纳米材料结构研究与正电子寿命谱学

从纳米材料的结构特点，重要性和所使用的现代实验手段出发，简要地介绍了已被广泛采用的正电子寿命谱学的基本原理，实验方法和数据分析，给出了微结构分析，温度稳定性，压力效应和动态观察等方面的研究工作，指出了研究纳米材料的微结构对基础学科和技术应用都非常重要，正电子寿命谱学是研究纳米材料的有用工具。     

掺铽氧化钇多晶的正电子寿命谱及阴极射线发光

在不同条件下灼烧多晶掺铽氧化钇，并用正电子寿命谱和阴极射线发光来检验，正电子寿命和发光线强度１５００－１６００℃之间的高温烧结使颗粒快速生长，相关的结果证明，正电子寿命测量对研究材料微结构的实用性以及这些性能对发光的重要性。     

用正电子研究NaCl在NaY沸石上的固溶过程

用正电子湮没谱学研究NaCl与NaY沸石机械混合后, NaCl在NaY中的固溶扩散过程.分别测量不同质量比的NaCl/NaY［(1—20)%］经500℃烘烤1h，NaCl/NaY(15%)经不同温度烘烤1h,以及NaCl/NaY(15%)经500℃烘烤不同时间后的正电子寿命谱.所有寿命谱都出现了5个寿命分量, 其中第3，4，5寿命分别与β笼、超笼及沸石微粒界面空洞的大小和数量相关.实验表明正电子湮没谱学能敏感地表征NaCl在NaY中的固溶扩散过程. 关键词： 正电子湮没谱学 氯化钠 沸石     

不同气氛下多孔硅中电子偶素湮没行为研究

使用正电子湮没谱学方法,在不同气氛下对电化学腐蚀法制备的多孔硅中电子偶素的湮没行为进行了系统的研究.正电子湮没寿命谱测试结果表明,样品中存在长达40 ns的电子偶素湮没成分,并且进入多孔硅膜层的正电子约有80%形成电子偶素,具有非常高的电子偶素产额;在氧气气氛下,由于气体导致o-Ps发生自旋转化猝灭是使多孔硅样品中电子偶素寿命缩短的主要原因.结合正电子寿命-动量关联谱测量结果,分析了不同气氛下多孔硅样品中电子偶素湮没寿命及动量变化关系,讨论了多孔硅中电子偶素的湮没机理以及气氛对孔径计算理论模型的影响. 关键词： 电子偶素 正电子湮没谱学方法 多孔硅     

第五届全国正电子湮没谱学会议简讯

第五届全国正电子湮没谱学会议简讯受中国核学会，中国物理学会及中国核物理学会的委托，由兰州大学材料科学系主办的第五届全国正电子湮没谱学学术会议于１９９３年１０月１０日至１５日在甘肃酒泉市举行，全国３１个单位５８名代表出席了会议，共收到论文９３篇。会议采...     

CVD金刚石膜的结构分析

利用x射线广角衍射和低角掠入射散射谱、正电子湮没谱、定性分析软件和Positronfit程序，研究了生长在Si（100）基底上的金刚石膜微结构.研究发现，在样品邻近基底区域为纳米 多晶结构，具有弱的［111］织构；在邻近表面区域为微米多晶结构，具有强的［220］织构 .金刚石膜样品有空位、空位团和空洞3种缺陷，其中主要缺陷是大约10个空位形成的空位团 . 关键词： 金刚石膜 化学气相沉积 x射线掠入射 正电子湮没谱     

正电子湮没谱学在金属材料氢/氦行为研究中的应用

用于核反应堆的金属结构材料中氢/氦泡的前躯体——(氢/氦)-空位复合体的形成受到温度、辐照剂量等多方面因素的影响,研究其在材料中的形成和演化行为对气泡形核的理解及先进核反应堆材料的发展起着至关重要的作用.然而,受到分辨率的局限,这种原子尺度的微结构很难用电镜等常规方法进行表征,以致于该问题的研究上可利用的数据相对较少.正电子湮没谱学是一种研究材料中微观缺陷的特色表征方法,近些年来慢正电子束流和新型核探测谱仪技术的不断发展以及基于慢束发展起来的多种实验测试方法的改进,使正电子湮没技术应用已拓展到金属材料中氢/氦行为的研究领域,在金属材料表面氢/氦辐照损伤的研究中发挥了重要作用.本文结合国内外相关进展以及本课题组的一些研究成果评述了正电子湮没谱学在金属材料氢氦行为研究中的应用,着重讨论了正电子湮没寿命谱、多普勒展宽谱、符合多普勒展宽三种测量方法在如下金属材料氢/氦行为研究中的优势:1)氢/氦气泡尺寸和浓度的估算; 2)高能氢/氦离子辐照损伤缺陷及缺陷的退火、时效的演化行为; 3)不同形变程度样品中氢/氦与形变缺陷的相互作用; 4)不同能量或剂量氢/氦离子辐照对材料造成的损伤以及氢氦协同作用.     

液晶相变的微结构研究

用正电子湮没和差示扫描量热(DSC)变温测量液晶(EBBA)样品的正电子湮没寿命谱及DSC曲线,结果表明正电子湮没的短寿命(τ_s)基本不变,而长寿命(τ₁)和强度(I₁)明显地有两次跳变,其跳变的温度范围与DSC所测定的相转变温度范围基本一致,在加热和冷却过程中样品在晶体相←→向列相之间的相互转变的相转变温度范围显著不同。用正电子湮没的ORE模型讨论了由于液晶相转变所引起的微结构变化,从而提出正电子是研究液晶(EBBA)相变的探针。 关键词：     

用正电子湮没探测高聚物的自由体积特性

简要介绍了用正电子湮没谱探测高聚物的微观结构的方法，给出了几种具有简单链结构的高聚物的玻璃化转变，自由体移浓度的标度行为，自由体积形成能的直接测量等方面的最新应用结果，由此表明，正电子湮没谱学在高分子物理研究领域具有十分广阔的应用前景。     

正电子湮没谱学研究半导体材料微观结构的应用进展

<正>电子湮没谱学技术在研究材料微观缺陷、微观结构方面有着独特的优势,尤其是在针对阳离子空位等负电性空位型缺陷的研究中,可以获取材料内部微观缺陷的种类与分布的关键信息.正电子湮没寿命和多普勒展宽能谱是正电子湮没谱学的最基本的分析方法,在半导体材料的空位形成、演化机理以及分布等研究方面能够发挥独特的作用;此外,慢正电子束流技术在半导体薄膜材料的表面和多层膜材料的界面的微观结构和缺陷的深度分布的研究中有广泛的应用.通过正电子技术所得到的微观结构和缺陷、电子密度和动量分布等信息对研究半导体微观结构、优化半导体材料的工艺和性能等方面有着指导作用.本文综述了正电子湮没谱学技术在半导体材料方面的应用研究进展,主要围绕正电子研究平台在半导体材料微观缺陷研究中对材料的制备工艺、热处理、离子注入和辐照情况下,各种缺陷的微观结构的表征及其演化行为的研究成果展开论述.     

Glassy dynamics of model colloidal polymers:Effect of controlled chain stiffness

Colloidal polymers with tunable chain stiffness have been successfully assembled in experiments recently.Similar to molecular polymers,chain stiffness is an important feature which can distinctly affect the dynamical behaviors of colloidal polymers.Hence,we model colloidal polymers with controlled chain stiffness and study the effect of chain stiffness on glassy behaviors.For stiff chains,there are long-ranged periodic intrachain correlations besides two incompatible local length scales,i.e.,monomer size and bond length.The mean square displacement of monomers exhibits sub-diffusion at intermediate time/length scale and the sub-diffusive exponent increases with chain stiffness.The data of localization length of stiff polymers versus rescaled volume fraction for different monomer sizes can gather close to an exponential curve and decay slower than those of flexible polymers.The increase of chain stiffness linearly increases the activation energy of the colloidal-polymer system and thus makes the colloidal polymers vitrify at lower volume fraction.Static and dynamic equivalences between stiff colloidal polymers of different monomer sizes have been checked.     

功能聚合物:从薄膜器件到纳米器件

文章简要回顾了功能聚合物的发现和发展历程,着重介绍了其在发光二极管、太阳能电池、场效应晶体管、传感器件、纳米材料与器件中的应用。     

光在大分子聚合物中的解偏和散射

文章报道了光在大分子聚合物中的前向散射和解偏现象,并用Mie散射和Fraunhofe衍射理论对其进行了解释,提出了小角度散射的光解偏理论。     

Polymer ablation: From fundamentals of polymer design to laser plasma thruster

UV-Laser ablation of polymers is a well-established method to structure and deposit polymers, but the mechanisms of ablation are still controversial, i.e. photothermal or photochemical processes. An approach to probe the ablation mechanisms and to improve ablation is to incorporate photoactive groups into the polymer structure.The investigation of the ablation behavior of designed triazene polymers showed that the ablation mechanism is always a combination of both photothermal and photochemical processes, but the ratio can be changed by using different polymers and irradiation wavelengths. Also the quality of structures in the triazene polymers is superior at an irradiation wavelength of 308 nm compared to commercially available polymers.Polymers can be designed not only for UV irradiation, but also for applications in the IR range, but with different requirements. One application for designed polymers in the near-IR range is as fuel for the laser plasma thruster, which is used as propulsion system for small satellites. With commercially available polymers the necessary thrust could not be achieved. A specially designed polymer-absorber system for this application produce more energy in the form of thrust, than the laser delivered.     

导电高聚物的微波吸收机理的研究

本文以“导电孤岛”物理模型阐明界面极化率对导电高聚物电损耗的影响。通过物理模型的数学解析表明,导电高聚物中的“导电孤岛”是导电高聚物的介电损耗的主要来源,并发现“导电孤岛”所引起的介电损耗依赖于“导电孤岛”本身的电导率、介电常数以及它的体积分数。“导电孤岛”物理模型所揭示的介电特性与实验中所观祭到的微波吸收率和导电高聚物的室温电导率有关的实验事实相符合。 关键词：     

Calculation of the Band Intensities of the IR Spectra of Oriented Polymers

An attempt has been made to extend the theory of IR spectra of polymers to oriented polymers. Formulas for the absorption-band intensities in polarization IR spectra of oriented polymers reflecting the dependence of the polarized absorption-band intensity on the structural and orientation characteristics of polymers have been obtained. These formulas permit calculating the intensity of polarized absorption bands at different degrees of orientation of the polymer.     

The Statistical Mechanics of Semiflexible Equilibrium Polymers

We give an overview of studies of models for semiflexible, equilibrium polymers with special emphasis on our work on both lattice and continuum models for such systems. We show, principally by Monte Carlo simulations, that, once monomers self assemble to form polymers, their semiflexibility leads to nematic phases at low temperatures. Attractive wall potentials encourage the adsorption of these equilibrium polymers on surfaces. Rapid cooling leads to the formation of glasses with entangled polymers. Shear promotes nematic ordering, but, at high shear rates, this tendency decreases since the equilibrium polymers are torn apart. A version of our model in which the polymers are directed shows the polymer analog of bosonic Mott-insulating, mass-density-wave, and supersolid phases. We give a brief comparison of our work with other studies and also explore the experimental implications of our study.     

Polymer packaging and ejection in viral capsids: shape matters

We use a mesoscale simulation approach to explore the impact of different capsid geometries on the packaging and ejection dynamics of polymers of different flexibility. We find that both packing and ejection times are faster for flexible polymers. For such polymers a sphere packs more quickly and ejects more slowly than an ellipsoid. For semiflexible polymers, however, the case relevant to DNA, a sphere both packs and ejects more easily. We interpret our results by considering both the thermodynamics and the relaxational dynamics of the polymers. The predictions could be tested with biomimetic experiments with synthetic polymers inside artificial vesicles. Our results suggest that phages may have evolved to be roughly spherical in shape to optimize the speed of genome ejection, which is the first stage in infection.     

Doping-dedoping-driven optic effect of pi-conjugated polymers prepared in cholesteric-liquid-crystal electrolytes

Chiral conjugated polymers were synthesized by electrochemical polymerization in a cholesteric-liquid-crystal (CLC) electrolyte. The polymers display a characteristic finger print texture similar to that of CLC. The natural optical activity of the polymers was successfully controlled by the electrochemical doping-dedoping procedure. The finding of this unprecedented mechanism, involving doping of pi-conjugated systems, can be an important advance in the development of plastic optoelectronics based on conductive polymers.     

Buckling Behavior of Carbon Nanotubes Functionalized with Carbene under Physical Adsorption of Polymer Chains: a Molecular Dynamics Study

The buckling analysis of functionalized carbon nanotubes (CNTs) is of great importance for the better understanding of mechanical behavior of nanocomposites. The buckling behavior of carbene-functionalized CNTs (cfCNTs) under physical adsorption of polymer chains (cfCNTs/polymers) is studied in this paper by the classical molecular dynamics (MD) simulations. In this regard, to investigate the interactions between non-covalent polymer chains and cfCNTs, two different non-covalent functional groups, i.e. polycarbonate (PC) and polypropylene (PP), are selected. The findings are compared with those of pure CNTs under the physical adsorption of polymer chains (pCNTs/polymers). The obtained results show that at a given weight percentage of non-covalent functional groups, the gyration radius of cfCNTs/polymers is higher than that of pCNTs/polymers. Furthermore, an increase in the critical buckling force of cfCNTs/polymers is dependent on the type of non-covalent polymer chains. For cfCNTs/PC and cfCNTs/PP, the critical buckling force is respectively lower and higher than that of pCNTs/polymers for the similar weight percentage of non-covalent functional groups. In addition, it is found that the critical buckling strain of cfCNTs/polymers is smaller than that of pCNTs/polymers for the same weight percentage of non-covalent polymer chains.