掺Fe(Ⅲ)的A-TiO_2的水热法制备、表征及其光催化活性分析

一定条件下用水热法制备了的掺Fe(Ⅲ)的TiO2晶体,XRD分析结果表明它是锐钛矿型Fe(Ⅲ)的TiO2(A-TiO2).研究了以自制的掺Fe(Ⅲ)的A-TiO2为光催化剂对罗丹明B溶液的降解性能.结果表明,在5 mg/L的罗丹明B溶液中,加入0.1650 g自制的掺Fe(Ⅲ)的5%的A-TiO2,用硝酸调节溶液PH=5后,可见光照射下,43℃恒温磁力快速搅拌反应6 h,罗丹明B降解率为76.5%;同样条件下经254nm紫外光照6 h,降解率达到95.7%.     

高超声速再入试验的辐射光谱定量测量

利用膨胀管对宽度为45 mm和90 mm的半圆柱模型进行了地球再入高超声速流动试验,再入速度为8 km/s。试验利用配有ICCD相机的光谱仪,测量了具有空间分辨的激波后辐射光谱,光谱范围为250~550 nm,得到了沿流体方向的激波辐射轮廓线。分析发现在该光谱范围内辐射主要为CN(B-X)带系分子光谱。利用卤钨灯对该波段光谱进行定标,得到了激波层辐射的绝对辐射亮度。通过采用两种模型辐射亮度对模型宽度归一化后发现,绕流场高温气体辐射存在较强的自吸收现象,同时观测到了绕流场激波的三维效应。通过实验发现,CN(B-X)Δv=0带系的3-3振动带系385.2 nm波长位置和0-0带系388.4 nm波长位置辐亮度之比随着流场靠近模型边缘而逐渐下降,这表明激波层内辐射的动态非平衡特征。     

氧化锌量子点和碳量子点及其复合物的制备与发光性能的研究

采用溶胶凝胶方法和水热法制备了水溶性荧光氧化锌量子点(Zn O-QDs)和碳量子点(C-QDs),其量子效率分别达到38%和61%。基于所合成的Zn O-QDs和C-QDs制备了氧化锌和碳量子点复合物(Zn O/CQDs),并分别对其发光特性进行了研究。透射电镜(TEM)图像表明,所合成的Zn O-QDs和碳量子点尺寸分布在3~6 nm之间,分散均匀。光致发光光谱表明,Zn O-QDs和碳量子点的发光峰中心分别位于540 nm和450 nm,两者发光峰的最佳激发波长为370 nm和350 nm。通过调整Zn O-QDs和C-QDs的体积比,所制备的Zn O/C-QDs能够实现荧光光谱的连续可调,并产生了白色荧光。     

新型蓝色磷光嘧啶铱(Ⅲ)配合物的合成及发光性质

设计并合成了以2-(2,4-二氟苯基)嘧啶(DFPPM)为主配体的两种新型二嗪铱配合物 (Ph:苯基)和,用核磁共振(NMR)和质谱等方法对其进行了表征,并用紫外-可见吸收光谱和光致发光光谱对其光学性质进行了研究。光致发光光谱结果显示:配合物 的发射峰波长为472 nm和489 nm;而配合物 的发射峰波长为447 nm和472 nm,1931CIE色度坐标为(0.14,0.15),是一种深蓝色磷光材料。以 为客体材料、PVK为主体材料制备了电致发光器件,研究了其电致发光光谱。结果表明,电致发光光谱与光致发光光谱相比有较大程度的红移。     

Ce:YAG晶体和透明陶瓷的光学和闪烁性能

采用温梯法生长了Ce:YAG晶体和真空烧结法制备了Ce:YAG透明陶瓷,并对晶体和透明陶瓷的光学和闪烁性能进行了对比研究.Ce:YAG晶体和陶瓷都具有位于230,340和460 nm波段的Ce³⁺离子的特征吸收带和540 nm附近的发射峰,但Ce:YAG晶体同时存在296和370 nm的色心吸收,其发射峰位于398 nm,而透明陶瓷中不存在.Ce:YAG晶体和陶瓷的X射线荧光中均存在520 nm附近的Ce³⁺离子发射,但晶体中还存在由反格位缺陷引起的300 nm 关键词： Ce:YAG 闪烁晶体 透明陶瓷     

Quantitative measurement of CN radical in a low-pressure methane/air flame by cavity ring-down spectroscopy

The ultrasensitivity of the cavity ring down spectroscopy technique has been used to detect the minor CN species in a premixed rich (φ=1.2) methane/air flame stabilized at 53 hPa. The CN radical has been probed around 387 nm on the B–X (0–0) band. A peak concentration of 4.7·10⁹ cm⁻³ has been measured which corresponds to a mole fraction of 0.022 ppm. A detection limit of a few ppb has been reached despite the presence of an important off-resonance background due to the flame.     

Diode-pumped femtosecond Yb:CaNb2O6 laser

We report to our knowledge a diode-pumped passively mode-locked Yb:CaNb(2)O(6) (Yb:CN) laser for the first time. Both CW and passive mode-locking operation of the laser are experimentally investigated. A maximum CW output power of 1.4 W with a slope efficiency of 20% is obtained on a 7 mm long 1.5 at.% Yb:CN crystal, while stable passive mode-locking with a commercial semiconductor saturable absorption mirror (SESAM) was achieved on a 3 mm long 3 at.% Yb:CN crystal. The mode-locked pulses have pulse width of 251 fs and an average output power of 44 mW at 1038 nm.     

室温氧化还原反应制备AgCuSe三元纳米棒

在室温下通过氧化还原反应制备了AgCuSe三元纳米棒.用X射线粉末衍射、透射电镜和X射线光电子能谱对产物进行了表征.X射线粉末衍射结果表明,产物是四方相AgCuSe;透射电镜结果表明,产物是纳米棒,其直径为5～20nm,长度为200～600nm;X射线光电子能谱结果表明,产物的纯度是很高的,没有单质Ag、Cu等杂质.应用化学热力学原理讨论了产物AgCuSe的生成机理.热力学计算表明,在这个反应体系中最终产物是纯AgCuSe.溶剂乙二胺不仅作为双齿配体与Ag+和Cu+形成稳定的配合物,而且还能溶解金属硒、增强硒的反应性,乙二胺在控制AgCuSe的成核和纳米棒的生长过程中起着重要的作用.     

Nature of the adhesion bond between epoxy adhesive and steel

The potential difference that appears in the epoxy resin located between two grade 3 steel plates is studied. One of them is stored in epoxy resin to reach equilibrium, and the second plate is coated with an asprepared mixture of epoxy resin with a hardener. It is found that the potential difference decreases in time because of charge transfer by Fe²⁺ ions through epoxy resin. The luminescence and infrared absorption spectra of the epoxy adhesive on the grade 3 steel surface are recorded. An analysis of these spectra shows that Fe²⁺ ions penetrate into the as-prepared mixture of epoxy resin with the hardener, and interact with CN groups in the mixture, and form coordination compounds. As a result, a diffusion layer saturated by the coordination compounds forms at the interface between the steel and the adhesive.     

Synthesis of porous and trigonal TiO2 nanoflake, its high activity for sonocatalytic degradation of rhodamine B and kinetic analysis

Porous and trigonal TiO(2) nanoflakes (p-TiO(2)) have been synthesized via a simple hydrothermal calcination process, and characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), and UV-vis absorption/reflection spectroscopy (UV-vis). The X-ray diffraction patterns of the as-prepared samples show that p-TiO(2) has an anatase structure. Transmission electron microscopy images indicate that p-TiO(2) consists of sheet-like particles with numerous pores about 100nm in diameter. Ultraviolet-visible reflection spectroscopy exhibits that the absorption edge acquires a blue shift with increased calcination temperature. The effects of the calcination temperature, catalyst dosage, and initial rhodamine B (RhB) concentration on the sonocatalytic activity for removing RhB are investigated in detail. The results show that the as-prepared p-TiO(2) obtained at the optimal calcination temperature of 600°C exhibits a higher sonocatalytic activity than commercial P25. Based on the effects of the initial RhB concentration on sonocatalytic activity, the sonocatalytic degradation kinetics of RhB is also investigated.     

225∽260 nm波段溴化氰光解动力学系统性研究

本文报道了在自行搭建的时间切片离子速度成像装置上进行的225∽260 nm波段内溴化氰光解动力学的研究. 在该波段内选取了若干溴原子(²P_3/2或²P_1/2)的共振线对产物溴原子的共振电离并采集其切片影像,得到了光解产物的总平动能谱,进而获得了产物氰基的振转态布居等信息. 本文发现了在Br^*通道,产物氰基的内能激发比Br通道低;Br和Br^*通道产物氰基振动的最高布居分别为v=0和1. 另外,还发现对于Br通道,溴化氰分子在长波处与短波处解离时,氰基产物的振转激发差异很大,这揭示了其显著不同的光解动力学.     

亚稳态能量转移发射光谱法的研究—挥发性有机物的分析特性

本文提出了采用微波放电获得亚稳态活化氮。有机化合物与活化氮混合后产生CN基团,考察了各实验参数对CN发射强度的影响。在388.3nm处测定CN带发射,对一些挥发性有机化合物测试结果表明,检出限为ng级。并对活化氮的化学活性进行了初步的探讨。     

Growth,structure, and cathodoluminescence of Dy-doped ZnO nanowires

Dy-doped ZnO nanowires have been prepared using high-temperature and high-pressure pulsed-laser deposition. The morphology, structure, and composition of the as-prepared nanostructures are characterized by field emission scanning electron microscopy, X-ray diffraction, Raman scattering spectrometry, X-ray photoelectron spectrometry, transmission electron microscopy, and energy dispersive X-ray spectroscopy. The alloying droplets are located at the top of the as-prepared Dy-doped ZnO nanowires, which means that the growth of the Dy-doped ZnO nanowires is a typical vapor-liquid-solid process. The luminescence properties of Dy-doped ZnO nanowires are characterized by cathodoluminescence spectra and photoluminescence spectra at low temperature (8 K). Two peaks at 481 and 583 nm, respectively, are identified to be from the doped Dy³⁺ ions in the CL spectra of Dy-doped ZnO nanowires.     

Eu3+掺杂2ZnO·2.2B2O3·3H2O红色荧光粉的发光性能

采用水热法合成2ZnO.2.2B2O3·3H2O:Eu3+红色荧光粉.其形貌、结构和光学性能分别用扫描电镜、X射线衍射和荧光光谱进行表征.扫描电镜图片显示样品的尺寸分布在0.1～1 μm范围内.随着Eu3+掺杂浓度的升高,样品向无定形的玻璃态转变.当激发波长为253 nm(属于Eu3+ -O2 -电荷迁移带吸收)时,样...     

BaWO4∶Eu3+红色荧光粉的水热制备及其发光性能

采用水热法,通过变化水热反应时间制备出不同的BaWO₄∶Eu³⁺样品,利用XRD和SEM分析了样品的晶体结构和表面形貌,研究了基质晶体生长取向对BaWO₄中Eu³⁺离子特征发射的影响。实验结果表明:BaWO₄∶Eu³⁺样品在395 nm近紫外光或464 nm蓝光激发下发射578,592,612 nm的红光,其中612 nm(⁵D₀→⁷F₂)发射强度明显高于592 nm (⁵D₀→⁷F₁)。在水热温度160 ℃的情况下,所制备的样品均为四方相,不同的水热反应时间将影响晶体在各晶向的生长速度,进而影响晶体的对称性和发光性能。水热时间为10 h时的发射强度最大。     

Synthesis, characterization, and luminescent properties of Lu2O3:Eu phosphors

Eu-doped lutetia (Lu₂O₃:Eu) nano-phosphors were synthesized by the sol-gel combustion process from a mixed aqueous solution of europium and lutetium nitrates, using organic glycine as the fuel. Powder X-ray diffraction shows that cubic Lu₂O₃:Eu crystallites are directly obtained by the sol-gel combustion process without further calcination. Electron microscopy reveals that the as-prepared phosphors are agglomerated and have a fluffy, fine, and porous morphology, consisting of primary particle size of 8-10 nm. The excitation spectrum is characterized by three dominant bands centered at 395, 466, and 534 nm, respectively. Both the photoluminescent and radioluminescent spectra are very similar and exhibit intense emission peaks centered at 612 nm due to ⁵D₀→⁷F₂ transition of Eu³⁺ ions. The energy transfer from Lu₂O₃ host to Eu³⁺ activator is more efficient in the case of calcined phosphors than for the as-prepared phosphors due to their improved lattice perfection.     

Charge transport and prototypical optical absorptions in functionalized zinc phthalocyanine compounds: A density functional study

Metal phthalocyanines are considered to be prominent candidates for designing organic semiconductors. However, enhancing n‐type characteristics and air stability in these compounds have been the major challenges. Earlier studies on zinc phthalocyanines (ZnPc) reported enhancement in electron mobility due to fluorination. We present a theoretical study of the charge transfer and optical properties of functionalized zinc phthalocyanines (XZnPc, with X = F₁₆, Cl₁₆, Br₁₆, I₈, and (CN)₈) within the framework of the density functional theory. Substitutions with electron‐withdrawing groups at the peripheral sites of ZnPc was found to lower both E_HOMO and E_LUMO in the compounds. Computed values of electron affinity (EA) > 3 eV in all XZnPcs indicated effective electron injection inferring enhanced n‐type characteristics and air stability in these compounds. However, cyanation ((CN)₈), as compared to the other EWGs, is found to enhance the electron mobility more prominently in the compound. In addition, studied optical absorption spectra of all XZnPc compounds at different exchange‐correlation functionals such as B3LYP, PBE0, CAM‐B3LYP, wB97xD, M06, and M06‐2X exhibited Q‐band in visible region (～600‐700 nm) and B‐band (Soret) in ultraviolet (～300‐400 nm) region, and a few shows an N‐band below 300 nm. Upon functionalization, the B‐band and Q‐band maxima show bathochromic shift both in gas phase and dimethyl sulfoxide. All these optical absorptions were found to be prototypical in nature, and the spectra are assigned to character.     

Tailoring optical properties of TiO2 nanowires coated with Ag nanoparticles by plasmon coupling of Ag nanoparticles

TiO₂ nanowires were grown on titanium foil by an alkali hydrothermal growth method. The as-synthesized nanowires are structurally uniform with diameters of 50-100 nm and lengths of up to a few micrometers. The as-prepared TiO₂ nanowires were coated with Ag nanoparticles by reducing AgNO₃ in solution. The experimental results indicate that the Ag nanoparticles can aggregate together on the surfaces of TiO₂ nanowires by interconnection between nanoparticles. The degree of aggregation of Ag nanostructures can be controlled by changing the concentrations of Ag nanoparticles. The as-prepared nanostructures exhibit a wide optical absorption from 387 to 580 nm that can be easily tuned by controlling the degree of aggregation of Ag nanostructures. The results reveal that optical properties of the Ag-coated TiO₂ nanowires can be enhanced by plasmon coupling of Ag nanoparticles. The as-prepared nanostructures may find potential applications in the field of solar cells.     

以巯基丙酸为稳定剂的水溶性CdTe量子点的水热合成及表征

以巯基丙酸(MPA)为稳定剂,采用水热合成方法在160 ℃下合成水溶性CdTe量子点。研究了不同反应时间及反应前驱体溶液的不同pH值对合成的CdTe量子点光学性质的影响。结果表明:所制得的CdTe量子点的荧光发射波长在510~661 nm范围内连续可调,并且CdTe量子点的光学性质强烈地依赖于反应前驱体溶液的pH值,最佳pH值为9。透射电子显微镜和X射线衍射分析表明所制备的CdTe量子点的形状接近于球形,粒径分布较均匀。与回流方法制备的水溶性量子点相比,高温条件下的水热合成方法简单,反应时间短,CdTe量子点生长速度快,100 min就可生长到3.5 nm,并且所制得的CdTe量子点荧光强度高,稳定性好,荧光量子产率也较高,最高可达44.6%。     

硅包覆上转换纳米晶制备和表征及生物特异性标记研究

以NaYF₄为代表的上转换纳米晶作为细胞及组织标记的研究越来越热。但易团聚,水溶性、生物兼容性差,没有与生物偶联官能团等缺点限制了其应用,因而表面修饰显得尤为重要。作者通过水热和共沉淀相结合方法,制备了NaYF₄∶Yb3+, Er3+上转换纳米晶,并对其包覆二氧化硅壳层。SEM表征硅包覆前后分别为25和250 nm的单分散粒子,说明硅已成功地包覆于纳米晶表面。980 nm激光照射下,样品的PBS胶体溶液呈可视上转换绿光。上转换荧光光谱和寿命均表明二氧化硅壳层对其发光性质影响很小。圆二色谱说明蛋白分子通过戊二醛与纳米晶偶联前后的二级结构基本不变。基于硅片上的抗原抗体荧光免疫识别试验进一步验证了偶联蛋白分子的特异性,表明该上转换纳米晶适合于生物标记。