Er3+单掺、Er3+/Yb3+共掺杂Ca12Al14O32F2的 制备及上转换发光性质

利用高温固相法成功制备了Er~(3+)单掺、Er~(3+)/Yb~(3+)共掺杂Ca_(12)Al_(14)O_(32)F_2上转换发光样品。在980 nm激光激发下,Er~(3+)单掺和Er~(3+)/Yb~(3+)共掺杂样品均呈现出较强的绿光(528,549 nm)和较弱的红光(655 nm)发射,分别归因于Er~(3+)离子的~2H_(11/2),~4S_(3/2)→~4I_(15/2)和~4F_(9/2)→~4I_(15/2)能级跃迁。随着Er离子浓度的增加,单掺杂样品上转换发光强度先增大后减小,最佳掺杂浓度为0.8%。共掺杂Yb~(3+)后,Er~(3+)的发光强度明显增大。还原气氛下合成的样品上转换发光强度增大约两倍,可能和笼中阴离子基团变化有关。发光强度和激发光功率的关系表明所得上转换发射为双光子吸收过程,借助Er~(3+)-Yb~(3+)体系能级结构详细讨论了上转换发射的跃迁机制。     

Study on the mechanism of catalytic synthesis of dimethyldichlorosilane by AlCl3/MIL‐53(Al)@γ‐Al2O3

Dimethyldichlorosilane, one of the most consumed organosilicon monomers in the industry, can be prepared in a highly efficient and environmentally friendly synthesis method of disproportionating methylchlorosilanes. However, the internal mechanism of the reaction remains unclear. In this paper, the mechanism catalyzed by AlCl₃/MIL‐53(Al) and AlCl₃/MIL‐53(Al)@γ‐Al₂O₃ catalysts was calculated at B3LYP/6‐311++G(3df, 2pd) level by using the density functional theory (DFT). The results showed that although the two catalysts had similar active structures, the catalytic effects were significantly different. The Lewis acid center on the surface of γ‐Al₂O₃ in the core‐shell catalyst is complementary to the classic Lewis acid AlCl₃ through the spatial superposition effect, which greatly improves the Lewis acid catalytic activity of AlCl₃/MIL‐53(Al)@γ‐Al₂O₃.     

Surface passivation in n-type silicon and its application in silicon drift detector

Based on the surface passivation of n-type silicon in a silicon drift detector(SDD), we propose a new passivation structure of SiO2/Al2O3/SiO2 passivation stacks. Since the SiO2 formed by the nitric-acid-oxidation-of-silicon(NAOS)method has good compactness and simple process, the first layer film is formed by the NAOS method. The Al2O3 film is also introduced into the passivation stacks owing to exceptional advantages such as good interface characteristic and simple process. In addition, for requirements of thickness and deposition temperature, the third layer of the SiO2 film is deposited by plasma enhanced chemical vapor deposition(PECVD). The deposition of the SiO2 film by PECVD is a low-temperature process and has a high deposition rate, which causes little damage to the device and makes the SiO2 film very suitable for serving as the third passivation layer. The passivation approach of stacks can saturate dangling bonds at the interface between stacks and the silicon substrate, and provide positive charge to optimize the field passivation of the n-type substrate.The passivation method ultimately achieves a good combination of chemical and field passivations. Experimental results show that with the passivation structure of SiO2/Al2O3/SiO2, the final minority carrier lifetime reaches 5223 μs at injection of 5×10¹⁵ cm^-3. When it is applied to the passivation of SDD, the leakage current is reduced to the order of nA.     

激光驱动复合飞片冲击起爆HNS-Ⅳ实验研究

激光驱动飞片冲击起爆技术具有很强的抗电磁干扰能力和可以直接起爆钝感炸药等优点，能够满足现代战场对火工系统的高安全性和高可靠性要求。HNS-Ⅳ是最适合激光驱动飞片冲击起爆技术的药剂。本文中在6种不同激光能量下，测试了Al/Al₂O₃/Al复合飞片和Al单层飞片对HNS-Ⅳ药剂(装药密度为1.5 g/cm3)的冲击起爆情况。实验实现了激光驱动飞片对HNS-Ⅳ的成功起爆。在217~245 mJ激光能量范围内，激光驱动Al/Al₂O₃/Al复合飞片均可成功完全起爆HNS-Ⅳ药柱。Al单层飞片均未成功起爆HNS-Ⅳ药柱。飞片冲击压力对激光驱动飞片冲击起爆HNS-Ⅳ起决定作用。     

Facile synthesis,characterization, and decolorization activity of Mn2+ and Al3+ co-doped hexagonal-like ZnO nanostructures as photocatalysts

A good photocatalyst with high efficiency can be synthesized easily using eco-friendly materials and processes. Our synthesized samples exhibit all of the aforementioned features. In this work, manganese co-doped ZnO at different weight percentages (3, 6, 9, and 15 wt.%) with and without 1.5 wt.% aluminum was synthesized by hydrothermal method, and their photocatalytic activity in aqueous solutions of methyl orange (MO) was investigated under visible light. The structural and optical properties of the samples were characterized using X-ray powder diffraction, Fourier-transform infrared spectroscopy, scanning electron microscopy, energy-dispersive X-ray analysis, and diffuse reflectance spectroscopy. In this work, Mn²⁺ ions in the 9%Mn/ZnO sample and Mn²⁺, Al³⁺ ions in the (9%Mn, 1.5%Al)/ZnO sample calcined at 800 °C were replaced instead with some Zn²⁺ ions in hexagonal wurtzite structures of ZnO. These structures were found next to each other in the form of a hexagonal shape that created 3D-hexagonal-like ZnO nanostructures. Finally, nanoparticles (NPs) and nano hexagonal-like ZnO nanostructures were, respectively, dispersed on the surface of 3D-hexagonal-like structure of 9%Mn/ZnO and (9%Mn, 1.5%Al)/ZnO. Diffuse reflectance spectroscopy analysis showed that the (9%Mn, 1.5%Al)/ZnO sample had more light absorption than 9%Mn/ZnO. However, contrary to our expectations, the 9%Mn/ZnO sample had better decolorization efficiency (94%) after 60 min under visible light, which could be attributed to a significant increase in the level of recombination by the aluminum ions.     

固体核磁共振结合密度泛函理论计算研究SSZ-39分子筛的钠离子落位与铝分布

具有AEI结构的SSZ-39分子筛的骨架外阳离子落位和铝分布对其催化性能影响显著.AEI笼中有三个结晶学不等价位，且铝取代T位具有一定的倾向性.本文结合固体核磁共振（NMR）技术（²⁷Al/²³Na MQ MAS NMR），以及密度泛函理论（DFT）计算，研究了不同硅铝比Na-SSZ-39分子筛中的Na⁺落位和铝分布.在孤立铝分布的情况下，铝原子优先占据于T3位，Na⁺主要落位于AEI笼中的SIIa0和SIII'a0位点上，其中SIII'a0位点的优先度较高，此外少部分Na⁺还落位于六棱柱内部的SIa0.当铝对存在时，AlSiSiAl分布的铝对占据六元环的对位（T3-T3），对应的Na⁺分别落位于SIIa1和SⅢ'a1位点.随着分子筛结构的部分破坏，游离的Na⁺可能形成明显的SIII'b位点.本文可加深对SSZ-39分子筛构效关系的理解，为更好地调控催化性能奠定基础.     

Manipulating OH−-Mediated Anode-Cathode Cross-Communication Toward Long-Life Aqueous Zinc-Vanadium Batteries

The anode-cathode interplay is an important but rarely considered factor that initiates the degradation of aqueous zinc ion batteries (AZIBs). Herein, to address the limited cyclability issue of V-based AZIBs, Al₂(SO₄)₃ is proposed as decent electrolyte additive to manipulate OH⁻-mediated cross-communication between Zn anode and NaV₃O₈ ⋅ 1.5H₂O (NVO) cathode. The hydrolysis of Al³⁺ creates a pH≈0.9 strong acidic environment, which unexpectedly prolongs the anode lifespan from 200 to 1000 h. Such impressive improvement is assigned to the alleviation of interfacial OH⁻ accumulation by Al³⁺ adsorption and solid electrolyte interphase formation. Accordingly, the strongly acidified electrolyte, associated with the sedated crossover of anodic OH⁻ toward NVO, remarkably mitigate its undesired dissolution and phase transition. The interrupted OH⁻-mediated communication between the two electrodes endows Zn||NVO batteries with superb cycling stability, at both low and high scan rates.     

低温加氢裂解脱除高硅ZSM-5分子筛内TPAOH模板剂

Zeolite membranes, especially the MFI-type zeolite membranes, have attracted significant attention for decades because of their special properties. While organic templates such as tetrapropylammonium hydroxide (TPAOH) have typically been used for the synthesis of ZSM-5 zeolite and zeolite membranes, the templates remain trapped in the as-synthesized zeolite crystals. A common method for removing organic templates and generating porous frameworks is calcination; however, during this process, the channel structure may be affected. In particular, for ZSM-5 membranes, membrane defects may be produced and the separation efficiency therefore may decrease to some extent. In this study, the low-temperature hydrocracking of TPAOH in ZSM-5 zeolite crystals was studied under H₂/N₂, while N₂ adsorption, thermogravimetric (TG) analysis, Fourier transform infrared (FTIR) spectroscopy, temperature-programmed desorption of ammonia (NH₃-TPD), and Raman spectroscopy were used to characterize zeolite samples. The results show that the organic template in the pores of ZSM-5 can be effectively removed below 350 ℃ by low-temperature hydrocracking. Characterization analyses by BET specific surface area, TG, FTIR, and Raman spectroscopy demonstrated that a reducing atmosphere containing H₂ was more conducive to template removal at low temperature than atmospheres of air or N₂. The degree of template removal increased with temperature increasing. The BET surface area of the crystal after hydrocracking at 280 ℃ reached 252 m²·g^-1, although a small amount of organic residue remained. Furthermore, after hydrocracking at 350 ℃, the BET surface area reached 399m2·g^-1, and only trace amount of inorganic carbon residue remained. In addition, the introduction of hydrogen at low temperatures could prevent coke deposits on acid sites and thus ZSM-5 zeolite crystals had greater numbers of acidic sites after low-temperature hydrocracking.     

水热合成制备Al掺杂α-MnO2纳米管及其超级电容器电化学性能

α-MnO₂ and Al-doped α-MnO₂ were synthesized via a hydrothermal method. The morphologies, structures, and electrochemical performances of as-synthesized un-doped and doped α-MnO₂ were studied. Scanning electron microscopy (SEM) and high-resolution transmission electron microscopy (HRTEM) show that these un-doped and doped α-MnO₂ are nanotube shaped. The band gaps of α-MnO₂ are investigated by ultraviolet-visible absorption spectroscopy, which indicates that the band gap of α-MnO₂ decreases upon Al doping. The electrochemical performances of un-doped and doped α-MnO₂ as electrode materials for supercapacitors were measured by cyclic voltammetry (CV) and galvanostatical charge/discharge tests. The specific capacitances of un-doped and Al-doped α-MnO₂ respectively reach 204.8 and 228.8 F·g^-1under a current density of 50 mA·g^-1. It was discovered that the electrochemical impedance of Al-doped α-MnO₂ was decreased by Al doping analyzed using electrochemical impedance spectra (EIS), which provides a beneficial increase to its electrochemical specific capacitance. Enhanced specific capacitance and preferable cycling stability (up to 1000 cycles) for Al-doped α-MnO₂ mean that these systems are favorable prospects for application in supercapacitors.     

X射线荧光光谱法快速测定铜基催化剂中金属含量

本文使用X射线荧光光谱仪,采用人工制备标样,以粉末直接压片和经验系数校正基体效应的方法,建立了铜基催化剂中CuO、ZnO和Al2O3含量的快速测定方法。考察了样品厚度的影响及方法的精密度和准确度。该法待测元素线性范围较宽,分别为:CuO:13.0%~97.0%,ZnO:0~63.0%,Al2O3:0~25.0%,且相关系数均大于0.99。测定各元素的相对标准偏差均小于0.3%,且测定结果与化学滴定分析结果吻合。该方法快速、简便,可应用于工业生产质量监控。