一种非连续纳米氧化层自旋阀的显微结构研究

利用高分辨电子显微学方法(HREM)研究了纳米氧化层镜面反射自旋阀多层结构Ta(35nm)Ni80Fe20(2nm)Ir17Mn83(6nm)Co90Fe10(15nm)NOL1Co90Fe10(2nm)Cu(22nm)Co90Fe10(15nm)NOL2Ta(3nm).该自旋阀的巨磁电阻(GMR)效应高达15%,较无此镜面反射纳米氧化层(NOL)的自旋阀提高近1倍,同时交换偏置场亦有所增强.高分辨显微结构分析表明,介于钉扎层与被钉扎层之间的氧化层(NOL1)并未完全氧化,即除氧化过程生成的CoFe氧化物 关键词： 自旋阀 纳米氧化层 高分辨电子显微学 巨磁电阻效应     

Analysis of nano channel formation in quartz cubes by laser-induced process

A novel laser processing technique was developed for making channels in the nano regime in this paper. A Nd:YAG laser was used to dry fabricate micro channels (25μm～100μm di ameter) in a 1 cm^3 fused silica substrate by thermal-induced processing. By controlling the locations of these initiating micro channels on a silica cube, 1D-controllable self-connecting nano fractures can be formed as rectangular channels. These nano channels are smooth and with extremely high aspect ratio (～10^4 depth to width ratio). A possible mechanism is proposed to explain the formation of the nano channels. This laser-based nano channel fabrication technique is fast and inexpensive, and with potential applications in capillary electrophoresis and electro-osmosis driven nano-filtration.     

纳米ZnO／环氧树脂复合材料的力学性能和摩擦学性能

在超声波作用下，利用偶联剂将ZnO纳米微粒同环氧树脂进行复合，制备了纳米ZnO／环氧树脂复合材料，用M-2000型摩擦磨损试验机评价了复合材料在干摩擦条件下同不锈钢对摩时的摩擦学性能，测定了复合材料的力学性能，并用正电子湮没寿命技术(PALT)分析了试样的微观结构．结果表明：纳米ZnO／环氧树脂复合材料的耐磨性优于环氧树脂；当纳米ZnO的质量分数为10％时，复合材料的磨损率最小，仅为环氧树脂的15％，且摩擦系数也有所降低；摩擦后复合材料试样的自由体积孔穴尺寸有所增大，而且随着ZnO含量的增加，自由体积孔穴尺寸呈增大趋势．     

纳米氧化铈在催化氧化木质素制备芳香化合物中的应用研究

木质素是自然界中唯一大规模可再生的含芳环聚合物.通过催化氧化的方法,定向解聚木质素得到芳香类化合物,具有非常重要的价值.近年来,氧化铈作为载体在木质素的多相催化氧化反应中表现较好性能.然而,对于氧化铈直接作为催化剂,并探讨其纳米结构与性能之间的研究未见报道.研究结果表明:纳米氧化铈直接作为催化剂时,对于木质素的催化氧化反应具有较好的性能,顺序为氧化铈纳米八面体纳米四方体纳米球纳米棒.纳米八面体表现出最优的催化性能,以其作为催化剂,对乙醇木质素进行催化氧化,得到了大量芳香酸及其酯类化合物.     

原子力／摩擦力显微图象的分析与测量

用表面粗糙度评定方法和分形几何方法，结合原子力／摩擦力显微图象的特点，编制了包括Ｒａ，Ｒｑ，Ｓｍ，Ｓ，λａ，λｑ及高度分布、承载率曲线、相关函数、功率谱和分形维数等参数的图象分析与测量的ＦＯＲＴＲＡＮ程序；用ＳＴＲ－１８０和ＳＴＲ－１０００标样作了高度标定，对国产Ｎａｔｕｒｅ磁带和进口Ｓｏｎｙ磁带的原子力／摩擦力显微图象进行了分析测量．结果表明：Ｎａｔｕｒｅ磁带的粗糙度和粒度均比Ｓｏｎｙ磁带的大；微摩擦力与表面轮廓及表面轮廓斜率之间均有良好的对应关系．     

质子与金属布线层核反应对微纳级静态随机存储器单粒子效应的影响分析

金属布线层对微纳级静态随机存储器(static random access memory, SRAM) 质子单粒子效应敏感性的影响值得关注. 利用Geant4针对不同能量(30 MeV, 100 MeV, 200 MeV和500 MeV)的质子与微纳级SRAM器件的核反应过程开展计算, 研究了核反应次级粒子的种类、线性能量传输值(linear energy transfer, LET)及射程情况, 尤其对高LET 值的核反应次级粒子及其射程开展了详细分析. 研究表明, 金属布线层的存在和质子能量的增大为原子序数大于或等于30的重核次级粒子的产生创造了条件, 器件体硅区中原子序数大于60的重核离子来源于质子与钨材料的核反应, 核反应过程中的特殊作用机理会生成原子序数在30至50之间的次级粒子, 且质子能量的增大有助于这种作用机理的发生, 原子序数在30至50之间的次级粒子在器件体硅区的LET值最大约为37 MeV·cm²/mg, 相应射程可达到几微米, 对于阱深在微米量级的微纳级SRAM器件而言, 有引发单粒子闩锁的可能. 研究结果为空间辐射环境中宇航器件的质子单粒子效应研究提供理论支撑.     

花状CeO2/TiO2异质结的构筑及光催化性能

采用溶剂热法制备了三维花状CeO₂/TiO₂异质结光催化剂,然后以甲基橙(MO)为模拟有机污染物,在氙灯照射下考察了其光催化活性。结果表明,花状结构由纳米片和纳米颗粒复合而成,纳米片上均匀地附着CeO₂颗粒。Ce/Ti的物质的量之比(n_Ce/n_Ti)和溶剂热时间影响异质结的光催化性能,当n_Ce/n_Ti=0.1、溶剂热时间为6 h时,CeO₂/TiO₂的光催化活性达到最佳,氙灯照射50 min的降解率达95%,光催化活性优于纯TiO₂,这主要是CeO₂和TiO₂形成了异质结,有利于光生电子和空穴的分离。     

碳包覆纳米铁镍磁性颗粒的合成

通过在双温控的化学气相沉积炉中热解四吡啶并卟啉铁镍混合物,合成了碳包覆铁镍纳米颗粒。原料中四吡啶并卟啉铁镍的质量比为7∶3;扫描电镜和透射电镜的结果显示碳包覆铁镍纳米颗粒形貌均匀,直径为100~300 nm;能谱结果显示碳包覆铁镍纳米颗粒是由铁、镍和碳组成;拉曼光谱证明产物有大量的缺陷存在,可能是由于球状结构上的碎片引起的;此外,磁性能测试表明室温下,碳包覆铁镍纳米颗粒有很高的饱和磁化强度,为56.3 emu·g^-1;而其产物的矫顽力趋近于零,呈超顺磁性,适合用于催化剂载体。     

Combustion Derived Nanocrystalline‐ZrO2 and Its Catalytic Activity for Biginelli Condensation under Microwave Irradiation

Nanocrystalline zirconium(IV) oxide (nc‐ZrO₂) possessing high surface area was synthesized by a low temperature eco‐friendly solution combustion method using a new organic fuel alanine. The powder XRD, SEM and surface area measurements were carried out for characterization of nc‐ZrO₂. The powder XRD results revealed that, the nc‐ZrO₂ has the pure tetragonal phase. The crystallite size calculated by Scherrer's formula and BET surface area were found to be ca. 53–57 nm and ca. 275 m²/g, respectively. SEM micrograph exhibited the macroporous nature of the powder. nc‐ZrO₂ has been employed as a catalyst for the solvent‐free synthesis of 3,4‐dihydro‐ pyrimidin‐2‐ones (DHPMs) by a microwave (MW) assisted one‐pot, multicomponent Biginelli condensation reaction of araldehydes, ethylacetoacetate and urea or thiourea. DHPMs are obtained in good to excellent yields (85%–96%) under this reaction condition within short interval of time (10–20 min).     

Nano‐emulsion use for the synthesis of polyaniline nano‐grains or nano‐fibers

We report that nano‐emulsions can be creatively used as a morphology selective synthesis method to prepare not only nano‐grains but also nano‐fibers with high selectivity. Synthesis of the two different morphological materials was demonstrated using polyaniline synthesis as a model case. Polyaniline nano‐grains were synthesized from aniline molecules in nano‐size aqueous droplets as polymerization sites whose droplets were generated by inverse water‐in‐oil nano‐emulsion use, and polyaniline nano‐fibers were synthesized from aniline in aqueous nano‐dimensional channels as polymerization sites whose channels were generated by direct oil‐in‐water nano‐emulsion use containing high population of oil droplets. Using the approaches, we successfully synthesized nano‐fibers of 60 nm diameter with 0.5 µm length and also nano‐grains having diameter of 60–80 nm. The two different polymerization sites of nano‐scale dimension were made by changing the ratio among surfactant, aqueous aniline/HCl solution, and oil, i.e. organic solvent. We found the nano‐fibers synthesized from the channels formed by the direct oil‐in‐water nano‐emulsion have higher bulk electrical conductivity than the nano‐grains which were synthesized from the droplets formed by the inverse water‐in‐oil emulsion. We also found that the emulsion use allows us to use a room temperature synthesis unlike conventional synthesis methods which require to use ice bath temperature. Physical properties of both nano‐fibers and nano‐grains synthesized were characterized by Fourier transform infrared (FTIR), UV–Vis spectra, scanning electron microscopy (SEM), and four probes conductivity measurement. Copyright © 2009 John Wiley & Sons, Ltd.