基于非线性偏振旋转效应的多波长光纤激光器

多波长光纤激光器是未来波分复用光通信系统的理想光源,提出和展示了一个基于非线性偏振旋转效应的多波长光纤激光器,非线性偏振旋转诱导的强度相关非均匀损耗能有效地抑制均匀加宽增益介质掺铒光纤中的模式竞争,从而使光纤激光器在室温下产生稳定的多波长输出,实验实现了最多18个波长的多波长输出.另外,此激光器没有使用传统的滤波器,而是在激光腔内插入一段保偏光纤,保偏光纤与偏振相关隔离器构成一等效Lyot双折射光纤周期性滤波器.利用这种在线型的双折射光纤滤波器简化了光纤激光器的结构,使它更易于集成.还实验研究了多波长输出随抽运功率的演化,发现抽运功率对多波长的均匀性影响很大.     

倒V形四能级亚飞秒极化拍的三光子吸收和色散

基于孪生色锁噪声场的互相关效应,从理论上研究了倒V形(RV)四能级飞秒量级差频极化拍与极化拍中五阶非线性极化率,并提出了用一种相位敏感的方法来研究多能级原子相干造成的三光子六波混频过程.在抽泵光束为窄带末端情况下,场关联对信号和极化率的影响都很弱,在非窄带情况下,场关联会使极化强度自相干信号和极化拍信号产生关于零延时的不对称性和时域扫描上的辐射与物质失谐阻尼振荡(RDO),而极化率会产生频域扫描上的RDO振荡.参考光信号是一路传播方向和六波混频信号稍有区别的双光于非简并四波混频信号.五阶非线性响应则由享生 关键词： 外差法 吸收 色散 非线性极化     

Multisites Cr3+ in GGG and GSGG garnets

The emission and excitation spectra of Cr³⁺ -doped Gd₃Ga₅O₁₂ (GGG) and Gd₃Sc₂Ga₃O₁₂ (GSGG) are explained in the light of multisite effects. The situation is particularly complicated in the case of GSGG, where the different sites have²E energy levels near each other which overlap with the⁴A₂ ⁴T₂ absorption bands. The spectra obtained under selective excitations are interpreted on the multisite assumption.     

Effect of hydroxyl groups on Er doped Bi2O3-B2O3-SiO2 glasses

A series of Er³⁺-doped Bi₂O₃-B₂O₃-SiO₂-Na₂O glasses with different hydroxyl groups were prepared and the interaction between the Er³⁺ ions and OH groups was investigated. Infrared spectra were measured in order to calculate the exact content of OH groups in samples. The observed increase of the fluorescence lifetime with the oxygen bubbling time has been related to the reduction in the OH content concentration evidenced by infrared (IR) absorption spectra, which confirmed that the OH groups were dominant quenching centers of excited Er³⁺ and a cause of concentration quenching of 1.5 μm band emission. Various nonradiative decay rates from ⁴I_13/2 of Er³⁺ with the change of OH content were determined from the fluorescence lifetimes and radiative decay rates, which were calculated on the basis of Judd-Ofelt theory.     

Enhanced in vitro biocompatibility of ultrafine-grained biomedical NiTi alloy with microporous surface

Bulk ultrafine-grained Ni_50.8Ti_49.2 alloy (UFG-NiTi) was successfully fabricated by equal-channel angular pressing (ECAP) technique in the present study, and to further improve its surface biocompatibility, surface modification techniques including sandblasting, acid etching and alkali treatment were employed to produce either irregularly roughened surface or microporous surface or hierarchical porous surface with bioactivity. The effect of the above surface treatments on the surface roughness, wettability, corrosion behavior, ion release, apatite forming ability and cytocompatibility of UFG-NiTi alloy were systematically investigated with the coarse-grained NiTi alloy as control. The pitting corrosion potential (E_pit) was increased from 393 mV (SCE) to 704 mV (SCE) with sandblasting and further increased to 1539 mV (SCE) with following acid etching in HF/HNO₃ solution. All the above surface treatment increased the apatite forming ability of UFG-NiTi in varying degrees when soaked them in simulated body fluid (SBF). Meanwhile, both sandblasting and acid etching could promote the cytocompatibility for osteoblasts: sandblasting enhanced cell attachment and acid etching increased cell proliferation. The different corrosion behavior, apatite forming ability and cellular response of UFG-NiTi after different surface modifications are attributed to the topography and wettability of the resulting surface oxide layer.     

Projective synchronization of two coupled excitable spiral waves

Interaction of two identical excitable spiral waves in a bilayer system is studied. We find that the two spiral waves can be completely synchronized if the coupling strength is sufficiently large. Prior to the complete synchronization, we find a new type of weak synchronization between the two coupled systems, i.e., the spiral wave of the driven system has the same geometric shape as the spiral wave of the driving system but with a much lower amplitude. This general behavior, called projective synchronization of two spiral waves, is similar to projective synchronization of two coupled nonlinear oscillators, which has been extensively studied before. The underlying mechanism is uncovered by the study of pulse collision in one-dimensional systems.     

求解波束波导中激励-传输-辐射问题的积分方程方法

针对波束波导系统结构和馈电特性,应用体面积分方程建立了任意结构波束波导中电磁波的激励、传输和辐射问题所对应的物理模型.在激励端,采用模式展开方法描述输入口面场分布,并利用模式匹配方法精确模拟波束波导馈电端的匹配状况.通过对波束波导内部的实际结构的精确拟合,基于积分方程建立了激励-传输-辐射的电磁模型,并以高效数值解法给...     

Be(d,n)反应中子源能谱测量及应用

 利用中子飞行时间技术和BC501A液体闪烁探测器的粒子分辨特性,测量了0°方向、20 MeV氘束轰击厚金属铍靶反应产生的中子源能谱,测量的中子能谱范围为0.7～25.0 MeV。在60°方向放置芪晶体闪烁探测器,由刻度好的BC501A液体闪烁探测器归一校正后,用于中子源强度监测。利用Be(d, n) 反应中子源,采用单粒子灵敏度标定方法,实验标定了0.75~15.75 MeV能量范围内的薄膜闪烁探测器中子能量响应曲线,实验结果与蒙特卡罗模拟计算结果在8%的不确定度范围内一致。     

Comparative analysis of (p,d), (d,t) and (3He, α) reactions on13C nucleus

The angular distributions of the (p, d), (d, t) and(³He, ) reactions on¹³C have been analysed within the framework of DWBA in which additional information on nuclear vertex constants was introduced. Although all these reactions seem to be similar single nucleon transfer, their mechanism is shown to be quite different and so is the information extracted thereof. While from the (p, d) reactions spectroscopic factors may be extracted unambiguously, from the (d, t) reactions it is possible to obtain directly the values of vertex constants only, which in turn are consistent with those determined by extrapolation of the experimental cross sections of the (p, d) reactions to the pole.In the case of (³He, ) reactions, however, the analysis indicates inadequacy of the DWBA concerning the calculations of central partial amplitudes. For a more reliable extraction of structural information, besides the correct normalization of peripheral amplitudes, a contribution of more complex mechanisms must be taken into account.     

Effect of nonstoichiometry on Raman scattering of VO2 films

We report on Raman scattering of VO2 films prepared by radio frequency magnetron sputtering under different conditions. Our investigations revealed that the dominated Raman peaks shift towards high frequency for both V-rich and O-rich VO2 films, compared with the stoichiometry VO2 films. The experimental evidence is presented and the cause for nonstoichiometry dependence of Raman spectra of VO2 films is discussed.