CO Oxidation Research Articles

Pd-CeO2 catalyst facilely derived from one-pot generated Pd@Ce-BTC for low temperature CO oxidation

Due to the capacity to offer abundant catalytic sites within porous solids featuring high surface areas, metal-organic frameworks (MOFs) and their derivatives have garnered considerable attention as prospective catalysts in environmental catalysis. To promote the industrial application of MOFs, there is an urgent need for an effective and environmental-friendly preparation approach. Breaking through the limitation of the traditional two-step preparation method that Pd was introduced to the already prepared Ce-BTC (Pd/Ce-BTC, BTC = 1, 3, 5 benzenetricarboxylate), in this work, we present a novel one-pot solvothermal method for synthesizing the Pd material supported by Ce-BTC (Pd@Ce-BTC). After pyrolysis in N2 flow or air flow, Pd-CeO2 catalysts derived from Pd@Ce-BTC exhibited much higher CO oxidation activity than those from Pd/Ce-BTC. Moreover, Pd/Ce-BTC and Pd@Ce-BTC pyrolyzed in N2 flow (Pd/Ce-BTC-N and Pd@Ce-BTC-N) could better catalyze the oxidation of CO than Pd/Ce-BTC and Pd@Ce-BTC pyrolyzed in air flow (Pd/Ce-BTC-A and Pd@Ce-BTC-A). Further characterizations revealed that the abundant surface Ce3+ species, rich surface adsorbed oxygen species and superior redox properties were the main reasons for the superior CO oxidation activity of Pd@Ce-BTC-N.

Trinary metal oxides of Co, Ni, and Mn as efficient overall water splitting catalyst

Trinary metal oxides of Co, Ni, and Mn as efficient overall water splitting catalyst

Multi-band Metasurface-Driven Surface-Enhanced Infrared Absorption Spectroscopy for Improved Characterization of in-Situ Electrochemical Reactions.

Surface-enhanced spectroscopy techniques are the method-of-choice to characterize adsorbed intermediates occurring during electrochemical reactions, which are crucial in realizing a green and sustainable future. Characterizing species with low coverage or short lifetimes has so far been limited by low signal enhancement. Recently, single-band metasurface-driven surface-enhanced infrared absorption spectroscopy (SEIRAS) has been pioneered as a promising technology to monitor a single vibrational mode during electrochemical CO oxidation. However, electrochemical reactions are complex, and their understanding requires the simultaneous monitoring of multiple adsorbed species in situ, hampering the adoption of nanostructured electrodes in spectro-electrochemistry. Here, we develop a multi-band nanophotonic-electrochemical platform that simultaneously monitors in situ multiple adsorbed species emerging during cyclic voltammetry scans by leveraging the high resolution offered by the reproducible nanostructuring of the working electrode. Specifically, we studied the electrochemical reduction of CO2 on a Pt surface and used two separately tuned metasurface arrays to monitor two adsorption configurations of CO with vibrational bands at ∼2030 and ∼1840 cm-1. Our platform provides a ∼40-fold enhancement in the detection of characteristic absorption signals compared to conventional broadband electrochemically roughened platinum films. A straightforward methodology is outlined starting with baselining our system in a CO-saturated environment and clearly detecting both configurations of adsorption. In contrast, during the electrochemical reduction of CO2 on platinum in K2CO3, CO adsorbed in a bridged configuration could not be detected. We anticipate that our technology will guide researchers in developing similar sensing platforms to simultaneously detect multiple challenging intermediates, with low surface coverage or short lifetimes.

Nickel- and/or iron-based ceria-supported catalysts for CO oxidation in combustion exhaust gases

We present a series of Ni, Fe, and mixed NiFe-based catalysts, deposited onto ceria prepared with either soft templated (with CTAB) or hard templated (with SBA-15) syntheses. The prepared materials were thoroughly characterized with SEM, HRTEM, EDX, ICP-MS, PXRD, and N2 adsorption techniques, to fully comprehend their physicochemical properties. All catalysts were then tested for carbon monoxide oxidation reaction at different temperatures, aiming to reach temperature and feed composition conditions typical of combustion exhausts from industrial and power plants (350–400 °C, in the presence of competitive species such as CO2 and H2O in the feed). Advanced reaction tests highlighted outstanding materials (especially NiFe catalyst deposited onto hard-templated ceria), displaying catalytic performances able to compete with those typical of noble metal–based catalysts. Such catalysts were further investigated by means of Raman, NEXAFS, H2–TPR, and CO@FT-IR, unraveling their surface and reduction properties, which make them excellent candidates for replacing more costly noble metal-based catalysts currently employed for CO oxidation reaction.

Elucidation of site structures and CO oxidation kinetics of the Ir1/TiO2 single-atom catalyst

Elucidation of site structures and CO oxidation kinetics of the Ir1/TiO2 single-atom catalyst

Remarkable SO2 and H2S Resistant Ability on CO Oxidation by Unique Pd/WO3 3D Hollow Sphere Nanocatalyst: Correlating Structure–Activity Relationships on SO2 Exposure

Remarkable SO₂ and H₂S Resistant Ability on CO Oxidation by Unique Pd/WO₃ 3D Hollow Sphere Nanocatalyst: Correlating Structure–Activity Relationships on SO₂ Exposure

Removal of CO in flue gas by catalytic oxidation: a review

Abstract Most coal-fired industrial flue gases contained low concentration CO. How to deal with it effectively was a research hotspot in recent years. Catalytic oxidation was considered as the most promising method in the 21st century for the removement of CO with the high efficiency, environmentally friendly, easy to operate and low cost. In this review, the reaction mechanisms of CO oxidation were described, which could provide ideas for the development of new catalysts. The effects of supports and preparation methods on catalysts activity was also reviewed systematically. In addition, some suggestions and outlooks were provided for future development of CO catalytic oxidation.

Synergistic hydroxyl mechanism on halloysite-confined PtFe alloy boosting low-temperature CO-PROX performance

Both structural and adsorbed surface hydroxyl groups in solid materials are important carriers for oxygen species transport. The role of identifiable structural hydroxyl groups in catalytic reactions, however, is often underestimated. Here, we propose a synergistic hydroxyl reaction mechanism on Pt1Fe0.33/HNTs catalyst in CO-PROX reaction, which is critical to reveal the new way of oxygen transport in the oxidation reaction. Particularly, the Pt1Fe0.33 nanoparticles (NPs) have been confined in the cavity of halloysite nanotubes (HNTs) to activate structural hydroxyl groups linked to the AlVI via a two-step reduction treatment. The activated structural hydroxyl groups exhibit sensitivity to CO, as revealed by in situ DRIFTS and MS data. The experimental and DFT data demonstrate that the cooperation of Pt, Fe, and hydroxyl sites in the active units on Pt1Fe0.33/HNTs can induce a synergistic participation of structural and adsorbed hydroxyl groups in CO oxidation through the formate pathway. In such catalytic process, the oxygen mobility is dominated by oxygen-containing hydroxyl species rather than reactive oxygen species. This work contributes to a deeper understanding of the role of hydroxyl groups in catalysis and lays the foundation for establishing a comprehensive oxidation reaction mechanism in the future.

Single-and double transition metal atoms anchored C2N as a high-activity catalyst for CO oxidation: A first-principles study

The oxidation of CO has attracted great interest in recent years due to its important role in enhancing the catalyst durability in fuel cells and solving the growing environmental problems caused by CO emissions. Consequently, the catalytic oxidation of CO at double non-noble metal atoms anchored C2N is investigated using density functional theory (DFT) computations. All the screened Ti@C2N and Ti2@C2N are thermodynamically stable based on their binding energy calculations. The electronic characteristics, the natural bond orbital analyses (NBO), Frontier orbital, statistical thermodynamics, projected densities of states (PDOS) characteristics, non-covalent interactions (NCI), and quantum theory of atoms in molecules (QTAIM) descriptors of these systems have been examined to analyze the interaction process. Our comparative study suggested that the newly predicted double-atom catalyst (Ti2@C2N) is highly active for CO oxidation, which is a useful guideline for further development. The calculated static first-order hyperpolarizability (βo) illustrated that the double-atom catalyst under investigation can be considered a potential candidate for non-linear optical behavior and could be used for NLO applications. CO oxidation on Ti2@C2N along the Eley–Rideal (ER) mechanism with a low energy barrier of 0.16 eV, which is smaller than the maximum energy barrier (0.73 eV) of CO oxidation along the Langmuir–Hinshelwood (LH) mechanism. Consequently, the ER mechanism is more favorable both thermodynamically and dynamically. This work can provide useful insights and guidelines for future theoretical and experimental investigations to promote the design and development of highly effective and low-cost non-precious-metal Ti2@C2N nanocatalysts towards CO oxidation at ambient temperature.

Decoration of Gold and Platinum Nanoparticle Catalysts by 1 nm Thick Metal Oxide Overlayer and Its Effect on the CO Oxidation Activity.

Exfoliated M-Al layered double hydroxide (M-Al LDH; M = Mg, Co, Ni, and Zn) nanosheets were adsorbed on Au/SiO2 and calcined to transform LDH into mixed metal oxides (MMOs) and yield Au/SiO2 coated with a thin MMO overlayer. These catalysts showed a higher catalytic activity than pristine Au/SiO2. In particular, the 50% CO conversion temperature decreased by more than 250 °C for Co-Al MMO-coated Au/SiO2. In contrast, the deposition of CoAlOx on Au/SiO2 by impregnation or the deposition of Au on Co-Al MMO-coated SiO2 resulted in a worse catalytic activity. Moreover, the presence of a thick MMO overlayer decreased the catalytic activity, suggesting that the control of the overlayer thickness to less than 1 nm is a requisite for obtaining a high catalytic activity. Moreover, the thin Co-Al MMO overlayer on Au/SiO2 possessed abundant oxygen vacancies, which would play an important role in O2 activation, resulting in a highly active interface between Au and the defect-rich MMO on the Au NP surface. Finally, this can be applied to Pt/SiO2, and the obtained Co-Al MMO-coated Pt/SiO2 also exhibited a much improved catalytic activity for CO oxidation.

Role of surface species in CO oxidation over CuO@LaMnO3 nanocomposites: Effect of calcination temperature

As one of the main atmospheric pollutants, CO poses great hazards to the living environment. This study synthesized a series of CuO@LaMnO3 nanocomposites via a well-optimized one-step synthesized sol-gel method. All catalysts were calcined at different temperatures (600–800 °C) to analyze their impact on the material properties. The appropriate elevation of calcination temperature visibly enhanced the catalytic behavior, due to the greatest activity being gathered on the sample calcinated at 700 °C, with nearly 100% conversion for CO at 150 °C. Further characterization results revealed that the change in surface species induced by the calcination temperature was a key factor in enhancing catalytic behavior. The coupling of CuO and LaMnO3 induced electron migration and released more Mn4+, Cu+ and OS, boosting the upgraded adsorption capacity of CO, which served as the inherent motivation for the high activity observed over the CuO@LaMnO3 catalyst. Finally, a possible mechanism model of CO oxidation over the CuO@LaMnO3 catalyst was proposed. Adoption of the innovative composite method herein indeed led to a rich variation in the valence state of the elements on the catalyst surface without the inclusion of copper into the lattice, which in turn caused a significant alteration in the reaction mechanism.

Atomic-scale understanding of the impact of CoO phase in cobalt-catalyzed Fischer-Tropsch synthesis: A combined computational and experimental study

In cobalt-catalyzed Fischer-Tropsch synthesis (FTS), the active metallic cobalt phase always suffers from oxidation under FTS reaction conditions, leading to the coexistence of metallic cobalt and cobalt oxide (CoO) phases. However, there still exist contradictory views on the impact of CoO phase in FTS. Some researchers proposed that the oxidation of metallic Co to CoO causes the deactivation of cobalt-based FTS catalysts, while some held the view that CoO phase could act as the potential active phase in FTS. In this study, by combining theoretical calculations and experiments, we systematically investigated the fundamental FTS reactions including CO adsorption and activation, C-C coupling, and CxHy hydrogenation on CoO phase, and compared them with those on metallic cobalt phase, aiming at identifying the exact role of CoO, understanding how CoO influences the activity and selectivity, and unraveling the intrinsic mechanism that determines the catalytic behaviors of CoO phase in FTS. The results reveal that the CoO(200) crystal facet is the dominantly exposed surface structure for CoO phase under FTS reaction conditions. The d-band center of CoO(200) surface shifts downward in comparison with that of active metallic Co surface, which causes difficulties in adsorbing and activating CO and gives rise to high energy barriers for the dissociation of C-O bond. This determines the inactive nature of CoO phase in FTS reaction. As for the product selectivity, the CoO(200) surface restricts the C-C chain growth due to its higher barriers for C-C coupling, facile desorption ability for light olefins, and lower energy barrier for CH4 formation compared with metallic cobalt, and consequently leads to the loss of selectivity to C5+ hydrocarbons and enhancement of selectivity to light olefins and undesired methane. Moreover, a strong linear relationship between the experimental observed selectivity change and the DFT-calculated energy difference of CoO and metallic cobalt phases was found, validating the DFT-calculated results. This study provides a comprehensive understanding of the nature and intrinsic catalytic behaviors of CoO phase in cobalt-catalyzed FTS.

CO Oxidation Promoted by NO Adsorption on RhMn2O3- Cluster Anions.

CO oxidation represents an important model reaction in the gas phase to provide a clear structure-reactivity relationship in related heterogeneous catalysis. Herein, in combination with mass spectrometry experiments and quantum-chemical calculations, we identified that the RhMn2O3- cluster cannot oxidize CO into gas-phase CO2 at room temperature, while the NO preadsorbed products RhMn2O3-[(NO)1,2] are highly reactive in CO oxidation. This discovery is helpful to get a fundamental understanding on the reaction behavior in real-world three-way catalytic conditions where different kinds of reactants coexist. Theoretical calculations were performed to rationalize the crucial roles of preadsorbed NO where the strongly attached NO on the Rh atom can greatly stabilize the products RhMn2O2-[(NO)1,2] during CO oxidation and at the same time works together with the Rh atom to store electrons that stay originally in the attached CO2- unit. The leading result is that the desorption of CO2, which is the rate-determining step of CO oxidation by RhMn2O3-, can be greatly facilitated on the reactions of RhMn2O3-[(NO)1,2] with CO.

Structure characterization of aged automobile exhaust catalysts using electron probe microanalysis

BackgroundDriven by emission regulations, the technology of emission control catalysts has been under increasing need for development. Understanding the deactivation mechanism of aged or spent automobile exhaust catalysts is the key to extending their service lifetime. However, the lack of comprehensive microstructural characterization results in an incomplete understanding of their physicochemical properties. Deactivation mechanism of automobile exhaust catalysts is a considerably complex phenomenon, it can be classified into three groups based on its origin: thermal sintering, chemical poisoning and mechanical deactivation. ResultsIn this study, an aged high-mileage automobile exhaust catalyst with Pd and Rh active phases supported on a cerium zirconium oxide doped alumina coating on cordierite was analysed; six consecutive monolithic blocks along the inlet to the outlet of the aged catalyst were extracted, and the corresponding metallographic samples were fabricated using the vacuum impregnation resin method. The purpose of this study was to accurately characterize the different regions of the monolith via electron probe microanalysis and to infer potential causes of catalyst deactivation. Two major causes of deactivation were found: (1) aggregation and alloying of precious-metal particles caused by thermal sintering and (2) chemical poisoning caused by sulphur and phosphorus. Other mechanisms, such as mechanical degradation, which mainly manifests as the loss or wear of the washed coating, were also found to be involved in deactivation. Additionally, the catalytic activity tests showed a considerable decrease in the aged catalyst. The poison concentration trends in the washcoat indicated that P is detrimental to CO oxidation, while S accumulation affects propane oxidation. SignificanceThis analysis method can be of substantial practical significance in developing advanced washcoat materials. Meanwhile, it has great potential in the washcoat analysis of honeycomb-shaped monolithic catalyst, such as natural gas catalyst, diesel vehicle oxidation catalyst and other honeycomb catalysts applied in chemical industry.

Graphene/Hexagonal Boron Nitride Heterostructures for O2 Activation and CO Oxidation: Metal-Free Catalysts by Design.

Pristine graphene and h-BN monolayers are chemically inert to oxygen and thus exhibit very limited catalytic activity toward O2 activation. Herein, we show that graphene/h-BN heterostructures exhibit a surprising O2 activation capability. We theoretically designed ten graphene/h-BN heterostructures with three types of interfaces and investigated their catalytic activities toward O2 activation and CO-oxidation. In general, O2 can be molecularly chemisorbed and activated on electron-rich graphene/h-BN heterostructures. Electron-deficient graphene/h-BN heterostructures can lead to dissociative O2 adsorption with relatively low dissociation energy barriers (<0.4 eV). For CO-oxidation, the computed energy barrier can be as low as 0.67 eV. The high catalytic activities toward O2 stem from either electron-deficient heterostructures' accumulated electrons or electron richness and low work function for the electron-rich heterostructures. Although the catalytic activities of graphene/h-BN heterostructures depend strongly on the interface type, they are insensitive to the patterns of BN-substitutes, hence benefiting applicability of a wide range of heterostructures.

Manufacturing AAl2O4 (A=Cu, Co, Ni, Zn) Spinel Catalysts for Toluene Combustion: Elucidating the A‐site Replacement Effect on the Reactivity

AbstractTo decode the A‐site substitution effect on the reactivity of Al‐based spinel complex oxides, a series of AAl2O4 (A=Cu, Co, Ni, Zn) compounds were manufactured and tested by toluene combustion. It was confirmed that a pure spinel crystalline phase has been successfully synthesized for all the catalysts. The toluene and CO oxidation activity are sequenced as CuAl2O4&gt;CoAl2O4&gt;NiAl2O4&gt;ZnAl2O4. As discovered, both active surface O2− and acid sites are the two critical factors to determine the reactivity, which can adsorb and activate the reactants effectively to form active intermediates, possibly following a Mars‐van‐Krevelen pathway. The activity improves positively with the amount increasing of these two kinds of active sites, thus showing an evident A‐site replacement effect. CuAl2O4 owns the biggest numbers of these two kinds of active sites, thereby exhibiting the optimal catalytic activity. Moreover, it also shows good stability in a dry feed, and considerable ability to resist water vapor and sulfur poisoning. In‐situ DRIFTS results have indicated that benzyl, benzoate, benzaldehyde and benzoquinone might be the major reaction intermediates.

Versatile Spectroscopic Cell for Operando Studies in Heterogeneous Catalysis Using Tender X‐ray Spectroscopy in Fluorescence Mode

AbstractThe design and commissioning of a cell suitable for operando studies using high‐energy‐resolution fluorescence‐detected X‐ray absorption near‐edge structure (HERFD‐XANES) spectroscopy in the tender X‐ray regime is reported. The cell is optimized for measurements within the energy range of 1.5 keV to 4.5 keV. It has a plug‐flow geometry and can be used for sieved powder samples, analogous to reactors employed for laboratory tests. The functionality of the spectroscopic cell is demonstrated in the area of emission control using CO oxidation as target reaction over 1 wt.% Rh/γ‐Al2O3 as catalyst. We show how HERFD‐XANES at the Rh L3‐edge captures variations in the noble metal structure resulting from the interaction with the support material and reactant molecules. Moreover, distinct structural changes were identified along the catalyst bed as a function of temperature and local gas mixture.

Mining wastes as CO oxidation mesoporous catalysts from the Fe-skarns of Serifos Island, Cyclades, Greece

The Fe-skarns from the Greek Island of Serifos in Cyclades has been utilized only for the exploitation of magnetite ores, while significantly vast amounts of red and yellow hematite ores remained unexploited as mining wastes. This study explores the effective utilization of such mining wastes per se, as active mesoporous catalysts for energy applications, taking CO oxidation as a model reaction. The results of our multi-analytical study have illustrated that the physicochemical characteristics of the hematite materials can be positively influenced by the implementation of a simple calcination step, while the characteristics of magnetite remained unaffected. The calcined yellow and red mineral hematite from Serifos Fe-skarns mining wastes per se, act beneficial in the catalytic activity with respect to calcined magnetite catalyst. The calcinated counterparts of hematite, and especially yellow hematite, can efficiently be used as a support for depositing Au nanoparticles, and thus achieving even higher activity for CO oxidation (90% CO conversion), at much lower temperatures (T ∼62.0 °C). The mining wastes per se of Serifos, mainly of mesoporous hematite, are particularly active for CO oxidation, without any complex pretreatments or activation or functionalization in the context of circular economy.

Active nanointerfaces sites for low-temperature water-gas shift reaction over inverse configuration Nb–CeO2/Cu catalysts

A comparative investigation of inverse Nb–CeO2/Cu catalysts obtained via sol–gel, coprecipitation, hydrothermal, and incipient wetness impregnation methods was performed against a normal configuration for hydrogen production through a water–gas shift reaction. Exposed oxygen-deficient Nb–CeO2 (111) facet sites deposited on Cu (111) facets with enhanced densities of Ce3+, Cu+, and Ov species for high reducibility were confirmed using X-ray diffraction, transmission electron microscopy, and X-ray photoelectron spectroscopy. Nb–CeO2/Cu catalyst prepared by coprecipitation exhibited the highest activity of 68 % CO conversion, 100 % H2 selectivity at 360 °C, and gas hourly space velocity of 43,535 h−1. The lowest activation energy (39.67 kJ/mol) and high turnover frequency illustrate facilitated water dissociation and CO oxidation in close vicinity across nanointerfaces. For the Nb–CeO2/Cu catalyst prepared by the coprecipitation method, nanosized Nb–CeO2 stabilized over the porous Cu support was optimum for generating interfaces and facilitating catalytic performance. It is to underscore that the catalyst prepared by coprecipitation exhibited constant H2 production under realistic conditions for 102 h, demonstrating the robust structural features of the configuration Nb–CeO2/Cu.

Single atom sites as CO scavenger to allow for crude hydrogen usage in PEMFC

Nanosized Pt catalysts are the catalyst-of-choice for proton exchange membrane fuel cell (PEMFC) anode, but are limited by their extreme sensitivity to CO in parts per million (ppm) level, thereby making the use of ultrapure H2 a prerequisite to ensure acceptable performance. Herein, we confront the CO poisoning issue by bringing the Ir/Rh single atom sites to synergistically working with their metallic counterparts. In presence of 1000 ppm CO, the catalyst represents not only undisturbed H2 oxidation reaction (HOR) catalytic behavior in electrochemical cell, but also unparalleled peak power density at 643 mW cm−2 in single cell, 27-fold in mass activity of the best PtRu/C catalysts available. Pre-poisoning experiments and surface-enhanced Raman scattering spectroscopy (SERS) and calculation results in combine suggest the presence of adjacent Ir/Rh single atom sites (SASs) to the nanoparticles (NPs) as the origin for this prominent catalytic behavior. The single sites not only exhibit superb CO oxidation performance by themselves, but can also scavenge the CO adsorbed on approximated NPs via supplying reactive OH* species. We open up a new route here to conquer the formidable CO poisoning issue through single atom and nanoparticle synergistic catalysis, and pave the way towards a more robust PEMFC future.