TiO_2/石墨烯/Ag复合结构SERS实验

基于氧化物半导体的光催化特性,能够降解有机物分子,使表面增强拉曼散射基底得以重复使用。提出了银纳米颗粒有效修饰覆盖有石墨烯的二氧化钛纳米棒阵列(TiO_2/石墨烯/Ag)复合结构作为表面增强拉曼散射基底,并对其进行了实验研究。利用水热法制备了二氧化钛纳米棒阵列;采用湿法转移石墨烯和光照还原方法制备了TiO_2/石墨烯/Ag复合结构。用罗丹明6G(R6G)分子作为探测分子,结果表明:随着紫外光照沉积时间增加,探针分子的拉曼信号先增强后减弱;计算得到最大增强因子值约为2.6×106。此外,还对TiO_2/石墨烯/Ag复合结构的紫外自清洁特性进行了初步实验,结果表明,紫外光照射20min后,其拉曼强度下降到42.3%,具有一定的紫外清洁效果。     

Synthesis and characterization of multifunctional silica core-shell nanocomposites with magnetic and fluorescent functionalities

Multifunctional core-shell nanocomposites with a magnetic core and a silica shell doped with lanthanide chelate have been prepared by a simple method. First, citric acid-modified magnetite nanoparticles were synthesized by a chemical coprecipitation method. Then the magnetite nanoparticles were coated with silica shells doped with terbium (Tb³⁺) complex by a modified Stöber method based on hydrolyzing and condensation of tetraethyl orthosilicate (TEOS) and a silane precursor. These multifunctional nanocomposites are potentially useful in a variety of biological areas such as bio-imaging, bio-labeling and bioassays because they can be simultaneously manipulated with an external magnetic field and exhibit unique phosphorescence properties.     

Structure and Mechanical Properties of 50/50 NR/SBR Blend/Pristine Clay Nanocomposites

A blend/clay nanocomposites of 50/50 (wt%) NR/SBR was prepared via mixing the latex of a 50/50 NR/SBR blend with an aqueous clay dispersion and co‐coagulating the mixture. The structure of the nanocomposite was characterized by transmission electron microscopy (TEM) and X-ray diffraction (XRD). Nanocomposites containing less than 10 phr clay showed a fully exfoliated structure. After increasing the clay content to 10 phr, both nonexfoliated (stacked layers) and exfoliated structures were observed in the nanocomposites. The results of mechanical tests showed that the nanocomposites presented better mechanical properties than clay‐free NR/SBR blend vulcanizate. Furthermore, tensile strength, tensile strain at break, and hardness (shore A) increased with increasing clay content, up to 6 phr, and then remained almost constant.     

Large scale silver nanowires network fabricated by MeV hydrogen(H~+) ion beam irradiation

A random two-dimensional large scale nano-network of silver nanowires(Ag-NWs) is fabricated by MeV hydrogen(H~+) ion beam irradiation. Ag-NWs are irradiated under H~+ion beam at different ion fluences at room temperature. The Ag-NW network is fabricated by H~+ion beam-induced welding of Ag-NWs at intersecting positions. H~+ion beam induced welding is confirmed by transmission electron microscopy(TEM) and scanning electron microscopy(SEM). Moreover, the structure of Ag NWs remains stable under H~+ion beam, and networks are optically transparent. Morphology also remains stable under H~+ion beam irradiation. No slicings or cuttings of Ag-NWs are observed under MeV H~+ion beam irradiation.The results exhibit that the formation of Ag-NW network proceeds through three steps: ion beam induced thermal spikes lead to the local heating of Ag-NWs, the formation of simple junctions on small scale, and the formation of a large scale network. This observation is useful for using Ag-NWs based devices in upper space where protons are abandoned in an energy range from MeV to GeV. This high-quality Ag-NW network can also be used as a transparent electrode for optoelectronics devices.     

Double peaks on ac magnetization in a superconducting Pb-porous glass nanocomposite

Studies of temperature dependences of ac magnetization were carried out for a superconducting lead-porous glass nanocomposite. Double peaks were found on the imaginary part of ac magnetization which were accompanied with double steps on the real part. The lower-temperature anomalies in ac magnetization differed noticeably when they were obtained upon cooling and warming. The double peaks were treated as two phase transitions in the vortex system: the liquid-solid transition which occurs close to the onset of superconductivity and solid-solid one which is triggered by superconductivity in confined lead islands.     

Effect of Mn on the magnetic properties of Fe3B/Nd2Fe14B nanocomposites

The magnetic properties of Nd_4.5Fe_77−xMn_xB_18.5 (x=0, 1 and 2) nanocomposites prepared by the crystallization of amorphous precursors were investigated. Addition of Mn is found to decrease the crystallization temperature of the amorphous ribbons. The intrinsic coercivity _iH_c and maximum energy product (BH)_max increase from 2.6 kOe and 9.1 MGOe for x=0 to 3.1 kOe and 10.3 MGOe for x=1, respectively, and the remanence ratio M_r/M_s increases from 0.70 to 0.72. The effect of Mn on Curie temperature T_C and the thermal stability of M_r and _iH_c were also studied. ⁵⁷Fe Mössbauer spectra have been recorded for x=0, 1 and 2 ribbons at room temperature and site preference of the Mn atoms in Fe₃B and Nd₂Fe₁₄B phases is discussed using the Mössbauer spectroscopy.     

Hard magnetic properties in Pr2Fe14B/α-Fe nanocomposite magnets with a combined addition of V and C

Nanostructured Pr₈Fe_86−xV_xB_6−yC_y (x=0, 1; y=0, 1) ribbons composed of Pr₂Fe₁₄B and α-Fe phases with a high coercivity are fabricated by direct melt spinning. The effects of a single addition of V and a combined addition of V and C on the structures and magnetic properties of melt-spun Pr₈Fe₈₆VB_6−xC_x (x=0 and 1) ribbons have been investigated. Compared with addition-free ribbons, 1 at% V addition is found to reduce the grain sizes of the samples and improve their magnetic properties due to a strong exchange coupling between the hard and the soft phase. A remanence ratio of 0.82, a coercive field of 6.2 kOe and a maximum energy product of 23.4 MGOe in melt-spun Pr₈Fe₈₅VB₆ ribbons are obtained at room temperature. The combined addition of V and C is found to lead to the formation of an intermediate phase of VC at grain boundaries, which appears as a pinning barrier during magnetization and results in an increase of the coercivity value to 6.9 kOe for melt-spun Pr₈Fe₈₅VB₅C ribbons.     

银纳米粒子/碳纳米管阵列SERS基底增强因子分析和实验

为了直观、准确地定量分析表面拉曼增强散射基底结构的拉曼增强,利用磁控溅射和高温退火的方法制备了银纳米粒子修饰垂直排列的碳纳米管阵列三维复合结构样品;实验采用罗丹明6G(R6G)溶剂作为探针分子,结合共聚焦显微拉曼系统,开展了表面增强拉曼增强因子(EF)分析计算的相关实验。SEM结果表明：在有序碳纳米管阵列的表面和外壁均匀地负载了大量银纳米粒子。对退火温度为450 ℃,退火时间为30 min的样品进行了EF计算,得到其增强因子约为2.2×103,并分析了EF值低的原因主要是：在碳纳米管上溅射的银膜膜厚不均匀,导致退火后银颗粒分布不均,使得样品粗糙度值偏大,EF值较低;实验中所用的激励光源并非银纳米颗粒的优化光源。     

低能离子束诱导Ag表面纳米金字塔微结构

利用离子束溅射诱导实验方法,在单晶Si(100)基底上辅助沉积银膜,研究了低能Ar+离子束30°入射时,不同离子束能量和束流密度以及基底温度对Ag纳米结构的影响.结果表明:在较低基底温度下(32~100℃)辅助沉积银膜,膜层表面会呈现排列紧密、晶粒尺寸一致的金字塔状纳米结构.当温度升高时(32~200℃),纳米微结构横向尺寸λc迅速增加,而粗糙度先减小(32~100℃)后迅速增大(100~200℃);当离子束能量1 400eV、束流密度15~45μA/cm2时,在相同温度下,随着离子束束流密度的增大,纳米晶粒横向尺寸基本不变,粗糙度略有增加;当离子束流密度为15μA/cm2、能量1 000~1 800eV时,在相同温度下,随着离子束能量的增加,银纳米结构尺寸增加,而表面粗糙度先增加,然后缓慢减小.自组织纳米结构的转变是溅射粗糙化和表面驰豫机制相互作用的结果.     

CoPt(FePt)-C纳米复合膜的结构与磁性

用磁过滤脉冲真空电弧沉积方法制备了CoPt(FePt) C纳米复合薄膜，并在不同温度下进行了退火处理，研究了薄膜中碳的含量以及退火温度对薄膜结构与磁性能的影响.制备态薄膜经过足够高的温度退火后，x射线衍射和磁力显微镜分析发现，在碳基质中生成了面心四方相的CoPt(FePt)纳米颗粒.对于特定组分为Co24Pt31C45和Fe43Pt35C22的薄膜，矫顽力以及颗粒尺寸都随退火温度的升高而增大，当退火温度为700℃时，Co24Pt31C45薄膜的矫顽力为21×105A/m，晶粒尺寸为17nm;当退火温度为650℃时，Fe43Pt35C22相应值分别为28×105A/m和105nm. 关键词： 磁记录材料 磁性薄膜 CoPt FePt纳米复合薄膜