One-Step Synthesis of Highly Active NiFe Electrocatalysts for the Oxygen Evolution Reaction.

Electrochemical water splitting is a key technology for the conversion of renewable energy into chemical resources such as hydrogen. However, the oxygen evolution reaction (OER), a half-reaction of water splitting, is so slow that various effective catalysts for the OER have been explored. In this study, we demonstrate a simple and direct process for the synthesis of OER-active NiFe catalysts over electrodes. A NiFe/C catalyst layer was formed on a glassy carbon electrode by simply dropping the catalyst ink containing only metal nitrates and carbon black. The catalyst layer exhibited higher OER performance than the state-of-the-art Ir/C catalyst. The presence of carbon black is essential to enhance the OER activity of NiFe because carbon black helps to disperse the NiFe active sites. Cyclic voltammetry indicated that Ni and Fe are adjacent to each other on the surface of carbon black, resulting in significantly higher activity of NiFe/C compared to those of Ni/C and Fe/C. The effects of the Ni/Fe ratio, amount of carbon black, and type of carbon black on the OER activity of NiFe/C were examined in detail. Furthermore, we discuss the factors that determine the OER performance of NiFe/C.

Facile synthesis of nanostructured perovskites by precursor accumulation on nanocarbons.

Perovskite-type oxides have impacted various research fields, including materials and energy science. Despite their vast potential in various applications, general and simple synthesis methods for nano-perovskites remain limited. Herein, various nano-perovskites were synthesized by a facile approach involving the use of nanocarbons. The calcination of the nanocarbon deposited with metal salts yielded nano-perovskites, emulating the morphology of nanocarbons. The accumulation of precursors (i.e., metal salts) on the surface of the nanocarbon during the evaporation of the solvent is the key step in which the precursors are homogeneously mixed prior to calcination. The homogeneity of the precursors facilitated low-temperature calcination that resulted in the formation of nano-perovskites. Various nano-perovskites, including LaMnO3, LaCoO3, LaFeO3, LaNiO3, LaAlO3, LaGaO3, CaMnO3, BaMnO3, SrMnO3, La0.7Sr0.3FeO3, La2CuO4, and Ca2Fe2O5, were successfully synthesized, demonstrating the simplicity and novelty of the method for the general synthesis of nano-perovskites.

Upgrading of Ethanol to 1,1-Diethoxyethane by Proton-Exchange Membrane Electrolysis.

The direct acetalization of ethanol is a significant challenge for upgrading bioethanol to value-added chemicals. In this study, 1,1-diethoxyethane (DEE) is selectively synthesized by the electrolysis of ethanol using a proton-exchange membrane (PEM) reactor. In the PEM reactor, a Pt/C catalyst promoted the electro-oxidation of ethanol to acetaldehyde. The Nafion membrane used as the PEM served as a solid acid catalyst for the acetalization of ethanol and electrochemically formed acetaldehyde. DEE was obtained at high faradaic efficiency (78 %) through sequential electrochemical and nonelectrochemical reactions. The DEE formation rate through PEM electrolysis was higher than that of reported systems. At the cathode, protons extracted from ethanol were reduced to H2 . The electrochemical approach can be utilized as a sustainable process for upgrading bioethanol to chemicals because it can use renewable electricity and does not require chemical reagents (e. g., oxidants and electrolytes).

A case of accessory pathway mapped with ultra-high-resolution mapping led to a coronary sinus diverticulum.

Ultra-high-resolution mapping is useful in the ablation of accessory pathways. However, in patients with accessory pathways in the coronary sinus (CS) diverticulum, treatment with endocardial ablation may be challenging. Patients suspected of having subepicardial accessory pathways may require the examination of the venous anomaly using CS angiography.

Precursor accumulation on nanocarbons for the synthesis of LaCoO3 nanoparticles as electrocatalysts for oxygen evolution reaction.

Oxygen evolution reaction (OER) is a key step in energy storage devices. Lanthanum cobaltite (LaCoO3) perovskite is an active catalyst for OER in alkaline solutions, and it is expected to be a low-cost alternative to the state-of-the-art catalysts (IrO2 and RuO2) because transition metals are abundant and inexpensive. For efficient catalysis with LaCoO3, nanosized LaCoO3 with a high surface area is desirable for increasing the number of catalytically active sites. In this study, we developed a novel synthetic route for LaCoO3 nanoparticles by accumulating the precursor molecules over nanocarbons. This precursor accumulation (PA) method for LaCoO3 nanoparticle synthesis is simple and involves the following steps: (1) a commercially available carbon powder is soaked in a solution of the nitrate salts of lanthanum and cobalt and (2) the sample is dried and calcined in air. The LaCoO3 nanoparticles prepared by the PA method have a high specific surface area (12 m2 g-1), comparable to that of conventional LaCoO3 nanoparticles. The morphology of the LaCoO3 nanoparticles is affected by the nanocarbon type, and LaCoO3 nanoparticles with diameters of less than 100 nm were obtained when carbon black (Ketjen black) was used as the support. Further, the sulfur impurities in nanocarbons significantly influence the formation of the perovskite structure. The prepared LaCoO3 nanoparticles show excellent OER activity owing to their high surface area and perovskite structure. The Tafel slope of these LaCoO3 nanoparticles is as low as that of the previously reported active LaCoO3 catalyst. The results strongly suggest that the PA method provides nanosized LaCoO3 without requiring the precise control of chemical reactions, harsh conditions, and/or special apparatus, indicating that it is promising for producing active OER catalysts at a large scale.

Efficacy of isoproterenol in the evaluation of dormant conduction and arrhythmogenic foci identification in atrial fibrillation ablation.

BACKGROUND: Catheter ablation for atrial fibrillation (AF) is an established therapy. However, postoperative recurrence is a serious issue caused by the reconduction of the isolated pulmonary veins (PV) and the onset of non-PV foci. The objectives of this study were to elucidate dormant conduction, confirm PV arrhythmia substrate, induce non-PV foci after PV isolation, and assess the acute efficacy of high dose isoproterenol (ISP) when administered in addition to adenosine. METHODS: The study consisted of 100 patients with drug-refractory AF (paroxysmal and persistent) who underwent ablation therapy (either radio-frequency or cryoballoon ablation) as the first-line of therapy at our hospital. All patients first underwent PV isolation (PVI) and were administered adenosine followed by ISP (6 µg × 5 min). The effects were observed, and the therapeutic strategy was evaluated. RESULTS: Persistent dormant conduction due to ISP administration was observed in 13 patients. In over half of the patients, arrhythmia substrates were identified in the PV. Ten patients presented with persistent PV firing. The ablation of non-PV foci was additionally performed in 23 patients. CONCLUSIONS: We found that dormant conduction, as a result of ISP administration, is persistent and ISP is useful when performing an ablation. In addition, ISP administration is useful for the identification of PV arrhythmia substrates and induction of non-PV foci. However, the effectiveness of ISP may be partially due to the complementary effect of adenosine, and, therefore, a combination of the two drugs seems preferable.

The appearance of a single left atrial tachycardia as two different types on preoperative surface and intracardiac ECG of pacemaker due to progressive cardiac conduction disturbance.

We treated a patient with PCCD whose single left AT appeared as two different types on preoperative surface and intracardiac ECG from a pacemaker. The diagnosis was hindered by the fact that the conduction block encompassed interatrial block and the pacemaker A-wave was captured at the right atrial appendage.

Coating of Silica Nanolayers on Carbon Nanofibers via the Precursor Accumulation Method.

Surface modification of nanocarbons, for example, by coating with oxide nanolayers, is a research topic of significant interest because of the drastic changes in the physicochemical properties of the modified nanocarbons. One simple method of creating these oxide nanolayer coatings on nanocarbons is the precursor accumulation (PA) technique, which entails the following: (1) a precursor solution is added dropwise onto nanocarbon powder; (2) the solvent is dried, leaving the accumulated precursor on the nanocarbon surface; and (3) hydrolysis or decomposition of the precursor in air leads to the formation of oxide nanolayers on the nanocarbons. In this study, tetraethoxysilane (TEOS) was used as a precursor for coating silica nanolayers onto carbon nanofibers (CNFs). TEOS is so stable that it hardly undergoes hydrolysis on the surface of pristine CNFs. By treating CNFs with H2SO4/HNO3, acidic functional groups were introduced onto the CNF surfaces. Silica nanolayers were successfully synthesized on these acid-treated CNFs via PA coating because the acidic functional groups catalyzed the hydrolysis of TEOS accumulated on the CNF surfaces. Scanning transmission electron microscopy indicated that the thickness of silica layer is approximately several nanometers. Pore size distribution analysis for the silica nanolayer suggested the presence of nanopores with 3-5 nm. The TEOS molecules could have accessed the functional groups through the nanopore; therefore, the number of silica nanolayers formed increased with the number of PA coatings. Finally, we compared the PA coating with conventional sol-gel and atomic layer deposition techniques.

Safe and rapid development of capillary electrophoresis for ultratrace uranyl ions in radioactive samples by way of fluorescent probe selection for actinide ions from a chemical library.

After the serious nuclear accident at the Fukushima Daiichi Nuclear Power Plant caused by the Great East Japan Earthquake in 2011, the development of feasible, safe, and highly sensitive analytical methods (in terms of low levels of radiation exposure and radioactive waste generation) for radioactive samples, especially actinide (An) ions, represents an important challenge. Here we propose a methodology for selecting appropriate emissive probes for An ions with very low consumption and emission of radioactivity by capillary electrophoresis-laser-induced fluorescence detection (CE-LIF), using a small chemical library of probes with eight different chelating moieties. It was found that the emissive probe L1, which possesses the tetradentate chelating moiety 1,10-phenanthroline-2,9-dicarboxylic acid (PDA), was suitable for detecting uranyl ions. The detection limit for the uranyl-L1 complex using CE-LIF combined with dynamic ternary complexation and on-capillary concentration techniques was determined to be 2.9 × 10-12 M (0.7 ppt). No interference from the large excess of matrix metal ions was observed. This method was successfully applied to real radioactive liquid samples collected from nuclear facilities, including the Fukushima Daiichi Nuclear Power Plant. This strategy not only permitted the development of a safe and rapid analytical method but also provided insight into the coordination chemistry of An ion complexes. Specifically, the PDA structure provided substantial kinetic inertness to its uranyl complex; the formation of a ternary complex between uranyl-L1 and carbonate was revealed; and unusual interactions were observed between the π-electron systems of uranyl and the phenanthroline ring, which stabilized the uranyl-PDA interaction.