetallic nanoparticles, focusing on the effect of atomic and electronic structure on catalytic selectivity for methanol steam reforming (MSR) and hydrodechlorination of trichloroethylene. Emphasis is placed on the in situ characterization of functioning catalysts, mainly by (polarization modulated) infrared spectroscopy, ambient pressure X-ray photoelectron spectroscopy, X-ray absorption near edge structure, and X-ray diffraction. In the present contribution, we pursue a two-fold, fundamental and applied, approach investigating technologically applied catalysts as well as model catalysts, which provides comprehensive and complementary information of the relevant surface processes at the atomic or molecular level. Comparison to results of theoretical simulations yields further insight.
Several key aspects were identified that control the nanoparticle functionality: (i) alloying (IMC formation) leads to site isolation of specific (e.g. Pd) atoms but also yields very specific electronic structure due to the (e.g. Zn or Ga or Cu) neighboring atoms; (i) for intermetallic PdZn, the thickness of the surface alloy, and its resulting valence band structure and corrugation, turned out to be critical for MSR selectivity; (ii) the limited stability of phases, such as Pd_{2}Ga under MSR conditions, also limits selectivity; (iii) favorably bimetallic catalysts act bifunctional, such as activating methanol AND water or decomposing trichlorothylene AND activating hydrogen; (iv) bifunctionality is achieved either by the two metals or by one metal and the metal–oxide interface; (v) intimate contact between the two interacting sites is required (that cannot be realized by two monometallic nanoparticles being just located close by).
The current studies illustrate how rather simple bimetallic nanoparticles may exhibit intriguing diversity and flexibility, exceeding by far the properties of the individual metals. It is also demonstrated how complex reactions can be elucidated with the help of in situ spectroscopy, in particular when complementary methods with varying surface sensitivity are applied.},
keywords = {P08, P10, pre-TACO},
pubstate = {published},
tppubtype = {article}
}
Several key aspects were identified that control the nanoparticle functionality: (i) alloying (IMC formation) leads to site isolation of specific (e.g. Pd) atoms but also yields very specific electronic structure due to the (e.g. Zn or Ga or Cu) neighboring atoms; (i) for intermetallic PdZn, the thickness of the surface alloy, and its resulting valence band structure and corrugation, turned out to be critical for MSR selectivity; (ii) the limited stability of phases, such as Pd2Ga under MSR conditions, also limits selectivity; (iii) favorably bimetallic catalysts act bifunctional, such as activating methanol AND water or decomposing trichlorothylene AND activating hydrogen; (iv) bifunctionality is achieved either by the two metals or by one metal and the metal–oxide interface; (v) intimate contact between the two interacting sites is required (that cannot be realized by two monometallic nanoparticles being just located close by).
The current studies illustrate how rather simple bimetallic nanoparticles may exhibit intriguing diversity and flexibility, exceeding by far the properties of the individual metals. It is also demonstrated how complex reactions can be elucidated with the help of in situ spectroscopy, in particular when complementary methods with varying surface sensitivity are applied.