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101.
AMT在青铜器文物表面形成缓蚀膜的计算分析   总被引:1,自引:0,他引:1  
利用密度泛函(DFT)、概念DFT、Electron Localization Function(ELF)和Fukui函数中的亲电反应函数及Multiwfn软件,在B3LYP/6-311+G(d,p)基组水平上研究了5-氨基-2-巯基-1,3,4-噻二唑[AMT(a)]及其同分异构体[AMT(b)]和四面体型配合物i Thiol-Cu-2AMT的几何构型和反应特性.通过计算研究发现,首先AMT(b)与青铜器表面的Cu2+形成平面型配合物i Thiol-Cu后再与AMT(b)相互作用,并最终形成不规则的四面体型i Thiol-Cu-2AMT.在i Thiol-Cu-2AMT中Cu19能与AMT(b)中的亲核性原子有效地结合,形成四面体结构后将Cu19离子保护起来,达到了保护青铜器不受腐蚀的目的;对i Thiol-Cu-2AMT结构中的活性位置分析及ELF拓扑研究后发现,在i Thiol-Cu-2AMT中N6、N15、S26和S35原子又可以与其它的Cu2+相互作用,逐步形成配位型聚合物保护膜[i Thiol-Cu-2AMT]n.  相似文献   
102.
尼启良 《中国光学》2015,8(5):847-872
本项目对我国空间探测的极紫外(EUV)波段大视场相机所需求的球面光子计数成像探测器的关键技术进行了研究。首先,建立了光阴极材料次级电子产出模型,利用该模型计算了软X射线-EUV波段常用的光电阴极材料—碱卤化物的次级电子产出,分析了微通道板(MCP)的次级电子产出。建立了测量MCP量子探测效率的装置,并推导出MCP量子探测效率的计算公式,测量了MCP在软X射线-EUV波段的量子效率以及MCP量子效率随掠入射角的变化。其次,建立了球面实芯微通道板的制备装置,利用高温热成型方法制备出曲率半径为150 mm球面MCP,利用光刻技术制备出有效直径为48 mm的楔条形感应电荷位置灵敏阳极,在此基础上集成了一套使用球面MCP和感应电荷位置灵敏阳极的两维光子计数成像探测器。再次,研制出包括快速前端模拟电路与后续数字电路的成像读出电路,编制了能矫正图像畸变的图像实时采集和处理软件。最后,建立了MCP探测器空间分辨率、图像线性的检测装置,对研制出的探测器性能进行了检测,检测结果表明:探测器的各项技术指标完全满足要求。  相似文献   
103.
《Current Applied Physics》2015,15(12):1580-1586
The characteristics of gasification reactions for carbon–carbonate mixtures were experimentally investigated at high temperatures up to 900 °C, considering the application of the mixtures to the external anode media of a direct carbon fuel cell. A thermo-gravimetric analysis (TGA) was conducted in either a nitrogen or carbon dioxide ambient environment for Li2CO3, K2CO3 and a mixture of these two substances with carbon black. Changes in the exit gas composition were also monitored during the heating process. It was shown that gasification in the mixture media occurs much more rapidly than carbonate decomposition at elevated temperatures, even for low concentrations of CO2. It was also shown that the loading of carbonates to carbon significantly affects the global gasification reaction; it increased the reaction rate by an order of magnitude and decreased its activation energy. Based on the experimental observations, a simplified reaction model of gasification was suggested for the anode media of a DCFC, regarding carbonate-catalysed and metal-catalysed pathways of Boudouard reactions.  相似文献   
104.
A spray‐pyrolysis process is introduced as an effective tool for the preparation of yolk–shell‐structured materials with electrochemical properties suitable for anode materials in Li‐ion batteries (LIBs). Yolk–shell‐structured ZnO–Mn3O4 systems with various molar ratios of the Zn and Mn components are prepared. The yolk–shell‐structured ZnO–Mn3O4 powders with a molar ratio of 1:1 of the Zn and Mn components are shown to have high capacities and good cycling performances.  相似文献   
105.
Mesoporous SnO microspheres were synthesised by a hydrothermal method using NaSO4 as the morphology directing agent. Field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM) and high‐resolution transmission electron microscopy (HRTEM) analyses showed that SnO microspheres consist of nanosheets with a thickness of about 20 nm. Each nanosheet contains a mesoporous structure with a pore size of approximately 5 nm. When applied as anode materials in Na‐ion batteries, SnO microspheres exhibited high reversible sodium storage capacity, good cyclability and a satisfactory high rate performance. Through ex situ XRD analysis, it was found that Na+ ions first insert themselves into SnO crystals, and then react with SnO to generate crystalline Sn, followed by Na–Sn alloying with the formation of crystalline NaSn2 phase. During the charge process, there are two slopes corresponding to the de‐alloying of Na–Sn compounds and oxidisation of Sn, respectively. The high sodium storage capacity and good electrochemical performance could be ascribed to the unique hierarchical mesoporous architecture of SnO microspheres.  相似文献   
106.
The synthesis of colloidal nanocrystals (NCs) of lithiated group 14 elements (Z=Si, Ge, and Sn) is reported, which are Li4.4Si, Li3.75Si, Li4.4Ge, and Li4.4Sn. LixZ compounds are highly reactive and cannot be synthesized by existing methods. The success relied on separating the surface protection from the crystal formation and using a unique passivating ligand. Bare LixZ crystals were first produced by milling elemental Li and Z in an argon‐filled jar. Then, under the assistance of additional milling, hexyllithium was added to passivate the freshly generated LixZ NCs. This ball‐milling‐assisted surface protection method may be generalized to similar systems, such as NaxZ and KxZ. Moreover, Li4.4Si and Li4.4Ge NCs were conformally encapsulated in carbon fibers, providing great opportunities for studying the potential of using LixZ to mitigate the volume‐fluctuation‐induced poor cyclability problem confronted by Z anodes in lithium‐ion batteries.  相似文献   
107.
A simple, green, and efficient method for the N-tert-butoxycarbonylation of amines by pyridinium 2,2,2- trifluoroacetate ([Py][OTf]) as an efficient and reusable catalyst is reported. In general, electron donating groups on aryl group give rise to the higher yields than electron withdrawing groups. Clean reaction, short reaction times, high yields, reusability of catalyst, and easy preparation of it are some advantages of this work.  相似文献   
108.
In the present work,an interconnected sandwich carbon/Si-SiO2/carbon nanospheres composite was prepared by template method and carbon thermal vapor deposition(TVD).The carbon conductive layer can not only efficiently improve the electronic conductivity of Si-based anode,but also play a key role in alleviating the negative effect from huge volume expansion over discharge/charge of Si-based anode.The resulting material delivered a reversible capacity of 1094 mAh/g,and exhibited excellent cycling stability.It kept a reversible capacity of 1050 mAh/g over 200 cycles with a capacity retention of 96%.  相似文献   
109.
Electrolyte modulation simultaneously suppresses polysulfide the shuttle effect and lithium dendrite formation of lithium–sulfur (Li-S) batteries. However, the sluggish S redox kinetics, especially under high S loading and lean electrolyte operation, has been ignored, which dramatically limits the cycle life and energy density of practical Li-S pouch cells. Herein, we demonstrate that a rational combination of selenium doping, core–shell hollow host structure, and fluorinated ether electrolytes enables ultrastable Li stripping/plating and essentially no polysulfide shuttle as well as fast redox kinetics. Thus, high areal capacity (>4 mAh cm−2) with excellent cycle stability and Coulombic efficiency were both demonstrated in Li metal anode and thick S cathode (4.5 mg cm−2) with a low electrolyte/sulfur ratio (10 μL mg−1). This research further demonstrates a durable Li-Se/S pouch cell with high specific capacity, validating the potential practical applications.  相似文献   
110.
Because of containing urea groups, flame resistance and smoke releasing behaviors of isocyanate-based polyimide foam (IBPIF) produced using free foaming technology require further improvement. In this work, silica aerogel layers were incorporated into cells of IBPIF through an in situ growth process of silica sol (SS). Compared with silica aerogel particles directly mixed into the foaming slurry, the silica aerogel layers that firmly attached to the pores and surfaces of cells not only provided exceptional thermal insulation and flame protection, but also kept original cellular structure. With increase in ratio of SS mass to IBPIF volume, silica aerogel incorporation dosage was gradually increased. Accompanied by flame resistance was obviously improved and smoke releasing behavior was effectively suppressed. Those were indicated by the improved limiting oxygen index (LOI), decreased heat release rate (HRR), peak of HRR, and specific optical density of smoke (Ds) in trials with pilot flames. Compared with pure IBPIF, when the ratio reached to 5/15 g/cm3, it resulted in LOI increasing from 22.0% to 33.0%, peak of HRR, total smoke production (TSP), and maximum value of Ds decreasing from 174 to 72 kW/m2, 1.11 to 0.37 m2/m2, 45.90 to 17.45, respectively.  相似文献   
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