退火对Pb辐照Al2O3单晶发光特性的影响

研究了230MeV的²⁰⁸Pb²⁷⁺辐照Al₂O₃样品及随后在600,900,1100K高温条件下退火后的光致发光特性。从辐照样品的测试结果可以清楚地看到在波长为390,450nm处出现了强的发光峰。辐照量为1×10¹³ions/cm²时,样品的发光峰最强。经过600K退火2h后测试结果显示,380nm发光峰剧烈增强,而其他发光峰显示不明显。在900K退火条件下,380nm的发光峰开始减弱,而在360,510nm出现了明显的发光峰,至到1100K退火完毕后380nm的发光峰完全消失,而360,510nm的发光峰相对增强。从被辐照样品的FTIR谱中看到,波数在460~510cm^-1间的吸收是振动模式,经过离子辐照后,吸收带展宽,随着辐照量的增大,Al₂O₃振动吸收峰消失,说明Al₂O₃振动模式被完全破坏。1000~1300cm^-1之间为Al—O—Al桥氧的伸缩振动模式,辐照后吸收带向高波数方向移动,说明其振动模式受到影响。辐照剂量较小的样品,损伤程度相对较低,经退火晶化后,振动模式基本恢复到单晶状态;辐照剂量较高的样品,损伤程度大,退火处理后表面变得较粗糙,振动模式并未出现,说明结构破坏严重。     

85MeV19F重离子辐照α–Al2O3的空洞研究

5.28×10¹⁶cm^－2 85MeV¹⁹F辐照的αAl₂O₃中,在其热退火过程中采用正电子湮没方法首次观察到了空洞.450℃退火开始产生空洞,550℃到750℃空洞半径约为0.29nm不随温度变化,但浓度随温度增加而增加;高于750℃,空洞半径随温度升高迅速增大,1050℃时空洞的半径达1.10nm.     

钨酸铅晶体的本征色心和辐照诱导色心

根据钨酸铅晶体(PbWO4,简称PWO)的缺陷化学和晶体结构特点,用光吸收谱、广延X射线吸收精细结构(EXAFS)和精密X射线衍射(XRD)方法对高温退火后PWO晶体进行微结构研究,获得了其退火前后缺陷变化的情况,据此提出生成态(asgrown)晶体中350nm本征色心吸收带起源于V-F空穴心,并指出PWO中紫外区色心吸收带的强度取决于晶体中铅空位和氧空位浓度之差:[VPb]-[VO];然后,结合晶体在紫外光(UV)辐照过程中色心的转化规律和偏振吸收谱的实验结果,提高420nm辐照诱导色心吸收带起源于V0F双空穴心.并对所提出的PWO晶体色心模型的合理性进行了讨论. 关键词： 钨酸铅 本征色心 辐照诱导色心 色心模型     

蓝宝石中子辐照色心的研究

研究了中子辐照对蓝宝石(α-Al2O3)单晶体缺陷形成及光学性能的影响,对采用提拉法与温度梯度法生长的蓝宝石晶体进行中子辐照,通过对比辐照前后的吸收及荧光光谱变化,发现辐照使得蓝宝石晶体内形成F、F^ 和F2^ 色心缺陷,但不同方法生长的晶体样品中色心浓度差异明显。其中提拉法样品的F心浓度要高于温度梯度法样品,而温度梯度法样品中F^ 色心浓度要高于提拉法样品。分析表明,这与两种方法生长的晶体中杂质含量差异有关。通过研究辐照后晶体的热致发光谱发现提拉法与温度梯度法生长的蓝宝石晶体分别在145℃与150℃有明显的热致发光出现,采用初始上升法计算出两种方法生长的晶体的热致发光陷阱深度分别为1．15eV及1．05eV。     

重离子辐照SiO2 的光致发光(英文)

基于荷能离子与固体相互作用特点 ,提出了一种新的制备光致发光材料的方法——高能重离子辐照 .用这种方法研究了SiO₂ 薄膜的光致发光特性 ,发现高能 84Kr和40Ar离子辐照可在注碳Si O₂ 薄膜样品中产生强的蓝-紫光发射带 ,掺杂碳增强了辐照样品的发光特性.     

脉冲激光辐照TiO2/SiO2薄膜热效应研究

 采用1.06 μm单脉冲激光在不同能量密度下辐照特殊光电系统中典型薄膜光学元件，理论分析了激光辐照薄膜元件产生的温度场和热应力场，在此基础上建立了激光辐照多层薄膜的物理模型，计算软件使用ANSYS软件的热分析模块对激光辐照薄膜元件产生的温度场和热应力场进行了模拟，分别给出不同激光能量密度下薄膜表面光斑中心的温度场、径向温度场和轴向温度场分布；同时给出不同能量密度下薄膜的轴向、径向和环向热应力分布。并对激光辐照薄膜元件产生的温度场、热应力场进行了分析，阐明了原因。     

脉冲激光辐照TiO2/SiO2薄膜热效应研究

采用1.06 μm单脉冲激光在不同能量密度下辐照特殊光电系统中典型薄膜光学元件,理论分析了激光辐照薄膜元件产生的温度场和热应力场,在此基础上建立了激光辐照多层薄膜的物理模型,计算软件使用ANSYS软件的热分析模块对激光辐照薄膜元件产生的温度场和热应力场进行了模拟,分别给出不同激光能量密度下薄膜表面光斑中心的温度场、径向温度场和轴向温度场分布;同时给出不同能量密度下薄膜的轴向、径向和环向热应力分布。并对激光辐照薄膜元件产生的温度场、热应力场进行了分析,阐明了原因。     

BaClxBr2-x∶Eu2+材料光激励光谱及色心研究

采用高温固相法制备了BaClxBr2-x∶Eu2+光激励发光材料,利用XRD、激发、发射以及激励光谱研究了所制备材料的结构和光学性能。XRD图像表明所制备的材料为单一纯相,随X值增大,衍射角向大角度偏移。发射光谱中位于405nm的窄带谱峰,由Eu2+的4f65d→4f7能级跃迁所引起,监测405nm发射峰,所得激发光谱是位于250～380nm之间的宽带,谱峰位于303nm;光激励波段位于480～800nm,激励峰位于575nm。通过光谱曲线拟合,发现激励光谱由550,610和685nm左右的光谱叠加而成,分别对应F(Cl-),F(Cl-Br),F(Br-)色心,激励峰随Cl/Br比值增加而蓝移。     

重离子辐照SiO2的光致发光

基于荷能离子与固体相互作用特点,提出了一种新的制备光致发光材料的方法-- 高能重离子辐照. 用这种方法研究了SiO2薄膜的光致发光特性,发现高能84K r和40Ar离子辐照可在注碳SiO2薄膜样品中产生强的蓝-紫光发射带,掺杂碳增强了辐照样品的发光特性.     

快重离子辐照引起Ni/SiO2界面原子混合及相变研究

在室温下用308 MeV的Xe离子和853 MeV的Pb离子辐照Ni/SiO2样品, 用卢瑟福背散射和X射线衍射技术对样品进行了分析。 通过分析Ni/SiO2样品中元素成分分布和结构随离子辐照剂量和电子能损的变化, 探索了离子辐照在Ni/SiO2样品中引起的界面原子混合与结构相变现象。 实验结果显示, Xe和Pb离子辐照均能引起明显的Ni原子向SiO2基体的扩散并导致界面附近Ni, Si和O原子的混合。 实验观测到低剂量Xe离子辐照可产生NiSi2相, 而高剂量Xe离子辐照则导致了Ni3Si和NiO相的形成。 根据热峰模型, Ni原子的扩散和新相的形成可能由沿离子入射路径强电子激发引起的瞬间热峰过程驱动。Ni/SiO2 interface were irradiated at room temperature with 308 MeV Xe ions to 1×1012, 5×1012 Xe/cm2 and 853 MeV Pb ions to 5×1011 Pb/cm2, respectively. These samples were analyzed using Rutherford Backscattering Spectrometry (RBS) and X ray diffraction spectroscopy (XRD), from which the intermixing and phase change were investigated. The obtained results show that both Xe and Pb ions could induce diffusion of Ni atoms to SiO2 substrates and result in intermixing of Ni with SiO2. Furthermore, 1.0×1012 Xe/cm2 irradiation induced the formation of NiSi2 and 5.0×1012 Xe/cm2 irradiation created Ni3Si and NiO phases. The diffusion of Ni atoms and the formation of new phase may be driven by a transient thermal spike process induced by the intense electronic energy loss along the incident ion path.     

Photoluminescence properties of SHI induced F2 and F3 color centers in nano-granular LiF thin films

Photoluminescence (PL) properties of swift heavy ions-induced F₂ and F₃⁺ color centers in nano-granular lithium fluoride (LiF) thin film were studied. LiF films were deposited on glass and silica substrates and irradiated with various ion species (Ag, Ni and Au) at different irradiation temperatures. The role of ion species, their fluence and the irradiation temperature on the PL intensity of color centers induced in LiF thin films is discussed.     

Effect of neutron-irradiation on optical properties of SiO2-Na2O-MgO-Al2O3 glasses

Silica based glasses are used as nuclear shielding materials. The effect of radiation on these glasses varies as per the constituents used in these glasses. Glasses of different composition of SiO₂-Na₂OMgO-Al₂O₃ were made by melt casting techniques. These glasses were irradiated with neutrons of different fluences. Optical absorption measurements of neutron-irradiated silica based glasses were performed at room temperature (RT) to detect and characterize the induced radiation damage in these materials. The absorption band found for neutron-irradiated glasses are induced by hole type color centers related to non-bridging oxygen ions (NBO) located in different surroundings of glass matrix. Decrease in the transmittance indicates the formation of color-center defects. Values for band gap energy and the width of the energy tail above the mobility gap have been measured before and after irradiation. The band gap energy has been found to decrease with increasing fluence while the Urbach energy shows an increase. The effects of the composition of the glasses on these parameters have been discussed in detail in this paper.      

CVD法单层MoS2在209Bi离子辐照下的损伤效应研究

通过光学显微镜、拉曼光谱确定了CVD（化学气相沉积法）制备的不同厚度MoS₂的层数,采用拉曼分析结合原子力显微镜观测分析了由HIRFL提供的高能209Bi离子辐照CVD制备的单层MoS₂样品随辐照注量的损伤规律。随辐照注量增加,E_2g1和A_1g两种声子振动模式对应的拉曼峰逐渐蓝移,且拉曼特征峰强度减弱,这是由于带正电荷的209Bi辐照产生潜径迹型晶格缺陷吸附空气中氧分子而引入p型掺杂引起的。同时,在辐照注量为5×1010 ions/cm2的单层MoS₂的AFM图像中观察到潜径迹主要以凹坑形式出现,与机械剥离法观测到的凸起径迹明显不同,分析了不同制备工艺对径迹形貌的影响。比较了机械剥离法制备MoS₂样品的拉曼光谱和AFM成像的实验数据和结果,认为不同制备方法会影响单层或少层MoS₂的电子密度。The layer number of MoS₂ with different thickness was determined by the optical microscope and Raman spectra. And the damage effect of the CVD (chemical vapor deposition) prepared single-layer MoS₂ sample irradiated by 209Bi ions was analyzed by the combination of Raman analysis and AFM observations. With the increase of irradiation fluence, the Raman characteristic peaks of E_2g1 and A_1g corresponding to both phonon vibration modes gradually bluely shift, and the intensity of the peaks obviously decreased. This is due to the fact that the 209Bi ion irradiation results in the latent track type lattice defects and they adsorb the oxygen molecules in the air ended with the p-type doping. Meanwhile, from the AFM image of the mono-layer of irradiated MoS₂ under the 5×1010 ions/cm2, it can been seen that latent tracks mainly occur in the form of pits, which different from the hillock tracks observed by mechanical stripping method. The influence of different preparation technology to the track morphology is analyzed. Compared with the Raman and AFM results of MoS₂ prepared by mechanical stripping, it is considered that different preparation methods will affect the electron density in single or few layers of MoS₂.     

组装条件对涂布法制备SiO2结构色涂层光谱性质影响研究

为了实现结构色涂层在纸张表面的快速制备,研究不同组装条件对SiO₂结构色涂层呈色效果的影响,采用快速涂布的方法,在纸张表面制备出了大面积且具有随角异色特性的结构色涂层。探讨SiO₂微球粒径、分散液浓度及涂布次数等因素对结构色涂层光学特性的影响,通过优化自组装条件和分析周期性结构构筑类型,阐明快速涂布法构建的SiO₂微球在激光打标纸上的自组装过程及结构色呈色机理。应用数码相机、3D激光共聚焦形貌测量显微镜等仪器对样品的颜色外观和微观结构进行测量,表征样品的呈色性能及表面结构。使用X-Rite MA68Ⅱ多角度分光光度仪及光纤光谱仪测量反射光谱,进而用CIEL*a*b*色度值对制备的结构色涂层的光学性能进行分析。结果表明,通过快速涂布自组装法制备所得的结构色涂层,SiO₂微球粒径尺度对样品色调影响显著,随着微球粒径的增加,反射光谱中心波长发生红移,且该涂层有角度依赖特性,当固定入射角度为45°时,随着探测方向与镜面反射方向夹角的增大,中心波长发生红移;微球溶液的浓度可以调控结构色涂层反射光谱曲线的半高宽及反射率峰值,进而影响样品的亮度和彩度,而对于光子带隙的位置无明显影响。微球浓度为4%时,样品表面呈现出基材本身的黑色,微球浓度为8%时,200,220和250 nm粒径的样品表面分别可以呈现彩度较低的蓝色、绿色、黄色,微球浓度增加到10%时,纸张表面的结构色涂层彩度提高,色调不变;随着涂布次数的增加,反射光谱曲线的半高宽变窄,且反射峰位发生蓝移,涂布次数达到3次时,反射峰位最接近于根据布拉格定律计算出的理论值,但涂布次数的增加也使得结构色涂层表面产生白色的不均匀现象。     

Energy of excitons and acceptor-exciton complexes to explain the origin of ultraviolet photoluminescence in ZnO quantum dots embedded in a SiO2 matrix

Assuming finite depth and within the effective mass approximation, the energies of exciton states and of the acceptor-exciton complexes confined in spherical ZnO quantum dots (QDs) embedded in a SiO₂ matrix are calculated using a matrix procedure, including a three-dimensional confinement of carrier in the QDs. This theoretical model has been designed to illustrate the two emission bands in the UV region observed in our experimental Photoluminescence spectrum (PL), with the first emission band observed at 3.04 eV and attributed to the bound ionized acceptor-exciton complexes, and the second one located at 3.5 and assigned to the free exciton. Our calculations have revealed a good agreement between the matrix element calculation method and the experimental results.     

Mn2+离子掺杂的NaTaOGeO4:Tb3+的发光性能

采用高温固相法制备了颜色可调的NaTaOGeO₄∶Tb³⁺,Mn²⁺荧光粉,并研究了其发光特性以及能量传递机理。在244 nm激发下,NaTaOGeO₄∶Tb³⁺的发射光谱的发射峰分别位于380,413,436,492,544 nm,分别属于Tb³⁺的⁵D₃→⁷F_J和⁵D₄→⁷F_J（J=6,5,4）能级跃迁,为蓝光和绿光发射。在280 nm波长激发下,在492 nm和544 nm处有较强的发射峰,分别属于Tb³⁺的⁵D₄→⁷F₆、⁵D₄→⁷F₅能级跃迁,为绿光发射。在248 nm波长激发下,NaTaOGeO₄∶Mn²⁺的发射光谱由位于576 nm处的宽带组成,属于Mn²⁺的⁴T₁→⁶A₁能级跃迁。当在NaTaOGeO₄∶Tb³⁺荧光粉中共掺杂Mn²⁺时,可以同时观察到Mn²⁺和Tb³⁺的发射峰,通过改变浓度掺杂比,可以得到颜色可调控的荧光粉。     

Ba9Y2(SiO4)6: Ce3+,Mn2+荧光粉的发光特性及能量传递

利用高温固相法制备了Ba₉Y₂(SiO₄)₆:Ce³⁺,Mn²⁺(BYS:Ce³⁺,Mn²⁺)荧光粉,并通过X射线衍射(XRD)谱、激发和发射光谱及荧光寿命的测试对材料的结构、发光特性和能量传递进行了研究。在327 nm激发下,BYS:Ce³⁺,Mn²⁺发射光谱中包含2个发射峰,分别为位于407 nm的Ce³⁺的蓝紫光发射和位于597 nm的Mn²⁺的红光发射。在该体系中,发现了Ce³⁺向Mn²⁺的有效能量传递,使得Mn²⁺在597 nm处的红光发射显著提高,当x(Mn²⁺)=0.25时,BYS:Ce³⁺,xMn²⁺的能量传递效率可达39%。实验表明,该荧光粉可为紫外基白光LED提供良好的红光光源。     

Ge dots on Si (1 1 1) and (1 0 0) surfaces with SiO2 coverage: Raman study

Germanium quantum dots formed on Si (1 1 1) and (1 0 0)-oriented surfaces coated with ultra-thin oxide layers are studied using Raman spectroscopy technique. Some structural properties (height, stoichiometry and mechanical stresses) of the dots were estimated from Raman data. For analysis of the experimental data, the Raman spectra of Ge nanoclusters containing some hundreds of Ge atoms were calculated numerically. The effects of the resonance enhancement of the intensity of Raman scattering in the Ge-nanoclusters–SiO₂–Si system were discussed. The influence of the lateral sizes of Ge nano-clusters on the frequencies of phonons localized in them was studied using numerical simulation. The influence of multi-layer growth on the structure of the Ge quantum dots was investigated.     

Improved photoluminescence and afterglow in CaTiO3:Pr with addition of nanosized SiO2

Enhancement of the ¹D₂-³H₄ red emission in CaTiO₃:Pr³⁺ with addition of nanosized SiO₂ fabricated by a solid state reaction method is reported. The dynamical processes for the improvement of red emission were systematically investigated using photoluminescence (PL) and PL excitation spectra, and diffused reflectance spectra as well as time decay patterns of PL and persistent afterglow. Higher efficiency of energy transfer from CaTiO₃ host to the activator Pr³⁺ due to the improvement of crystallinity by SiO₂ addition was discussed in comparison with that of the SiO₂ free sample. The enhancement of persistent afterglow after the cessation of excitation in SiO₂ added CaTiO₃:Pr³⁺ was also analyzed by theoretically fitted results.