Christoph Rameshan

How to Control the Selectivity of Palladium-based Catalysts in Hydrogenation Reactions: The Role of Subsurface Chemistry

Discussed are the recent experimental and theoretical results on palladium‐based catalysts for selective hydrogenation of alkynes obtained by a number of collaborating groups in a joint multi‐method and multi‐material approach. The critical modification of catalytically active Pd surfaces by incorporation of foreign species X into the sub‐surface of Pd metal was observed by in situ spectroscopy for X=H, C under hydrogenation conditions. Under certain conditions (low H2 partial pressure) alkyne fragmentation leads to formation of a PdC surface phase in the reactant gas feed. The insertion of C as a modifier species in the sub‐surface increases considerably the selectivity of alkyne semi‐hydrogenation over Pd‐based catalysts through the decoupling of bulk hydrogen from the outmost active surface layer. DFT calculations confirm that PdC hinders the diffusion of hydridic hydrogen. Its formation is dependent on the chemical potential of carbon (reactant partial pressure) and is suppressed when the hydrogen/alkyne pressure ratio is high, which leads to rather unselective hydrogenation over in situ formed bulk PdH. The beneficial effect of the modifier species X on the selectivity, however, is also present in intermetallic compounds with X=Ga. As a great advantage, such PdxGay catalysts show extended stability under in situ conditions. Metallurgical, clean samples were used to determine the intrinsic catalytic properties of PdGa and Pd3Ga7. For high performance catalysts, supported nanostructured intermetallic compounds are more preferable and partial reduction of Ga2O3, upon heating of Pd/Ga2O3 in hydrogen, was shown to lead to formation of PdGa intermetallic compounds at moderate temperatures. In this way, Pd5Ga2 and Pd2Ga are accessible in the form of supported nanoparticles, in thin film models, and realistic powder samples, respectively.

Enhancing Electrochemical Water-Splitting Kinetics by Polarization-Driven Formation of Near-Surface Iron(0): An In Situ XPS Study on Perovskite-Type Electrodes

In the search for optimized cathode materials for high-temperature electrolysis, mixed conducting oxides are highly promising candidates. This study deals with fundamentally novel insights into the relation between surface chemistry and electrocatalytic activity of lanthanum ferrite based electrolysis cathodes. For this means, near-ambient-pressure X-ray photoelectron spectroscopy (NAP-XPS) and impedance spectroscopy experiments were performed simultaneously on electrochemically polarized La0.6Sr0.4FeO3−δ (LSF) thin film electrodes. Under cathodic polarization the formation of Fe0 on the LSF surface could be observed, which was accompanied by a strong improvement of the electrochemical water splitting activity of the electrodes. This correlation suggests a fundamentally different water splitting mechanism in presence of the metallic iron species and may open novel paths in the search for electrodes with increased water splitting activity.

Hydrogen Production by Methanol Steam Reforming on Copper Boosted by Zinc-Assisted Water Activation

For use of polymer electrolyte membrane fuel cells (PEMFC) in mobile power applications, an efficient source of CO-depleted hydrogen is needed. To avoid technical and safety problems of hydrogen handling, storage, and transport, methanol can be used as practical and abundant energy carrier for on-board H2 generation, as it has the advantage of a high energy density. Hydrogen generation from methanol can be performed by catalytic methanol steam reforming (MSR): CH3OH+H2O→CO2+3 H2. Methanol conversion must be carried out with very high CO2/H2 selectivity to avoid CO poisoning of the fuel-cell anode. A number of promising selective MSR catalysts are already available. Apart from advanced copper-based catalysts,1, 2 special attention is presently paid to the highly MSR-selective reduced state of Pd/ZnO,3 containing a particularily stable intermetallic PdZn (1:1) active phase.3, 4 Therefore, we recently studied related “inverse” near-surface PdZn intermetallic phases, showing that three-dimensional PdZn active site ensembles are equally important for selective dehydrogenation of methanol (thus avoiding CO) and for efficient water activation.5 For the less costly Cu/ZnO catalysts, originally designed for methanol synthesis, improvements towards a technical MSR application regarding sintering stability, pyrophoricity, and selectivity are still required. Empirical development of Cu/ZnO catalyst preparation and activation has aimed in a particularily large Cu0–ZnO contact.6 Nevertheless, it is very difficult to derive an unambiguous causality for the role of the contact on technical catalysts. It is known that zinc leads to an improvement in the desired properties, but a clear assignment of a predominant promotional effect (both from the theoretical and experimental side) is still missing. In the Cu/ZnO literature, seemingly incompatible model interpretations can be found, involving the “metallic copper model”,7 the “special site model”,8 the “morphology model”,7, 9 the “spillover model”,10 and last but not least the “Cu-Zn alloy model”.8, 11 Consequently, the Cu-ZnO(H) contact most likely constitutes a combination of promotional effects. The central aim of our study is to highlight the aspect of zinc-promoted water activation. This is achieved by using an ultrahigh-vacuum (UHV) “inverse” model catalyst approach, which, in contrast to investigations on real catalyst systems, allows the zinc segregation behavior and the changes in redox chemistry of both copper and zinc to be better followed. This provides a solid basis for directional promotion of microkinetic steps leading to enhanced CO2 selectivity.

Ambient Pressure XPS Study of Mixed Conducting Perovskite-Type SOFC Cathode and Anode Materials under Well-Defined Electrochemical Polarization

The oxygen exchange activity of mixed conducting oxide surfaces has been widely investigated, but a detailed understanding of the corresponding reaction mechanisms and the rate-limiting steps is largely still missing. Combined in situ investigation of electrochemically polarized model electrode surfaces under realistic temperature and pressure conditions by near-ambient pressure (NAP) XPS and impedance spectroscopy enables very surface-sensitive chemical analysis and may detect species that are involved in the rate-limiting step. In the present study, acceptor-doped perovskite-type La0.6Sr0.4CoO3-δ (LSC), La0.6Sr0.4FeO3-δ (LSF), and SrTi0.7Fe0.3O3-δ (STF) thin film model electrodes were investigated under well-defined electrochemical polarization as cathodes in oxidizing (O2) and as anodes in reducing (H2/H2O) atmospheres. In oxidizing atmosphere all materials exhibit additional surface species of strontium and oxygen. The polaron-type electronic conduction mechanism of LSF and STF and the metal-like mechanism of LSC are reflected by distinct differences in the valence band spectra. Switching between oxidizing and reducing atmosphere as well as electrochemical polarization cause reversible shifts in the measured binding energy. This can be correlated to a Fermi level shift due to variations in the chemical potential of oxygen. Changes of oxidation states were detected on Fe, which appears as FeIII in oxidizing atmosphere and as mixed FeII/III in H2/H2O. Cathodic polarization in reducing atmosphere leads to the reversible formation of a catalytically active Fe0 phase.

Growth of an Ultrathin Zirconia Film on Pt3Zr Examined by High-Resolution X-ray Photoelectron Spectroscopy, Temperature-Programmed Desorption, Scanning Tunneling Microscopy, and Density Functional Theory

Ultrathin (∼3 Å) zirconium oxide films were grown on a single-crystalline Pt3Zr(0001) substrate by oxidation in 1 × 10–7 mbar of O2 at 673 K, followed by annealing at temperatures up to 1023 K. The ZrO2 films are intended to serve as model supports for reforming catalysts and fuel cell anodes. The atomic and electronic structure and composition of the ZrO2 films were determined by synchrotron-based high-resolution X-ray photoelectron spectroscopy (HR-XPS) (including depth profiling), low-energy electron diffraction (LEED), scanning tunneling microscopy (STM), and density functional theory (DFT) calculations. Oxidation mainly leads to ultrathin trilayer (O–Zr–O) films on the alloy; only a small area fraction (10–15%) is covered by ZrO2 clusters (thickness ∼0.5–10 nm). The amount of clusters decreases with increasing annealing temperature. Temperature-programmed desorption (TPD) of CO was utilized to confirm complete coverage of the Pt3Zr substrate by ZrO2, that is, formation of a closed oxide overlayer. Experiments and DFT calculations show that the core level shifts of Zr in the trilayer ZrO2 films are between those of metallic Zr and thick (bulklike) ZrO2. Therefore, the assignment of such XPS core level shifts to substoichiometric ZrOx is not necessarily correct, because these XPS signals may equally well arise from ultrathin ZrO2 films or metal/ZrO2 interfaces. Furthermore, our results indicate that the common approach of calculating core level shifts by DFT including final-state effects should be taken with care for thicker insulating films, clusters, and bulk insulators.

From Oxide-Supported Palladium to Intermetallic Palladium Phases: Consequences for Methanol Steam Reforming

This Minireview summarizes the fundamental results of a comparative inverse‐model versus real‐model catalyst approach toward methanol steam reforming (MSR) on the highly CO2‐selective H2‐reduced states of supported Pd/ZnO, Pd/Ga2O3, and Pd/In2O3 catalysts. Our model approach was extended to the related Pd/GeO2 and Pd/SnO2 systems, which showed previously unknown MSR performance. This approach allowed us to determine salient CO2‐selectivity‐guiding structural and electronic effects on the molecular level, to establish a knowledge‐based approach for the optimization of CO2 selectivity. Regarding the inverse‐model catalysts, in situ X‐ray photoelectron spectroscopy (in situ XPS) studies on near‐surface intermetallic PdZn, PdGa, and PdIn phases (NSIP), as well as bulk Pd2Ga, under realistic MSR conditions were performed alongside catalytic testing. To highlight the importance of a specifically prepared bulk intermetallicoxide interface, unsupported bulk intermetallic compounds of PdxGay were chosen as additional MSR model compounds, which allowed us to clearly deduce, for example, the water‐activating role of the special Pd2Ga‐β‐Ga2O3 intermetallicoxide interaction. The inverse‐model studies were complemented by their related “real‐model” experiments. Structure–activity and structure–selectivity correlations were performed on epitaxially ordered PdZn, Pd5Ga2, PdIn, Pd3Sn2, and Pd2Ge nanoparticles that were embedded in thin crystalline films of their respective oxides. The reductively activated “thin‐film model catalysts” that were prepared by sequential Pd and oxide deposition onto NaCl(001) exhibited the required large bimetaloxide interface and the highly epitaxial ordering that was required for (HR)TEM studies and for identification of the structural and catalytic (bi)metalsupport interactions. To fully understand the bimetalsupport interactions in the supported systems, our studies were extended to the MeOH‐ and formaldehyde‐reforming properties of the clean supporting oxides. From a direct comparison of the “isolated” MSR performance of the purely bimetallic surfaces to that of the “isolated” oxide surfaces and of the “bimetaloxide contact” systems, a pronounced “bimetaloxide synergy” toward optimum CO2 activity/selectivity was most evident. Moreover, the system‐specific mechanisms that led to undesired CO formation and to spoiling of the CO2 selectivity could be extracted.

Surface-assisted laser desorption/ionization-mass spectrometry using TiO2-coated steel targets for the analysis of small molecules

Matrix-assisted laser desorption/ionization-mass spectrometry (MALDI–MS) measurements in the low-molecular-mass region, ranging from 0 to 1000 Daltons are very often difficult to perform because of signal interferences originating from matrix ions. In order to overcome this problem, a stainless steel target was coated with a homogeneous titanium dioxide layer. The layer obtained was further investigated for its ability to desorb small molecules, e.g., amino acids, sugars, poly(ethylene glycol) (PEG) 200, or extracts from Cynara scolymus leaves. The stability of the layer was determined by repeated measurements on the same target location, which was monitored by X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM) before and after surface-assisted laser desorption/ionization (SALDI) analysis. In addition, this titanium dioxide layer was compared with an already published method with titanium dioxide nanopowder as inorganic matrix. As a result of this work, the titanium dioxide layer produced minimal background interference, enabling simple interpretation of the detected mass spectra. Furthermore, the TiO2 coating provides a target that can be reused many times for SALDI–MS measurements.

Reversible modification of the structural and electronic properties of a boron nitride monolayer by CO intercalation.

We demonstrate the reversible intercalation of CO between a hexagonal boron nitride (h-BN) monolayer and a Rh(111) substrate above a threshold CO pressure of 0.01 mbar at room temperature. The intercalation of CO results in the flattening of the originally corrugated h-BN nanomesh and an electronic decoupling of the BN layer from the Rh substrate. The intercalated CO molecules assume a coverage and adsorption site distribution comparable to that on the free Rh(111) surface at similar conditions. The pristine h-BN nanomesh is reinstated upon heating to above 625 K. These observations may open up opportunities for a reversible tuning of the electronic and structural properties of monolayer BN films.

Surface Chemistry of Perovskite-Type Electrodes During High Temperature CO2 Electrolysis Investigated by Operando Photoelectron Spectroscopy

Any substantial move of energy sources from fossil fuels to renewable resources requires large scale storage of excess energy, for example, via power to fuel processes. In this respect electrochemical reduction of CO2 may become very important, since it offers a method of sustainable CO production, which is a crucial prerequisite for synthesis of sustainable fuels. Carbon dioxide reduction in solid oxide electrolysis cells (SOECs) is particularly promising owing to the high operating temperature, which leads to both improved thermodynamics and fast kinetics. Additionally, compared to purely chemical CO formation on oxide catalysts, SOECs have the outstanding advantage that the catalytically active oxygen vacancies are continuously formed at the counter electrode, and move to the working electrode where they reactivate the oxide surface without the need of a preceding chemical (e.g., by H2) or thermal reduction step. In the present work, the surface chemistry of (La,Sr)FeO3−δ and (La,Sr)CrO3−δ based perovskite-type electrodes was studied during electrochemical CO2 reduction by means of near-ambient pressure X-ray photoelectron spectroscopy (NAP-XPS) at SOEC operating temperatures. These measurements revealed the formation of a carbonate intermediate, which develops on the oxide surface only upon cathodic polarization (i.e., under sufficiently reducing conditions). The amount of this adsorbate increases with increasing oxygen vacancy concentration of the electrode material, thus suggesting vacant oxygen lattice sites as the predominant adsorption sites for carbon dioxide. The correlation of carbonate coverage and cathodic polarization indicates that an electron transfer is required to form the carbonate and thus to activate CO2 on the oxide surface. The results also suggest that acceptor doped oxides with high electron concentration and high oxygen vacancy concentration may be particularly suited for CO2 reduction. In contrast to water splitting, the CO2 electrolysis reaction was not significantly affected by metallic particles, which were exsolved from the perovskite electrodes upon cathodic polarization. Carbon formation on the electrode surface was only observed under very strong cathodic conditions, and the carbon could be easily removed by retracting the applied voltage without damaging the electrode, which is particularly promising from an application point of view.

CO Adsorption on Reconstructed Ir(100) Surfaces from UHV to mbar Pressure: A LEED, TPD, and PM-IRAS Study

Clean and stable surface modifications of an iridium (100) single crystal, i.e., the (1 × 1) phase, the (5 × 1) reconstruction, and the oxygen-terminated (2 × 1)-O surface, were prepared and characterized by low energy electron diffraction (LEED), temperature-programmed desorption (TPD), infrared reflection absorption spectroscopy (IRAS) and polarization modulation IRAS (PM-IRAS). The adsorption of CO in UHV and at elevated (mbar) pressure/temperature was followed both ex situ and in situ on all three surface modifications, with a focus on mbar pressures of CO. The Ir(1 × 1) surface exhibited c(4 × 2)/c(2 × 2) and c(6 × 2) CO structures under low pressure conditions, and remained stable up to 100 mbar and 700 K. For the (2 × 1)-O reconstruction CO adsorption induced a structural change from (2 × 1)-O to (1 × 1), as confirmed by LEED, TPD, and IR. For Ir (2 × 1)-O TPD indicated that CO reacted with surface oxygen forming CO2. The (5 × 1) reconstruction featured a reversible and dynamic behavior upon CO adsorption, with a local lifting of the reconstruction to (1 × 1). After CO desorption, the (5 × 1) structure was restored. All three reconstructions exhibited CO adsorption with on-top geometry, as evidenced by IR. With increasing CO exposure the resonances shifted to higher wavenumber, due to adsorbate–adsorbate and adsorbate–substrate interactions. The largest wavenumber shift (from 2057 to 2100 cm–1) was observed for Ir(5 × 1) upon CO dosing from 1 L to 100 mbar.