Unusual resistive switching induced by voltage in La0.7Sr0.3MnO3 thin films

The hysteretic and reversible resistive-switching effect was observed in La_0.7Sr_0.3MnO₃ films at room temperature. The resistive switching was found to be most obvious in films fabricated at 30 Pa oxygen pressure, and more distinct in films fabricated on SrTiO₃ substrates than those fabricated on LaAlO₃ substrates. Moreover, La_0.7Sr_0.3MnO₃ films fabricated at a certain oxygen pressure with indium electrodes showed double ‘8’ type current-voltage loops. Some of the results are explained by considering the influence of the interface effect, electrodes and oxygen vacancies, but the mechanism of the double ‘8’ type current-voltage loops remains an open question.     

Cobalt-Catalyzed Regio- and Stereoselective Hydroboration of Allenes

An efficient pincer-ligand-based cobalt-complex-catalyzed allene hydroboration affording Z-allylic boronates is described. The reaction demonstrates an excellent regio- as well as Z-stereoselectivity and a wide substrate scope that tolerates many functional groups. Based on solvent-assisted electrospray ionization mass spectrometry (SAESI-MS) studies, a rationale for the cobalt-catalyzed hydroboration involving the highly selective insertion of an allene into the Co−H bond to form Z-allylic cobalt intermediates is proposed.     

N-substituted-3(10H)-acridones as visible-light photosensitizers for organic photoredox catalysis

N-Substituted-3(10H)-acridones have been established as visible-light organic photocatalyst. These photosensitizers are efficient for oxidative coupling reaction of N-aryl tetrahydroisoquinolines with various nucleophiles. Notably, N-methyl-3(10H)-acridone (Ia) is stable and can be effectively prepared. It is a water-soluble and atom-economic catalyst, and thus holds promise for green chemical applications. Mechanistic studies confirm a single electron transfer (SET)-induced radical process and a rate-limiting step. Analysis of the photocatalytic reactivity?structure relationship reveals that the acridones are robust and tunable photosensitizers for photoredox catalysis.     

A nonnormal look at polychoric correlations: modeling the change in correlations before and after discretization

Two algorithms for establishing a connection between correlations before and after ordinalization under a wide spectrum of nonnormal underlying bivariate distributions are developed by extending the iteratively found normal-based results via the power polynomials. These algorithms are designed to compute the polychoric correlation when the ordinal correlation is specified, and vice versa, along with the distributional properties of latent, continuous variables that are subsequently ordinalized through thresholds dictated by the marginal proportions. The method has broad applicability in the simulation and random number generation world where modeling the relationships between these correlation types is of interest.     

Link Homologies and the Refined Topological Vertex

We establish a direct map between refined topological vertex and sl(N) homological invariants of the of Hopf link, which include Khovanov-Rozansky homology as a special case. This relation provides an exact answer for homological invariants of the Hopf link, whose components are colored by arbitrary representations of sl(N). At present, the mathematical formulation of such homological invariants is available only for the fundamental representation (the Khovanov-Rozansky theory) and the relation with the refined topological vertex should be useful for categorizing quantum group invariants associated with other representations (R ₁, R ₂). Our result is a first direct verification of a series of conjectures which identifies link homologies with the Hilbert space of BPS states in the presence of branes, where the physical interpretation of gradings is in terms of charges of the branes ending on Lagrangian branes.     

Bianchi type III models with anisotropic dark energy

The general form of the anisotropy parameter of the expansion for Bianchi type-III metric is obtained in the presence of a single diagonal imperfect fluid with a dynamically anisotropic equation of state parameter and a dynamical energy density in general relativity. A special law is assumed for the anisotropy of the fluid which reduces the anisotropy parameter of the expansion to a simple form (D μ H^-2V^-2{\Delta\propto H^{-2}V^{-2}}, where Δ is the anisotropy parameter, H is the mean Hubble parameter and V is the volume of the universe). The exact solutions of the Einstein field equations, under the assumption on the anisotropy of the fluid, are obtained for exponential and power-law volumetric expansions. The isotropy of the fluid, space and expansion are examined. It is observed that the universe can approach to isotropy monotonically even in the presence of an anisotropic fluid. The anisotropy of the fluid also isotropizes at later times for accelerating models and evolves into the well-known cosmological constant in the model for exponential volumetric expansion.     

Non-existence of a massive scalar field for the Marder universe in Lyra and Riemannian geometries

In this paper, we have studied a massive scalar field for a Marder type universe in the context of Lyra and Riemannian geometries. From the exact solutions obtained we show that the massive scalar field does not survive in Lyra and Riemannian geometries for an anisotropic Marder type universe. Therefore we have solved the massless scalar field problem in Lyra and Riemann geometries for two cases. Also we have obtained vacuum solutions for homogeneous and anisotropic Marder space-time in Lyra geometry and the solutions obtained are compared by considering Lyra and Riemann geometries. Finally, some physical and kinematical properties are discussed by using graphics.     

Highly sensitive sensor for detection of NADH based on catalytic growth of Au nanoparticles on glassy carbon electrode

In this work, an electrochemical dihydronicotinamide adenine dinucleotide (NADH) sensor based on the catalytic growth of Au nanoparticles (Au NPs) on glassy carbon electrode was developed. Catalyzed by Au NPs immobilized on pretreated glassy carbon electrode, the reduction of AuCl₄ ^? in the presence of hydroquinone and cetyltrimethyl ammonium chloride led to the formation of enlarged Au NPs on the electrode surface. Spectrophotometry and high-resolution scanning electronic microscope (SEM) analysis of the sensor morphologies before and after biocatalytic reaction revealed a diameter growth of the nanoparticles. The catalytic growth of Au NPs on electrode surface remarkably facilitated the electron transfer and improved the performance of the sensor. Under optimal conditions, NADH could be detected in the range from 1.25?×?10^?6 to 3.08?×?10^?4 M, and the detection limit was 2.5?×?10^?7 M. The advantages of the proposed sensor, such as high precision and sensitivity, fast response, low cost, and good storage stability, made it suitable for on-line detection of NADH in complex biological systems and contaminant degradation processes.

Interface Engineering of a CoOx/Ta3N5 Photocatalyst for Unprecedented Water Oxidation Performance under Visible‐Light‐Irradiation

Cocatalysts have been extensively used to promote water oxidation efficiency in solar‐to‐chemical energy conversion, but the influence of interface compatibility between semiconductor and cocatalyst has been rarely addressed. Here we demonstrate a feasible strategy of interface wettability modification to enhance water oxidation efficiency of the state‐of‐the‐art CoO_x/Ta₃N₅ system. When the hydrophobic feature of a Ta₃N₅ semiconductor was modulated to a hydrophilic one by in situ or ex situ surface coating with a magnesia nanolayer (2–5 nm), the interfacial contact between the hydrophilic CoO_x cocatalyst and the modified hydrophilic Ta₃N₅ semiconductor was greatly improved. Consequently, the visible‐light‐driven photocatalytic oxygen evolution rate of the resulting CoO_x/MgO(in)–Ta₃N₅ photocatalyst is ca. 23 times that of the pristine Ta₃N₅ sample, with a new record (11.3 %) of apparent quantum efficiency (AQE) under 500–600 nm illumination.     

固体溶质在超临界三元系统中的溶解度

溶质在超临界流体中的溶解度数据是研究超临界流体技术的基础.本文对纯组分固体溶质有夹带剂存在的超临界流体三元系统中,夹带剂增大溶质溶解度的作用进行了总结,述评了夹带剂增大溶质溶解度的机理和常用的计算模型.此外,针对两种固体混合溶质共存于超临界流体中的三元系统,讨论了混合溶质共存对彼此溶解度的影响及其相关的理论假说和计算模型.