Nanoporous Gold: From Structure Evolution to Functional Properties in Catalysis and Electrochemistry.

Nanoporous gold (NPG) is characterized by a bicontinuous network of nanometer-sized metallic struts and interconnected pores formed spontaneously by oxidative dissolution of the less noble element from gold alloys. The resulting material exhibits decent catalytic activity for low-temperature, aerobic total as well as partial oxidation reactions, the oxidative coupling of methanol to methyl formate being the prototypical example. This review not only provides a critical discussion of ways to tune the morphology and composition of this material and its implication for catalysis and electrocatalysis, but will also exemplarily review the current mechanistic understanding of the partial oxidation of methanol using information from quantum chemical studies, model studies on single-crystal surfaces, gas phase catalysis, aerobic liquid phase oxidation, and electrocatalysis. In this respect, a particular focus will be on mechanistic aspects not well understood, yet. Apart from the mechanistic aspects of catalysis, best practice examples with respect to material preparation and characterization will be discussed. These can improve the reproducibility of the materials property such as the catalytic activity and selectivity as well as the scope of reactions being identified as the main challenges for a broader application of NPG in target-oriented organic synthesis.

Catalytic activity of 1D chains of gold oxide on a stepped gold surface from density functional theory.

The rich surface chemistry of gold at the nanoscale has made it an important catalyst for low-temperature applications. Recent studies point to the possible role of self-organized structures formed by chemisorbed O atoms on the surface of gold catalysts for their catalytic activity and/or deactivation. In this study, we investigate the reactivity of a double O chain running along a step on a Au(221) surface with oxygen vacancies as a prototypical model of a 1D surface gold oxide. We compare CO and O2 adsorption on such a chain with the oxygen-free Au(221) surface model. A systematic study of the reactivity of the double chain with O vacancies was done with respect to the regular Au(221) surface using CO as a probe. The CO oxidation was investigated assuming dissociative and associative mechanisms. Remarkably, O2 adsorbs stronger on the double oxygen vacancy than on the regular Au(221) surface, and its dissociation barrier reduces significantly from 1.84 eV to 0.87 eV, whereas the CO adsorption energy is similar on these surfaces. Calculations suggest that CO oxidation should occur more efficiently on the double O vacancy than on the regular Au(221) surface due to stronger adsorption of O2 and a low activation barrier for O2 + CO surface reaction.

Assessment of PBE+U and HSE06 methods and determination of optimal parameter U for the structural and energetic properties of rare earth oxides.

Rare earth oxides are attracting increasing interest as a relatively unexplored group of materials with potential applications in heterogeneous catalysis and electrocatalysis; therefore, a credible and universal computational approach is needed for modeling their reactivity. In this work, we systematically assessed the performance of the PBE+U method against the results of the hybrid HSE06 method with respect to the description of structural parameters and energetic properties of the selected hexagonal lanthanide sesquioxides and the cubic fluorite-type cerium dioxide. In addition, we evaluated the performance of PBE+U in describing the electronic structure and adsorption properties of the CeO2(111) and Nd2O3(0001) surfaces. The HSE06 method reproduces rather well the lattice parameters and selected energetic properties with respect to the experimental values. The PBE+U method is able to reproduce the results of HSE06 or the experimental values only if the U parameter is selected from an appropriate range of values. The U value around 3 eV gives the best description of the lattice parameters of most bulk oxides. 2 eV-3 eV is also found to be the optimal range of U for the reaction energies of bulk La2O3, Ce2O3, Nd2O3, Er2O3, and Ho2O3. U = 1 eV gives the best results for Pr2O3, Pm2O3, Eu2O3, Tm2O3, and Lu2O3, whereas Gd2O3 could not be accurately described by the PBE+U method. The U values (∼3 eV) found optimal for most bulk oxides also work well in the calculations of adsorption of small molecules on Nd2O3(0001) and CeO2(111), although larger U values are required to obtain sufficient localization of 4f electrons.

Nanoporous gold functionalized with praseodymia-titania mixed oxides as a stable catalyst for the water-gas shift reaction.

Dealloyed nanoporous metals hold great promise in the field of heterogeneous catalysis; however their tendency to coarsen at elevated temperatures or under catalytic reaction conditions sometimes limit further applications. Here, we report on a highly stable nanoporous gold catalyst (npAu) functionalized with praseodymia-titania mixed oxides as synthesized by a sol-gel method. Specifically, we used aberration-corrected transmission electron microscopy to study the morphology and the interface between the oxide deposits and the npAu substrate at the atomic level. Based on electron energy loss spectroscopy (EELS), it is concluded that Pr-TiOx mixed oxides form a solid solution. Flow reactor tests reveal that the Pr-TiOx functionalized nanoporous gold is not only highly active but also very stable for the water gas shift reaction in a large temperature range (180-400 °C). Our results demonstrate the potential of engineering the compositions of oxides coatings on npAu for advanced functional systems.

Ligand-Linked Nanoparticles-Based Hydrogen Gas Sensor with Excellent Homogeneous Temperature Field and a Comparative Stability Evaluation of Different Ligand-Linked Catalysts.

This paper presents a thermoelectric gas microsensor with improved stability where platinum nanoparticles linked by bifunctional ligands are used as a catalyst. The sensor design provides a homogeneous temperature field over the membrane, an important factor for the long-term stability of the catalyst. A comprehensive study of heat transfer from the chip is performed to evaluate the convection heat loss coefficient and to understand its effect on the homogeneity of the temperature field in a real-time situation. The effect of highly heat-conductive thermopiles is also analyzed by comparing the temperature distribution and power consumption with a thermoresistive sensor of the same dimensions and materials. Despite the thermopiles, the thermoelectric sensor gives better temperature homogeneity and consumes 23% less power than the thermoresistive sensor for 90 °C average temperature on the membrane. A comparative stability analysis among ligand-linked nanoparticles with 5 different ligands and unprotected nanoparticles was done through 3 consecutive 24 h tests under 1.5% continuous hydrogen gas flow. The sensors give very stable output, almost no degradation, through 72 h (3 × 24 h) tests for 3 different ligand-linked nanoparticles. The sensor design provides superb stability to the catalyst: Even catalysts of unprotected nanoparticles withstood more than 24 h and the sensor signal degradation is only 20%.

Catalysis by unsupported skeletal gold catalysts.

Catalysis is one of the key technologies for the 21st century for achieving the required sustainability of chemical processes. Critical improvements are based on the development of new catalysts and catalytic concepts. In this context, gold holds great promise because it is more active and selective than other precious metal catalysts at low temperatures. However, gold becomes only chemically and catalytically active when it is nanostructured. Since the 1970s and 1980s, the first type of gold catalysts that chemists studied were small nanoparticles on oxidic supports. With the later onset of nanotechnology, a variety of nanostructured materials not requiring a support or organic stabilizers became available within about the last 10 years. Among these are gold nanofoams generated by combustion of gold compounds, nanotube membranes prepared by electroless deposition of gold inside a template, and corrosion-derived nanoporous gold. Even though these materials are macroscopic in their geometric dimensions (e.g., disks, cubes, and membranes with dimensions of millimeters), they are comprised of gold nanostructures, for example, in the form of ligaments as small as 15 nm in diameter (nanoporous gold, npAu). The nanostructure brings about a high surface to volume ratio and a large fraction of low coordinated surface atoms. In this Account, we discuss how unsupported materials are active catalysts for aerobic oxidation reaction in gas phase (oxidation of CO and primary alcohols), as well as liquid phase oxidation and reduction reactions. It turns out that the bonding and activation of molecular oxygen for gas phase oxidations strongly profits from trace amounts of an ad-metal residue such as silver. It is noteworthy that these catalysts still exhibit the special gold type chemistry, characterized by activity at very low temperatures and high selectivity for partial oxidations. For example, we can oxidize CO over these unsupported catalysts (npAu, nanotubes, and powder) at temperatures well below water's freezing point (-30 °C) and with turnover frequencies up to 0.5 s(-1) (at 30 °C). Yet, we can anticipate the surface chemistry of these unsupported and extended gold surfaces based on model experiments under UHV conditions. We have demonstrated this for the selective oxidation of primary alcohols at low temperatures employing npAu catalysts. Chemists have paid growing interest to oxidation and reduction reactions in liquid phase catalysis, most suitable for synthetic organic chemistry. Early work on the aerobic oxidation of d-glucose in 2008 using Raney type npAu already showed the potential of this type of catalyst for liquid phase reactions. Since then, researchers have investigated further oxidation reactions (silanes to silanols) and reduction reactions of alkynes, as well as C-C coupling reactions ([4 + 2] benzannulation) and azo compound decomposition, with likely several more reactions to be reported in the next years. The advantage of this unsupported skeletal type of catalyst is its recyclability and retrievability without leaching of gold into the reaction medium, owing to its monolithic structure. Even though these materials contain nanoscopic structures, they are macroscopic in their geometric dimensions and pose no threat to the environment or health as discussed for other nanomaterials.

Influence of Sn content on the hydrogenation of crotonaldehyde catalysed by colloidally prepared PtSn nanoparticles.

Bimetallic PtSn nanoparticles (NPs) of well-defined size and metal composition were prepared by means of colloidal methods. The mean particle diameter was about 2 nm for all samples irrespective of the Pt/Sn-ratio, which enables a systematic study of the influence of the composition on the catalytic properties while excluding particle size effects. The hydrogenation of crotonaldehyde was investigated as a reaction for which chemoselectivity is known to be a challenging task. Already very low atomic Sn contents (≈10%) were found to lead to a significantly improved activity which may be attributed to an electronic effect of Sn on Pt. For further increasing tin contents the activity decreased gradually. This trend was accompanied by a steady increase in selectivity towards the desired product (crotylalcohol). The results show that the highest crotylalcohol time yields can be obtained by using catalysts with an atomic Sn content of approximately 23%. In contrast, maximum crotylalcohol selectivities are achieved by using catalysts with a high tin content (>50%).

Controlling the physics and chemistry of binary and ternary praseodymium and cerium oxide systems.

Rare earth praseodymium and cerium oxides have attracted intense research interest in the last few decades, due to their intriguing chemical and physical characteristics. An understanding of the correlation between structure and properties, in particular the surface chemistry, is urgently required for their application in microelectronics, catalysis, optics and other fields. Such an understanding is, however, hampered by the complexity of rare earth oxide materials and experimental methods for their characterisation. Here, we report recent progress in studying high-quality, single crystalline, praseodymium and cerium oxide films as well as ternary alloys grown on Si(111) substrates. Using these well-defined systems and based on a systematic multi-technique surface science approach, the corresponding physical and chemical properties, such as the surface structure, the surface morphology, the bulk-surface interaction and the oxygen storage/release capability, are explored in detail. We show that specifically the crystalline structure and the oxygen stoichiometry of the oxide thin films can be well controlled by the film preparation method. This work leads to a comprehensive understanding of the properties of rare earth oxides and highlights the applications of these versatile materials. Furthermore, methanol adsorption studies are performed on binary and ternary rare earth oxide thin films, demonstrating the feasibility of employing such systems for model catalytic studies. Specifically for ceria systems, we find considerable stability against normal environmental conditions so that they can be considered as a "materials bridge" between surface science models and real catalysts.

Stabilizing catalytically active nanoparticles by ligand linking: toward three-dimensional networks with high catalytic surface area.

A general approach for the linking of Pt nanoparticles (NPs) with bifunctional amine ligands (organic molecules with two amine groups) is presented that allows for the preparation of NP catalysts without inorganic supports and high densities of the catalytically active metal. Advantage was taken of the use of "unprotected" NPs, which enables us to prepare different ligand-functionalized NPs from the same particle batch and thus to relate changes of the resulting material properties exclusively to the influence of the ligand. Three bifunctional ligands with similar functional groups (amines) but different hydrocarbon skeletons were used and compared to monofunctional ligands of similar molecular structures (alkyl and aryl amines) showing significantly different material properties. Monofunctional molecules with minor steric demand cover almost completely the NP surface and lead to two-dimensional assembling of the NPs. In contrast, the use of bifunctional amine ligands leads to the formation of porous, three-dimensional NP networks (ligand-linked NPs) with a high density of ligand free surface atoms, thus enabling for the application as catalytic materials. The stabilizing effect of bifunctional ligands serves as an alternative to the use of inorganic support materials and enables for catalytic applications of ligand-linked NP networks.

Ligand-stabilized Pt nanoparticles (NPs) as novel materials for catalytic gas sensing: influence of the ligand on important catalytic properties.

Different mono- and bifunctional amine ligands have been used to stabilize Pt NPs for catalytic H2 gas sensing. Depending on the chemical structure and properties of the ligand, the catalysts show different overall sensor performances, activation periods, and long-term stabilities. These sensor characteristics are put into relation with chemical processes like cleaning of the surface, degradation processes of the ligands and nanoparticle (NP) sintering. It has been found that during activation free adsorption sites are formed primarily due to desorption of synthetic residues. Furthermore, partial desorption of the ligands followed by their degradation may occur. For monoamines the latter process results in destabilization of the NPs followed by catalyst deactivation through particle sintering. The use of bifunctional ligands that link individual NPs shows significantly enhanced stabilities which can be related to the reduction of the ligand desorption rates and degradation. Besides the functionality of the ligands it was observed that the chemical nature of their hydrocarbon skeleton affects the catalyst stability: aromatic substructures remain intact upon H2 oxidation, while alkyl fragments undergo oxidation and decomposition. The advantages of bifunctionality and an aromatic hydrocarbon skeleton can be combined by the use of para-phenylenediamine (PDA) as a linking ligand. Networks formed by this ligand were indeed found to be stable under the applied catalytic conditions for more than 24 h.

In-operando FTIR study of ligand-linked Pt nanoparticle networks employed as catalysts in hydrogen gas micro sensors.

Microporous networks of Pt nanoparticles (NP) interlinked by aromatic diamines have recently shown prospects of application as hydrogen combustion catalysts in H2 gas microsensors. In particular with respect to long-term sensor performance, they outperformed plain Pt NP as catalysts. In this paper, electron microscopy and Fourier transform infrared (FTIR) spectroscopy data on the stability of p-phenylene diamine (PDA) and of the PDA-linked Pt NP network structure during catalyst activation and long-term sensor operation at elevated temperature (up to 120-180 °C) will be presented. For the first time, all data were collected directly from microsensor catalysts, and FTIR was performed in operando, i.e., during activation and sensor operation. While the data confirm high long-term catalyst activity far superior to that of plain Pt NP over 5 days of testing, they reveal that PDA fully decomposed during long-term sensor operation and that the network of discrete Pt nanoparticles changed to a sponge-like Pt nanostructure already during catalyst activation. These findings are at variance with previous work which assumed that stability of the PDA-linked Pt NP network is prerequisite for catalyst stability and performance.

Pt based PEMFC catalysts prepared from colloidal particle suspensions--a toolbox for model studies.

A colloidal synthesis approach is presented that allows systematic studies of the properties of supported proton exchange membrane fuel cell (PEMFC) catalysts. The applied synthesis route is based on the preparation of monodisperse nanoparticles in the absence of strong binding organic stabilizing agents. No temperature post-treatment of the catalyst is required rendering the synthesis route ideally suitable for comparative studies. We report work concerning a series of catalysts based on the same colloidal Pt nanoparticle (NP) suspension, but with different high surface area (HSA) carbon supports. It is shown that for the prepared catalysts the carbon support has no catalytic co-function, but carbon pre-treatment leads to enhanced sticking of the Pt NPs on the support. An unwanted side effect, however, is NP agglomeration during synthesis. By contrast, enhanced NP sticking without agglomeration can be accomplished by the addition of an ionomer to the NP suspension. The catalytic activity of the prepared catalysts for the oxygen reduction reaction is comparable to industrial catalysts and no influence of the particle size is found in the range of 2-5 nm.

Self-diffusion of carbon dioxide in samaria/alumina aerogel catalyst using high field NMR diffusometry.

Pulsed field gradient (PFG) NMR was used to investigate the self-diffusion of carbon dioxide in alumina stabilized samaria aerogel catalyst, a promising porous catalyst for gas-phase reactions featuring high porosity and high surface area. For diffusion studies, the catalyst was prepared in two sample packing types, macroscopic monoliths (i.e., macroscopic cylindrical particles) and powder beds with particle sizes around 200 µm that are considered for catalytic applications. Studies of diffusion in these samples revealed how macroscopic packing influences the catalyst transport properties. Application of a high magnetic field of 17.6 T in the reported PFG NMR studies enabled diffusion measurements for relatively low carbon dioxide densities in the catalyst samples corresponding to a gas loading pressure of around 0.1 atm. As a result, it was possible to perform diffusion measurements for a large range of carbon dioxide loading pressures between 0.1 and 10 atm. The measured carbon dioxide diffusivities in the beds of catalyst particles are interpreted in the context of a simple diffusion-mediated exchange model previously used for zeolites and other porous materials.

New Perspectives for Evaluating the Mass Transport in Porous Catalysts and Unfolding Macro- and Microkinetics.

In this article we shed light on newly emerging perspectives to characterize and understand the interplay of diffusive mass transport and surface catalytic processes in pores of gas phase metal catalysts. As a case study, nanoporous gold, as an interesting example exhibiting a well-defined pore structure and a high activity for total and partial oxidation reactions is considered. PFG NMR (pulsed field gradient nuclear magnetic resonance) measurements allowed here for a quantitative evaluation of gas diffusivities within the material. STEM (scanning transmission electron microscopy) tomography furthermore provided additional insight into the structural details of the pore system, helping to judge which of its features are most decisive for slowing down mass transport. Based on the quantitative knowledge about the diffusion coefficients inside a porous catalyst, it becomes possible to disentangle mass transport contributions form the measured reaction kinetics and to determine the kinetic rate constant of the underlying catalytic surface reaction. In addition, predictions can be made for an improved effectiveness of the catalyst, i.e., optimized conversion rates. This approach will be discussed at the example of low-temperature CO oxidation, efficiently catalysed by npAu at 30 °C. The case study shall reveal that novel porous materials exhibiting well-defined micro- and mesoscopic features and sufficient catalytic activity, in combination with modern techniques to evaluate diffusive transport, offer interesting new opportunities for an integral understanding of catalytic processes.

ALD functionalized nanoporous gold: thermal stability, mechanical properties, and catalytic activity.

Nanoporous metals have many technologically promising applications, but their tendency to coarsen limits their long-term stability and excludes high temperature applications. Here, we demonstrate that atomic layer deposition (ALD) can be used to stabilize and functionalize nanoporous metals. Specifically, we studied the effect of nanometer-thick alumina and titania ALD films on thermal stability, mechanical properties, and catalytic activity of nanoporous gold (np-Au). Our results demonstrate that even only 1 nm thick oxide films can stabilize the nanoscale morphology of np-Au up to 1,000°C, while simultaneously making the material stronger and stiffer. The catalytic activity of np-Au can be drastically increased by TiO(2) ALD coatings. Our results open the door to high-temperature sensor, actuator, and catalysis applications and functionalized electrodes for energy storage and harvesting applications.

Colloidal synthesis and structural control of PtSn bimetallic nanoparticles.

PtSn bimetallic nanoparticles with different particle sizes (1-9 nm), metal compositions (Sn content of 10-80 mol %), and organic capping agents (e.g., amine, thiol, carboxylic acid and polymer) were synthesized by colloidal chemistry methods. Transmission electron microscopy (TEM) measurements show that, depending on the particle size, the as-prepared bimetallic nanocrystals have quasi-spherical or faceted shapes. Energy-dispersive X-ray (EDX) analyses indicate that for all samples the signals of both Pt and Sn can be detected from single nanoparticles, confirming that the products are actually bimetallic but not only a physical mixture of pure Pt and Sn metal nanoparticles. X-ray diffraction (XRD) measurements were also conducted on the bimetallic particle systems. When compared with the diffraction patterns of monometallic Pt nanoparticles, the bimetallic samples show distinct shifts of the Bragg reflections to lower degrees, which gives clear proof of the alloying of Pt with Sn. However, a quantitative analysis of the lattice parameter shifts indicates that only part of the Sn atoms are incorporated into the alloy nanocrystals. This is consistent with X-ray photoelectron spectroscopy (XPS) measurements that reveal the segregation of Sn at the surfaces of the nanocrystals. Moreover, short PtSn bimetallic nanowires were synthesized by a seed-mediated growth method with amine-capped bimetallic particles as precursors. The resulting nanowires have an average width of 2.3 nm and lengths ranging from 5 to 20 nm.

Silver residues as a possible key to a remarkable oxidative catalytic activity of nanoporous gold.

Recently, several forms of unsupported gold were shown to display a remarkable activity to catalyze oxidation reactions. Experimental evidence points to the crucial role of residual silver present in very small concentrations in these novel catalysts. We focus on the catalytic properties of nanoporous gold (np-Au) foams probed via CO and oxygen adsorption/co-adsorption. Experimental results are analyzed using theoretical models represented by the flat Au(111) and the kinked Au(321) slabs with Ag impurities. We show that Ag atoms incorporated into gold surfaces can facilitate the adsorption and dissociation of molecular oxygen on them. CO adsorbed on top of 6-fold coordinated Au atoms can in turn be stabilized by co-adsorbed atomic oxygen by up to 0.2 eV with respect to the clean unsubstituted gold surface. Our experiments suggest a linking of that most strongly bound CO adsorption state to the catalytic activity of np-Au. Thus, our results shed light on the role of silver admixtures in the striking catalytic activity of unsupported gold nanostructures.

Rational design of functional oxide thin films with embedded magnetic or plasmonic metallic nanoparticles.

Getting into films: semiconductor thin films containing magnetic or plasmonic metal nanoparticles are key materials for the development of high-efficiency solar cells, bright light-emitting diodes, and new magnetoelectric devices. The catalytically driven chemical vapor deposition offers a unique way to combine deposition of the metallic nanoparticles with that of functional oxides to produce such films.

Synthesis and Characterization of Ligand-Linked Pt Nanoparticles: Tunable, Three-Dimensional, Porous Networks for Catalytic Hydrogen Sensing.

Porous networks of Pt nanoparticles interlinked by bifunctional organic ligands have shown high potential as catalysts in micro-machined hydrogen gas sensors. By varying the ligand among p-phenylenediamine, benzidine, 4,4''-diamino-p-terphenyl, 1,5-diaminonaphthalene, and trans-1,4-diaminocyclohexane, new variants of such networks were synthesized. Inter-particle distances within the networks, determined via transmission electron microscopy tomography, varied from 0.8 to 1.4 nm in accordance with the nominal length of the respective ligand. While stable structures with intact and coordinatively bonded diamines were formed with all ligands, aromatic diamines showed superior thermal stability. The networks exhibited mesoporous structures depending on ligand and synthesis strategy and performed well as catalysts in hydrogen gas microsensors. They demonstrate the possibility of deliberately tuning micro- and mesoporosity and thereby transport properties and steric demands by choice of the right ligand also for other applications in heterogeneous catalysis.

Colloidally prepared Pt nanowires versus impregnated Pt nanoparticles: comparison of adsorption and reaction properties.

Ligand-capped Pt nanowires, prepared by colloidal synthesis and deposited on a high surface area γ-Al(2)O(3) support, were subjected to surface characterization by electron microscopy and FTIR spectroscopy using CO as a probe molecule. The structural, adsorption, and catalytic reaction properties of the colloidal Pt nanowires were compared to those of conventional, impregnated Pt nanoparticles on the same Al(2)O(3) support. In situ FTIR spectroscopy indicated ligand effects on the CO resonance frequency, irreversible CO-induced surface roughening upon CO adsorption, and a higher resistance of colloidal catalysts toward oxidation (both in oxygen and during CO oxidation), suggesting that the organic ligands might protect the Pt surface. Elevated temperature induced a transformation of Pt nanowires to faceted Pt nanoparticles. The colloidal catalyst was active for hydrodechlorination of trichloroethylene (TCE), but no ligand effect on selectivity was obtained.