ZnS:Er3+的激光选择激发—一种立方对称Er3+中心

本文首次报导了用激光选择激发技术研究Ⅱ-Ⅵ族化合物中三价稀土离子中心的结果.用激光选择激发技术分辨出ZnS:Er3+中一种具有立方对称的中心,确定了基态和激发态的晶场分裂。根据点电荷模型计算和实验结果,该中心的结构是Er3+离子处于填隙位置,最近邻配位体是四个带正一价电荷的电荷补偿离子.该中心的发射光谱中发现由于发射局域声子产生的声子伴线。     

SryBa1－yFCl0.5Br0.5:Sm2+在光谱

本文对无机光谱烧孔系列材料SryBa1－yFCl0.5Br0.5:Sm2+中不同组份的样品(y=0,0.25.0.5,0.75.1.00)4f5d能带的激发光谱、不同温度下5D2、5D1、5D0→7F0跃迁的荧光衰减进行了测量,研究了组份的变化对4f5d能带的位置,5D2、5D1、5D0→7F0跃迁的几率和烧孔效率的影响,并得出结论:在该系列材料中,随组份y的增加,4f5d带与5DJ能级更加接近,5D0→7F0的电子跃迁几率增大,烧孔效率提高。     

具有两参数的非线性椭圆型方程边值问题解的渐近性态

讨论一类具有双参数的非线性椭圆型方程边值问题. 引入多重尺度变量, 构造问题的形式渐近解. 利用微分不等式理论, 证明边值问题渐近解的存在性和一致有效性. 由解的结构指出, 在两参数一定的情况下,相应问题的解只具有一个边界层.     

一类非线性奇摄动分数阶微分方程的渐近解

研究了一类奇摄动非线性分数阶微分方程边值问题.在适当的条件下,首先求出了原问题的外部解,然后利用伸长变量、合成展开法和幂级数展开理论构造出解的边界层项,并由此得到解的渐近展开式.最后利用微分不等式理论,讨论了问题解的渐近性态,得到了原问题解的一致有效的渐近估计式.     

Solvent‐Responsive Behavior of Polymer‐Brush‐Modified Amphiphilic Gold Nanoparticles

Amphiphilic polymer brushes grafted onto gold nanoparticles impart distinct solvent‐responsive behavior via the change to particle size and surface chemistry and, therefore, wide application prospects can be expected. Coarse‐grained simulations are performed for block and/or mixed polystyrene (PS)/poly(ethylene oxide) (PEO)‐modified amphiphilic gold nanoparticles (AuNP) to investigate their responsive behavior in five different solvents by analyzing their morphology, distribution density profiles, and gyration radii. Typical core–shell, Janus‐type, buckle‐like, ring‐like, jellyfish‐like, and octopus‐like morphologies are formed. Influence of block sequence, mixing mode, and several other effects are discussed. Responsive particle size and surface hydrophilicity can be successfully reproduced by altering solvents.

     

Selective enrichment and quantification of okadaic acid in shellfish using an immunomagnetic‐bead‐based liquid chromatography with tandem mass spectrometry assay

Okadaic acid is a marine biotoxin that primarily occurs in shellfish and can cause diarrheic shellfish poisoning in humans. When analyzing biological samples using liquid chromatography with tandem mass spectrometry, the presence of complex matrices is a major issue. Thus, it is crucial to selectively and simply extract the target analyte from samples and minimize matrix effects simultaneously. To meet this need, an immunomagnetic‐bead‐based liquid chromatography with tandem mass spectrometry method was developed to detect okadaic acid in shellfish. Magnetic beads bound to monoclonal antibody against okadaic acid were used as affinity probes to specifically enrich okadaic acid in samples, which effectively eliminated matrix effects. A magnetic separator was used to aggregate and separate magnetic particles from sample matrices, and methanol was used to elute okadaic acid from the magnetic beads. Standard solution prepared with methanol was employed directly for quantitative analysis. Several experimental conditions were optimized to improve performance. The method is of interest as a rapid (10 min) sample clean‐up and selective enrichment tool, and it showed good linearity and sensitivity, with reported limits of detection and quantitation of 3 and 10 μg/kg, respectively. Fifty‐three shellfish samples from an aquatic products market were tested using this method, and four samples positive for okadaic acid were found.     

水热法制备二氧化锡/钨酸铋复合光催化材料及其催化活性研究

本文用水热法制备了正交晶系的纳米球状结构的二氧化锡和正交晶系的由片状聚集成球状结构的钨酸铋,并且对二者进行了复合,制备出了二氧化锡/钨酸铋复合光催化材料。采用X射线衍射(XRD)、扫描电子显微镜(SEM)、比表面积测试仪(BET)、紫外可见分光光度计等技术对复合样品的结构、形貌、比表面积、孔容孔径和光学性质进行了表征。用碘钨灯模拟太阳光,分别以二氧化锡、钨酸铋和二氧化锡/钨酸铋复合材料为催化剂降解罗丹明B(RhB),研究所制备的二氧化锡/钨酸铋复合材料的光催化活性。光催化90 min时二氧化锡、钨酸铋和二氧化锡/钨酸铋对罗丹明B的降解率分别是9%、22%和30%。实验结果表明,在可见光下,二氧化锡/钨酸铋复合材料的光催化活性要高于单一的二氧化锡和钨酸铋。     

Biotemplated Fabrication of ZnO Microstructures with Enhanced Photocatalytic Properties from Rape Pollen

Crystallography Reports - Sodium dodecyl sulfonate and rape pollen were selected as soft and hard templates to induce ZnO formation under hydrothermal conditions, respectively. In the preparation...     

Polyethylene Terephthalate Deconstruction Catalyzed by a Carbon-Supported Single-Site Molybdenum-Dioxo Complex

Polyethylene terephthalate (PET) is selectively depolymerized by a carbon-supported single-site molybdenum-dioxo catalyst to terephthalic acid (PTA) and ethylene. The solventless reactions are most efficient under 1 atmosphere of H₂. The catalyst exhibits high stability and can be recycled multiple times without loss of activity. Waste beverage bottle PET or a PET + polypropylene (PP) mixture (simulating the bottle + cap) proceeds at 260 °C with complete PET deconstruction and quantitative PTA isolation. Mechanistic studies with a model diester, 1,2-ethanediol dibenzoate, suggest the reaction proceeds by initial retro-hydroalkoxylation/β-C−O scission and subsequent hydrogenolysis of the vinyl benzoate intermediate.     

Improved Reversible Zinc Storage Achieved in a Constitutionally Crystalline-Stable Mn(VO3)2 Nanobelts Cathode

Rechargeable zinc-ion batteries (ZIBs) are potential for grid-scale applications owing to their safety, low price, and available sources. The development of ZIBs cathode with high specific capacity, wide operating voltage window and stable cyclability is urgently needed in next-generation commercial batteries. Herein, we report a structurally crystalline-stable Mn(VO₃)₂ nanobelts cathode for ZIBs prepared via a facile hydrothermal method. The as-synthesized Mn(VO₃)₂ exhibited high specific capacity of 350 mAh g⁻¹ at 0.1 A g⁻¹, and maintained a capacity retention of 92 % after 10,000 cycles at 2 A g⁻¹. It also showed good rate performance and obtained a reversible capacity of up to 200 mAh g⁻¹ after 600 cycles at 0.2 A g⁻¹ under −20 °C. The electrochemical tests suggest that Mn(VO₃)₂ nanobelts impart fast Zn²⁺ ions migration, and the introduction of manganese atoms help make the structures more indestructible, leading to a good rate performance and prolonged cycle lifespan.