CO activation by copper oxide clusters: size, composition, and charge state dependence.

The interaction of CO with copper oxide clusters of different size, composition, and charge is investigated infrared multiple-photon dissociation (IR-MPD) spectroscopy and density functional theory (DFT) calculations. Laser ablation of a copper target in the presence of an O/He mixture leads to the preferred formation of oxygen-rich copper oxide cluster cations, CuO ( > ; ≤ 8), while the anionic cluster distribution is dominated by stoichiometric ( = ) and oxygen-deficient ( < ; ≤ 8) species. Subsequent reaction of the clusters with CO in a flow tube reactor results in the preferred formation of near-stoichiometric CuO(CO) complexes.

Gas-Phase Production of Hydroxylated Silicon Oxide Cluster Cations: Structure, Infrared Spectroscopy, and Astronomical Relevance.

The interaction of free cationic silicon oxide clusters, Si O ( = 2-5, ≥ ), with dilute water vapor, was investigated in a flow tube reactor. Product mass distributions indicate cluster size-dependent dissociative water adsorption. To probe the structure and vibrational spectra of the resulting Si O H ( = 2-4) clusters, we employed infrared multiple photon dissociation spectroscopy and density functional theory calculations.

Antimicrobial effects of silver nanoparticle-microspots on the mechanical properties of single bacteria.

Silver nanoparticles (AgNPs) conjugated with polymers are well-known for their powerful and effective antimicrobial properties. In particular, the incorporation of AgNPs in biocompatible catecholamine-based polymers, such as polydopamine (PDA), has recently shown promising antimicrobial activity, due to the synergistic effects of the AgNPs, silver(I) ions released and PDA. In this study, we generated AgNPs-PDA-patterned surfaces by localised electrochemical depositions, using a double potentiostatic method scanning electrochemical cell microscopy (SECCM).

Cluster size dependent coordination of formate to free manganese oxide clusters.

The interaction of free manganese oxide clusters, MnO ( = 1-9, = 0-12), with formic acid was studied infrared multiple-photon dissociation (IR-MPD) spectroscopy together with calculations using density functional theory (DFT). Clusters containing only one Mn atom, such as MnO and MnO, bind formic acid as an intact molecule in both the - and -configuration. In contrast, all clusters containing two or more manganese atoms deprotonate the acid's hydroxyl group.

Structural Evolution of Iron-Loaded Metal-Organic Framework Catalysts for Continuous Gas-Phase Oxidation of Methane to Methanol.

Catalytic partial oxidation of methane presents a promising route to convert the abundant but environmentally undesired methane gas to liquid methanol with applications as an energy carrier and a platform chemical. However, an outstanding challenge for this process remains in developing a catalyst that can oxidize methane selectively to methanol with good activity under continuous flow conditions in the gas phase using O as an oxidant. Here, we report a Fe catalyst supported by a metal-organic framework (MOF), Fe/UiO-66, for the selective and on-stream partial oxidation of methane to methanol.

Switchable Polyacrylonitrile-Copolymer for Melt-Processing and Thermal Carbonization-3D Printing of Carbon Supercapacitor Electrodes with High Capacitance.

Polyacrylonitrile (PAN) represents the most widely used precursor for carbon fibers and carbon materials. Carbon materials stand out with their high mechanical performance, but they also show excellent electrical conductivity and high surface area. These properties render carbon materials suitable as electrode material for fuel cells, batteries, and supercapacitors.

Nanoporous Au Formation on Au Substrates via High Voltage Electrolysis.

Nanoporous Au (NPG) films have promising properties, making them suitable for various applications in (electro)catalysis or (bio)sensing. Tuning the structural properties, such as the pore size or the surface-to-volume ratio, often requires complex starting materials such as alloys, multiple synthesis steps, lengthy preparation procedures or a combination of these factors. Here we present an approach that circumvents these difficulties, enabling for a rapid and controlled preparation of NPG films starting from a bare Au electrode.

A Carbon Nanodot Based Near-Infrared Photosensitizer with a Protein-Ruthenium Shell for Low-Power Photodynamic Applications.

Near-infrared (NIR) light-activated photosensitization represents an encouraging therapeutic method in photodynamic therapy, especially for deep tissue penetration. In this context, two-photon activation, i.e.

Reversible Growth of Gold Nanoparticles in the Low-Temperature Water-Gas Shift Reaction.

Supported gold nanoparticles are widely studied catalysts and are among the most active known for the low-temperature water-gas shift reaction, which is essential in fuel and energy applications, but their practical application has been limited by their poor thermal stability. The catalysts deactivate on-stream via the growth of small Au nanoparticles. Using operando X-ray absorption and in situ scanning transmission electron microscopy, we report direct evidence that this process can be reversed by carrying out a facile oxidative treatment, which redisperses the gold nanoparticles and restores catalytic activity.

Resolving the structure of VO·HO and Mo-substituted VO·HO.

Vanadate compounds, such as VO·HO, are of high interest due to their versatile applications as electrode material for metal-ion batteries. In particular, VO·HO can insert different ions such as Li, Na, K, Mg and Zn. In that case, well resolved crystal structure data, such as crystal unit-cell parameters and atom positions, are needed in order to determine the structural information of the inserted ions in the VO·HO structure.

Spin-Gated Selectivity of the Water Oxidation Reaction Mediated by Free Pentameric CaMnO Clusters.

We report on the first preparation of isolated ligand-free CaMnO gas-phase clusters, as well as other pentameric CaMnO ( = 0-4) clusters with varying Ca contents, which serve as molecular models of the natural CaMnO inorganic cluster in photosystem II. Ion trap reactivity studies with DO and HO reveal a pronounced cluster composition-dependent ability to mediate the oxidation of water to hydrogen peroxide. First-principles density functional theory simulations elucidate the mechanism of water oxidation, proceeding via formation of a terminal oxyl radical followed by oxyl/hydroxy (O/OH) coupling.

Enhanced Electrochemical Capacity of Spherical Co-Free Li Mn Ni O Particles after a Water and Acid Treatment and its Influence on the Initial Gas Evolution Behavior.

Li-rich layered oxides (LRLO) with specific energies beyond 900 Wh kg are one promising class of high-energy cathode materials. Their high Mn-content allows reducing both costs and the environmental footprint. In this work, Co-free Li Mn Ni O was investigated.

Zinc-Ion Hybrid Supercapacitors Employing Acetate-Based Water-in-Salt Electrolytes.

Halide-free, water-in-salt electrolytes (WiSEs) composed of potassium acetate (KAc) and zinc acetate (ZnAc ) are investigated as electrolytes in zinc-ion hybrid supercapacitors (ZHSs). Molecular dynamics simulations demonstrate that water molecules are mostly non-interacting with each other in the highly concentrated WiSEs, while "bulk-like water" regions are present in the dilute electrolyte. Among the various concentrated electrolytes investigated, the 30 m KAc and 1 m ZnAc electrolyte (30K1Zn) grants the best performance in terms of reversibility and stability of Zn plating/stripping while the less concentrated electrolyte cannot suppress corrosion of Zn and hydrogen evolution.

Nonmetal-to-Metal Transition of Magnesia Supported Au Clusters Affects the Ultrafast Dissociation Dynamics of Adsorbed CHBr Molecules.

The detection of intermediate species and the correlation of their ultrafast dynamics with the morphology and electronic structure of a surface is crucial to fully understand and control heterogeneous photoinduced and photocatalytic reactions. In this work, the ultrafast photodissociation dynamics of CHBr molecules adsorbed on variable-size Au clusters on MgO/Mo(100) is investigated by monitoring the CH transient evolution using a pump-probe technique in conjunction with surface mass spectrometry. Furthermore, extreme-UV photoemission spectroscopy in combination with theoretical calculations is employed to study the electronic structure of the Au clusters on MgO/Mo(100).

On-Chip Direct Laser Writing of PAN-Based Carbon Supercapacitor Electrodes.

The carbonization of polyacrylonitrile (PAN) by direct laser writing to produce microsupercapacitors directly on-chip is reported. The process is demonstrated by producing interdigitated carbon finger electrodes directly on a printed circuit board (PCB), which is then employed to characterize the supercapacitor electrodes. By varying the laser power, the process can be tuned from carbonization to material ablation.

Impact of the Transition Metal Dopant in Zinc Oxide Lithium-Ion Anodes on the Solid Electrolyte Interphase Formation.

Conversion/alloying materials (CAMs) provide substantially higher specific capacities than graphite, the state-of-the-art lithium-ion battery anode material. The ability to host much more lithium per unit weight and volume is, however, accompanied by significant volume changes, which challenges the realization of a stable solid electrolyte interphase (SEI). Herein, the comprehensive characterization of the composition and evolution of the SEI on transition metal (TM) doped zinc oxide as CAM model compound, is reported, with a particular focus on the impact of the TM dopant (Fe or Co).

Low-temperature nucleation and growth of Zn on Au(111) and thermal stability toward (surface) alloy formation.

As part of an extensive study of the interaction between Zn and Au in Zn/Au(111) model systems, we have systematically investigated the low-temperature (LT) nucleation and growth behavior of Zn on the Au(111) surface as well as the thermal stability of the resulting structures toward sintering, intermixing, and dissolution by scanning tunneling microscopy (STM) and x-ray photoelectron spectroscopy (XPS). Zn deposition at LT, at 105 K (STM) or 80 K (XPS), leads to nucleation and two-dimensional growth of Zn islands mainly at the elbows of the Au(111) herringbone reconstruction, with a slight preference for island formation at pinched-in (pi) rather than bulged-out (bu) elbows. Local surface intermixing during LT Zn deposition leads to local perturbations of the Au(111) herringbone reconstruction, which results in the formation of additional nucleation sites (edge sites).

Chimera states in a neuronal network under the action of an electric field.

The phenomenon of the chimera state symbolizes the coexistence of coherent and incoherent sections of a given population. This phenomenon identified in several physical and biological systems presents several variants, including the multichimera states and the traveling chimera state. Here, we numerically study the influence of a weak external electric field on the dynamics of a network of Hindmarsh-Rose (HR) neurons coupled locally by an electrical interaction and nonlocally by a chemical one.

Size, Stoichiometry, Dimensionality, and Ca Doping of Manganese Oxide-Based Water Oxidation Clusters: An Oxyl/Hydroxy Mechanism for Oxygen-Oxygen Coupling.

Gas-phase ion-trap reactivity experiments and density functional simulations reveal that water oxidation to HO mediated by (calcium) manganese oxide clusters proceeds via formation of a terminal oxyl radical followed by oxyl/hydroxy O-O coupling. This mechanism is predicted to be energetically feasible for MnO ( = 2-4) and the binary CaMnO, in agreement with the experimental observations. In contrast, the reaction does not proceed for the tetramanganese oxides MnO ( = 4-6) under these experimental conditions.

Long-range interaction effects on coupled excitable nodes: traveling waves and chimera state.

In this paper, analytical and numerical studies of the influence of the long-range interaction parameter on the excitability threshold in a ring of FitzHugh-Nagumo (FHN) system are investigated. The long-range interaction is introduced to the network to model regulation of the Gap junctions or hemichannels activity at the connexins level, which provides links between pre-synaptic and post-synaptic neurons. Results show that the long-range coupling enhances the range of the threshold parameter.

Cluster Size Dependent Interaction of Free Manganese Oxide Clusters with Acetic Acid and Methyl Acetate.

We have employed infrared multiple-photon dissociation (IR-MPD) spectroscopy together with density functional theory (DFT) calculations to study the interaction of series of subnanometer sized manganese oxide clusters, MnO ( = 1-6, = 0-9) with acetic acid (HOAc) and methyl acetate (MeOAc). Reaction with HOAc leads to strongly cluster size and composition dependent IR-MPD spectra, indicating molecular adsorption on MnO clusters and thermodynamically favorable but kinetically hampered HOAc dissociation (deprotonation) on MnO and MnO. Other cluster sizes exhibit the preferred formation of a dissociative bidentate chelating structure.

Fundamental Aspects of Ceria Supported Au Catalysts Probed by In Situ/Operando Spectroscopy and TAP Reactor Studies.

The discovery of the activity of dispersed gold nanoparticles three decades ago paved the way for a new era in catalysis. The unusual behavior of these catalysts sparked many questions about their working mechanism. In particular, Au/CeO proved to be an efficient catalyst in several reactions such as CO oxidation, water gas shift, and CO reduction.

Bifunctional versus Defect-Mediated Effects in Electrocatalytic Methanol Oxidation.

The most prominent and intensively studied anode catalyst material for direct methanol oxidation fuel cells consists of a combination of platinum (Pt) and ruthenium (Ru). Classically, their high performance is attributed to a bifunctional reaction mechanism where Ru sites provide oxygen species at lower overpotential than Pt. In turn, they oxidize the adsorbed carbonaceous reaction intermediates at lower overpotential; among these, the Pt site-blocking carbon monoxide.