The investigation of photoluminescence centers in porous alumina membranes

To investigate the origin of blue photoluminescence (PL) in porous alumina membrane, we have prepared an anodic aluminum oxide film with a pore diameter of 40 nm in oxalic acid solution by a two-step anodization process. Our results show that the as-prepared alumina membrane is amorphous and exhibits a broad emission band peaking at around 452 nm with two sub-peaks located at 443 nm and 470 nm. As indicated by the PL excitation spectra, there are two excitation peaks which can account for the sub-peaks observed in the PL emission band. We have proposed that the broad emission band with two sub-peaks can be attributed to two luminescence centers in porous alumina membranes, namely, oxygen defects and oxalic impurities. Furthermore, we have rationalized that the two emission centers show similar influence on the PL band in the blue region based on a simple model. PACS 81.07.-b; 81.16.Dn; 79.60.Jv     

液相基质中重金属元素激光诱导击穿光谱实验参数的优化

针对混合溶液中重金属元素的激光诱导击穿光谱(LIBS)测量系统,为提高测量系统的检测灵敏度,以提高混合溶液中Ca和Cr金属元素LIBS光谱线强度的信噪比为目标,对LIBS测量系统中的激光脉冲能量、液相样品流速、ICCD门宽、延时等实验参数进行了优化,得到最优化参数激光脉冲能量、样品流速、ICCD门宽、延时分别为35 m J、30 ml/min、1400 ns和2400 ns,为降低LIBS技术应用于混合溶液中痕量重金属元素的检出限提供了实验参数支撑.     

二氧化碳分子离子经由Ã2Πu1/2电子态振动能级共振的光解动力学：一项时间切片离子速度成像技术研究

We report on the photodissociation dynamics of CO₂⁺ via its òΠ_u,1/2 state using the scheme of [1+1] photon excitation that is intermediated by the mode-selected òΠ_u,1/2( u1,u2,0) vibronic states. Photodissociation fragment exciation spectrum and images of photofragment CO⁺ have been measured to obtain reaction dynamics parameters such as the available energy and the average translational energy. Combining with the potential energy functions of CO₂⁺, the dissociation mechanism of CO₂⁺ is discussed. The conformational variation of CO₂⁺ from linear to bent on the photodissociation dynamics of CO₂⁺ is verified.     

BSA-SDS-Ag聚合物纳米微粒的制备及水凝胶性质的研究(Ⅱ)

本文报道用X－射线衍射（XRD），TEM和FTIR光谱考察了在不同的制备条件下BSA－SDS－Ag的SDS－Ag聚合物纳米微粒的结构，形貌以及表面性质，随制备条件的不同，微粒的表面形貌有很大的差异。体系在微也液状态下，用甲醛作还原剂，可把银离子还原为单质，进而聚集成包裹型的团状微粒，微粒粒径32－60nm；微粒表面结构复杂，表明Ag^＋先后与蛋白质中的某些氨基酸残基产生化学键合，再还原为Ag粒，进而聚合成网状结构的聚合物。     

源气体对沉积的a-C∶F∶H薄膜结构的影响

采用微波电子回旋共振等离子体化学气相沉积(MWPECRCVD)方法,使用不同的源气体(CHF3CH4,CHF3C2H2,CHF3C6H6)体系制备了aC∶F∶H薄膜.由于CH4,C2H2,C6H6气体在等离子体中的分解反应不同导致了薄膜的沉积速率和结构上的差异.红外吸收谱的结果表明,用C6H6CHF3作为源气体沉积的薄膜中几乎不含H,而用C2H2CHF3所沉积的薄膜中的含氟量最高,其相应的CF振动峰位向高频方向偏移.薄膜的真空退火结果表明,aC∶F∶H薄膜的热稳定性除了取决于薄膜的CC键浓度外,还与CC键 关键词： 氟化非晶碳膜 电子回旋共振化学气相沉积 红外吸收光谱     

氢离子与碳膜相互作用的实验研究

此文报道了H+、H+2和H+3离子通过碳膜后,在其中产生的各种微量产物的测量结果.讨论了离子与碳膜作用中的电荷交换过程.分析了这些微量产物的形成机理.实验证明在产物的形成中电荷交换过程起关键作用.研究了离子与碳膜作用中的团簇效应和尾流效应.     

植物研究用γ射线成像系统设计

为了利用正电子发射断层成像技术在植物生理功能研究中的优势,正在开发由两个探测器相向放置构成的γ射线成像系统.系统中采用的探测器是由10×10的氧正硅酸镥(LSO)晶体阵列与滨松R5900-C12耦合组成.单个LSO尺寸为1.8mm×1.8mm×10mm.根据PET应用的特点,测试了该探测器的性能.所有闪烁晶体的图像在位置图谱中清楚可见;511keV全能峰处的能量分辨率位于14.5%—22%之间;符合时间分辨率随着位置灵敏光电倍增管的供给电压的增加而得到改善.这些实验结果表明,该LSO探测器适于构造高分辨率的双探测器成像系统.     

聚酰胺酸合成工艺研究

 采用超声波在线测量溶液粘度的方法，研究了合成聚酰胺酸过程中实验条件的影响，并对实验结果进行分析，由此确定了合成高分子量聚酰胺酸的最佳实验条件。研究表明：在加料次序为先加二胺后加二酐（二酐与二胺的摩尔比为1.01～1.02：1）、试剂中含水量尽可能少，反应温度0～5℃、反应时间以溶液粘度到达最大值为止的条件下，所合成的聚酰胺酸溶液粘度最大，可满足惯性约束聚变（ICF）充气腔靶端口膜的需要。     

高温高压下绿辉石成因研究

在3 GPa,1 200 ℃条件下,分别以碱性玄武岩粉末和等化学计量光谱纯试剂为原料进行高温高压熔融结晶实验,对实验产物进行了电子探针测试和拉曼光谱分析,确定结晶产物为绿辉石,其拉曼谱峰的半高宽较窄且形态尖锐,表明绿辉石晶体中Si—O四面体结构稳定,矿物内部有序度高。结合前人研究成果探讨了绿辉石成因的影响因素及其原始岩浆,结果表明绿辉石的形成可能受母岩成分、体系流体含量和温压条件等多种因素影响。本实验结果为绿辉石和榴辉岩成因学研究提供可能的实验依据。     

Brittle-Ductile Transition of Ferroelectric Ceramics Induced by Thermally Activated Dislocation Emission

Thermally activated dislocation emission in high-temperature ferroelectric ceramics is investigated through an assumption of thermal stability and a novel analytical method. The stress intensity factor (SIF) arising from domain switching is evaluated by using a Green's function method, and the critical applied electric field intensity factor (CAEFIF) for brittle fracture at room temperature is obtained. Besides, the lowest temperature for single dislocation emission before brittle fracture is also obtained by constructing an energy balance. The multi-scale analysis of facture toughness of the ferroelectric ceramics at high temperature is carried out. Through the analysis, the CAEFIF for crack extension is recalculated. The results show that the competition and interaction effects between dislocation emission and brittle fracture are very obvious. Besides, the higher critical activation temperature, the more columns of obstacles will be overcome. Additionally, the shielding effect arising from thermally activated dislocations is remarkable, thus, the brittle-ductile transition can promote the fracture toughness of high-temperature ferroelectric ceramics.