激光遥感偏振成像系统光学元件调整及误差分析

改进了利用双旋转波片方法进行偏振成像的实验装置,提出了通过一次测量获得目标偏振度和强度编码图像的方法.运用光强法对激光遥感偏振成像装置的光学元件进行调整,通过斯托克斯和穆勒矩阵在偏振光学元件中的应用,给出了相应光学元件的调整原理、方法及过程.分析了激光器中心波长变动、偏振片的角度误差和波片的相位延迟及角度误差对整个系统的影响.结果表明,由偏振片角度和波片角度误差造成的出射光斯托克斯误差较小,不超过0.001,可以忽略;由波片相位延迟不精确造成的误差在0.02左右,所以应采用延迟精度较高的波片;激光器中心波长变化的影响最大,不能忽略,必须加滤光片使接收光的中心波长控制在808nm;镀有铝膜望远镜对接收到的散射光偏振度影响较小,适于激光遥感偏振成像系统的应用.     

Enhancement of bioelectrochemical dioxygen reduction with oxygen-enriching materials

Bioelectrochemical dioxygen reduction reaction (ORR) catalyzed by multi-copper oxidases (MCOs) is a process of paramount importance occurring at the cathode of enzymatic biofuel cells (EBFCs), which is an energy harvester that holds promise of self-sustained implantable and wearable medical devices. The MCO biocathode is, however, frequently the limiting factor of a working EBFC. Besides the operational stability issue, enzymatic biocathodes are largely constrained by the relatively low solubility of dioxygen in aqueous solution. As an emerging topic, we here review the introduction of dioxygen-enriching materials to the cathodic bioelectrode for overcoming the dioxygen supply limitation, leading to improved ORR performance.     

Isobaric Vapor–Liquid Equilibrium for the Mixture of Neohexane,Cyclopentane and N,N-Dimethylformamide at 101.3 kPa

The vapor–liquid phase equilibrium (VLE) data for binary systems of neohexane?+?cyclopentane, neohexane?+?N,N-dimethylformamide (DMF), cyclopentane?+?DMF and ternary system of neohexane?+?cyclopentane?+?DMF were determined with a modified Rose still at 101.3 kPa, and all the binary data passed the Wisniak’s test (D?<?5), which accorded with the thermodynamic consistency. Three activity coefficient models namely, Wilson, NRTL and UNIQUAC were used to correlate VLE data and get binary interaction parameters, then the ternary VLE data of neohexane?+?cyclopentane?+?DMF were estimated based on these model parameters using Aspen Plus software. The estimation values of the three models agree well with the experimental data (σ(T)?<?0.5 K). Moreover, the analysis of the effect of DMF on the vapor–liquid phase equilibrium shows that DMF can act as an effective extractant for the system studied.

     

Highly efficient and thermal stable guanidinium-based two-dimensional perovskite solar cells via partial substitution with hydrophobic ammonium

Layered two-dimensional(2D)perovskite solar cells(PVSCs)with a chemical formula of C(NH_2)_3(CH_3NH_3)_3Pb_3I_(10)(n=3)have been fabricated through additive engineering,wherein stoichiometrically equivalent guanidinium(GA~+)and methylammonium(MA~+)serve as spacer cations.The crystallinity of the perovskite films is dramatically enhanced with proper amount of methylammonium thiocyanate(MASCN)added into the precursor solution.In addition,we substitute a small amount of MA~+with hydrophobic phenylethylammonium(PEA~+),which can passivate trap states of the perovskite films.As a result,the open circuit voltage increases to 1.1 V and the best power conversion efficiency(PCE)of 10.12%is yielded.Furthermore,superior thermal stability and balanced moisture stability of the PEA-substituted GA-based PVSCs are demonstrated,compared to the popular 3D MAPbI_3and 2D PEA-based PVSCs.They retain approximately 80%of the original PCE after 30 d at 20%relative humidity(RH),and 50%of the original PCE after 3200 min at 85°C without any encapsulation.This work suggests a new route to achieve both heat and humidity stable PVSCs by simply mixing different spacer cations.     

Selective Photocatalytic Oxidation of Sulfides in Lanthanide Metal -Organic Frameworks Incorporating Ru(2,2′-bpy)3 photosensitizer

Three isostructural lanthanide metal-organic frameworks (Ln-MOFs) were synthesized with uncoordinated N^N site, and the Ru(N^N)₃ photosensitizer was introduced via coordination link. These functionalized frameworks showed excellent performance in the photocatalytic oxidation of sulfides with good conversion and high sulfoxide selectivity.     

Tuning the morphology of amphiphilic copolymer aggregates by compound emulsifier via emulsion–solvent evaporation

A series of poly(4-vinylpyridine)-b-poly{6-[4-(4-butyloxyphenylazo)phenoxy]hexyl methacrylate} (P4VP-b-PAzoMA) were employed to fabricate aggregates via the emulsion–solvent evaporation method. The emulsion was stabilized by compound emulsifier composed of SDS and span60. By tuning the ratio of two emulsifiers, P4VP-b-PAzoMA could self-assemble into various morphologies including porous microspheres, tremella-like aggregates, bowl-like aggregates and wrinkled microspheres. The transformation of the morphologies could be ascribed to three major aspects: the stability of emulsified chloroform droplets, the permeation of water into chloroform and the dispersity of the interior water droplets with regard to different HLB values. Besides, the morphology could even be tuned by changing the block ratio and the concentration of P4VP-b-PAzoMA, and the HLB dependent morphology changing was also proved within other block ratio or different concentration. The study uncovers a convenient and effective technique to manipulate the morphology of amphiphilic copolymer aggregates.     

Boundedness of Marcinkiewicz integral related to multilinear commutators with variable kernels on Hardy spaces

Let→b=(b1,b2,…,bm),bi∈∧βi(Rn),1≤I≤m,βi＞0,m∑I=1βi=β,0＜β＜1,μΩ→b(f)(x)=(∫∞0|F→b,t(f)(x)|2dt/t3)1/2,F→b,t(f)(x)=∫|x-y|≤t Ω(x,x-y)/|x-y|n-1 mΠi=1[bi(x)-bi(y)dy.We consider the boundedness of μΩ,→b on Hardy type space Hp→b(Rn).     

Novel ring B abeo-sterols as growth inhibitors of Mycobacterium tuberculosis isolated from a Caribbean Sea sponge, Svenzea zeai

Assay-guided fractionation of a moderately strong anti-tubercular extract obtained from the Caribbean Sea sponge Svenzea zeai afforded two novel 5(6 → 7)abeo-sterols, named parguesterols A (1) and B (2), as its active components. Their structures were elucidated on the basis of extensive spectroscopic analysis.     

Studies on the interactions between lactam analogs and the N-terminal extracellular tail of CC chemokine receptor 4 by CZE

CC chemokine receptor 4 (CCR4) is a kind of G-protein-coupled receptors with a characteristic seven-transmembrane structure and selectively expressed on Th2-type CD4+ T-cells, which play a pivotal role in allergic inflammation. In this study, the interactions between 2-(2-(2,4-dichloro-phenyl)-4-{[(2-methyl-3-chloro-phenyl)-1-ylmethyl]-carbamoyl}-methyl)-5-oxo-pyrrole-1-yl)-N-(3-piperidinyl-propyl)-acetamide (compound A), a known CCR4 antagonist, and ML40 were studied by CZE for the first time. Both qualitative and quantitative characterizations of the drug-peptide binding were determined. The binding constant of the interaction between the trans-diastereomer of compound A and ML40, calculated from the Scatchard plot by regression, was (1.06 +/- 0.11)x10(5)/M. Also, it was confirmed that the trans-diastereomer was more potent affinity with CCR4 than its cis-counterpart. The experimental results show that this reported method by CZE for the determination of the compound A and ML40 interactions is powerful, sensitive, and fast, requires less amounts of reagents, and further, it can be employed as one of the reliable screening methods to a series of lactam analogs in the drug discovery for allergic inflammation diseases.