飞秒激光参数对非绝热耦合分子态布居的影响

利用含时波包法研究强飞秒泵浦-探测激光场中激光脉宽、波长和场强对非绝热耦合NaI分子各态布居的影响.波包在势能面上做周期性运动,周期约为1 000 fs.延时为200 fs时,波包第一次到达交叉区域分裂成两部分.波包在交叉区域的分裂情况影响各态布居.脉宽增长,NaI分子的激发概率增大,而解离概率减小.泵浦波长为共振波长318 nm时,激发概率最大.泵浦波长增长,NaI分子的解离概率减小.泵浦场强增大,激发概率增大,但解离概率不变.探测激光波长和场强不影响NaI分子各态布居分布.调节激光场参数可实现对波包运动的控制从而控制态布居的选择性分布.研究结果为实验上实现分子的光控制过程提供参考.     

Near-infrared ultrabroadband luminescence spectra properties of subvalent bismuth in CsI halide crystals

We observed two ultrabroadband near-infrared (NIR) luminescence bands around 1.2 and 1.5 μm in as-grown bismuth-doped CsI halide crystals, without additional aftertreatment. Dependence of the NIR emission properties on the excitation wavelength and measurement temperature was studied. Two kinds of NIR active centers of subvalent bismuth and color centers were demonstrated to coexist in Bi:CsI crystal. The eye-safe 1.5 μm emission band with an FWHM of 140 nm and lifetime of 213 μs at room temperature makes Bi:CsI crystal promising in the applications of the ultrafast laser and ultrabroadband amplifier.     

飞秒激光脉宽对非绝热耦合分子波包运动的影响研究

利用含时波包法研究了强飞秒泵浦-探测激光场中激光脉宽对非绝热耦合NaI分子波包运动的影响.发现波包的振荡周期随脉宽增长而增大,而振荡幅度随脉宽增长而减小.非绝热效应引起的波包在交叉区域的分裂情况影响各态布居.脉宽增长,NaI分子的激发概率增大,而解离概率减小.研究表明调节激光场脉宽可实现对波包运动的控制从而控制态布居的选择性分布.研究结果可以为实验上实现分子的光控制以及量子调控过程提供一定的参考.     

基于非线性放大环镜和Lyot滤波器的多波长与耗散孤子锁模态开关型掺铥光纤激光器

报道了一种基于非线性放大环镜和Lyot滤波器技术的态开关型掺铥光纤激光器.通过仔细调节偏振控制器和泵浦功率,掺铥光纤激光器可以分别在多波长态和耗散孤子锁模态运行,并且两种态之间可以相互切换.对于多波长态,在光谱半功率值范围内能生成8个稳定的波长;对于耗散孤子锁模态,在1996 nm的中心波长处产生脉冲能量高达41.49 nJ,脉冲持续时间为2.4 ns,光谱带宽为29 nm的耗散孤子.不同运行态间的切换归因于偏振控制器导致的非线性放大环镜的功能的改变.     

A mathematical simulation of intramolecular proton phototransfer

A system of equations for the matrix elements of the density operator of a seven-level model molecule interacting with a light pulse was solved numerically to determine the time dependences of the populations of molecule states at various radiation pulse parameters and parameters characterizing radiative and nonradiative spontaneous molecule transitions and reversible transitions between some of its states. The results were used to characterize the photoisomerization of molecules between states with different positions of the proton of the intramolecular H-bond (the keto and enol forms). Examples of oscillating molecular state population modulation in isomer-isomer tunnel proton shifts are given. Changes in the development of photoionization in time as molecular parameters and radiation pulse width and intensity changed were considered. An analysis of the results obtained is an example of the use of mathematical simulation of intramolecular dynamics for increasing the effectiveness of using spectral-time data in the determination of the mechanism of proton phototransfer in molecules with intramolecular H-bonds     

高灵敏高稳定的碘化铯阴极密封式分幅变像管研制

为解决采用Au光电阴极、开放式结构的分幅变像管探测效率低、稳定性差的问题,研制了一种采用CsI光电阴极的密封式分幅变像管。为了对比不同光电阴极对X射线的响应强度,密封式分幅变像管制作有一条Au微带阴极和一条CsI微带阴极。完成了密封式分幅变像管的结构设计、工艺制作和实验测试。研究结果表明:当加载半高宽度200 ps、幅值?2.7 kV的选通脉冲时测得其时间分辨为65 ps;在非单色高能X射线源照射下,CsI阴极的静态响应强度是Au阴极的3.4倍;大气环境中存储1000 h后密封式分幅变像管的静态响应强度仅降低到完成制作时的83%。上述结果表明采用CsI阴极的密封式分幅变像管具有更高的探测效率和稳定性,可有效提升X射线分幅成像质量和可靠性。     

New method for solving the time-dependent Schrödinger equation for molecules in a strong pulsed light field

A new approach to solution of the time-dependent Schrödinger equation for a quantum system affected by a strong electromagnetic laser field modulated in amplitude and frequency is proposed. This approach is based on application of the Floquet method and approximation of the Hamiltonian parameters slowly varying with time by step functions within the (t, t′) formalism. A relationship between the method developed and representation of the evolution operator in the form of the T-ordered product of operators acting at short time intervals is demonstrated. The method proposed is used to describe the response of a LiH molecule to the action of a radiation pulse and calculate the populations of the electronic states of the molecule under the pulse action. The evolution of the populations and dynamic susceptibility of the molecule and its relationship with the probabilities of Landau-Zener transitions between the electronic quasienergy states of the molecule have been analyzed.     

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.     

Optical properties of CsI(Na) and heat-treated pure CsI

On the basis of the similarity of luminescence properties of CsI(Na) crystals and heat-treated crystals of pure CsI excited in the long wavelength tail of the fundamental absorption, the effect of sodium in CsI(Na) is tentatively explained.     

Generation of a Super Strong Attosecond Pulse from an Atomic Superposition State Irradiated by a Shape-Optimized Short Pulse

Using a linearly polarized, phase-stabilized 3-fs driving pulse of 800 nm central wavelength shape-optimized on its＇ascending edge by its an amplitude-reduced pulse irradiating on a superposition state of the helium atom, we demonstrate theoretically the generation of a super strong isolated 176-attosecond pulse in the spectral region of 93-124 eV. The unusually high intensity of this attosecond pulse is marked by the Rabi-like oscillations emerging in the time-dependent populations of the ground state and the continuum during the occurrence of the electron recombination, which is for the first time observed in this work.     

激光场强度对NO电子态粒子数布居影响的理论研究

用含时波包方法研究了激光场强度对NO各电子态上粒子数布居的影响.在计算中,采用了四态模型.利用分裂算符傅里叶变换方法求解Schrdinger方程,得到各个电子态的波函数,从而求得各个电子态上粒子数的布居.计算结果表明,不同强度的抽运光对各个电子态上粒子数布居会产生不同的影响.通过改变激光强度可以实现对电离产率的控制,这种思想对实现原子分子过程的激光操控具有重要意义.     

Time-resolved X-ray spectrometry of UV laser produced plasmas

Preliminary experiments using an X-ray streak filter spectrometer employing a Au/CsI bifurcated photocathode to investigate the X-ray history of UV (350 nm) laser produced plasmas are reported. Novel use of the streak spectrometer permits a direct and precise fiducial record of the laser pulse to be made from specularly scattered laser light, in true streak time relative to the X-ray record. Initial data indicates a constant 700 eV temperature during the laser pulse; time-resolved particulars are compared to simulations made by the design code LILAC.     

An atom/molecule/DNA probing and transportation using dynamic optical tweezers via a wavelength router

A dark soliton pulse beam that has potential applications in the probing and transport of atoms or molecules as an optical tweezers is demonstrated. The trapped pulse beam is formed in the gap between a BP signal at 1500.00 nm and Stokes signal at 1500.09 nm, which has peak powers of −12 dBm. The generated beam is seen to be stable with no fluctuations over a test period of 10 min, which is important to ensure that the transported atom/molecule is not lost in the link media, therefore, the dynamic optical tweezers are now plausible. The theoretical background of the trapped atom/molecule is also analyzed and described in details. The atomic/molecular network via a wavelength router is also described.     

Experimental study on the Stokes effect in disordered birefringent microstructure fibers

In this paper, a 120-fs pulse transmission experiment is carried out using disordered birefringent microstructure fibers with cladding ventages. Through this experiment, it is found for the first time that remarkable Stokes and anti-Stokes waves can also be produced when the central wavelength of the incident pulse is in the normal dispersion regime of the microstructure fiber. The generation of the two waves can be explained by the four-wave mixing phase matching theory. Properties of the two waves under the action of femtosecond laser pulses with different parameters are studied. The results show that the central wavelength of anti-Stokes waves and Stokes waves produced under the two orthogonal polarization states shift by 63 nm and 160 nm, respectively. The strengths and central positions of the two waves in birefringent fibers can be controlled by adjusting the phase match condition and the polarization directions of incident pulses.     

Size-induced effect on cathode luminescence spectra of CsI(Na) and CsI(Tl) crystals

We investigated the cathode luminescence characteristics of CsI(Na)and CsI(Tl)crystals by the spectrum and structure properties at room temperature.We fabricated three different sizes of CsI(Na)and CsI(Tl)crystals and measured their luminescence spectra under cathode rays.We found that CsI(Na)cathode luminescence peaks appear at 420 and 305 nm,and CsI(Tl)cathode luminescence peaks are 540 and 410 nm,the grain size affects CsI(Na)luminescence significantly,and the Na-related420 nm luminescence intensified relatively when the average grain size reaches~20μm,which becomes weak when the grain size is down to nano-scale.But the cathode luminescence spectra of CsI(Tl)crystals with different size have no obvious changes.Our explanations for these phenomena are that the different impurities in the same host material CsI lead to different luminescence mechanisms.These cathode luminescence characteristics indicate the suitability of CsI(Na)and CsI(Tl)crystals to match photomultiplier tube for large area crystal detector development.     

利用NOLM实现连续光到归零码脉冲和波长的同时变换

利用非线性光学环路镜成功地实现了连续光到超短光脉冲和波长的同时变换.最大波长变换间距大于35nm.实验系统中采用增益开关分布反馈半导体激光器(GSDFB-LD)产生的超短光脉冲作为控制光,采用波长可调半导体激光器作为信号光.在变换过程中在1.55μm附近首次观测到了波长的反相变换.当信号光和控制光脉冲走离大于40.7ps时,变换信号脉冲发生畸变,变换脉冲展宽.     

高阶群速度色散引起的高斯超短脉冲宽度的展宽和形变

基于动量守恒和光参变过程中的三波耦合波方程,和负单轴非线性光学晶体CsLiB6O10的色散方程,研究了在光参变效应中超短激光脉冲由于群速度色散引起的展宽和形变。数值模拟显示,在超短脉冲波形为双曲正割形和无啁啾调制时,高阶群速度色散引起的超短脉冲为50fs时,晶体长度为10mm,紫外光213nm作为基波入射时的脉冲展宽是波长为532nm绿光在同等条件下的1.6倍。脉冲展宽程度与入射波长和晶体长度有关,波长越短和晶体长度越长则脉冲展宽和波形变化越严重,高阶色散引起的超短高斯脉冲展宽,将破坏其波形对称性并引起旁瓣现象。     

The 193 nm photolysis of NO2: NO(ν) vibrational distribution,O(1D) quantum yield and emission from vibrationally excited NO2

Time resolved Fourier transform infrared emission has been used to study the photolysis of NO2 and its dimer N2O4 at 193 nm. NO(ν) populations from the photolysis of NO2 show a bimodal distribution, peaking at ν = 5 and with a subsidiary maximum at ν = 14, close to the energetically allowed limit. The results are discussed in terms of previous measurements near this photolysis wavelength of the kinetic energies of the two possible O atomic fragments, O(3P) and O(1D), and on the electronic states of the parent molecule which can be populated. The O(1D) yield has been measured as 0.51 ± 0.04, in good agreement with previously reported values. Emission from vibrationally excited NO2 arises from the dissociation of N2O4 and is similar to that observed from photolysis at 248 nm.     

Numerical simulation of intramolecular dynamics during dual fluorescence

The dynamics of transformation of a light pulse by a five-level model molecule whose secondary emission spectrum can contain two fluorescence bands is simulated. The system of equations that determine the time behavior of the matrix elements of the statistical operator of the molecule interacting with the light pulse is numerically solved. From this solution, the time dependences of the populations of the molecular states are determined for different values of the parameters of the irradiation pulse, which is described in terms of the classical theory, and of the parameters that characterize the rates of radiative and nonradiative spontaneous transitions of the molecule. Based on particular examples of the choice of these parameters, it is demonstrated that the mechanism by which dual fluorescence occurs in molecules with intramolecular hydrogen bonds can be efficiently established from the numerically simulated intramolecular dynamics.     

Experiment Study of Dual Wavelength and Dual Pulse Q-switched Intracavity Frequency Doubling of a Tunable Cr:LiSAF Laser

In this paper, a flashlamp-pumped Q-switched Cr: LiSAF laser system with intracavity frequency doubling is designed to obtain dual pulse and dual wavelength laser output. The behaviors of second harmonic output of dual pulse and dual wavelength are studied experimentally. Good results are obtained in experiments: the output energy of each second harmonic pulse a round 448.1 nm is 10.2 mJ, the dual pulse time interval can be tuned widely, and the tunable range of each second harmonic wavelength is 448.1 to 465 nm.