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硅烷偶联剂表面接枝包覆纳米SiO2的研究 总被引:18,自引:0,他引:18
采用硅烷偶联剂γ-(甲基丙烯酰氧)丙基三甲氧基硅烷(MPS)处理纳米SiO2,并用FT-IR、ζ-电势、TG、TEM对纳米SiO2的处理效果进行了表征.结果表明,纳米SiO2的接枝率随偶联剂MPS加入量的增加而增加;当pH值为4,MPS/SiO2为50%,反应温度为110 ℃、时间为90 min时,纳米SiO2表面MPS的接枝包覆率达到35.7%;此时纳米SiO2粒子在乳液中的分散更为均匀. 相似文献
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纳米TiO2表面包覆致密SiO2膜的试验研究 总被引:16,自引:0,他引:16
用液相沉积法对纳米二氧化钛进行了表面改性.用XRD、FT-IR分析手段对其进行了表面结构表征,采用X衍射荧光光谱仪(XRF)测定SiO2包覆量随陈化时间的变化.通过煅烧失重法比较改性前后样品的失重,并用动态法测量样品与水的湿润角.结果表明在TiO2表面存在致密非晶态的硅氧化合物膜,纳米TiO2与水的湿润角增大,并且充分分散后在水中的稳定性却得到了很大提高. 相似文献
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纳米SiO2氢氧化铝/十二烷基苯磺酸钠的表面包覆改性 总被引:1,自引:0,他引:1
通过氢氧化铝和十二烷基苯磺酸钠(SDBS)对纳米SiO2进行表面包覆和改性处理,改善纳米SiO2的表面结构和分散性.使用IR、FESEM、EDS、Malvern Zetasize 3000HSA自动电位粒度仪等表征手段,对表面包覆改性后纳米SiO2的表面结构、形貌及等电点等进行了测试和分析.结果表明,经Al(OH)3表面包覆后,纳米SiO2粉体等电点(IPE)的pH值从1.58变为7.1;经SDBS对表面包覆Al(OH)3的纳米SiO2进行改性后,纳米SiO2粉体团聚现象减少,单个纳米SiO2颗粒的粒径约为30nm. 相似文献
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利用简单的物理气相沉积制备了多种纳米结构的8-羟基喹啉铝(AlQ3),主要考察了温度对其微结构的影响.运用傅立叶红外光谱仪、环境扫描电子显微镜、紫外光致发光仪等对其进行了结构、形貌和光致发光特性的研究.结果表明:成功制备了AlQ3纳米链,AlQ3纳米片,AlQ3微米球与纳米线的复合结构.PL谱没有明显的变化,可能是因为AlQ3分子间结合力是较弱的范德华力. 相似文献
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铝酸锶是典型的长余辉发光材料,已经广泛应用于日常生活中,但是铝酸锶在水中极易发生水解,抗湿性差,严重限制了其应用。采用化学气相沉积法和物理蒸汽沉积法在长余辉发光材料表面包覆膜,对设备要求高,价格贵,不易推广。因此,采用液相沉积法在长余辉荧光粉铝酸锶表面包覆SiO2膜和A l2O3膜来提高其耐水性能,采用电镜扫描(SEM)、X射线衍射(XRD)表征膜的存在,并对包膜试样进行了耐水性和发光性能的测试。结果表明:铝酸锶荧光粉包覆了致密的复合膜层后,耐水性得到显著的提高,同时,包膜对荧光粉的发光性能影响较小,发射光和激发光强度损失均在10%以下。 相似文献
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采用液相法成功的在球形Gd2O3Eu荧光粉颗粒表面包覆一层纳米SiO2保护膜.扫描电镜分析可见包覆SiO2后颗粒粒径略微变大说明表面包覆一层纳米级的包覆层.XPS分析表明SiO2包覆层与Gd2O3Eu颗粒表面以Gd(Eu)-O-Si化学键的方式键合在一起的.荧光光谱分析表明包覆后的Gd2O3Eu3+颗粒仍旧是一种很好的发光材料. 相似文献
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《Journal of Experimental Nanoscience》2013,8(5):578-585
We fabricated 8-hydroxyquinoline (HQ) wires by two methods, decomposition of tris(HQ) aluminium at low pressure in a tube furnace and heating of HQ powder at atmospheric pressure. Fabricated wires were crystalline, and exhibited the same optical properties (absorption and photoluminescence) as HQ powder. While the properties of wires prepared by two different methods were the same, it should be noted that synthesis by decomposition of tris(HQ) aluminium required elimination of mechanical vibration of the growth tube. Implications of decomposition of tris(HQ) aluminium during organic vapour phase deposition growth on organic optoelectronic device performance are discussed. 相似文献
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Antti Tolkki Kimmo KaunistoJuha P. Heiskanen Walaa A.E. Omar Kirsi HuttunenSuvi Lehtimäki Osmo E.O. HormiHelge Lemmetyinen 《Thin solid films》2012,520(13):4475-4481
Tris(8-hydroxyquinoline)aluminum (Alq3) is a frequently used material for organic light emitting diodes. The electronic properties and solubility can be tuned by chemical tailoring of the quinoline part, which makes it an interesting candidate for organic solar cells. Steady-state absorption and fluorescence, as well as time-resolved fluorescence properties of the parent Alq3 and a series of complexes consisting of derivatives, such as 4-substituted pyrazol, methylpyrazol, arylvinyl, and pyridinoanthrene moieties, of the quinoline ligand, were studied in solutions and in thin films. Suitability of the complexes as anodic buffer layers or dopants in inverted organic solar cells based on the well known bulk heterojunction of poly(3-hexylthiophene) (P3HT) and phenyl-C61-butyric acid methyl ester (PCBM) was tested. The devices equipped with the derivatives showed higher power conversion efficiency (η) compared to the photocells containing the parent Alq3. Open circuit voltage (Voc) was increased when the derivatives were utilized as the anodic buffer layer. Doping of the P3HT:PCBM with a small amount of Alq3 or its derivative improved short circuit current density, Voc, fill factor, and η, while the series resistance decreased. In addition, the devices were stable in air over several weeks without encapsulation. Possible mechanisms leading to the improvements in the photovoltaic performance by using the parent Alq3 or its derivative as buffer layer or dopant are discussed. 相似文献
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We fabricated electron-only tris (8-hydroxyquinoline) aluminum (Alq3) single-layer devices with a device structure of glass substrate/MgAg anode (100 nm)/Alq3 layer (100 nm)/metal cathode (100 nm), and systematically varied the work functions (WF) of the metal cathodes from WF = − 1.9 (Cs) to − 2.9 (Ca), − 3.8 (Mg), − 4.4 (Al), − 4.6 (Ag), and − 5.2 eV (Au) to investigate how electron injection barriers at the cathode/Alq3 interfaces influence their current density–voltage (J–V) characteristics. We found that current densities at a certain driving voltage decrease and the temperature dependence of J–V characteristics of the devices gradually becomes weaker as the work functions of the metal cathodes are decreased. The device with the highest-work-function Au cathode exhibited virtually temperature-independent J–V characteristics, suggesting that a current flow mechanism of this device is mainly controlled by electron tunneling injection at the Au/Alq3 interface. 相似文献
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A well-known red fluorescent dye 4-(dicy-anomethylene)-2-t-butyl-6(1,1,7,7-tetramethyljulolidyl-9-enyl)-4H-pyran (DCJTB) was codoped with an electron transport organic molecule tris(8-hydroxyquinoline) aluminum (Alq(3)) in a host matrix of polystyrene (PS), and the amplified spontaneous emission (ASE) was studied by optically pumping. It was found that the ASE performance was significantly improved by the introduction of Alq(3). The Alq(3):DCJTB:PS blending thin films showed a low threshold (2.4 microJ/pulse) and a high net gain coefficient (109.95 cm(-1)) compared with the pure DCJTB:PS system (threshold of 15.2 microJ/pulse and gain of 35.94 cm(-1)). The improvement of the ASE performance was considered to be attributable to the effective F?ster energy transfer from Alq(3) to DCJTB. Our results demonstrate that the Alq(3):DCJTB could be a promising candidate as gain medium for red organic diode lasers. 相似文献
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