溶胶—凝胶法制备高强度二氧化硅增透膜的研究

以正硅酸乙酯（ＴＥＯＳ）为原料，用溶胶－凝胶（ＳＯＬ－ＧＥＬ）法在碱性催化条件下制睾一氧化硅膜，经氨气氛和热处理工艺，提高了二氧化硅透膜的拭和抗氙灯辐照能力，可用于激光器泵浦光学元件的增透。在５７０－８００ｎｍ范围内，双面涂的Ｋ９下班的平均透过率可提高到９８％以上。     

二氧化硅增透膜微观结构与激光损伤阈值的调控

采用溶胶-凝胶技术制备了二氧化硅增透膜,通过向溶胶中添加高分子聚乙烯醇缩丁醛（PVB）,调控胶体的粒径,进而控制膜层微观结构,研究膜层微观结构与激光损伤阈值的关系。纳米粒度仪和扫描探针显微镜测试表明：PVB加入溶胶后,控制了二氧化硅胶粒的生长,使二氧化硅胶粒生长更均匀,因而膜层的微观结构更均匀。当PVB质量分数为1%时,胶体粒径为15 nm,分散系数小于0.1。用该胶体镀膜,膜层均匀,表面粗糙度小于3.25 nm。并且PVB加入后增加了膜层胶粒间的黏附性,使得膜层强度增大。PVB加入使膜层的激光损伤阈值有所增加。当PVB的添加量为1%时,膜层的激光损失阈值从30.0 J/cm2增加到40.1 J/cm2。膜层激光损伤阈值的增加与膜层微观均匀性和物理强度的增加有关。     

二氧化硅增透膜微观结构与激光损伤阈值的调控

采用溶胶-凝胶技术制备了二氧化硅增透膜,通过向溶胶中添加高分子聚乙烯醇缩丁醛（PVB）,调控胶体的粒径,进而控制膜层微观结构,研究膜层微观结构与激光损伤阈值的关系。纳米粒度仪和扫描探针显微镜测试表明:PVB加入溶胶后,控制了二氧化硅胶粒的生长,使二氧化硅胶粒生长更均匀,因而膜层的微观结构更均匀。当PVB质量分数为1%时,胶体粒径为15 nm,分散系数小于0.1。用该胶体镀膜,膜层均匀,表面粗糙度小于3.25 nm。并且PVB加入后增加了膜层胶粒间的黏附性,使得膜层强度增大。PVB加入使膜层的激光损伤阈值有所增加。当PVB的添加量为1%时,膜层的激光损失阈值从30.0 J/cm2增加到40.1 J/cm2。膜层激光损伤阈值的增加与膜层微观均匀性和物理强度的增加有关。     

新型溶胶-凝胶二氧化硅微孔增透膜的制备及性能研究

以正硅酸乙酯为前驱体,二甲基二乙氧基硅烷为造孔剂,采用溶胶凝胶技术在酸催化条件下制备了二氧化硅溶胶;采用提拉法在K9玻璃基片上双面镀膜,经500 ℃热处理,制备得到一种新型单层微孔二氧化硅增透膜。通过改变造孔剂加入量,膜层峰值透过率可达到99.7％,而硬度仍保持在2H以上,同时具有良好的耐摩擦性及粘附性。加速腐蚀实验表明,膜层的环境稳定性是常规膜层的10倍以上。由于该新型增透膜兼具高透过率、良好的机械性能以及很强的环境稳定性,因而在改善太阳能玻璃增透性能方面有极大的应用价值。     

掺氟SiO2增透膜真空环境抗污染能力

以正硅酸乙酯为前驱体,采用氨水为催化剂配制SiO2溶胶,在胶体陈化过程中掺入十二氟庚基丙基三甲氧基硅烷对胶体进行改性,并采用溶胶 凝胶法在K9基片上制备了改性的二氧化硅增透膜,用红外光谱仪、分光光度计、原子力显微镜、椭偏仪、静滴接触角测量仪、N2吸附-脱附对膜层性质进行了分析。结果表明：掺氟的二氧化硅膜层增透膜峰值透光率为99.7%;与水的接触角为129°;与二甲基硅油的接触角达到86°;膜层真空抗污染能力比掺氟前大大提高。     

利用氟硅烷提高溶胶-凝胶SiO2增透膜的疏水性

 以正硅酸乙酯为前驱体，氨水为催化剂，采用溶胶 凝胶法制备了二氧化硅增透膜；通过自组装技术，用氟硅烷对膜层进行表面修饰，制得了疏水增透膜，克服了常规增透膜亲水的缺点。采用红外光谱、分光光度计、扫描探针显微镜和静滴接触角测量仪等测试手段分析了薄膜的特性。结果表明：疏水增透膜的峰值透光率为99.7％，疏水角为110°；氟硅烷自组装改性不影响二氧化硅增透膜的光学性能。     

利用氟硅烷提高溶胶-凝胶SiO2增透膜的疏水性

以正硅酸乙酯为前驱体,氨水为催化剂,采用溶胶 凝胶法制备了二氧化硅增透膜;通过自组装技术,用氟硅烷对膜层进行表面修饰,制得了疏水增透膜,克服了常规增透膜亲水的缺点。采用红外光谱、分光光度计、扫描探针显微镜和静滴接触角测量仪等测试手段分析了薄膜的特性。结果表明：疏水增透膜的峰值透光率为99.7％,疏水角为110°;氟硅烷自组装改性不影响二氧化硅增透膜的光学性能。     

SiO_2光学增透膜的制备及光学性能

在碱催化体系中以正硅酸乙酯 (TEOS)为前驱体制得SiO2 溶胶 ,采用旋转镀膜法 (spin coating)制备SiO2 光学增透膜。研究了在不同制备条件下对膜层光学性质的影响 ,推算了膜层的折射率及厚度 ,并由此给出膜层孔隙率以及膜层的厚度与转速的关系     

掺氟SiO_2增透膜真空环境抗污染能力

以正硅酸乙酯为前驱体,采用氨水为催化剂配制SiO2溶胶,在胶体陈化过程中掺入十二氟庚基丙基三甲氧基硅烷对胶体进行改性,并采用溶胶-凝胶法在K9基片上制备了改性的二氧化硅增透膜,用红外光谱仪、分光光度计、原子力显微镜、椭偏仪、静滴接触角测量仪、N2吸附-脱附对膜层性质进行了分析。结果表明:掺氟的二氧化硅膜层增透膜峰值透光率为99.7%;与水的接触角为129°;与二甲基硅油的接触角达到86°;膜层真空抗污染能力比掺氟前大大提高。     

水解反应温度对溶胶-凝胶SiO2增透膜光学性能的影响

在制备高激光损伤阈值溶胶-凝胶二氧化硅增透膜的工艺中,水解反应温度对镀膜溶胶的形成和薄膜的光学性能都有很大影响。本文较为详细地研究了这一重要工艺多数对镀膜溶胶的颗粒度、分散性、稳定性的影响,以及它对薄膜增速效果的影响。     

单甲基原位改性SiO2疏水减反膜的制备与性能研究

 在碱性条件下通过TEOS和MTES的共水解缩聚反应制备了单甲基原位改性的SiO₂溶胶，并使用提拉法在K9玻璃基片上镀制了疏水减反膜。通过透射电镜（TEM）考察了镀膜溶胶的微结构，分别使用红外光谱（FTIR）分析了薄膜的组分，用原子力显微镜（AFM）观察了薄膜的表面形貌和起伏状况，用紫外可见光谱（UV-vis）考察了薄膜的减反射性能，用接触角仪测量了薄膜对水的接触角。并使用“R-on-1”的方式测量了薄膜在Nd:YAG激光（1 064 nm，1 ns）作用下的损伤阈值。结果表明，通过共水解缩聚反应可以把甲基引入镀膜溶胶簇团中，改善了溶胶簇团的网络结构，使薄膜得到相当好的疏水性能和更好的抗激光损伤性能，同时薄膜能保持较好的减反射性能。     

抗真空有机物污染增透膜特性分析

 采用溶胶-凝胶法,结合氨水后处理工艺制备了抗真空有机物污染的二氧化硅增透膜。该膜峰值透光率为99.8%,在有机污染的真空系统中(10^-3 Pa)保持168 h,透光率曲线变化微小,而同样条件下常规二氧化硅增透膜的峰值透光率下降至95.5%。并采用分光光度计、红外光谱、扫描探针显微镜、静滴接触角测量仪、椭偏仪等测试手段分析了薄膜的特性。     

Study on antireflective coatings of PbTe/PbSnTe heterojunction infrared detectors

ZnS antireflective coatings and passivation layer are developed on self-made PbTe/PbSnTe heterojunction infrared detectors and following experiments have been finished: WaterProof properties of ZnS coatings; Anti-reflective properties of PbSnTe materials and their detectors with ZnS coatings, respectively; ageing and stability tests of the PbSnTe detectors with ZnS coatings.All experimental results are excellent: The typical detectivity (D^*) of PbSnTe detector is 2.83×10¹⁰ cmHz^1/2W^–1. (with peak wavelength p=9.8 m and cut-off wavelength c=11.7 m). Average detectivity of the PbSnTe detector with ZnS anti-reflective coatings is increased by 45%. Ageing tests indicated that the PbSnTe detectors with ZnS coatings have still high stabilities after several years. They are used successfully in medical infrared imaging systems and other applications.     

PEG200改性SiO_2溶胶制备光学增透膜的研究

采用ＴＥＭ、ＳＤＰ 等分析手段对ＰＥＧ２００ 改性的ＳｉＯ２ 溶胶制备参数与光学增透膜的性质进行了研究。结果表明：ＰＥＧ２００ 改性后的ＳｉＯ２ 溶胶簇团粒度分布与交联状况发生显著变化,形成不同的网络结构特征,由此影响膜层的光学增透性能。     

Preparation and Characterization of Poly(Vinyl Alcohol) (PVA)/SiO2, PVA/Sulfosuccinic Acid (SSA) and PVA/SiO2/SSA Membranes: A Comparative Study

Abstract

New organic–inorganic nanocomposites based on PVA, SiO₂ and SSA were prepared in a single step using a solution casting method, with the aim to improve the thermomechanical properties and ionic conductivity of PVA membranes. The structure, morphology, and properties of these membranes were characterized by Raman spectroscopy, small- and wide-angle X-ray scattering (SAXS/WAXS), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA), water uptake (Wu) measurements and ionic conductivity measurements. The SAXS/WAXS analysis showed that the silica deposited in the form of small nanoparticles (～ 10?nm) in the PVA composites and it also revealed an appreciable crystallinity of pristine PVA membrane and PVA/SiO₂ membranes (decreasing with increasing silica loading), and an amorphous structure of PVA/SSA and PVA/SSA/SiO₂ membranes with high SSA loadings. The thermal and mechanical stability of the nanocomposite membranes increased with the increasing silica loading, and silica also decreased the water uptake of membranes. As expected, the ionic conductivity increased with increasing content of the SSA crosslinker, which is a donor of the hydrophilic sulfonic groups. Some of the PVA/SSA/SiO₂ membranes had a good balance between stability in aqueous environment (water uptake), thermomechanical stability and ionic conductivity and could be potential candidates for proton exchange membranes (PEM) in fuel cells.     

PVA nano composite membrane for DMFC application

A new PEM composite membrane comprising of polyvinyl alcohol (PVA), sulfonic acid functionalized CNT and fluorinated MMT has been fabricated. Composite polymer membrane has been prepared by simple solution casting method. Composite properties have been evaluated by using thermal gravimetric analysis (TGA), scanning electron microscopy (SEM), and FTIR techniques. The proton conductivity, methanol crossover and water uptake properties of newly fabricated membrane have been studied. The polymer membrane shows good thermal properties. The water content is in the range of 35-45%. Especially, it has been found that the fluorinated MMT used in this study plays a decisive role in water uptake and acts as a hydrophobic surface for controlling the swelling. The proton conductivities and the methanol permeabilities of all the membranes are in the range of 10^− 3 to 10^− 2 S/cm and 2.08 × 10^− 6 cm²/s at room temperature, respectively.     

溶胶凝胶法制备PMMA/SiO2杂化材料

 针对目前PMMA/SiO₂杂化材料制备过程中容易出现的相分离问题，采用原位聚合和同步溶胶凝胶过程制备了聚合物链段与无机组分间有化学键作用的PMMA/SiO₂杂化材料，并应用透射电子显微镜、红外光谱分析仪、X射线衍射分析仪、热失重分析仪等对不同SiO₂含量的PMMA/SiO₂杂化材料的形貌及结构进行了研究。结果表明：SiO₂含量在20%～60%间的PMMA/SiO₂杂化体系没有明显的相分离现象，SiO₂含量在20%～40%间的杂化体系的透光性较好。