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非线性克尔效应对飞秒激光偏振的超快调制 被引量:3
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作者 林贤 金钻明 +6 位作者 李炬赓 郭飞云 庄乃锋 陈建中 戴晔 阎晓娜 马国宏 《物理学报》 SCIE EI CAS CSCD 北大核心 2018年第23期212-218,共7页
研究了近红外飞秒激光的偏振在太赫兹频率的超快调制.利用抽运-探测光谱技术,通过改变两个脉冲之间的延迟时间可以控制光脉冲的旋转角.在Li:NaTb (WO_4)_2磁光晶体中观察到探测光的偏振随延迟时间变化的高速振荡,振荡信号的中心频率为0.... 研究了近红外飞秒激光的偏振在太赫兹频率的超快调制.利用抽运-探测光谱技术,通过改变两个脉冲之间的延迟时间可以控制光脉冲的旋转角.在Li:NaTb (WO_4)_2磁光晶体中观察到探测光的偏振随延迟时间变化的高速振荡,振荡信号的中心频率为0.19 THz.这种超快偏振调制现象可以解释为,抽运-探测实验构置中,前向传播的抽运光诱导的光学克尔非线性引起被晶体远端表面所反射的背向传播的探测光脉冲偏振面的额外旋转.通过改变抽运光的圆偏振旋性可以控制探测光调制信号的相位和振幅.实验结果表明,非线性光学克尔效应可以作为一种全新的手段,在磁光晶体中实现近红外飞秒激光以太赫兹频率的超快偏振调控.这将在超快磁光调制器等全光器件中得以应用.实验结果将有助于偏振依赖的超快动力学过程的研究. 展开更多
关键词 超快光谱 克尔效应 磁光效应 太赫兹
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Probing Effect of Solvation on Photoexcited Quadrupolar Donor-Acceptor-Donor Molecule via Ultrafast Raman Spectroscopy
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作者 Wei Zhang Jie Kong +4 位作者 Wenqi Xu Xinmiao Niu Di Song Weimin Liu Andong Xia 《Chinese Journal of Chemical Physics》 SCIE EI CAS CSCD 2022年第1期69-76,I0003-I0012,I0062,共19页
The symmetric and quadrupolar donor-acceptordonor(D-A-D)molecules usually exhibit excitedstate charge redistribution process from delocalized intramolecular charge transfer(ICT)state to localized ICT state.Direct obse... The symmetric and quadrupolar donor-acceptordonor(D-A-D)molecules usually exhibit excitedstate charge redistribution process from delocalized intramolecular charge transfer(ICT)state to localized ICT state.Direct observation of such charge redistribution process in real-time has been intensively studied via various ultrafast time-resolved spectroscopies.Femtosecond stimulated Raman spectroscopy(FSRS)is one of the powerful methods which can be used to determine the excited state dynamics by tracking vibrational mode evolution of the specific chemical bonds within molecules.Herein,a molecule,4,4′-(buta-1,3-diyne-1,4-diyl)bis(N,N-bis(4-methoxyphenyl)aniline),that consists of two central adjacent alkyne(-C≡C-)groups as electron-acceptors and two separated,symmetric N,N-bis(4-methoxyphenyl)aniline at both branches as electron-donors,is chosen to investigate the excited-state photophysical properties.It is shown that the solvation induced excited-state charge redistribution in polar solvents can be probed by using femtosecond stimulated Raman spectroscopy.The results provide a fundamental understanding of photoexcitation induced charge delocalization/localization properties of the symmetric quadrupolar molecules with adjacent vibrational markers located at central position. 展开更多
关键词 Donor-acceptor-donor Intramolecular charge transfer Femtosecond stimulated Raman spectroscopy
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