Can NiFe-Layered-Double-Hydroxide Catalysts Suppress Carbon Corrosion in Electrochemical Oxygen Evolution?

Sustainable energy societies demand rechargeable batteries using ubiquitous-material electrodes of geopolitical-risk-free elements. We aim to develop low-overpotential oxygen-evolution-reaction (OER) catalysts that suppress carbon corrosion of gas-diffusion electrodes (GDEs) to realize two-electrode rechargeable Zn-air batteries (r-ZABs). Herein, single-walled-carbon-nanotube (SWNT) thin films are used as a scaffold for a benchmark OER catalyst, doping-free NiFe-layered double hydroxide (NiFeLDHs), operating in r-ZABs using alkali aqueous electrolytes.

A solvent-compatible filter-transfer method of semi-transparent carbon-nanotube electrodes stacked with silver nanowires.

Low-density films of single-walled carbon nanotubes (SWNTs) can be used as a semi-transparent top electrode for all-solution-processed film devices; however, their semiconductor characteristics vary depending on the experimental factors in their dispersion into solvents, and the sublayers are damaged as a result of solvent incompatibility. In this study, we report a solvent-compatible filter-transfer method for SWNT films stacked with silver nanowires (AgNWs), and evaluate the semiconductor characteristics through the p/n heterojunction with a Si wafer (SWNT/Si). AgNWs and SWNTs were successively filtered through their aqueous dispersion solutions using a membrane filter.

Effect of Static Jahn-Teller Distortion on the Li Transport in a Copper Hexacyanoferrate Framework.

Prussian blue (PB) and its analogues (PBAs) are potential cathode-active materials for rechargeable lithium-ion batteries. Although a body of research has assessed the performances of various PB/PBA cathodes with an eye to practical use, the underlying Li-transport mechanism is still unclear. Focusing on copper hexacyanoferrate (CuHCF), a PBA that exhibits static Jahn-Teller (JT) distortion, we theoretically investigate how the framework's distortion affects the pathways and energetics of the Li transport.

Size-tunable synthesis of iron oxide nanocrystals by continuous seed-mediated growth: role of alkylamine species in the stepwise thermal decomposition of iron(II) oxalate.

The properties of inorganic nanoparticles (NPs) are governed by their size. Therefore, tuning the size of NPs is a fundamental technique in nanoscience. However, the size-tunable synthesis of inorganic NPs is generally carried out in a dilute solution, which produces large quantities of waste.

Microvascular Decompression for Glossopharyngeal Neuralgia in the Semi-Sitting Position: A Report of Two Cases.

The semi-sitting position is well known to neurosurgeons. However, there are few reports of microvascular decompression surgery for glossopharyngeal neuralgia performed using the semi-sitting position. The semi-sitting position is not widely adopted in Japan, but it is considered to be a very useful neurosurgical position.

Estimation of the head elevation angle that causes clinically important venous air embolism in a semi-sitting position for neurosurgery: a retrospective observational study.

Introduction: The benefits of a sitting position for neurosurgery involving the posterior fossa remain controversial. The main concern is the risk of venous air embolism (VAE). A recent study showed that the rate of VAE was higher when the head was elevated to 45° than when it was elevated to 30°.

An exclusive deposition method of silver nanoparticles on TiO particles low-temperature decomposition of silver-alkyldiamine complexes in aqueous media.

An exclusive deposition method of Ag nanoparticles (NPs) on TiO particles has been developed. Ag NPs supported on TiO particles, Ag /TiO, with various Ag weight ratios total weights of Ag and TiO between = 2 and 16 wt% are prepared low-temperature thermal decomposition of Ag(i)-alkyldiamine complexes generated by a reaction between AgNO and ,-dimethyl-1,3-propanediamine (dmpda) in an aqueous medium suspending TiO particles. The thermal decomposition of the Ag(i)-alkyldiamine complexes is accelerated by TiO particles in the dark, indicating that the reaction catalytically occurs on the TiO surfaces.

Preparation of Hierarchically Assembled Silver Nanostructures based on the Morphologies of Crystalline Peptide-Silver(I) Complexes.

The preparation of a hierarchically assembled Ag nanostructures based on a nanocrystalline assembly was demonstrated using an Ag(I) complex of a dipeptide (AspDap). By heating under N gas, a spherical assembly of a nanocrystalline dipeptide-Ag(I) complex (diameter 4-5 μm), which has a morphology similar to the assembled structure of the dipeptide, was transformed to an assembly of Ag nanostructures, where the micrometre-order crystalline morphology was maintained. In addition, detailed scanning electron microscopy studies revealed that Ag nanoparticles (diameter ca.

Ion transportation by Prussian blue nanoparticles embedded in a giant liposome.

A new type of artificial giant liposome incorporating ion transport channels and using nanoparticles of metal organic frameworks was demonstrated. The micropores of Prussian blue nanoparticles served as ion transport channels between the outer and inner phases of liposomes.

Investigation of the Image Contrast in an Ultra-Low Voltage Scanning Electron Microscope Using an Auger Electron Spectrometer.

Surface-sensitive information on a bulk sample can be obtained by using a low incident electron energy (low accelerating voltage/landing voltage) in a scanning electron microscope (SEM). However, topography and composition contrast obtained at low incident electron energies may not be intuitive and should be analyzed carefully. By combining an Auger electron spectrometer (AES) with a low incident electron energy SEM (LE-SEM), we investigated the SEM contrast carefully by separating the secondary electron (SE) and back-scattered electron (BSE) components with high accuracy.

Interpretation of the Role of Composition on the Inclusion Efficiency of Monovalent Cations into Cobalt Hexacyanoferrate.

Cobalt hexacyanoferrate of various compositions was prepared in flow mode and the role of the vacancy on the structure, thermogravimetric (TG) properties, and the adsorption efficiency was studied. The material, Na Co[Fe(CN) ] ⋅z H O, with a minimum vacancy of x=0.014 to the highest x=0.

Ferrihydrite Particle Encapsulated within a Molecular Organic Cage.

Metal oxides with sizes of a few nanometers show variable crystal and electronic structures depending on their dimensions, and the synthesis of metal oxide particles with a desired size is a key technology in materials science. Although discrete metal oxide particles with an average diameter ( d) smaller than 2 nm are expected to show size-specific properties, such ultrasmall metal oxide particles are significantly limited in number. In nature, on the other hand, nanosized ferrihydrite (Fh), which is ferric oxyhydroxide, occurs as a result of biomineralization in ferritin, an iron storage protein cage.

Effects of the variation of metal substitution and electrolyte on the electrochemical reaction of metal hexacyanoferrates.

Metal hexacyanoferrates (MHCFs), also called Prussian blue analogs, are known as electrochemical electrodes and are ion-adsorbent. To investigate the effect of the ionic radius of the adsorbate (cations adsorbed upon reduction) and the pore size of the adsorbent (porous electrode that stores cations upon reduction), we investigated the electrochemical reactions with various alkali cations and by changing the metal sites of the MHCFs. First, we succeeded in controlling the pore sizes of the MHCFs, where the lattice constant could be estimated as = 0.

Unveiling Cs-adsorption mechanism of Prussian blue analogs: Cs-percolation vacancies to complete dehydrated state.

Metal hexacyanoferrates (MHCF) or Prussian blue analogs are excellent Cs-adsorbents used for radioactive Cs-decontamination. However, the adsorption mechanism is controversial. To clarify the issue, we quantitatively investigated the Cs-adsorption behaviors of potassium copper hexacyanoferrate (KCuHCF) and A Cu[Fe(CN)] ·HO.

Improvement of the Heat Resistance of Prussian Blue Nanoparticles in a Clay Film Composed of Smectite Clay and ε-Caprolactam.

Prussian blue (PB) is limited in its application by its breakdown at elevated temperatures. To improve the heat resistance of PB, we prepared a composite film comprising PB nanoparticles (NPs), smectite clay, and an organic compound. The composite film had a microstructure in which PB NPs were intercalated between smectite/organic compound layers.

Unique coexistence of dispersion stability and nanoparticle chemisorption in alkylamine/alkylacid encapsulated silver nanocolloids.

Surface encapsulation of metal nanoparticles (NPs) is fundamental to achieve sufficient dispersion stability of metal nanocolloids, or metal nanoink. However, the feature is incompatible with surface reactive nature of the metal NPs, although these features are both essential to realizing the functional applications into printed electronics technologies. Here we show that two different kinds of encapsulation for silver NPs (AgNPs) by alkylamine and alkylacid together are the key to achieve unique compatibility between the high dispersion stability as dense nanoclolloids and the AgNP chemisorption printing on activated patterned polymer surfaces.

Solvent-free synthesis of monodisperse Cu nanoparticles by thermal decomposition of an oleylamine-coordinated Cu oxalate complex.

Cu nanoparticles (NPs) are widely used in numerous applications because of their unique optical, catalytic, and electrical properties. However, the synthesis of monodisperse Cu NPs often involves harmful reducing agents under an inert atmosphere in a solution with low Cu ion concentrations. In this study, monodisperse Cu NPs were synthesized by the thermal decomposition of an oleylamine-coordinated Cu oxalate (Cu(ox)) complex (OA-Cu(ox)) in oleylamine in air with no reducing agent.

Wisely Designed Phthalocyanine Derivative for Convenient Molecular Fabrication on a Substrate.

An axial-substituted silicon phthalocyanine derivative, SiPc(OR) (R = CH), that is soluble in organic solvent is conveniently synthesized. This silicon phthalocyanine derivative reacts with a hydroxyl group on a substrate and then with another phthalocyanine derivative under mild conditions. The accumulation number of the phthalocyanine molecules on the substrates is easily controlled by the immersion time.

N,N-Diethyl-diaminopropane-copper(ii) oxalate self-reducible complex for the solution-based synthesis of copper nanocrystals.

Metal oxalates (CO, ox) have been explored as promising precursors for the direct transformation of their oxalate moieties into metallic or metal oxide crystals via thermal decomposition without the formation of any byproducts due to releasing CO gas. The copper(ii) oxalate (Cu(ox)) crystal is a coordination polymer composed of an infinite coordination network with a thermal decomposition temperature around 300 °C; however, their insoluble nature in any solvents and relatively high decomposition temperature do not allow the solution-based syntheses of surface-modified metallic Cu nanocrystals (NCs) in the presence of various surfactants such as long-chain alkylamines and alkylcarboxylates which have been used for increasing the dispersibility of NCs in organic solvents. In this study, the insoluble nature of Cu(ox) is overcome by mixing Cu(ox) crystals and N,N-diethyl-1,3-diaminopropane (dedap) to form a discrete complex, [Cu(ox)(dedap)], whose structure is determined by X-ray crystallographic analysis.

Grain-Boundary-Free Super-Proton Conduction of a Solution-Processed Prussian-Blue Nanoparticle Film.

A porous crystal family has been explored as alternatives of Nafion films exhibiting super-proton conductivities of ≥10  S cm . Here, the proton-conduction natures of a solution-processed film of nanoparticles (NPs) have been studied and compared to those of a Nafion film. A mono-particle film of Prussian-blue NPs is spontaneously formed on a self-assembled monolayer substrate by a one-step solution process.

Dual-Functional Surfactant-Templated Strategy for Synthesis of an In Situ N -Intercalated Mesoporous WO Photoanode for Efficient Visible-Light-Driven Water Oxidation.

N -Intercalated crystalline mesoporous tungsten trioxide (WO ) was synthesized by a thermal decomposition technique with dodecylamine (DDA) as a surfactant template with a dual role as an N-atom source for N intercalation, alongside its conventional structure-directing role (by micelle formation) to induce a mesoporous structure. N physisorption analysis showed that the specific surface area (57.3 m  g ) of WO templated with DDA (WO -DDA) is 2.

Characterization of Interfacial Charge-Transfer Photoexcitation of Polychromium-Oxo-Electrodeposited TiO as an Earth-Abundant Photoanode for Water Oxidation Driven by Visible Light.

Polychromium-oxo-deposited TiO (Cr O /TiO ) electrodes were fabricated by a simple electrochemical technique by using different TiO basal electrodes (anatase, rutile, and mixed polymorphic phases P25) as earth-abundant photoanodes for visible-light-driven water oxidation. The high-resolution transmission electron microscopy (HR-TEM) observation illustrated that an Cr O layer with approximately 2-3 nm thickness was formed on the surface of the crystalline TiO particles. Upon visible-light irradiation of the electrodes, the photoanodic current based on water oxidation was generated at the Cr O /TiO electrodes.

Nanoparticle chemisorption printing technique for conductive silver patterning with submicron resolution.

Silver nanocolloid, a dense suspension of ligand-encapsulated silver nanoparticles, is an important material for printing-based device production technologies. However, printed conductive patterns of sufficiently high quality and resolution for industrial products have not yet been achieved, as the use of conventional printing techniques is severely limiting. Here we report a printing technique to manufacture ultrafine conductive patterns utilizing the exclusive chemisorption phenomenon of weakly encapsulated silver nanoparticles on a photoactivated surface.

Potential Tuning of Nanoarchitectures Based on Phthalocyanine Nanopillars: Construction of Effective Photocurrent Generation Systems.

Nanopillars composed of a photoresponsive phthalocyanine derivative have been conveniently fabricated using a continuous silane coupling reaction on a substrate. The chemical potentials of phthalocyanine nanopillars (PNs) are precisely controlled by changing the number of phthalocyanine derivatives on the substrate. In addition, photocurrent generation efficiencies have been strongly influenced by the number of phthalocyanine derivatives.