KBe2BO3F2飞秒光参量放大中的群速匹配

提出了KBe₂BO₃F₂ （KBBF）飞秒光参量放大中三波群速完全匹配的方法.对于Ⅰ类相位匹配方式采用非共线结构及倾斜抽运光脉冲波面,对于Ⅱ类相位匹配方式采用共线结构同时倾斜抽运光和信号光脉冲波面,可实现参量带宽最大时三波群速的完全匹配,从而获得更高增益,更窄脉宽的参量光. 关键词： 群速匹配 相位匹配 脉冲波面倾斜 飞秒光参量放大     

BBOⅠ类相位匹配光参量放大中群速失配的补偿

描述了在BBOⅠ类相位匹配的飞秒光参量放大（OPA）中，利用非共线结构和倾斜抽运光的脉 冲波面来完全补偿三波群速失配的方法.理论计算了三波群速匹配时，非共线角、相位匹配 角、抽运光的脉冲波面倾斜角随信号光波长的变化，并分析了对抽运光光斑尺寸的要求和对 空间走离长度的影响.结果表明，利用该方法不仅能够实现最大的参量带宽，而且能够完全 补偿飞秒OPA中三波的群速失配.此外，选取合适的抽运光光斑尺寸和非线性晶体的长度对提 高参量增益也至关重要. 关键词： 群速匹配 非共线相位匹配 脉冲波面倾斜 飞秒光参量放大     

飞秒光参量放大中三波群速失配的补偿

为了消除群速失配对参量放大的不利影响，描述了利用脉冲波面倾斜与非共线相位匹配相结 合，完全补偿飞秒光参量放大（OPA）中三波群速失配的新方法.计算了在BBOⅠ类、Ⅱ类相 位匹配条件下， 三波实现群速匹配时，相位匹配角、脉冲波面倾斜角以及非共线角随信号 光波长的变化.并分析了三波群速匹配对空间走离长度、参量增益和参量带宽的影响.结果表 明，在BBOⅠ类、Ⅱ类相位匹配条件下，利用该方法均能实现飞秒OPA连续调谐时三波的群速 匹配，从而大大增加了三波的有效互作用长度，为能够获得高增益，窄脉宽的参量光脉冲提 供了理论依据和指导. 关键词： 群速匹配 脉冲波面倾斜 非共线相位匹配 飞秒光参量放大     

非线性光学 非线性光学器件

O437.42006010281BBOⅡ类共线相位匹配结构中群速失配的补偿=Compen-sating group velocity mismatch in BBO type-Ⅱcollinearphase-matched configuration[刊,中]/马晶(天津大学精密仪器与光电子工程学院超快激光研究室,光电信息技术科学教育部重点实验室.天津(300072)),章若冰…∥中国激光.—2005,32(7).—913-916为了消除群速失配对飞秒光参量放大(OPA)的不利影响,描述了在Ⅱ类共线相位匹配的飞秒BBO光参量放大中,同时倾斜抽运光和信号光的脉冲波面完全补偿三波群速失配的方法。理论计算了三波群速匹配时,相位匹配角、抽运光和信…     

BBOⅠ类相位匹配非共线参量产生中的群速自匹配

利用重复频率为1kHz的钛宝石激光的倍频蓝光抽运Ⅰ类相位匹配的偏硼酸钡(BBO)晶体，获得了可见光区的非共线参量超荧光.给出了最强光强处参量超荧光的非共线角，波长随相位匹配角的变化.理论计算了在参量超荧光中三波的群速失配随非共线角和相位匹配角的变化规律.结果表明，Ⅰ类非共线相位匹配的参量超荧光关于抽运光中心对称.并且沿光强最强的参量超荧光方向三波的群速失配最小，有效互作用长度最大，即参量超荧光的强度角分布是三波的相速和群速自匹配的结果.该理论和实验研究为减小飞秒光参量放大中三波的群速失配提供了一个理想的几何模型，为获得高增益、窄脉冲宽度的参量光输出提供了理论依据和实验验证. 关键词： 群速自匹配 参量超荧光 非共线相位匹配 飞秒光参量放大     

非线性光学 位相共轭、自聚焦等相关效应

O437 2005042689 飞秒光参量放大中三波群速失配的补偿=Compensation of group velocity mismatching of three pulses in femtosec- ond optical parametric amplification[刊,中]／马晶(天津大学精密仪器与光电子工程学院超快激光研究室,光电信息技术科学教育部重点实验室(天津大学),天津(300072)), 章若冰…／／物理学报,-2005,54(2),-755-762 为了消除群速失配对参量放大的不利影响,描述了利用脉冲波面倾斜与非共线相位匹配相结合,完全补偿飞秒光参量放大(OPA)中三波群速失配的新方法。计算了在 BBOⅠ类、Ⅱ类相位匹配条件下,三波实现群速匹配时,相位匹配角、脉冲波面倾斜角以及非共线角随信号光波长的     

基于单晶体的可调谐参量超荧光的产生

研究了一种基于单晶体的可调谐超荧光产生机理，在一个偏硼酸钡(BBO)晶体中实现了飞秒脉冲倍频过程和光参量产生过程.实验中采用kHz高功率钛宝石激光系统输出的飞秒脉冲光倍频后的蓝光作为抽运光，获得了可调谐范围为480—530 nm参量超荧光光谱输出.理论上分析了这种超荧光产生机理，并利用放大传递函数模拟出参量超荧光环的产生过程.结果表明，在一个BBO晶体中，当抽运光源输出光入射晶体角度同时满足倍频相位匹配角和非共线光参量产生相位匹配角时可产生参量超荧光环，通过微调相位匹配角可控制参量超荧光光谱调谐输出.该理论和实验研究为控制参量超荧光和量子纠缠态的产生提供了理论依据，对于量子成像和量子通讯等领域的发展具有重要意义.     

周期性极化铌酸锂晶体中半非共线型宽带光学参变放大理论研究

基于周期性极化铌酸锂晶体(PPLN)的准相位匹配光参变放大过程,通过倾斜周期极化铌酸锂晶体中极化域(极化光栅)一定角度,实现了介于共线匹配方式和非共线匹配方式之间的一种半非共线型准相位匹配方式,并以该匹配方式下的各光矢量几何关系得出相位匹配曲线,找到在特定抽运光和信号光波长下能获得宽带增益放大的周期极化长度。并研究其极化倾斜角度与温度特性。模拟计算表明,在合适的角度与温度条件下,该方式可以532 nm抽运光抽运的信号光在800 nm和1064 nm处均获得宽带光参变放大。     

飞秒BBO光参量放大中闲频光二次谐波的产生

由于相位匹配条件和非线性晶体透光范围的限制，400nm蓝光抽运的飞秒β-BaB₂O₄（BBO）光参量放大（OPA）输出的参量光调谐范围有限，很难得到波长小于460nm的蓝光和近紫外光.实验采用1kHz钛宝石九通啁啾脉冲放大器的倍频蓝光作抽运光，超连续白光 作种子光，在Ⅰ类非共线相位匹配条件下，利用宽带的飞秒BBO OPA，在一定的实验参数下 获得了530—810nm放大的信号光，以及810nm—17μm波段范围的闲频光.与此同时 ，还获得了410—700nm连续可调的闲频光的二次谐波，其与闲频光层叠分布，单脉冲能量 为26μJ，转换效率大于5%.仅利用单块晶体的飞秒BBO OPA就可以获得410—810nm连 续可调的飞秒脉冲输出，从而为更多研究和应用的需要提供了重要的光源.对飞秒光参量放 大中闲频光二次谐波产生的条件也进行了理论分析. 关键词： 二次谐波 闲频光 非共线相位匹配 飞秒光参量放大     

非共线相位匹配LBO晶体飞秒光参变放大器的研究

对非共线相位匹配LBO晶体飞秒光参变放大器进行了系统地分析和理论研究，用数值方法得出了非共线角、相位匹配角、增益和增益带宽之间的关系，给出了放大器设计的各种最优化参量。研究结果表明，这种参变放大器不仅可以实现较高的参变增益和获得极宽的增益带宽，还具有较大的参变允许角、较小的走离角和小的群速色散。因此这种参变放大器对于以纳秒级高功率激光作为抽运光，利用光参变啁啾脉冲放大（OPCPA）技术高效率参变放大飞秒脉冲产生10^12W甚至10^15W级的超强超短激光脉冲具有重要的意义。建立的理论模型具有普遍意义，也为其他类似的参变过程提供了重要的理论依据。     

Magnetic ordering in HoRu2Si2, HoRh2Si2, TbRh2Si2 and TbIr2Si2 by neutron diffraction

Neutron diffraction study of polycrystalline HoRu₂Si₂, HoRh₂Si₂, TbRh₂Si₂, and TbIr₂Si₂ was performed in the temperature range between 4.2 and 300 K. For HoRu₂Si₂ the magnetic spin alignment of a linear transverse wave mode below the Néel temperature 19 K is observed. This static moment wave is propagating along the b-axis with k=(0, 0.2, 0) and is polarized in the c-axis. The root-mean-square and maximum saturation moments per Ho atom are 9.26 and 13.09μ_B, respectively. HoRh₂Si₂, TbRh₂Si₂ an TbIr₂Si₂ are simple collinear antiferromagnets of +-+- type with Néel temperatures of (27±1), (98±2) and (72±3) K, respectively. For TbRh₂Si₂ and TbIr₂Si₂ magnetic moments are localized on RE ions only and are aligned along the tetragonal axis, while for HoRh₂Si₂ they form an angle ø = (28±3)°.     

μ+SR study of LaNi2As2, URh2Si2 and CeRh2Si2

Muon spin relaxation experiments have been carried out in the paramagnetic and magnetically ordered states of URh₂Si₂ and CeRh₂Si₂. As the magnetic structure of these compounds is well known, these measurements can help to characterise their magnetic properties probed by μSR and to understand the μSR results of the heavy fermion compounds of the same crystallographic family. Our measurements show that the muons occupy two different crystallographic sites. The spectra of URh₂Si₂ and CeRh₂Si₂ in the magnetically ordered states are very different, probably reflecting their different magnetic structures. The spectra obtained on CeRh₂Si₂ are similar to the published spectra of the heavy fermion compound CeCu_2.1 Si₂. Muon spin rotation measurements on LaNi₂As₂ indicate that the muon is diffusing at 150 K.     

13C-selective IRMPD of CBr2F2/Cl2 and CCl2F2/Br2 systems

The CO₂ TEA laser irradiation of CBr₂F₂ in the presence of Cl₂ yielded ¹³C-enriched CBrClF₂ and ¹³C-enriched CCl₂F₂ under selected experimental conditions. As the photolysis proceeded, the ¹³C concentration of CBrClF₂ decreased gradually and that of CCl₂F₂ increased up to 90% or higher. These results can be explained by the mechanism involving the secondary ¹³C-selective IRMPD of the primary product CBrClF₂. On the other hand, the carbon-containing product for a CCl₂F₂/Br₂ system was only CBrClF₂; the further IRMPD of which probably regenerated CBrClF₂ in the presence of Br₂. The decomposition probabilities of ¹²C- and ¹³C-containing molecules in both systems were measured as functions of laser line, laser fluence, and reactant pressures.     

Polar optic phonons in Hg2Cl2 and Hg2Br2

Far infrared (30–430 cm^?1) reflectivity measurements of Hg₂Cl₂ and Hg₂Br₂ single crystals have been performed in polarized light. The spectra, which are in agreement with group-theoretical predictions, were analyzed by the oscillator fitting procedure and Kramers-Kronig method. The results are compared with the existing data from other measurements and the large anisotropy of polar modes is briefly discussed. The polarization vectors of all long-wavelength symmetry modes were determined group-theoretically.     

Magnetostriction of SmMn2Ge2 and GdMn2Ge2 intermetallic compounds

Longitudinal and transverse magnetostrictions of polycrystalline samples of intermetallic compounds RMn₂Ge₂ (R=Sm or Gd) are measured in pulsed magnetic fields up to 250 kOe. It is found that linear magnetostrictive strains of about 10^?3 arise in a temperature range in which the magnetic field causes a change in the magnetic state of a manganese magnetic subsystem. The results obtained are described within the model of a two-sublattice ferrimagnet with a negative exchange interaction in the manganese subsystem in terms of a strong dependence of this interaction on interatomic distances.     

Superconductivity in LaPd_2Bi_2 with CaBe_2Ge_2-type structure

正Since the discovery of superconductivity in LaFeAsO_(1-x)F_x,the high-T_c iron-based superconductors have been extensively studied from both experimental and theoretical viewpoints [1-8]. However, the mechanism of the unconventional superconductivity is still to be resolved. To     

Structural,magnetic and neutron diffraction studies on TbFe2-TbAl2, TbCo2-TbAl2 and HoCo2-HoAl2

Both pseudobinary systems exhibit large homogeneous regions of cubic and hexagonal Laves phases. Ordering tendencies on crystallographic sites between Al and the transition metals are observed in the hexagonal type.Electron transfer to the transition metals quenches their moments so that they become nonmagnetic at high Al concentrations. The peculiarities in the mechanism of magnetization which appear in rare earth dialuminides when Al is replaced by a transition metal have been studied in detail at cryogenic temperatures.The first replacement of Al results in a decrease in saturation moment. Neutron diffraction verifies the low ordered rare earth sublattice moments and reveals the ‘lost part’ as a disordered component. Considerable magnetic hardness develops in certain regions of concentration often connected with spontaneous increases in magnetization with field. All available evidence suggests the presence of unusual domain wall effects to be responsible for this effect. High remanences develop in both the hexagonal and in the cubic structures in the intermediate region. The development of disordered magnetic components is connected either with the disorder on crystallographic sites or changes in the free electron concentration.