501 resultados para Sol gel preparations
Resumo:
ZrO2 thin films were deposited bill using an electron beam evaporation technique on three kinds of lithium triborate (LiB3O5 or LBO) substrates with the surfaces at specified crystalline orientations. The influences of the LBO structure on the structural and optical properties of ZrO2 thin films are studied by spectrophotometer and x-ray diffraction. The results indicate that the substrate structure has obvious effects on the structural end optical properties of the film: namely. the ZrO2 thin film deposited on the X-LBO, Y-LBO and Z-LBO orients to m(-212), m(021) and o(130) directions. It is also found that the ZrO2 thin film with m(021) has the highest refractive index and the least lattice misfit.
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A novel fiber coated with novel sol-gel (5,11,17,23-tetra-tert-butyl-25,27-dihydroxy-26,28-diglycidyloxycalix[4]arene/hydroxy-terminated silicone oil; diglycidyloxy-C[4]/OH-TSO) was prepared for use with headspace solid-phase microextraction (HS-SPME) combined with gas chromatography (GC) and electron capture detection (ECD), which was applied in order to determine nine chlorobenzenes in soil matrices. Due to the improved fiber preparation, which increases the percentage of calixarene in the coating, the new calixarene fiber exhibits very high extraction selectivity and sensitivity to chlorine-substituted compounds. Various parameters affecting the extraction efficiency were optimized in order to maximize the sensitivity during the chlorobenzene analysis. Interferences from different soil matrices with different characteristics were investigated, and the amount extracted was strongly influenced by the matrix. Therefore, a standard addition protocol was performed on the real soil samples. The linear ranges of detection for the chlorobenzenes tested covered three orders of magnitude, and correlation coefficients > 0.9976 and relative standard deviations (RSD) < 8% were observed. The detection limits were found at sub-ng/g of soil levels, which were about an order of magnitude lower than those given by the commercial poly(dimethylsiloxane) (PDMS) coating for most of the compounds. The recoveries ranged from 64 to 109.6% for each analyte in the real kaleyard soil matrix when different concentration levels were determined over the linear range, which confirmed the reliability and feasibility of the HS-SPME/GC-ECD approach using the fiber coated with diglycidyloxy-C[4]/OH-TSO for the ultratrace analysis of chlorobenzenes in complex matrices.
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(Na1-xKx)(0.5)Bi0.5TiO3 (NKBT) (x = 0.1, 0.2, and 0.3) thin films with good surface morphology and rhombohedral perovskite structure were fabricated on quartz substrates by a sol-gel process. The fundamental optical constants (the band gaps, linear refractive indices and absorption coefficients) of the films were obtained through optical transmittance measurements. The nonlinear optical properties were investigated by Z-scan technique performed at 532 nm with a picosecond laser. A two-photon absorption effect closely related with potassium-doping content was found in thin films, and the nonlinear refractive index n(2) increases evidently with potassium-doping. The real part of the third-order nonlinear susceptibility chi((3)) is much larger than its imaginary part, indicating that the third-order optical nonlinear response of the NKBT films is dominated by the optical nonlinear refractive behavior. These results show that NKBT thin films have potential applications in nonlinear optics. (C) 2007 Elsevier B.V. All rights reserved.
Resumo:
SiO2-TiO2 sol-gel films are deposited on SiO2/Si by dip-coating technique. The SiO2-TiO2 strips are fabricated by laser direct writing using all ytterbium fiber laser and followed by chemical etching. Surface structures, morphologies and roughness of the films and strips are characterized. The experimental results demonstrate that the SiO2-TiO2 sol-gel film is loose in Structure and a shrinkage concave groove forms if the film is irradiated by laser beam. The surface roughness of both non-irradiated and laser irradiated areas increases with the chemical etching time. But the roughness of laser irradiated area increases more than that of non-irradiated area under the same etching time. After being etched for 28 s, the surface roughness value of the laser irradiated area increases from 0.3 nm to 3.1 nm.
Resumo:
Zn2SiO4:Mn2+, Zn2SiO4:Eu3+ and Zn2SiO4:Mn2+ Eu3+ phosphors were prepared by a sol-gel process and their luminescence spectra were investigated. The emission bands from intra-ion transitions of Mn2+ and Eu3+ samples were studied as a function of pressure. The pressure coefficient of Mn2+ emission was found to be -25.3 +/- 0.5 and -28.5 +/- 0.9 meV/GPa for Zn2SiO4:Mn2+ and Zn2SiO4:Mn2+ Eu3+, respectively. The Eu3+ emission shows only weak pressure dependence. The pressure dependences of the Mn2+ and Eu3+ emissions in Zn2SiO4:Mn2+ Eu3+ are slightly different from that in Zn2SiO4:Mn2+ and Zn2SiO4:Eu3+ samples, which can be attributed to the co-doping of Mn2+ and Eu3+ ions. The Mn2+ emission in the two samples, however, exhibits analogous temperature dependence and similar luminescence lifetimes, indicating no energy transfer from Mn2+ to Eu3+ occurs. (c) 2005 Elsevier B.V. All rights reserved.
Resumo:
The SnO2 material prepared by sol-gel method was modified by thiourea solution in different concentrations (0.05, 0.1 and 0.2 mol dm(-3)). Then the structure and the average grain size of the SnO2 material were investigated by X-ray power diffraction. In order to understand the nature of the species on the SnO2 surfaces, the thermal gravimetric and differential thermal analyzer (TG-DTA) and IR spectra of these modified and unmodified sample were taken. The result indicates that the stability of oxygen adsorbed on thiourea-modified surface was improved and the amount of surface hydroxyl groups adsorbed on this grain surface was decreased. The thiourea adsorbed on SnO2 grain surface is translated to SO42- after sintered at 600 degrees C. SO42- species stabilize the resistance of the SnO2 sensor. (c) 2005 Elsevier B.V. All rights reserved.
Resumo:
ZnO nanoparticles were synthesized in ethanolic solution using a sol-gel method. The structural and optical properties were investigated by X-ray diffraction, transmission electron microscopy, UV absorption, and photoluminescence. After annealing at 200 degrees C, the particle size is increased and the peak of defect luminescence in the visible region is changed. A yellow emission was observed in the as-prepared sample and a green emission in the annealed sample. The change of the visible emission is related to oxygen defects. Annealing in the absence of oxygen would increase oxygen vacancies. (c) 2006 Elsevier Ltd. All rights reserved.
Resumo:
Eu3+-doped zinc aluminate (ZnAl2O4) nanorods with a spinel structure were successfully synthesized via an annealing transformation of layered precursors obtained by a homogeneous coprecipitation method combined with surfactant assembly. These spinel nanorods, which consist of much finer nanofibres together with large quantities of irregular mesopores and which possess a large surface area of 93.2 m(2) g(-1) and a relatively narrow pore size distribution in the range of 6 - 20 nm, are an ideal optical host for Eu3+ luminescent centres. In this nanostructure, rather disordered surroundings induce the typical electric-dipole emission (D-5(0) --> F-7(2)) of Eu3+ to predominate and broaden.
Resumo:
ZnO nanoparticles were synthesized in ethanolic solution using a sol-gel method. The structural and optical properties were investigated by X-ray diffraction, transmission electron microscopy, UV absorption, and photoluminescence. After annealing at 200 degrees C, the particle size is increased and the peak of defect luminescence in the visible region is changed. A yellow emission was observed in the as-prepared sample and a green emission in the annealed sample. The change of the visible emission is related to oxygen defects. Annealing in the absence of oxygen would increase oxygen vacancies. (c) 2006 Elsevier Ltd. All rights reserved.
Resumo:
Low cost Si-based tunable InGaAs RCE photodetectors operating at 1.3similar to1.6 mum were fabricated using sol-gel bonding. A tuning range of 14.5 nm, a quantum efficiency of 44% at 1476 nm and a 3-dB bandwidth of 1.8 GHz were obtained.
Resumo:
TiO2 sol-gels with various Ag/TiO2 molar ratios from 0 to 0.9% were used to fabricate silver-modified nano-structured TiO2 thin films using a layer-by-layer dip-coating (LLDC) technique. This technique allows obtaining TiO2 nano-structured thin films with a silver hierarchical configuration. The coating of pure TiO2 sol-gel and Ag-modified sol-gel was marked as T and A, respectively. According to the coating order and the nature of the TiO2 sol-gel, four types of the TiO2 thin films were constructed, and marked as AT (bottom layer was Ag modified, surface layer was pure TiO,), TA (bottom layer was pure TiO,, surface layer was Ag modified), TT (pure TiO, thin film) and AA (TiO, thin film was uniformly Ag modified). These thin films were characterized by means of linear sweep voltammetry (LSV), X-ray diffraction (XRD), scanning electron microscopy (SEM), electrochemical impedance spectroscopy and transient photocurrent (I-ph). LSV confirmed the existence of Ago state in the TiO, thin film. SEM and XRD experiments indicated that the sizes of the TiO,, nanoparticles of the resulting films were in the order of TT > AT > TA > AA, suggesting the gradient Ag distribution in the films. The SEM and XRD results also confirmed that Ag had an inhibition effect on the size growth of anatase nanoparticles. Photocatalytic activities of the resulting thin films were also evaluated in the photocatalytic degradation process of methyl orange. The preliminary results demonstrated the sequence of the photocatalytic activity of the resulting films was AT > TA > AA > TT. This suggested that the silver hierarchical configuration can be used to improve the photocatalytic activity of TiO2 thin film.
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The thin films of TiO2 doped by Mn non-uniformly were prepared by sol-gel method under process control. In our preceding study, we investigated in detail, the effect of doping mode on the photocatalytic activity of TiO2 films showing that Mn non-uniform doping can greatly enhance the activity. In this study we looked at the effect of doping concentration on the photocatalytic activity of the TiO2 films. In this paper, the thin films were characterized by UV-vis spectrophotometer and electrochemical workstation. The activity of the photocatalyst was also evaluated by photocatalytic degradation rate of aqueous methyl orange under UV radiation. The results illustrate that the TiO2 thin film doped by Mn non-uniformly at the optimal dopant concentration (0.7 at %) is of the highest activity, and on the contrary, the activity of those doped uniformly is decreased. As a comparison, in 80 min, the degradation rate of methyl orange is 62 %, 12 % and 34 % for Mn non-uniform doping film (0.7 at %), the uniform doping film (0.7 at %) and pure titanium dioxide film, respectively. We have seen that, for the doping and the pure TiO2 films, the stronger signals of open circuit potential and transient photocurrent, the better photocatalytic activity. We also discusse the effect of dopant concentration on the photocatalytic activity of the TiO2 films in terms of effective separation of the photon-generated carriers in the semiconductor. (C) Versita Warsaw and Springer-Verlag Berlin Heidelberg. All rights reserved.
Resumo:
Al-doped and B, Al co-doped SiO2 xerogels with Eu2+ ions were prepared only by sol-gel reaction in air without reducing heat-treatment or post-doping. The luminescence characteristics and mechanism of europium doping SiO2 xerogels were studied as a function of the concentration of Al, B, the europium concentration and the host composition. The emission spectra of the Al-doped and B, Al codoped samples all show an efficient emission broad band in the blue violet range. The blue emission of the Al-doped sample was centered at 437 nm, whereas the B, Al co-doped xerogel emission maximum shifted to 423 nm and the intensity became weaker. Concentration quenching effect occurred in both the Al-doped and B, Al co-doped samples, which probably is the result of the transfer of the excitation energy from Eu2+ ions to defects. The highest Eu2+ emission intensity was observed for samples with the Si(OC2H5)(4):C2H5OH:H2O molar ratio of 1:2:4. (c) 2006 Elsevier B.V. All rights reserved.
Resumo:
A novel inorganic-organic hybrid hydrophobic anti-reflection silica film used for laser crystal was obtained by sol-gel process. The film consisted of silica sols mixed with a small amount of polymethyl methacrylate (PMMA) or polystyrene (PS). The optical transparency, hydrophobic property and surface morphology of the film were characterized by UV-VIS-NIR spectrophotometer; contact angle instrument and Scanning Electron Microscopy (SEM), respectively. The results showed that the anti-reflection coating had good hydrophobility and optical transparency from 400 nm to 1200 nm. The contact angle reached to 130-140 degrees. SEM images indicated the hydrophobic films modified with PMMA or PS had compact structure compared to the pure silica sol film. (C) 2008 Elsevier B.V. All rights reserved.
Resumo:
近年来,纳米杂化技术,尤其是溶胶-凝胶技术为发光材料的发展开辟了一个崭新的途径,但目前这些工作尚处于研究的初始阶段,还有许多问题有待克服,例如:有机染料的热稳定性差,稀土有机配合物在溶胶体系中的溶解性、分散性差,以及发光基质在杂化体系中具有浓度淬灭效应、渗出效应等。为此,我们从分子设计角度去有目的的合成一类新型Sol-gel前体,以此制备出系列有机/无机杂化发光材料,取得了一批有意义的结果。1.经γ-射线辐照原位制备有机/无机纳米杂化材料基于Sol-gel方法及γ-射线辐照技术发明了一种制备有机/无机杂化材料的新方法,并制备了两类有机/无机杂化材料,一类是有机/无机两相间无强相互作用(共价键)的杂化材料,一类是两相间有弱相互作用(氢键)的杂化材料。从材料制备上看,反应条件温和,易控制,解决了长期困扰的样品开裂问题,制备工艺简单,易操作,易于工业化。从材料的结构表征上看,经γ-射线辐照聚合的样品的聚合比较完全,紫外-可见光谱及透射电子显微镜观察结果表明杂化样品中有机相、无 机相分散性良好,杂化是在分了水平上进行的。无机网络的限制不仅提高了杂化样品中聚合物的热稳定性和相转蛮温度,还提高了杂化样品中聚合物的机械力学性能。所发明γ-射线辐照原位制备有机/无机纳米杂化材料技术可以作为相关材料制备的通用方法。2.含有机染料有机/无机纳米杂化发光材料 设计并合成了一种官能化有机染料(可作Sol-gel前体),采用所发明的γ-射线辐照技术制备了两类有机/无机杂化发光材料,一类是相间有强相互作用(共价键)有机/无机的杂化发光材料(HEMA/KH570),一类是两相间只有弱相互作用(氢键)有机/无机杂化发光材料(HEMMTEOS)。所得杂化发光样品透明性良好,在可见光范围内透光率在90%以上,在紫外光下能发射出较强的蓝色(偏紫)荧光。在所研究体系中,随着有机染料浓度的增加,样品的发光强度在逐渐增大,有机/无机组分、组成的变化对杂化材料的荧光行为:荧光发射、荧光激发、荧光寿命影响不大;同有机溶液相比,杂化基体的限制使得有机染料的荧光发射波长发生红移,纯无机基体使之红移位置更大。杂化材料的最强荧光发射波长较染料本体杂化材料的短,表明了有机染料是均匀分散在杂化基体中的。3.含稀土有机/无机纳米杂化发光材料通过所合成的含酰亚胺键的有机芳香羧酸化合物(NP)的稀土配合物的紫外-可见、荧光、磷光光谱探讨了稀土配合物中有机配体与稀土衷心离子的能量传递与能级匹配的关系。钆配合物的低温磷光光谱结果表明,所合成的酰亚胺类芳香羧酸化合物(NP)的最低三重态能级为24690cm~(-1),与稀土铕和铽的能级差分别为7426cm~(-1)和4190cm~(-1)。荧光光谱表明所合成芳香羧酸配体与稀土离子铽的能级匹配性好,与铕离子则较差,即铽的二元配合物的相对荧光效率比铕的高,荧光寿命则几乎相同在2ms左右。在芳香羧酸化合物(NP)的三元稀土配合物中,第二配体1,10-邻菲罗啉(Phen)是能量吸收,传递的主体。同相应二元配合物相比,铕的三元配合物的相对荧光效率提高了三倍,而铽的则降低了一半,三元配合物的荧光寿命为4ms,比二元的长近一倍。所研究稀土配合物的表现的均是基于中心稀土离子的特征跃迁的特征发光,即:Eu~(3+)的5D_0→7F_j (j = 0, 1, 2, 3, 4)跃迁,Tb~(3+)的~5D_4 → ~7F_j (j = 6, 5, 4, 3)跃迁。基于小分子模型配合物的研究,设计并合成了一种新型有机芳香羧酸Sol-gel前体(TAT),从而原位合成了含稀土有机/无机纳米杂化发光材料。荧光光谱表明所制得的有机/无机杂化膜的发光谱带较窄,色纯度较高。在含稀土有机/无机杂化膜中,随着稀土离子浓度的增加,样品相对荧光强度增大,浓度淬灭效应及发光基质的渗出效应在所研究体系中未出现。同小分子稀土配合物相比,含稀土杂化膜的荧光发射谱带窄化、不劈裂、对称性好,而且荧光寿命普遍变小,发光中心趋于单一.透射电镜结果表明所制备含稀土有机/无机杂化膜,不仅有机/无机基体杂化在分子水平上,稀土离子在杂化基体中的聚集结构也在纳米层次上,一般在50~100nm,随着稀土离子浓度的增加,这种聚集结构尺寸略有增大,但小于100nm。通过三基色原理成功地制备了发白色荧光有机/无机杂化材料,该杂化材料在紫外光的激发下可同时发出红、绿、蓝三种荧光,色坐标测试结果为:X = 0.314,Y = 0.316,该位置已接近等能量白光色坐标的理论值X = 0.33,Y = 0.33,又接近实际显示的需要,有一定的理论及实践意义。