Experimental and computational studies of naphthyridine derivatives as corrosion inhibitor for N80 steel in 15% hydrochloric acid

The inhibition effect of three naphthyridine derivatives namely 2-amino-4-(4-methoxyphenyl)-1,8-naphthyridine-3-carbonitrile (ANC-1), 2-amino-4-(4-methylphenyl)-1,8-naphthyridine-3-carbonitrile (ANC-2) and 2-amino-4-(3-nitrophenyl)-1,8-naphthyridine-3-carbonitrile (ANC-3) as corrosion inhibitors for N80 steel in 15% HCl by using gravimetric, electrochemical techniques (EIS and potentiodynamic polarization), SEM, EDX and quantum chemical calculation. The order of inhibition efficiency is ANC-1>ANC-2>ANC-3. Potentiodynamic polarization reveals that these inhibitors are mixed type with predominant cathodic control. Studied inhibitors obey the Langmuir adsorption isotherm. The quantum calculation is in good agreement with experimental results.     

Polarization and angle insensitive ultra-broadband mid-infrared perfect absorber

A new polarization and angle insensitive ultra-broadband perfect absorber (UPA) was proposed and demonstrated based on an alumina-chromium-alumina-chromium four-layer structure. The absorption bandwidth reached 3059 nm in the infrared range (from 939 nm to 3998 nm) with a spectral absorptivity greater than 90%. The average absorption was up to 94.0% in a range of 800 nm to 4200 nm. The physical mechanisms and influence of different structural configurations on the absorption performance of the UPA were analyzed in detail. When the oblique incidence angle was up to 60°, the average absorption rates of the TE and TM modes were 87.3% and 85.0%, respectively. The proposed UPA has potential applications in thermo-photovoltaics and infrared detection.     

考虑地表反射类型的气溶胶散射偏振特性

采用逐次阶散射法求解矢量辐射传输方程来研究气溶胶在不同地表反射模型下的散射偏振特性.首先,选取单一地表反射模型和耦合地表反射模型两种地表反射模型.然后,根据地表反射模型计算得到相应的地表反射率,进而采用逐次阶散射法对矢量辐射传输方程进行求解,得到散射光的Stokes矢量.最后,由Stokes矢量计算得出散射光的偏振度.仿真结果表明,两种地表反射模型下气溶胶单次散射的散射辐射强度和线偏振度均相等;耦合地表反射模型的总散射辐射强度和线偏振度总是大于单一地表反射模型;单一地表反射模型的气溶胶单次散射相对总散射的贡献总是大于耦合地表反射模型.研究结果对气溶胶光学特性的反演具有一定意义.     

Polarization-enhanced bulk photovoltaic effect of BiFeO3 epitaxial film under standard solar illumination

In this Letter, we report the polarization-enhanced bulk photovoltaic effect (BPV) in pristine BiFeO₃ (BFO) epitaxial film under standard 1 sun AM 1.5 G illumination. High-quality epitaxial BFO films are grown on (001)-oriented niobium doped-SrTiO₃ substrates by pulsed laser deposition. The best BFO film based photovoltaic device achieves a power conversion efficiency of 0.0062% under standard illumination. Besides, it is found that the number of bipolar pulses plays a key role in improving the short-circuit current density and open-circuit voltage. These results are beneficial for further understanding of physical origin of the photovoltaic properties in ferroelectric oxides.     

Wurtzite CuGaS2 with an In-Situ-Formed CuO Layer Photocatalyzes CO2 Conversion to Ethylene with High Selectivity

We present surface reconstruction-induced C−C coupling whereby CO₂ is converted into ethylene. The wurtzite phase of CuGaS_2. undergoes in situ surface reconstruction, leading to the formation of a thin CuO layer over the pristine catalyst, which facilitates selective conversion of CO₂ to ethylene (C₂H₄). Upon illumination, the catalyst efficiently converts CO₂ to C₂H₄ with 75.1 % selectivity (92.7 % selectivity in terms of R_electron) and a 20.6 μmol g⁻¹ h⁻¹ evolution rate. Subsequent spectroscopic and microscopic studies supported by theoretical analysis revealed operando-generated Cu²⁺, with the assistance of existing Cu⁺, functioning as an anchor for the generated *CO and thereby facilitating C−C coupling. This study demonstrates strain-induced in situ surface reconstruction leading to heterojunction formation, which finetunes the oxidation state of Cu and modulates the CO₂ reduction reaction pathway to selective formation of ethylene.     

Self-Polarization Triggered Multiple Polar Units Toward Electrochemical Reduction of CO2 to Ethanol with High Selectivity

Electrochemical conversion of CO₂ to highly valuable ethanol has been considered a intriguring strategy for carbon neutruality. However, the slow kinetics of coupling carbon-carbon (C−C) bonds, especially the low selectivity ethanol than ethylene in neutral conditions, is a significant challenge. Herein, the asymmetrical refinement structure with enhanced charge polarization is built in the vertically oriented bimetallic organic frameworks (NiCu-MOF) nanorod array with encapsulated Cu₂O (Cu₂O@MOF/CF), which can induce an intensive internal electric field to increase the C−C coupling for producing ethanol in neutral electrolyte. Particularly, when directly employed Cu₂O@MOF/CF as the self-supporting electrode, the ethanol faradaic efficiency (FE_ethanol) could reach maximum 44.3 % with an energy efficiency of 27 % at a low working-potential of −0.615 V versus the reversible hydrogen electrode (vs. RHE) using CO₂-saturated 0.5 M KHCO₃ as the electrolyte. Experimental and theoretical studies suggest that the polarization of atomically localized electric fields derived from the asymmetric electron distribution can tune the moderate adsorption of *CO to assist the C−C coupling and reduce the formation energy of H₂CCHO*-to-*OCHCH₃ for the generation of ethanol. Our research offers a reference for the design of highly active and selective electrocatalysts for reducing CO₂ to multicarbon chemicals.     

Polarization tensors of planar domains as functions of the admittivity contrast

(Electric) polarization tensors describe part of the leading order term of asymptotic voltage perturbations caused by low volume fraction inhomogeneities of the electrical properties of a medium. They depend on the geometry of the support of the inhomogeneities and on their admittivity contrast. Corresponding asymptotic formulas are of particular interest in the design of reconstruction algorithms for determining the locations and the material properties of inhomogeneities inside a body from measurements of current flows and associated voltage potentials on the body’s surface. In this work, we consider the two-dimensional case only and provide an analytic representation of the polarization tensor in terms of spectral properties of the double layer integral operator associated with the support of simply connected conductivity inhomogeneities. Furthermore, we establish that an (infinitesimal) simply connected inhomogeneity has the shape of an ellipse, if and only if the polarization tensor is a rational function of the admittivity contrast with at most two poles whose residues satisfy a certain algebraic constraint. We also use the analytic representation to provide a proof of the so-called Hashin–Shtrikman bounds for polarization tensors; a similar approach has been taken previously by Golden and Papanicolaou and Kohn and Milton in the context of anisotropic composite materials.     

基于散射实验极化靶的2.5T/1.3K的动态核极化(DNP)系统的开发

动态核极化法(Dynamic Nuclear Polarization, DNP)是利用热平衡下的电子在磁场中的高自旋极化率转移到原子核自旋的技术,从而极大的提高原子核自旋极化率。多种动态极化靶材料已广泛的用于自旋物理散射实验。本文介绍一种简单实用,共同开发的日本山形大学DNP系统,包括超导磁场,氦4蒸发恒冷器,微波系统以及NMR核磁共振检测系统,测得中子靶材料氘带丁醇(D-butanol)中氘核的极化率在2.5T/1.3K达到+6.5%。