层数相关黑磷双光子吸收的理论研究

原子层数是对黑磷物理性质宽波段可调谐的重要参量.基于5跳参数连续近似模型,从理论上研究了单层、双层和三层黑磷的双光子吸收系数对原子层数以及入射光偏振方向的依赖性.计算结果表明:黑磷的双光子吸收系数在扶手型方向上比锯齿型方向上大10个数量级,且双光子吸收系数随着层数的增加而增大,并且吸收峰发生红移;双光子吸收系数随入射线...     

基于单个BBO晶体载波包络相位稳定的高效率光参量放大器

基于单个BBO非线性晶体,利用非共线光参量放大技术,研究了载波包络相位稳定的高效率可调谐近红外脉冲产生.以载波包络相位稳定的飞秒激光放大系统产生的白光作为种子光,注入一个二类匹配的二级光参量放大器,在1350 nm波段获得抽运-信号光34%的转换效率.利用f—2f光谱相干测量技术,放大脉冲载波包络相位的抖动30 min内小于137 mrad.该方法提供了一种简单高效的载波包络相位稳定的红外脉冲产生技术.     

基于半导体光放大器四波混频原理的光采样

建立了可研究强超短光脉冲放大特性且包含自由载流子吸收、受激辐射、双光子吸收、光谱烧孔和超快非线性折射效应的半导体光放大器理论模型,用以建立脉冲四波混频模型,并进一步仿真了基于半导体光放大器的光采样过程,重点讨论了自由载流子吸收、双光子吸收效应对采样特性的影响。仿真结果与实验结果相符。     

利用双光子吸收效应测量激光脉冲的相干时间

研究了利用反向泵浦－探测双光子吸收材料的方法来测量脉冲激光的相干时间，并测量量了２３ｐｓ，５３２ｎｍ Ｎｄ：ＹＡＧ激光脉冲的相干时间。实验和理论分析表明，光束相干作用增加了双光子吸收，利用此方法可测量其它脉宽激光的相干时间。     

压缩态光场平衡零拍探测的位相锁定

平衡零拍探测是测量量子光场的重要方法之一. 通过对相位灵敏光学参量放大器注入的信号进行位相调制, 然后利用平衡零拍探测系统测量光学参量放大器输出的压缩光. 将相位灵敏光学参量分别运转在参量放大和参量缩小, 通过观察噪声谱中的调制信号就可确定测量的量子光场是正交振幅或位相分量. 通过解调位相调制信号可获得误差信号, 实现锁定平衡零拍探测系统本底光与待测光场相对位相为零(对应于待测光场振幅噪声分量). 关键词： 平衡零拍探测 位相锁定     

远红外自由电子激光太赫兹光源研究

基于射频电子直线加速器的可调谐相干太赫兹(THZ)光源实现了出光，该光源为远红外自由电子激光，具有辐射波长可设计并可以实现大范围调谐特性．利用光栅谱仪测量了受激辐射谱，中心波长为115μm，谱宽约为1％．     

控制光和信号光频差对太赫兹光非对称解复用器性能的影响

讨论了半导体光放大器中的带间效应，及载流子热效应、谱烧孔效应、双光子吸收以及超快非线性折射等带内效应对半导体光放大器的动态特性的影响，讨论了两种情况：1)保持控制光波长不变而改变信号光频率，2)保持控制光和信号光频率相同而同时改变它们的频率下半导体光放大器的增益、相位动态特性以及太赫兹光非对称解复用器的开关窗口特性。数值结果表明，为了得到较为平坦而窄的开关窗口，控制光波长应与信号光波长相同，且其与半导体光放大器增益谱中心波长的差值应该大一些。     

基于MgO:QPLN的多光参量振荡器电场调谐特性理论与实验研究

报道了基于掺氧化镁准周期极化铌酸锂(MgO:QPLN)的多光参量振荡器电场调谐特性理论与实验研究. 通过对电场调谐能力与极化结构参数间关联性的理论分析, 确定了高正负晶畴比MgO:QPLN电场调谐的可行性, 并模拟得到跨周期参量光输出波长与加载电压的关系曲线. 实验中通过对MgO:QPLN有效的电场加载, 实现了3.84 μm波段参量光的电场调谐, 频谱调谐带宽约6 nm, 调谐速率接近1 nm/kV, 进一步结合温度调谐, 实现了参量光宽谱段高精度的连续调谐. 所获得实验结果与理论模拟结果基本符合, 电场调谐在精度控制、快速响应方面相比于传统温度调谐更具技术优势.     

光参量振荡伴生拉曼激光

利用调QNd∶YAG倍频激光泵浦KTP非线性晶体为介质的参量振荡器,产生了608.3nm~903.1nm宽带参量调谐激光,线宽1.4nm,光-光转换效率30%。当泵浦光增强到12mJ时,在参量激光谱线的近傍,长波方向出现了一条新谱线,与参量调谐激光谱线同步移动,谱线间隔随参量激光波长的增加而增加,两条谱线波数(能量)差(720cm-1)是一个定值,这是参量激光激发出斯托克斯拉曼激光典型特征。     

射流冷却的OCS分子高分辨VUV吸收光谱研究

以双光子共振四波混频差频产生的高分辨、可调谐真空紫外激光(VUV)为光源,在151～156nm内测量了超声射流冷却的OCS分子1Σ+-1Σ+电子跃迁带的吸收光谱.由于采用射流冷却和高分辨激光,得到与前人吸收谱测量结果不同的光谱线线形,观察到两个呈现明显非对称结构的振动峰,通过Fano线型拟合,获得了这两个振动峰的半高峰宽和非对称参数q值,与前人光碎片激发谱测量结果基本一致.实验中,为了消除VUV激光强度波动的影响,通过记录参比光的方法,有效地提高了吸收光谱的信噪比,使得吸收测量的灵敏度达到1%左右.     

一种新型有机染料HEASPS在不同波长时的双光子吸收和频率上转换性质研究

报道了一种新型双光子吸收染料 ,即反式 - 4- [4′- (N-羟乙基 - N-乙基胺基 )苯乙烯基 ]- N-甲基吡啶对甲苯磺酸盐的非线性光学性质 ;测试了染料在 72 0～ 110 0 nm波段的非线性透过率曲线。结果发现 :双光子吸收最强波长相对线性吸收峰波长的两倍处有明显蓝移 ;计算出的相应波长的双光子吸收截面在 930 nm处染料有最大双光子吸收截面(2 .0 6× 10 - 4 7cm4·s/ photon) ;测量了染料在 90 0～ 110 0 nm波段的上转换效率 ,在 10 2 0 nm处有最高效率 (5 .1% ) ,最高激射效率的波长相对最强双光子吸收的波长有明显红移     

Two photon absorption spectrum ofp-dichlorobenzene

Two photon absorption spectrum ofp-dichlorobenzene has been studied in the spectral region 497–552 nm (one photon wavelength). Bands involving several frequencies of the excited electronic state not detected in the one photon absorption are seen. The observed two photon spectrum indicates that the electronic transition retains, to a large extent, the salient features of the two photon absorption spectrum of benzene and thus confirms chlorine as weak perturber (in the sense of Goodman and Rava [1]).     

NO分子A2Σ→X2Π双光子激光感生荧光光谱

以Nd∶YAG激光器抽运光学参变振荡器 /光学参变放大器做为激发源 ,得到了NO分子在 2 2 0～ 35 0nm波长范围内的双光子激光诱导荧光光谱 ,并将其归属于A2 Σ(ν′ =0 )→X2 Π(ν″ =1～ 8)跃迁 ,用最小二乘法拟合获得NO分子X2 Π态振动常量″ωe =(190 4 .7± 7.3)cm-1,″ωe ″xe =(14 .2± 1.2 )cm-1,″ωe″ye=- (0 .0 2 18± 0 .0 0 91)cm-1,及平衡位置的力常量k =(1.5 99± 0 .0 12 )× 10 3 N·m-1。计算了所得跃迁谱带的弗兰克康登因子及相对荧光强度 ,结果与实验观测值相符。这可为用激光诱导荧光光谱技术探测大气污染物NO分子提供理论及实验参考     

Two-photon absorption and nonlinear optical properties of a new organic dye PSPI

Trans-4-[p-(pyrrolidinyl)styryl]-N-methylpyridinium iodide (abbreviated as PSPI thereafter) is a two-photon absorption (TPA) dye newly synthesized by our research group. It possesses much larger TPA cross-section and much stronger upconversion fluorescence emission than those of common organic dye (such as rhodamine) when excited with near infrared (IR) radiation. TPA spectrum and upconversion efficiency spectrum of HEASPI solution at various wavelengths were measured. There is 34 nm blue shift for the central wavelength of the TPA induced absorption peak compared with two times of the linear absorption peak. The biggest molecular TPA cross-section σ₂^′ is 2.85×10⁻⁴⁷ cm⁴ s/photon at 930 nm. At 1064 nm, σ₂^′ is 3.12×10⁻⁴⁸ cm⁴ s/photon. The highest efficiency is 3.9% at 1010 nm, whereas 2.9% at 1064 nm. Its optical power limiting properties at 930 nm have also been illustrated.     

CdSe/ZnS核-壳结构量子点的非线性光学吸收

利用开孔Z扫描技术研究了吸收峰分别为553 nm和503 nm的两种尺寸CdSe/ZnS核-壳结构量子点溶液的非线性吸收性质.对于532 nm,6 ns激光脉冲,两种材料均表现出饱和吸收向反饱和吸收转化的现象.数值模拟结果表明：当吸收峰波长大于激光波长时,饱和吸收过程由快、慢两种机制组成,分别对应基态载流子被激发至不同的激发态,而强光下的反饱和吸收与快过程相关;当吸收峰波长小于激光波长时,饱和吸收主要由快过程机制引起,强光下的反饱和吸收源自激发态吸收和双光子吸收.我们的研究结果表明半导体量子点是研制光开关和光限制器件的理想候选材料.     

掺Tm激光晶体的可见与红外发光转换及双稳多色开关

理论研究了648nm激光抽运掺Tm晶体的可见与红外发光转换和发光双稳特性.根据系统的耦合速率方程理论,推导了发光转换阈值的解析表达式,数值研究了Tm³⁺能级布居数,辐射光谱以及发光强度等随抽运光强的变化.数值结果表明,648nm激光抽运下可以实现452/469nm蓝光与1716 nm红外光谱的发光转换.在光子雪崩阈值附近,可以观察到掺Tm晶体的辐射光谱双稳,荧光色度双稳和发光强度双稳等现象.利用掺Tm晶体的可见与红外发光转换与双稳特性,可以实现抽运功率控制的全固态发光转换器和双稳波长 关键词： 光学双稳 多色开关 掺Tm晶体 光子雪崩     

Photoacoustic detection of two photon absorption in formaldehyde using pulsed dye laser

Absorption spectra of formaldehyde molecule in the gas phase have been recorded using photoacoustic (PA) technique with pulsed dye laser at various power levels. The spectral profiles at higher power levels are found to be different from that obtained at lower laser powers. Two photon absorption (TPA) is found to be responsible for the photoacoustic signal at higher laser power while the absorption at lower laser power level is attributed to one photon absorption (OPA) process. Probable assignments for the different transitions are given in this paper.     

单光子波长调制吸收光谱用于1.5 μm激光器的波长锁定

提出了一种kHz调制频率量级的单光子调制技术,实现对激光器的实时锁定. 通过探测乙炔气体的单光子吸收光谱,对离散的单光子响应脉冲进行锁定放大, 获得激光器频率锁定的鉴频曲线.将1.5 μm分布反馈半导体激光器的输出频率稳定在乙炔气体 ν₁ + ν ₃带P5e支吸收峰上,在175 s内典型激光频率起伏小于25 MHz. 这种基于单光子波长高频调制吸收光谱的稳频技术消除了低频段较高背景的噪声, 可应用于单光子量级的量子保密通讯系统以及光学波分复用系统.     

Experimental and theoretical studies on the one‐photon and two‐photon properties of a series of carbazole derivatives containing styrene

Symmetric‐type carbazole derivatives show great potential for application in two‐photon absorption (TPA) materials and organic light‐emitting diodes. The absorption spectra and fluorescence emission spectra of three different N‐alkyl symmetric‐type carbazole derivatives were investigated. The density functional theory (DFT) time‐dependent‐DFT//Becke, three‐parameter, Lee–Yang–Parr/6‐31 G* method has been used to theoretically study one‐photon absorption properties. The computational results are in good agreement with the available experimental values. The two‐photon excited fluorescence of the compounds was surveyed by 120 fs pulse at 790 nm Ti: sapphire laser operating at 1 kHz repetition rate. Two‐photon excited fluorescence was obtained in the range of 380–600 nm, and TPA cross‐sections were calculated. The TPA properties of the series of compounds were investigated by the ZINDO/single and double electronic excitation configuration interaction method. The influence of the chemical structure of the compounds on two‐photon optical properties was discussed. The results show how the different changes in one‐photon absorption and TPA properties on the basis of lengthening the conjugated bridge and the different carbazole N‐alkyl substituents are attributed to the transition dipole moment in the excited process. Copyright © 2011 John Wiley & Sons, Ltd.     

Properties of two-photon fluorescence and superradiance of a new organic dye C46H51N2B

Linear and nonlinear optical properties of a new organic dye, trans-4-[p-(N-n-butyl-N-n-butylamino)-styryl]-N-methyl-pyridinium tetraphenylborate solution in dimethyl formamide (DMF) have been studied systematically. When excited with mode-locked picosecond 1 064 nm laser beam, intense upconversion fluorescence and superradiance can be obtained. The temporal behaviors of one-photon absorption and two-photon absorption (TPA) fluorescence and superradiance have been studied. The highest upconversion efficiency was found to be 4.1% at a pump energy of 4 mJ. By using an optical parameter amplifier (OPA) as the pump laser, the nonlinear transmittance and upconversion efficiencies of the dye solution at different wavelengths were measured. The strongest linear absorption was found at a wavelength of 930 nm whereas the highest upconversion efficiency was at 1 030 nm. The 100 nm red-shift for the highest upconversion efficiency wavelength compared with the strongest nonlinear absorption are caused by excited state absorption. Received 17 October 2001 and Received in final form 21 December 2001