纳米银导电膜的制备及其光谱学分析

为了以温和的化学反应制备纳米银导电膜,在PET薄膜上涂布柠檬酸银乳液,并用抗坏血酸(Vc)还原,用红外光谱仪、紫外-可见光分光光度计、X射线衍射仪(XRD)、扫描电子显微镜、原子力显微镜等,研究柠檬酸银乳液及其还原涂层的微观形貌、晶体结构和导电性能。发现PVP保护的柠檬酸银乳液粒径分布在60～150 nm。银膜的UV-Vis吸收峰位于430 nm,表明其具有纳米结构。XRD分析表明,还原后的涂层形成了不完整的银晶体,水洗比乙醇处理更能促进柠檬酸银的彻底还原和银膜的晶型完善,降低银膜表面电阻。     

碱石灰玻璃表面长方形银纳米颗粒的制备与表征

采用离子交换结合热处理的方法在碱石灰玻璃表面制备了银纳米颗粒。通过紫外-可见分光光度计、X射线衍射仪、扫描电子显微镜对样品进行了表征。结果表明:热处理时,银离子在玻璃表面成核并生长成近似长方形的纳米颗粒。吸收光谱在416nm附近出现明显的银纳米颗粒表面等离子体共振吸收特征峰。     

ICF靶用泡沫铜的制备与表征

 以次磷酸钠为还原剂的化学镀进行导电化处理,研究了ICF靶用泡沫铜的电沉积工艺。采用扫描电子显微境和X射线衍射仪对制备过程中各阶段泡沫铜的微观结构进行了表征。结果表明：经化学镀后可获得晶粒尺寸小、分布均匀的铜沉积层。电沉积后铜沉积层主要由0.55 μm的小颗粒组成,并且出现突出大颗粒的形貌特征。在氢气氛围下,经700 ℃热处理后,铜颗粒进一步长大,沉积层结晶致密。制备的泡沫铜呈3维网络状结构,分布均匀,密度为0.19 g/cm³,孔径分布为400～600 μm,孔隙率达97.9％。     

光色玻璃的X射线小角散射研究

用X射线小角散射SAXS)研究了光色玻璃中卤化银微晶尺寸同热处理温度的关系.发现在490℃以下热处理的玻璃,同原始玻璃一样,没有明显的散射.但由银含量仅为0.3(重量%)的玻璃能观察到散射干涉现象正说明银离子被富集在分散的Na_2O-B_2O_3液滴之中.从高温处理后冷却至440℃再快冷到室温的玻璃,其卤化银颗粒的尺寸比直接淬冷到室温的玻璃要大,后者约为110(?).玻璃中加入ZrO_2后,使卤化银颗粒尺寸达到近乎20O(?).基体玻璃中的-液分相,由于分散相与连续相之间的电子密度差太小,难以对其SAXS强度作定量处理.     

用SAXS和XRD方法研究TiO2纳米颗粒微观结构

用溶胶-凝胶方法制备了TiO₂纳米样品,并对该样品在300℃到800℃温度区域进行了退火处理.应用同步辐射X射线粉末衍射(XRD)方法研究了经不同热处理温度的TiO₂纳米颗粒的结构相变.应用同步辐射小角X射线散射(SAXS)方法研究了TiO₂纳米颗粒的表面分形与界面特性.得到纳米颗粒粒度与退火温度的变化规律,讨论了表面界面特征与相变的关系. 关键词： X射线小角散射 X射线衍射 2纳米颗粒')" href="#">TiO₂纳米颗粒     

溶胶-凝胶法合成Sr3MgSi2O8:Eu3+ 红色荧光粉及其发光性能

采用溶胶-凝胶法合成了Sr_3MgSi_2O_8∶Eu~(3+)红色荧光粉,并通过X射线衍射(XRD)、傅立叶变换红外光谱(FTIR)、扫描电镜(SEM)以及荧光光谱(PL)、X射线光电子能谱(XPS)等分析方法,对不同烧结温度(950,1 050,1 150,1 250℃)热处理4 h后得到的粉体的物相、形貌及发光性能进行了表征分析。由XRD表征结果可知,制备出的样品为正交晶系的Sr_3MgSi_2O_8;由扫描电镜及比表面积的测试结果可知,经过1 150℃热处理得到的荧光粉具有最大比表面积,可达到90.213 1 m~2/g,且粒径大小均一;由红外光谱图可知:样品中含有Si—O—Si、Mg—O和Sr—O化学键;在394 nm的激发波长下,所有样品在614 nm和702 nm处出现了强发射峰,分别对应于Eu~(3+)的~5D_0→~7F_2和~5D_0→~7F_4跃迁,属红光发射。随着热处理温度的升高,样品所对应的发射峰强度呈现出先增大后减小的变化趋势,即出现温度猝灭效应;经1 150℃热处理合成的Sr_3MgSi_2O_8∶Eu~(3+)红色荧光粉的发光性能最好,即最佳的热处理温度为1 150℃。     

银颗粒对Lu2O3:Eu薄膜光学性质影响

采用溶胶凝胶和提拉法制备了含有银颗粒的Lu2O3:Eu薄膜,利用X射线衍射,吸收光谱,光致发光光谱(PL)及荧光衰减光谱对其进行了表征,结果表明:所得材料在800℃下结晶完好,在发射光谱中观察到了银颗粒导致的Eu3 的发光增强效应,讨论了银颗粒对LU2O3:Eu薄膜发光性质的影响.     

热处理温度对化学镀磁性ICF玻璃靶丸特性的影响

 在300,700和1 000 ℃温度下,对化学镀Ni-P合金涂层后的磁性ICF玻璃靶丸进行热处理,通过X射线衍射仪（XRD）、扫描电子显微镜（SEM）和振动样品磁强计（VSM）对热处理后化学镀ICF玻璃靶丸的结构、形貌和磁性能进行了表征。结果表明：化学镀ICF玻璃靶丸经过热处理后,Ni-P涂层晶化为晶态合金层,涂层的组成颗粒直径和磁性能随着热处理温度的升高而不断增加,可望用于磁悬浮实验研究。     

竹节状α-Fe2O3纳米棒的制备、表征和性能研究

以硝酸铁为铁源,氨水为沉淀剂,聚乙二醇(PEG)为分散剂,采用共沉淀法制备氢氧化铁前驱体,然后将获得的前驱体在450℃、氮气保护下热处理2 h,最后利用透射电镜、X射线衍射、拉曼光谱和近边X射线精细结构光谱(NEXAFs)表征样品的形貌和结构,并使用HH-50型振动样品磁强计测量样品在室温下的磁学行为.透射电镜结果显示,获得的样品由氧化铁纳米颗粒和竹节状氧化铁纳米棒组成,纳米颗粒的粒径范围为50～100 nin,纳米棒的直径大约为10 nin.XRD表征显示样品中氧化铁纳米棒和纳米颗粒为赤铁矿型α-Fe2O3;光谱实验结果证实了样品中氧化铁纳米颗粒和纳米棒的结构是α-Fe2O3;磁学性能测试表明获得的样品表现为典型铁磁性材料的磁滞回线,其饱和磁感应强度约为64.65 emu·g-1,矫顽力的大小约为15.13 Oe.     

射频反应性溅射沉积的Cd2SnO4薄膜物理性质与缺陷特性研究

在Ar+O₂混合气氛中射频反应性溅射Cd-Sn合金靶制备了透明导电Cd₂SnO₄(简称CTO)薄膜。用X射线衍射测量了CTO膜的结构。实验结果表明,这种薄膜的电学和光学性质依赖于混合气体中的氧浓度、衬底温度以及沉积后的热处理。获得的CTO膜最低电阻率为1.74×10^-6Ω·cm,可见光光谱区最高透射率为95％。对于氧浓度为6％、衬底温度为400℃时沉积的CTO膜,经热处理后,其光隙能由热处理前的2.37eV增大为2.6 关键词：     

A promising approach to conductive patterns with high efficiency for flexible electronics

A promising approach for conductive patterns with high efficiency for flexible electronics was developed by direct-writing, silver(I) solution (silver nitrate, acetate silver, etc.) with no solid particles as a conductive ink, conductive pen as a writing implement, and polyimide (PI) film as a substrate. The physical properties of the conductive ink were investigated by a dynamic contact angle system, ubbelohde viscometer and surface tension instrument. Conductive properties of silver ink film were investigated by 4-point probe, scanning electron microscope (SEM) and surface profilometer. It is demonstrated how the design of solvent composition in conductive ink affects surface morphology, and conductivity of silver ink films. It can be obtained that conductive patterns drawn on PI substrate not only have good mechanical/electrical fatigue properties, but also have low resistivity. Especially, when the sintering condition is 200 °C for 60 min, the resistivity can be down to 6.6 μΩ cm, 4.25 times the silver bulk resistivity.     

Synthesis and characterization of copper ink and direct printing of copper patterns by inkjet printing for electronic devices

Among the conventional metallic inks used in the printing process, silver exhibits high conductivity and thermal stability. Nevertheless, due to the high cost of silver, it cannot be extensively used for the fabrication of inks. As a competitive alternative, copper can be considered as a substitute for silver; however, copper ink oxidizes under certain atmospheric conditions. To meet these shortcomings, a cost effective, highly conductive, and oxidation-free copper-based ink has been synthesized in this study, wherein, oxidation of the copper particles in the copper-based ink was prevented by using copper complexes. The copper ink thus fabricated was printed on chemically treated Si/SiO₂ substrates followed by the characterization of the printed copper films. The results of this study confirmed that the synthesized copper ink exhibited properties suitable for its use in the inkjet printing process for fabrication of various electronic devices.     

Synthesis and characterization of conductive silver ink for electrode printing on cellulose film

Silver nanoparticles with size less than 50 nm were synthesized from silver nitrate, polyvinylpyrrolidone (PVP) and ethylene glycol, where these chemicals acted as metal precursor, stabilizer and reducing agent, respectively. Then a conductive silver ink was prepared with a suitable solvent by adding a viscosifier, hydroxyethyl-cellulose (HEC), and a surfactant, diethylene glycol (DEG). The combined effect of both viscosifier and surfactant on the physical property of the silver ink was analyzed by measuring the contact angle of the silver ink on a cellulose film. Moreover, the influences of PVP molecular weight and reaction temperature on the size of the silver nanoparticles were analyzed. Then the silver ink was coated on the cellulose film by spin coating and the effects of different solvents, sintering temperatures and solid contents on its electrical resistivity were examined. It was found that, with 50 % co-solvent of deionized water and DEG and solid content of around 50 %, the silver ink exhibited the lowest resistivity. This ink can be used for inkjet printing of conductive patterns on cellulose films.     

溶剂对溶胶-凝胶法制备的掺铝氧化锌透明导电薄膜性质的影响

采用溶胶-凝胶法在玻璃基底上制备得到了高透光率,高导电性的掺铝氧化锌薄膜。研究了溶剂对薄膜晶体结构,薄膜厚度,表面形貌,光学性质和电学性质的影响,结果表明:在相同的制备条件下,薄膜的厚度随溶剂沸点的升高而降低;低沸点溶剂制备的薄膜由c轴择优取向的六角纤锌矿结构的晶体构成,且比较致密;所有薄膜可见光区的透光率在85%以上;乙二醇独甲醚为溶剂制备的薄膜电阻率最低,为3.0×1-0 4Ωm。     

基于铝浸润层的超薄银透明导电薄膜研究北大核心CSCD

超薄银薄膜具有高柔韧性和优良的光电性能,是用于透明导电电极的潜在材料。通过电阻热蒸发技术以金属铝作为浸润层制备超薄银透明导电薄膜。引入铝浸润层降低银薄膜的阈值厚度,使银薄膜在K9玻璃基底上以尽可能低的厚度达到连续。对不同厚度铝浸润层上银薄膜方块电阻进行测试,经SEM图像验证后得出,1 nm铝浸润层对银薄膜具有较好的浸润效果。随后采用相同的工艺在1 nm铝浸润层上制备了不同厚度的银薄膜,透过率和方阻测试结果表明,1 nm铝浸润层上制备的10 nm银薄膜方阻值可达到13Ω/,其在0.4μm~2.5μm波段内透过率可达到50%以上。     

Substrate pre-treatment of flexible material for printed electronics with carbon nanotube based ink

In this work, an innovative solution was developed in order to make paper-based material, used traditionally in the packaging and labelling industries, compatible with the printing of functional conductive inks. In order to avoid the deterioration of the ink functionalities due to different paper properties, a UV-curing inkjettable primer layer was developed. This pre-treatment enables homogeneous surface properties such as smoothness, absorption capacity and surface energy to be obtained, for almost all the examined substrates. To confirm the positive impact of such pre-treatment, conductivity has been measured when using a new conductive ink, combining the processability of the PEDOT-PSS conductive polymer with the high electrical properties of carbon nanotubes (CNTs). Significant improvement has been measured for all paper materials and similar conductivity (close to reference PET film) has been obtained whatever the substrate involved. This pre-treatment now makes it possible to consider paper-based material as a potential substrate for printed electronics. In this case, the substrate adaptation technique offers an innovative solution to produce low-cost and flexible electronics.     

Preparation of high quality Ag film from Ag nanoparticles

A simple route to the high quality Ag film was developed at room temperature by using Ag nanoparticles stabilized by polyvinylpyrrolidone (PVP) as Ag source. The scanning electron microscopy (SEM) images indicate that the silver film prepared on the quartz substrate is smooth and dense. Meanwhile, the X-ray diffraction (XRD) of the film shows a face-centered cubic (fcc) phase of Ag.     

质子酸功能化离子液体中银纳米颗粒的制备及其光学性能研究

以质子酸功能化离子液体1-丁基-3-甲基咪唑磷酸二氢盐([Bmim]H₂PO₄)为反应介质和表面活性剂,采用简单的化学还原法制备了具有形状各向异性的块状银纳米颗粒。通过X射线衍射(XRD)、扫描电镜(SEM)、紫外-可见(UV-Vis)吸收光谱等一系列手段对其结构、形貌及光吸收特性进行了表征。结果表明,所制备的银纳米块具有立方结构,其平均横向尺寸约为30 nm,在硅片上自组装形成密堆积结构的多层膜。以1,2-二(4-吡啶基)乙烯(BPE)作为探针分子,研究所制备银纳米颗粒的表面增强拉曼散射(SERS)活性。结果表明所制的银纳米颗粒是较好的SERS基底,具有良好的增强效果,痕检能力及稳定性。对BPE分子的最低检测浓度可低至10-9mol·L-1,而且保存了90天后,其检测灵敏度没有显著的降低。     

Synthesis and characterization of silver-polypyrrole film composite

In this work, we report the chemical polymerization of pyrrole to obtain thin film of polypyrrole (PPy) hydrochloride deposited onto the electrode of the quartz crystal microbalance (QCM). The film in the base form was exposed to a solution of AgNO₃. Electroless reduction for silver ions by the PPy film took place and silver particles were adsorbed onto the film surface. The silver particles content at the PPy films were analyzed by QCM and the results showed that the concentrations of silver uptakes increase as the original AgNO₃ solution increases. The morphology of the surface of the PPy film and the silver-PPy film composite were studied by the scanning electron microscopy (SEM) coupled with energy dispersive X-ray spectrometry (EDX). They showed that the obtained silver particles have spherical, cubic and tetrahedral structures. X-ray diffraction (XRD) and Fourier transformed infra-red spectroscopy (FTIR) were used to characterize the structure of the powder composite. This work reveals the capability of PPy film coating on QCM in sensing and removing silver from several environmental samples.