Supported Metal Nanoparticle Catalysts Research Articles

Rutile TiO2-Supported Pt Nanoparticle Catalysts for the Low-Temperature Oxidation of Ethane to Ethanol.

Structure-function relationships of supported metal nanoparticle catalysts in the CO-assisted oxidation of ethane to ethanol were investigated. A rutile TiO2-supported Pt nanoparticle catalyst exhibited the highest ethanol production rate and selectivity. During the reaction, sequential changes in the geometric/electronic states and the particle size of the Pt nanoparticles were observed. The comparison of the catalytic performances of model catalysts with controlled metal-support interactions revealed that Pt0 nanoparticles of 2-3 nm with a high fraction of the surface Ptδ+ species are highly active for the oxidation of ethane to ethanol. The coadded CO plays a pivotal role not only in tuning the oxidation state of the surface Pt but also in producing H2O2, which is the true oxidant for the reaction. The supported Pt nanoparticle uses in situ-generated H2O2 to activate ethane, where the C2H5OOH intermediate is formed through a nonradical mechanism and subsequently converted to C2H5OH. This reaction occurs even at 50 °C with an apparent activation energy of 32 kJ mol-1. The present study sheds light on the usefulness of surface-engineered Pt nanoparticles for the low-temperature oxidation of ethane to ethanol.

Rutile TiO2-Supported Pt Nanoparticle Catalysts for the Low-Temperature Oxidation of Ethane to Ethanol.

Structure-function relationships of supported metal nanoparticle catalysts in the CO-assisted oxidation of ethane to ethanol were investigated. A rutile TiO2-supported Pt nanoparticle catalyst exhibited the highest ethanol production rate and selectivity. During the reaction, sequential changes in the geometric/electronic states and the particle size of the Pt nanoparticles were observed. The comparison of the catalytic performances of model catalysts with controlled metal-support interactions revealed that Pt0 nanoparticles of 2-3 nm with a high fraction of the surface Ptδ+ species are highly active for the oxidation of ethane to ethanol. The coadded CO plays a pivotal role not only in tuning the oxidation state of the surface Pt but also in producing H2O2, which is the true oxidant for the reaction. The supported Pt nanoparticle uses in situ-generated H2O2 to activate ethane, where the C2H5OOH intermediate is formed through a nonradical mechanism and subsequently converted to C2H5OH. This reaction occurs even at 50 °C with an apparent activation energy of 32 kJ mol-1. The present study sheds light on the usefulness of surface-engineered Pt nanoparticles for the low-temperature oxidation of ethane to ethanol.

Atomic-Scale 3D Structure of a Supported Pd Nanoparticle Revealed by Electron Tomography with Convolution Neural Network-Based Image Inpainting.

Electron tomography based on scanning transmission electron microscopy (STEM) is used to analyze 3D structures of metal nanoparticles on the atomic scale. However, in the case of supported metal nanoparticle catalysts, the supporting material may interfere with the 3D reconstruction of metal nanoparticles. In this study, a deep learning-based image inpainting method is applied to high-angle annular dark field (HAADF)-STEM images of a supported metal nanoparticle to predict and remove the background image of the support. The inpainting method can separate an 11nm Pd nanoparticle from the θ-Al2 O3 support in HAADF-STEM images of the θ-Al2 O3 -supported Pd catalyst. 3D reconstruction of the extracted images of the Pd nanoparticle reveals that the Pd nanoparticle adopts a deformed structure of the cuboctahedron model particle, resulting in high index surfaces, which account for the high catalytic activity for methane combustion. Using the xyz coordinate of each Pd atom, the local Pd-Pd bond distance and its variance in a real supported Pd nanoparticle are visualized, showing large strain and disorder at the Pd-Al2 O3 interface. The results demonstrate that 3D atomic-scale analysis enables atomic structure-based understanding and design of supported metal catalysts.

Monitoring Structural and Electronic Changes of Supported Metal Catalysts Using Combined X‐Ray Techniques

Supported metal nanoparticle catalysts have become increasingly crucial for many catalytic applications. However, long‐term catalyst stability remains a problem due to catalyst deactivation caused by coke formation and sintering. The deposition of a thin overcoating via atomic layer deposition (ALD) onto metal‐supported nanoparticles has shown to greatly inhibit catalyst deactivation. This work utilizes a model catalyst system comprised of Pt nanoparticles supported on Al2O3 to demonstrate the effect of an atomically thin overcoating on supported metal nanoparticles. Continuous operando small‐angle X‐ray scattering (SAXS) and X‐ray absorption near edge spectroscopy (XANES) monitor structural and electronic changes to the catalyst and overcoating during calcination. SAXS data fitting reveals the formation of nanopores in the overcoating at high temperatures, while XANES monitors the oxidation state of the Pt catalyst. Herein, the usefulness of combined X‐ray techniques is demonstrated to characterize supported metal catalysts to further understanding of the synergistic effects of the ALD overcoating to aid in the design of new catalyst materials.

Oxygen‐Saturated Strong Metal‐Support Interactions Triggered by Water on Titania Supported Catalysts

AbstractStrong metal‐support interaction (SMSI) greatly improves the performances of various supported metal nanoparticle catalysts. Classical SMSI relies on the oxide species with substoichiometric oxygen concentration, which prefers to retreat off in humid and oxidative atmospheres. A SMSI is reported with oxygen‐saturated overlayers on Au/TiO2 catalyst achieved by steaming treatment, an opposite condition to the classical SMSI formation. Through a combination of experimental and theoretical methods, this study demonstrates that the strong interactions between the TiOxHy (x≥2) species and Au surface cause the support migration to encapsulate Au nanoparticles. The oxygen‐saturated oxide overlayers are stable in oxidative, reductive, and humid atmospheres, providing great vitality to stabilize metal nanoparticle catalysts under varied and complex reaction conditions to outperform the classical SMSI.

Cover Feature: Continuous Flow Single‐Atom Catalysis: A Viable Organic Process Technology? (ChemCatChem 21/2022)

The Cover Feature shows a flow reactor employing a single-atom catalyst schematically represented. In their Perspective, M. Pagliaro, C. Della Pina and R. Ciriminna try to answer the question: “Is single-atom catalysis under continuous flow conditions a technically and economically viable organic process technology?” Early results actually suggest valuable insight en route to its industrial uptake in the production of fine and specialty chemicals. Reviewing selected examples of the first utilization of single-atom catalysts (SACs) under continuous-flow conditions, the authors provide evidence that SACs are not different from state-of-the-art supported metal nanoparticle catalysts in affording significantly higher TOFs than the same catalysts in batch reactor conversions. Furthermore, continuous flow conditions enhance the lot-to-lot consistency and dramatically lowers production time thug improving customer delivery. More information can be found in the Perspective by M. Pagliaro, C. Della Pina and R. Ciriminna.

Perpetual hyperpolarization of allyl acetate from parahydrogen and continuous flow heterogeneous hydrogenation with recycling of unreacted propargyl acetate

A novel closed loop, continuous flow (CF) reactor system for parahydrogen enhanced nuclear magnetic resonance (NMR) of liquids via heterogeneous catalysis is introduced which enables recycling of unreacted liquid substrate reactant. This system consists of an HPLC pump, a liquid substrate reservoir incorporating a gas diffuser, an all-metal packed bed catalytic reactor, and an AF-2400 tube-in-tube gas permeable membrane for removal of normal H2. Two types of supported metal nanoparticle catalysts were tested: mesoporous silica encapsulated Pt3Sn intermetallic nanoparticles and a Rh on anatase TiO2 support. In the CF hydrogenation of propargyl acetate to allyl acetate, the hyperpolarized signals exhibited stability over 20 min of recirculation, with signal enhancements of up to 626 using 99% p-H2 and negligible leaching of the catalyst into the flowing solutions. These results demonstrate the practicality of performing systematic optimization of conditions for continuous flow catalysis and polarization transfer to heteronuclei with important implications for biomedical magnetic resonance imaging.

Swift reduction of nitroaromatics by gold nanoparticles anchored on steam-activated carbon black via simple preparation.

Gold (Au) nanoparticles supported on certain platforms display highly efficient activity on nitroaromatics reduction. In this study, steam-activated carbon black (SCB) was used as a platform to fabricate Au/SCB composites via a green and simple method for 4-nitrophenol (4-NP) reduction. The obtained Au/SCB composites exhibit efficient catalytic performance in reduction of 4-NP (rate constant kapp = 2.1925min-1). The effects of SCB activated under different steam temperature, Au loading amount, pH, and reaction temperature and NaBH4 concentration were studied. The structural advantages of SCB as a platform were analyzed by various characterizations. Especially, the result of N2 adsorption-desorption method showed that steam activating process could bring higher surface area (from 185.9689 to 249.0053 m2/g), larger pore volume (from 0.073268 to 0.165246 cm3/g), and more micropore for SCB when compared with initial CB, demonstrating the suitable of SCB for Au NP anchoring, thus promoting the catalytic activity. This work contributes to the fabrication of other supported metal nanoparticle catalysts for preparing different functional nanocomposites for different applications.

Ostwald ripening microkinetic simulation of Au clusters on MgO(0 0 1)

Sintering is one of the most common processes responsible for the loss of supported metal nanoparticle catalysts' activity. We have combined ab-initio calculations with microkinetic simulations to investigate the digestion and growth mechanism on Au clusters supported on MgO(001) following a bottom-up approach. The energy barrier for diffusing a single gold atom on the clean MgO surface was found to be 0.29 eV in full agreement with previous reports. Additionally, and as an extension to the entire energy profile related to Ostwald mechanisms, we found all of the activation energies to be below 1.05 eV in the cases investigated. An odd–even cluster trend was observed during ripening, attributed to the stability of pairing the unpaired electrons associated with the single gold atoms. Microkinetic analyses showed that Au single atoms are present on the surface of magnesia up to a temperature of 160 K. At higher temperatures, the system has enough energy for the single atom to diffuse across the surface and attach to other atoms or clusters. At temperatures akin to room temperature, the cluster undergoes ripening to form larger particles in order to achieve a more stable equilibrium.

Metal Nanoparticles Immobilized on Molecularly Modified Surfaces: Versatile Catalytic Systems for Controlled Hydrogenation and Hydrogenolysis.

ConspectusThe synthesis and use of supported metal nanoparticle catalysts have a long-standing tradition in catalysis, typically associated with the field of heterogeneous catalysis. More recently, the development and understanding of catalytic systems composed of metal nanoparticles (NPs) that are synthesized from organometallic precursors on molecularly modified surfaces (MMSs) have opened a conceptually new approach to the design of multifunctional catalysts (NPs@MMS). These complex yet fascinating materials bridge molecular (“homogeneous”) and material (“heterogeneous”) approaches to catalysis and provide access to catalytic systems with tailor-made reactivity through judicious combinations of supports, molecular modifiers, and nanoparticle precursors. A particularly promising field of application is the controlled activation and transfer of dihydrogen, enabling highly selective hydrogenation and hydrogenolysis reactions as relevant for the conversion of biogenic feedstocks and platform chemicals as well as for novel synthetic pathways to fine chemicals and even pharmaceuticals. Consequently, the topic offers an emerging field for interdisciplinary research activities involving organometallic chemists, material scientists, synthetic organic chemists, and catalysis experts.This Account will provide a brief overview of the historical background and cover examples from the most recent developments in the field. A coherent account on the methodological and experimental basis will be given from the long-standing experience in our laboratories. MMSs are widely accessible via chemisorption and physisorption methods for the generation of stable molecular environments on solid surfaces, whereby a special emphasis is given here to ionic liquid-type molecules as modifiers (supported ionic liquid phases, SILPs) and silica as support material. Metal nanoparticles are synthesized following an organometallic approach, allowing the controlled formation of small and uniformly dispersed monometallic or multimetallic NPs in defined composition. A combination of techniques from molecular and material characterization provides a detailed insight into the structure of the resulting materials across various scales (electron microscopy, solid-state NMR, XPS, XAS, etc.).The molecular functionalities grafted on the silica surface have a pronounced influence on the formation, stabilization, and reactivity of the NPs. The complementary and synergistic fine-tuning of the metal and its molecular environment in NPs@MMSs allow in particular the control of the activation of hydrogen and its transfer to substrates. Monometallic (Ru, Rh, Pd) monofunctional NPs@MMSs possess excellent activities for the hydrogenation of alkenes, alkynes, and arenes for which a nonpolarized (homolytic) activation of H2 is predominant. The incorporation of 3d metals in noble metal NPs to give bimetallic (FeRu, CoRh, etc.) monofunctional NPs@MMSs favors a more polarized H2 activation and thus its transfer to the C=O bond, while at the same time preventing the arrangement of noble metal atoms necessary for ring hydrogenation. The incorporation of reactive functionalities, such as, for example, a −SO3H moiety on NPs@MMSs, results in bifunctional catalysts enabling the heterolytic cleavage corresponding to a formal H–/H+ transfer. Consequently, such catalysts possess excellent deoxygenation activity with strong synergistic effects arising from an intimate contact between the nanoparticles and the molecular functionality.While many more efforts are still required to explore, control, and understand the chemistry of NPs@MMS catalysts fully, the currently available examples already highlight the large potential of this approach for the rational design of multifunctional catalytic systems.

Design and Characterization of ALD-Based Overcoats for Supported Metal Nanoparticle Catalysts

Supported metal nanoparticle (SMN) catalysts are enormously crucial for many catalytic applications. However, catalyst deactivation, caused by sintering and coke formation, is a ubiquitous problem ...

Selectively coupled small Pd nanoparticles on sp2-hybridized domain of graphene-based aerogel with enhanced catalytic activity and stability

The precisely coupling of metal nanoparticles with support domain are crucial to enhance the catalytic activity and stability of supported metal nanoparticle catalysts (MNPs). Here we selectively anchor Pd nanoparticles to the sp2 domain in graphene-based aerogel constructed with base-washed graphene oxide (BGO) by removing oxidative debris (OD). The effects of OD on the size and chemical composition of Pd nanoparticles in aerogels are initially unveiled. The removal of OD nanoparticles prompt selective coupling of Pd nanoparticles to the exposed sp2-hybridized domain on BGO nanosheets, and then prevent it from agglomeration. As a result, the Pd nanoparticle size of self-assembled Pd/BGA is 4.67 times smaller than that of traditional Pd/graphene oxide aerogel (Pd/GA). The optimal catalytic activity of Pd/BGA for the model catalytic reduction of 4-nitrophenol is 15 times higher than that of Pd/GA. Pd/BGA could maintain its superior catalytic activity and achieves 98.72% conversion in the fifth cycle. The superior catalytic performance could be ascribed to the small Pd nanoparticles and high percentage of Pd(0) in Pd/BGA, and the enhanced electronic conductivity of Pd/BGA. These integrated merits of Pd/BGA as heterogeneous catalysts are attributed to selectively anchor Pd nanoparticles on sp2-hybridized domain of graphene-based aerogel, and strongly coupled interaction of MNPs with support. The structure-regulated BGO nanosheets could serve as versatile building blocks for fabricating MNPs/graphene aerogels with superior performance for catalytic transformation of water pollutants.

In situ electrochemical redox tuning of Pd-Co hybrid electrocatalysts for high-performance methanol oxidation: Strong metal-support interaction

Construction of strong metal-support interaction (SMSI) is of fundamental interest in the preparation of supported metal nanoparticle catalysts with enhanced catalytic activity. Herein, we report a facile in situ electrochemical redox tuning approach to build strong interactions between metals and supports. As for a typical example, a composite electrocatalyst of Pd-Co hybrid nanoparticles directly developed on Ni substrate is found to follow a distinct surface self-reconstruction process in alkaline media via an in situ electrochemical redox procedure, which results in structural transition from the original nanoparticles (NPs) to nanosheets (NSs) coupled with a phase transformation of the Co component, Co → CoO/Co(OH)2. The SMSI is observed in the electrochemically tuned Pd-Co hybrid system and leads to significantly enhanced catalytic activity for methanol oxidation reaction (MOR) due to the modified atomic/electronic structure, increased surface area, and more exposed electroactive sites. Compared with commercial Pd/C catalyst, the electrochemically tuned Pd-Co hybrid catalyst with SMSI exhibits superior catalytic activity (2330 mA∙mgPd−1) and much better stability (remains 503 mA∙mgPd−1 after 1000 cycles and 172 mA∙mgPd−1 after 5000 s), and therefore has great potential in practical applications.

(Invited) In Situ Grown Metal Nanoparticle Catalysts from Perovskites: Properties and Control

The ability to produce supported metal nanoparticle catalysts via exsolution from a perovskite type oxide support under reducing conditions has been known for some time and is used in solid oxide electrochemical cells. The ability to re-dissolve and exsolve the metal via redox cycling has led to these systems being referred to as smart or regenerable catalysts. While this phenomenon is well known, the mechanism by which the transition metal is exsolved from the oxide host is still poorly understood. The relationships between the exsolution process and the resulting structure of the metal nanoparticles are also not well understood. In this talk I will discuss our recent mechanistic studies of the exsolution process. Using well-defined model systems and detailed structural analysis by electron microscopy and atomic force microscopy, the nucleation and exsolution of Ni particles from Ni-doped strontium titanate was monitored. These studies show how exsolution produces unique surface structures consisting of metal particles partially submerged in pits on the oxide surface. I will show that this particle-in-a-pit morphology imparts unusually high thermal stability as well as significantly decreased carbon filament formation. Metal exsolution control will be discussed for host oxide lattices in thin film form.

Strong metal-support interaction promoted via constructing biocarbon membrane for enhanced CO preferential oxidation activity of Rh/CaCO3@biocarbon

Precious metal nanoparticles, widely used as heterogeneous catalysts, are easy to aggregate and deactivate, restricting their applications in many important catalytic fields like preferential CO oxidation (CO-PROX) in H2-rich stream. In this work, well dispersed Rh nanoclusters anchored on CaCO3@biocarbon derived from waste eggshell (ESMC) were synthesized through a step carbonization and incipient wetness impregnation process. The obtained catalysts exhibited 3D macroporous architecture, which is favorable for exposure of more nucleation sites of precious metal Rh, thus minimizing the aggregation of Rh particles. Furthermore, a thick carbon shell attached to eggshells, with interesting electronic structure and surface chemistry, efficiently transfers electrons between Rh and biocarbon@CaCO3 support, and enhances the interaction between Rh NPs and support. Both effects synergistically allow Rh/ESMC to equip more active adsorption sites-asymmetric Rh(CO)2 gem-dicarbonyl, thus greatly promoting the catalytic performance of Rh/ESMC in CO-PROX (operation temperature window: 140–240 °C). The present finding offers an environmentally friendly approach to fabricate well dispersed Rh nanoclusters catalysts, and it can be extended to rationally design other supported metal nanoparticle catalysts.

Redispersion of Mo-Based Catalysts and the Rational Design of Super Small-Sized Metallic Mo Species

Supported metal nanoparticle catalysts are one of the most important classes of heterogeneous catalysts but suffer from agglomeration in many cases. Particle redispersion is of great importance for...

Wet-Chemistry Strong Metal–Support Interactions in Titania-Supported Au Catalysts

Classical strong metal-support interactions (SMSI), which play a crucial role in the preparation of supported metal nanoparticle catalysts, is one of the most important concepts in heterogeneous catalysis. The conventional wisdom for construction of classical SMSI involves in redox treatments at high-temperatures by molecular oxygen or hydrogen, sometimes causing sintered metal nanoparticles before SMSI formation. Herein, we report that the aforementioned issue can be effectively avoided by a wet-chemistry methodology. As a typical example, we demonstrate a new concept of wet-chemistry SMSI (wcSMSI) that can be constructed on titania-supported Au nanoparticles (Au/TiO2-wcSMSI), where the key is to employ a redox interaction between Auδ+ and Ti3+ precursors in aqueous solution. The wcSMSI is evidenced by covering Au nanoparticles with the TiO x overlayer, electronic interaction between Au and TiO2, and suppression of CO adsorption on Au nanoparticles. Owing to the wcSMSI, the Au-TiO x interface with an improved redox property is favorable for oxygen activation, accelerating CO oxidation. In addition, the oxide overlayer efficiently stabilizes the Au nanoparticles, achieving sinter-resistant Au/TiO2-wcSMSI catalyst in CO oxidation.

Sinter-resistant metal nanoparticle catalysts achieved by immobilization within zeolite crystals via seed-directed growth

Supported metal nanoparticle catalysts are widely used in industry but suffer from deactivation resulting from metal sintering and coke deposition at high reaction temperatures. Here, we show an efficient and general strategy for the preparation of supported metal nanoparticle catalysts with very high resistance to sintering by fixing the metal nanoparticles (platinum, palladium, rhodium and silver) with diameters in the range of industrial catalysts (0.8–3.6 nm) within zeolite crystals (metal@zeolite) by means of a controllable seed-directed growth technique. The resulting materials are sinter resistant at 600–700 °C, and the uniform zeolite micropores allow for the diffusion of reactants enabling contact with the metal nanoparticles. The metal@zeolite catalysts exhibit long reaction lifetimes, outperforming conventional supported metal catalysts and commercial catalysts consisting of metal nanoparticles on the surfaces of solid supports during the catalytic conversion of C1 molecules, including the water-gas shift reaction, CO oxidation, oxidative reforming of methane and CO2 hydrogenation. Supported metal nanoparticles are indispensable catalysts in industry, yet they are often subjected to severe sintering. Now, a general method based on metal immobilization within zeolite is reported for the preparation of highly sinter-resistant catalysts for a broad range of industrially relevant processes.

Origin and Abatement of Heterogeneity at the Support Granule Scale of Silver on Silica Catalysts

AbstractIncipient wetness impregnation is used commonly to form supported metal nanoparticle catalysts. Recently, it has been revealed that this approach may induce severe heterogeneity between catalyst granules of the same batch. At least a 10‐fold variation in metal loading was observed, which affect the catalytic performance of individual catalyst granules severely. However, the origin of this heterogeneity is still unclear. Here we show that every elementary step in the preparation procedure of a Ag on silica catalyst has an effect on the resulting interparticle heterogeneity, but the influence of the drying step is the most important. This is because drying by capillary force results in a heterogeneous sample. Specifically, the position of a granule in the stagnant drying bed influences the resulting color and, thus, Ag loading significantly. This is further demonstrated by varying the drying conditions: freeze‐drying and fluidized‐bed drying led to a more homogeneous Ag loading. An investigation of the fluidized‐bed‐dried sample by using optical microscopy revealed a large fraction of transparent granules (94 %), which indicates that almost all the Ag nanoparticles in this sample are confined within the 6 nm pores. The optimized supported Ag on silica catalyst shows a good catalytic performance. This adaptation of the drying step can be implemented easily on a laboratory scale, is scalable, and does not require the use of expensive solvents or metal precursors.

Revealing the Dynamics of Platinum Nanoparticle Catalysts on Carbon in Oxygen and Water Using Environmental TEM

Deactivation of supported metal nanoparticle catalysts, especially under relevant gas conditions, is a critical challenge for many technological applications, including heterogeneous catalysis, electrocatalysis, and fuel cells. It has been commonly realized that deactivation of catalysts stems from surface area loss due to particle coarsening; however, the mechanism for this remains largely unclear. Herein, we use aberration-corrected environmental transmission electron microscopy, at an atomic level, to observe in situ the dynamics of Pt catalysts under fuel cell relevant gas and temperature conditions. Particle migration and coalescence is observed to be the dominant coarsening process. In comparison with the case of H2O, O2 promotes Pt nanoparticle migration on the carbon surface. Surprisingly, coating Pt/carbon with a nanofilm of electrolyte (Nafion ionomer) leads to a faster migration of Pt in H2O than in O2, a consequence of a Nafion–carbon interface water “lubrication” effect. Atomically, the parti...