香豆素343敏化TiO2纳米粒子光致电子转移的荧光和拉曼光谱

通过对香豆素343(C343)染料敏化TiO₂纳米粒子光致电子转移的荧光和拉曼光谱特性的研究表明,C343染料敏化TiO₂纳米粒子稳态吸收光谱和稳态荧光光谱的红移归因于从被吸附的C343染料分子激发态和C343/TiO₂复合物到TiO₂纳米粒子导带的光致电子转移. 由时间分辨荧光光谱确定了C343染料敏化TiO₂纳米粒子的逆向电子转移速率常数为τ₁=31 ps. C343 染料敏化TiO₂纳米粒子体系拉曼光谱的研究表明, 被吸附在界面处的染料分子主链碳键的伸缩振动和碳环的呼吸运动的振动模式对超快界面光致电子转移有着重要的促进作用.     

溶剂对香豆素343染料光谱性质和最低激发态偶极矩的影响

通过对香豆素343(C343)在不同溶剂中的稳态吸收光谱、稳态荧光光谱和时间分辨荧光光谱的分析,研究了溶剂对C343的光谱性质的影响,并获得了光谱特性与溶剂极性之间的依赖关系. 吸收光谱峰值的红移随着溶剂极性的增加而发生较小的变化. 然而,荧光光谱的峰值对溶剂的极性却很敏感,并随着溶剂极性参数f(ε,n)的增加呈线性增长. 这是由于C343激发态电荷分布的变化导致了它在极性溶剂中第一激发单重态能级的变化. 用溶剂效应测量法和量子化学计算方法确定了C343最低激发态的偶极矩,这两方法所得的结果一致. C343在不同溶剂中的时间分辨荧光光谱研究表明荧光寿命随着溶剂极性的增加而增加,即从甲苯溶液的3.09 ns线性地增加到水溶液中4.45 ns;荧光寿命延长的根源可归因于C343与氢键给体溶剂之间的分子间氢键相互作用.     

Ultrafast multiplex CARS investigation of vibrational characteristics in chloroform and PMMA

This paper demonstrates the femtosecond time-resolved coherent anti-Stokes Raman scattering by using folded BOXCARS geometry where an ultrashort broadband coherent white light continuum was used as Stokes pulse, and carries out the non-contact detection at long distance. The CARS signal is so easy to be detected that it can be seen even by nude eye. The C-H bonds of chloroform or PMMA were detected and the vibration modes belonging to the side chain and the main chain in PMMA were also compared. Their vibrational characteristics involved decay process and quantum beating were discussed. This modified CARS experimental technique could make up the deficiency of traditional CARS technique.     

柱状交界面Richtmyer-Meshkov不稳定性的数值研究

采用基于有限体积法的二阶Godunov格式模拟了柱形密度交界面在同轴激波加速下的演化过程。得到了以下初步结果:在参数相同的情形下,内聚激波比中心爆炸波对界面的扰动更危险;内聚激波从轻质流体进入重质流体与从重质流体进入轻质流体相比,界面有更快的增长。周向波数大小对界面增长率有很大的影响,在计算的参数下,n=8～12有最大增长率,大于和小于这个范围的周向波长,增长率均明显减弱。     

Theoretical and experimental investigations of coherent phonon dynamics in sapphire crystal using femto- second time-resolved coherent anti-Stokes Raman scattering

We report on the theoretical and the experimental investigations of the coherent phonon dynamics in sapphire crystal using the femtosecond time-resolved coherent anti-Stokes Raman scattering (fs-CARS) technique. The temporal chirped white-light continuum (WLC) is used for the Stokes pulse, therefore we can perform the selective excitation of the phonon modes without using a complicated laser system. The expected quantum beat phenomenon is clearly observed. The theoretical formulas consist very well with the experimental results. The dephasing times of the excited phonon modes, the wavenumber difference, and the phase shift between the simultaneously excited modes are obtained and discussed. This work opens up a way to study directly high-frequency coherent phonon dynamics in bulk crystals on a femtosecond time scale and is especially helpful for understanding the nature of coherent phonons.     

Vibrational relaxation dynamics in transient grating spectroscopy studied by rate equations based on time-dependent correlation function

A modified model, a set of rate equations based on time-dependent correlation function, is used to study vibrational relaxation dynamics in transient grating spectroscopy. The dephasing, the population dynamics, and the vibrational coherence concerning two vibrational states are observed respectively in organic dye IR780 perchlorate molecules doped polyvinyl alcohol matrix. The result shows that in addition to the information concerning system-environment interac- tion and vibrational coherence, the vibrational energy transfer can be described by this modified model.     

Coherent coupling between vibrational modes of C-H bonds at different positions studied by femtosecond time-resolved coherent anti-Stokes Raman scattering

We performed femtosecond time-resolved coherent anti-Stokes Raman scattering(fs-CARS) measurements on liquid toluene and PVK film.For both samples,we selectively excited the CH stretching vibrational modes and observed the expected quantum beat signals.The frequency of the well-defined beats is in good agreement with the energy difference between the two simultaneously excited modes,which demonstrates that a coherent coupling between the vibrational modes of the C-H chemical bonds exists at the different positions of the molecules.The dephasing times of the excited modes are obtained simultaneously.     

5(6)羧基荧光素敏化TiO2纳米粒子的光致电子转移的荧光特性研究

通过水解TiCl₄制备了锐钛矿结构TiO₂纳米粒子, 并用时间分辨荧光光谱研究了5(6)CFL(5(6)-Carboxyfluorescein, 简称5(6)CFL)染料敏化TiO₂纳米粒子体系的光致电子转移动力学. 5(6)CFL染料敏化TiO₂纳米粒子能形成电荷转移复合物, 这归因于染料分子的激发电子态波函数Ψ(D^*)与电荷分离态波函数Ψ(D⁺ +e^-)之间的耦合作用. 当激发5(6)CFL染料敏化TiO₂纳米粒子体系时, 电子以两种不同方式注入TiO₂纳米粒子导带: 第一, 通过5(6)CFL染料分子的激发态注入; 第二, 从电荷转移复合物(5(6)CFL/TiO₂)直接注入. 时间分辨荧光光谱表明, 在水溶液中纯5(6)CFL染料的荧光以寿命为τ₁=41 ps (74.4%) 和τ₂=3.22 ns (25.6%) 的双e指数衰减, 而5(6)CFL染料敏化TiO₂纳米粒子体系的荧光分别以时间常数为τ₁=44 ps (90.4%), τ₂=478 ps (8.6%) 和τ₃=2.41 ns (1.0%) 的三e指数衰减. 本文的研究工作能够为染料敏化太阳能电池的光致电子转移机理提供有价值的参考.     

大学物理实验教学中学生专业思维训练的探索

大学物理实验实行分专业大类的模块教学,既考虑了物理实验课程的普遍性,又考虑了学生的专业性,使教学有层次、有针对性;学生选择适合自己的实验项目,能使学生的专业特点、兴趣爱好得到张扬.有利于学生对专业的理解和对大学物理实验课程的认识,强化专业思维意识,提高学生的学习积极性和主动性.     

固定时间梯度流在l1-l2范数中的稀疏重构

压缩感知（compressed sensing,CS）是一种全新的信号采样技术,对于稀疏信号,它能够以远小于传统的Nyquist采样定理的采样点来重构信号。在压缩感知中, 采用动态连续系统,对l₁-l₂范数的稀疏信号重构问题进行了研究。提出了一种基于固定时间梯度流的稀疏信号重构算法,证明了该算法在Lyapunov意义上的稳定性并且收敛于问题的最优解。最后通过与现有的投影神经网络算法的对比,体现了该算法的可行性以及在收敛速度上的优势.