ZnO/PAA复合体系的制备和光致发光研究

通过加热法在多孔氧化铝模板的纳米孔内组装了ZnO颗粒,形成了ZnO和多孔氧化铝模板(PAA)复合体系.用Y-2000型X射线衍射仪表征了复合体系的结构,用TU-1901型紫外-可见分光光度计测量了复合体系的光学透过率,用WFY-28型荧光分光光度计测量了复合体系的光致发光.结果显示,多孔氧化铝模板中的ZnO结晶良好,平均晶粒尺寸10.8 nm;多孔氧化铝模板组装ZnO后透过率明显下降,550 nm处只有45%左右;ZnO/PAA复合体系在短波长光激发下有一个强的430 nm峰位的发光峰,随着激发波长增大,发光峰位红移,并且逐渐分解为两个峰,峰位分别在410 nm和460 nm.     

金膜上亚波长周期性孔阵的模拟与研制

分析了980 nm波长的光在透过制作在金膜上的亚波长周期性孔阵时的透射增强现象.通过建立中心带缺陷孔的三角晶格的孔阵模型,并采用三维时域有限差分方法对该模型的透射情况进行模拟分析.结果表明通过优化孔阵周期参数可以对特定波长的光实现一定程度的选择透过性.当孔阵周期为450 am,中心缺陷孔径为400 nm,孔阵中单个孔孔径为150 nm时,980 nm波跃光透过该孔阵时具有明显的透射增强效应,并且距孔阵表面3μm的远场光斑尺寸被局限在亚波长尺度(880 nm).研究了使用聚焦离子束在金膜上制备孔阵的工艺,成功研制了与没计尺寸一致的孔阵.这种孔阵可以集成在980 nm垂直腔面发射激光器上,用于改善器件的远场光学特性.     

全天时紫外高光谱瑞利测温激光雷达系统EI北大核心CSCD

紫外高光谱瑞利测温激光雷达是一种探测大气温度廓线的有效工具。目前,紫外高光谱瑞利测温激光雷达通常采用355nm波长的光,然而白天太阳背景光辐射会影响雷达系统的信噪比(SNR),进而制约温度探测的距离和精度。针对大气温度的全天时探测,提出了基于法布里-珀罗标准具的266nm紫外高光谱瑞利测温激光雷达系统。由于到达地面的太阳背景光辐射不包含266nm波长的光,只需考虑臭氧对266nm波长光吸收的影响,进而实现全天时大气温度的探测。基于脉冲能量、望远镜直径、望远镜接收视场角、臭氧浓度以及太阳背景光强度等主要影响参数,对266nm和355nm两个波长紫外高光谱瑞利测温激光雷达系统的谱宽、透过率、回波信号SNR以及温度偏差参数进行数值仿真和对比分析。结果表明,大气分子和气溶胶散射对266nm波长光的影响远大于对355nm波长光的影响。白天266nm紫外高光谱瑞利测温激光雷达系统的有效探测距离为4km左右,比355nm紫外高光谱瑞利测温激光雷达系统的有效探测距离远2.9km;夜间266nm紫外高光谱瑞利测温激光雷达系统有效探测距离为6km。探测距离小于5km时,白天266nm紫外高光谱瑞利测温激光雷达的探测温度偏差比355nm紫外高光谱瑞利测温激光雷达的探测温度偏差小10K。266nm紫外高光谱瑞利测温激光雷达可实现全天时大气温度的探测。     

高稳定性低噪声的561 nm黄光激光器

鉴于目前561 nm激光器噪声较大,影响其实用性,提出一种高稳定性低噪声的561 nm黄光激光器。利用Nd:YAG晶体得到1 123 nm基频光,通过LBO晶体腔内倍频得到561 nm输出。理论分析了1 112 nm、1 116 nm与1 123 nm波长的阈值泵浦功率,提出1 123 nm的单波长振荡条件,确定谐振腔镀膜要求。根据理论计算,设计了合理的谐振腔膜系,通过抑制1 112 nm与1 116 nm谱线在谐振腔内的振荡实现1 123 nm谱线的单波长振荡。在泵浦功率为5 W时,实现了561 nm激光单波长输出,输出功率达到107 mW,功率不稳定性达到0.7%,噪声为1.2%。     

3.4μm处NO2吸收光谱特性及在差分吸收激光雷达中的应用

为使中红外差分吸收激光雷达能够精确测量NO_2气体浓度,对NO_2在中红外波段的吸收光谱特性进行测量分析.采用光参量放大激光器的λon和光参量振荡激光器λoff两路激光分别进行吸收谱线测量实验.用谱线宽小于0.05nm的λon激光测量了NO_2气体在3 410～3 433nm的吸收光谱,计算得到其吸收截面,采集分析了NO_2在291K、308K、363K三个温度下的光谱特性,用谱线宽约为10nm的λoff激光采集了3 400～3 435nm的吸收谱线.测量结果表明,在3 410～3 433nm波段,温度和吸收截面值呈负相关,测量的谱线与HITRAN数据库相关系数达到0.92以上;针对λoff激光下的吸收谱线,采用了改进的卷积修正方法,测量结果和拟合结果相关系数为0.97.将实测的on和off波长处的吸收截面应用于使用该波长对的中红外差分吸收激光雷达仿真上,拟合差分吸收激光雷达系统浓度测量误差,验证了基于该波长对的差分吸收激光雷达方案的可行性.     

Co/AAO纳米有序阵列复合结构的光致发光和光吸收特性

以草酸电解液制备的高度有序的纳米级多孔阳极氧化铝(AAO)为模板,采用交流电化学沉积工艺合成了Co/AAO纳米有序阵列复合结构。分别研究了AAO模板和Co/AAO结构的光致发光和光吸收特性。结果表明,AAO模板在350～550nm范围内存在较强的光致发光带,其峰位在395nm处;Co/AAO纳米有序阵列复合结构的光致发射峰位亦在395nm处,且发光峰强度随Co沉积量的增加而迅速减弱。实验发现,Co/AAO纳米有序阵列复合结构的光吸收边从近紫外至近红外的波段范围内发生大幅度红移,最大红移量甚至超过380nm。文章定性分析并解释了Co/AAO纳米有序阵列复合结构吸收边大幅度红移及其光发射峰位不变、而峰强减弱的主要原因。     

1 319和1 338 nm双波长Nd:YAG脉冲激光输出实验研究

 根据计算得到的双波长激光振荡的阈值条件,激光实验中对全反镜镀制1 319和1 338 nm的全反膜（其反射率大于99.73%,而对1 064 nm激光的反射率约为7%）;输出镜采用对1 064 nm强谱线95%的高透过率,而对1 319和1 338 nm谱线的透过率分别为34.7%,32.5%,有效抑制了强线1 064 nm振荡,成功实现了1 319和1 338 nm Nd:YAG同时双波长激光脉冲输出。当输入能量为125 J时,1 319和1 338 nm脉冲双波长激光的单脉冲总输出能量为0.89 J,电-光转换效率为0.71%,斜率效率为0.89%。输出的双波长激光的中心波长分别在1 318.8和1 338.2 nm处,谱线宽度（FWHM）分别为0.35和0.48 nm,强度之比为36:44。     

基于级联光纤Bragg光栅的外腔半导体激光器三波长同时激射

实现了使用3个级联的光纤Bragg光栅外腔半导体激光器3波长同时激射.3条谱线的峰值波长取决于光纤Bragg光栅的峰值反射波长,分别为1 531.5 nm、1 549.4 nm与1 554.8 nm.注入电流为52 mA时,激光器总输出功率为1 mW.该激光器的主要优点包括,由于输出波长被锁定在光纤Bragg光栅的Bragg波长上,因此输出波长稳定,谱线窄,成本低.可应用于多波长干涉测量以及全光通信等领域中.     

罗丹明6G在银纳米线阵列上的SERS光谱研究

制备出有序、均匀的活性衬底一直足表面增强拉曼散射(SERS)研究中的关键.阳极氧化法制备的多孔氧化铝膜的结构有序、均匀,为纳米金属SERS基底的制备提供了模板.以沉积了银的多孔氧化铝组装体为衬底,研究了罗丹明6G(Rh6G)分子的表面增强拉曼散射光谱.结果表明,沉积了银的多孔氧化铝模板是很好的SERS衬底,Rh6G分子在此衬底上的SERS谱强度与银纳米线在表面的显露高度有关,而其拉曼频移未受表面状态的影响,而PO43-离子的存在使SERS强度得到很大提高.     

菌紫质光致变色吸收特性的二能级理论研究

采用二能级模型(B态和M态)简化菌紫质(bR)光循环过程,建立了菌紫质光致变色吸收特性的数学方程,数值计算了bR膜对570nm单光束和对570nm与412nm双光束的吸收特性.计算表明,bR膜的光吸收特性与入射光波长、入射光强、摩尔消光系数、光密度和M态寿命有很大的关系.bR膜用于光存储时,读出光强和M态寿命是影响bR读出使用时间的两个重要因素.570nm与412nm双光束作用于bR膜时,可以实现以光控光操作,但由于570nm黄光的透过动态范围要比412nm紫光的透过动态范围大得多,因而在实际应用中应以黄光作为信息光,紫光作为控制光.基于bR膜对黄、紫光束的吸收特性,可以将其应用于亮背景滤除、反象器、图象相减、光寻址空间光调制器等光信息处理领域.     

Morphology and transmittance of porous alumina on glass substrate

The porous optical film has higher threshold of laser-induced damage than densified films, for the study of mechanism of laser-induced damage of porous optical film with ordered pore structure. Porous anodic alumina (PAA) film with high transmittance on glass substrate has been prepared. Aluminum film was deposited on glass substrate by means of resistance and electron beam heat (EBH) evaporation. Porous alumina was prepared in oxalic acid solution under different anodizing conditions. At normal incidence, the optical transmittance spectrum over 300-1000 nm spectra region was obtained by spectrophotometer. SEM was introduced to analysis the morphology of the porous alumina film. The pore aperture increased with the increase of anodizing voltage, which resulted in a rapid decrease of the pore concentration and the optical thickness of porous alumina film. Damage morphology of porous alumina film is found to be typically defects initiated, and the defect is the pore presented on the film.     

基于包络线法的多孔阳极氧化铝薄膜光学常数的计算

采用二步阳极氧化法在草酸溶液中制备了多孔阳极氧化铝(PAA)薄膜。借助于扫描电子显微镜(SEM)分析了多孔阳极氧化铝薄膜的微观形貌。结果发现,在其表面孔径为30~40nm的六边形孔洞分布均匀,且垂直于表面平行生长。依据PAA透射光谱的实验数据,采用极值包络线算法计算出了PAA薄膜的复折射率以及光学能隙等光学常数。通过分析吸收系数与入射光子能量之间的关系发现,PAA薄膜具有直接带隙半导体的电子结构特征,而且由理论计算得到的PAA的带隙能与其光致发光谱的峰位能是一致的。     

Synthesis of PS colloidal crystal templates and ordered ZnO porous thin films by dip-drawing method

Polystyrene spheres (PS) were synthesized by an emulsifier-free emulsion polymerization technique and the PS colloidal crystal templates were assembled orderly on clean glass substrates by dip-drawing method from emulsion of PS. Porous ZnO thin films were prepared by filling the ZnO sol into the spaces among the close-packed PS templates and then annealing to remove the PS templates. The effects of ZnO precursor sol concentration and dipping time in sol on the porous structure of the thin films were studied. The results showed an ordered ZnO porous thin film with designed pore size that depended on the sol concentration and PS size could be obtained. And the shrinkage of pore diameter was about 30-43%. X-ray diffraction (XRD) spectra indicated the thin film was wurtzite structure. The transmittance spectrum showed that optical transmittance decreased with the decrease of wavelength, but kept above 80% optical transmittances beyond the wavelength of 550 nm. Optical band gap of the porous ZnO thin film (fired at 500 °C) was 3.22 eV.     

Modification of erbium photoluminescence excitation spectra for the emission wavelength 1.54 μm in mesoscopic structures

Photoluminescence excitation (PLE) spectra for the emission wavelength 1.54 μm were studied for erbium-doped xerogels embedded in artificial opals and porous anodic alumina films. Opals were chosen with photonic stop-band in green spectral range, where excitation of 1.54 μm occurs most efficiently. In comparison to the structure erbium-doped titania xerogel/porous anodic alumina/silicon the photoluminescence excitation spectra for 1.54 μm emission wavelength significantly changes for the same xerogels embedded in artificial opals. Enhancement of erbium-related 1.54 μm emission was observed from the structure Fe₂O₃ xerogel/porous anodic alumina fabricated on silicon, having some incompletely anodized aluminium, under excitation with either the lasing source at 532 nm or xenon lamp. Evident difference in PLE spectra for erbium doped TiO₂ and Fe₂O₃ xerogels in porous anodic alumina is observed.     

Structural and optical properties of pulsed laser deposited SrBi2Nb2O9 thin films

SrBi₂Nb₂O₉ (SBN) thin films were prepared on fused quartz substrates at room temperature by pulsed laser deposition. The influence of deposition parameters such as target-to-substrate distance, oxygen pressure and annealing temperature on film crystallization behavior was investigated by X-ray diffraction. Results indicated that the films grown at the optimum processing conditions have polycrystalline structure with a single layered perovskite phase. The optical transmittance of the films prepared at various oxygen pressures was measured in the wavelength range 200–900 nm using UV–vis spectrophotometer. The results showed that there is a red shift in the optical absorption edge with a rise in the oxygen pressure. Refractive index as a function of wavelength and optical band gap of the films were determined from the optical transmittance spectra. The results indicated that the refractive index increases with increasing oxygen pressure at the same incident light wavelength, while the band gap reduces from 4.13 to 3.88 eV. It may be attributed to an increase in packing density and grain size, and decrease in oxygen defects.     

Elaboration and characterization of organic–inorganic quantum wells impregnated on porous anodic alumina nanostructures

An organic–inorganic quantum well embedded on porous anodic alumina was synthesized and studied by MEB, AFM, optical absorption and photoluminescence. The morphology determined by the MEB and the AFM, shows that the size of the pores is about 10 nm for alumina evaporated on glass substrate and about 35 nm for alumina template prepared in sulfuric acid (H₂SO₄). The optical properties are characterized from absorption and photoluminescence spectra measured at room and low temperature. The measured spectral characteristics demonstrate the influence of the pore size on the emission of the organic–inorganic quantum well ((C₁₂H₂₅NH₃)₂PbI₄). An obvious blueshifted photoluminescence (PL) of (C₁₂H₂₅NH₃)₂PbI₄ in nanometer-sized pores was observed. It results in a better quantum confinement.     

Fabrication and optical properties of platinum nanowire arrays on anodic aluminium oxide templates

Arrays of Pt nanowires, fabricated by electrodepositing Pt metal into nanoporous anodic aluminium oxide (AAO) templates, exhibit a preferable optical absorption band in the ultraviolet-visible (UV-VIS) spectra and present a blueshift as the wire aspect ratio increases or its radius decreases. This type of optical property of Pt nanowire/porous alumina composites has been theoretically explored using Maxwell－Garnett (MG) effective medium theory. The MG theory, however, is only applicable to nanowires with an infinitesimally small radius relative to the wavelength of an incident light. The nanowire radius is controlled by the pore radius of the host alumina, which depends on anodizing conditions such as the selected electrolyte, anodizing time, temperature and voltage. The nanowire aspect ratios depend on the amount of Pt deposited into the nanopores of AAO films. The optical absorption properties of the arrays of Pt nanowires with diameters of 24, 55 and 90 nm have been investigated by the UV-VIS spectra, which show that the extinction maximum (λ_max) shifts to shorter wavelength side as the wire aspect ratio increases or its radius decreases. The results are qualitatively consistent with those calculated based on the MG theory.     

Optical inhomogeneity of ZnS films deposited by thermal evaporation

Zinc sulfide (ZnS) films with optical thickness (reference wavelength is 620 nm) ranging from 310 to 1240 nm were deposited on quartz substrates at room temperature by a thermal evaporation system. The structure and morphology of the films were investigated by X-ray diffraction, atomic force microscopy, respectively. The optical properties of the films were determined by in situ transmittance measurements and wideband spectra photometric measurements, respectively. The experimental results show that the films exhibit cubic structure, and the intensity of the (2 2 0) diffraction peak enhances with the increase of optical thickness. Surface grain size and surface roughness increase monotonously with increasing film thickness. Refractive indices and extinction coefficients calculated by in situ transmittance measurements are well consistent with those calculated by wideband spectra photometric measurements. Both the refractive index and packing density of the film increase as the increase of film thickness, which confirms the film is positive inhomogeneous and has an expanding columnar structure. Extinction coefficients of the films increase with increasing film thickness, which results from the increase of surface roughness.     

退火对电子束热蒸发Al2O3薄膜性能影响的实验研究

 用电子束热蒸发方法镀制了Al₂O₃材料的单层膜，对它们在空气中进行了250~400 ℃的高温退火。对样品的透射率光谱曲线进行了测量，计算了样品的消光系数、折射率和截止波长。通过X射线衍射仪（XRD）测量分析了薄膜的微观结构,采用表面轮廓仪测量了样品的表面均方根粗糙度。结果发现随着退火温度的提高光学损耗下降，薄膜结构在退火温度为400 ℃时仍然为无定形态，样品的表面粗糙度随退火温度的升高而增加。引起光学损耗下降起主导作用的是吸收而不是散射，吸收损耗的下降主要是由于退火使材料吸收空气中的氧而进一步氧化，从而使薄膜材料的非化学计量比趋于正常。     

反应前驱物中n(S)∶n(Cd)对CdS薄膜结构及发光特性的影响

采用化学水浴以CdCl2·H2O、CS( NH2)2、NH4Cl、NH3·H2O和去离子水作为反应前驱物制备CdS纳米晶薄膜.采用扫描电镜( SEM)、X射线衍射(XRD)、透射光谱和稳态荧光光谱,研究了反应前驱物中不同的n(S)∶n(Cd)对所制备的CdS薄膜的形貌、结构和光学性能的影响.结果表明:反应前驱物中n(S...