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酞菁锌分子激发态的超快内转换和振动弛豫

Ultrafast Investigation of the Internal Conversion and Vibrational Relaxation in Excited States of Zinc Phthalocyanine Derivatives*

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【作者】 王朝晖衷庆华熊轶嘉孙亚孔繁敖

【Author】 Wang Zhaohui Zhong Qinghua Xiong Yijia Sun Ya Kong Fanao**(State Key Laboratory of Molecular Reaction Dynamics,Instituteof Chemistry,Chinese Academy of Sciences,Beijing 100080)

【机构】 中国科学院化学研究所分子反应动力学国家重点实验室

【摘要】 用飞秒时间分辨荧光亏蚀法研究了四特丁基酞菁(BuPc)、四特丁基酞菁锌(ZnBuPc)和四丙氧基酞菁锌(ZnPrPc)激发态的超快驰豫过程。用波长为398mm和796mm的超短脉冲激光激发分子,观察了S2态到S1态的内转换,其特征时间约为30fs。在796mm先于398mm作用于样品分子时,观察到了荧光强度渐变的过程,通过分析认为这一过程反映了S1的振动驰豫。通过对实验数据的拟合,得到了它们的振动驰豫特征时间,BuPc分子为1.5ps,ZnBuPc和ZnBuPc的特征时间分别为13.4和7.6ps。

【Abstract】 An internal conversion(IC)process from the S2 state to the S1 state of tetratertbutylphthalocyanine(BuPc),Zinc tetratertbutylphthalocyanine(ZnBuPc)and Zinc tetratpropoxyphthalocyanine(ZnPrPc)has been investigated respectively using femtosecond timeresolved fluorescence depletion methodThe S2 state of BuPc,ZnBuPc and ZnPrPc was prepared by the excitation of a 398nm laser pulse of 100fs durationVia a fast IC process from S2 to S1,the excited molecule emitted fluorescence from the S1 stateHowever,an ultrafast 796nm laser pulse depopulated the S2 state and therefore weakened the fluorescenceThe time scale of IC is estimated to be tens of femtosecondsThe vibrational relaxation in the S1 state was also studied by two 796nm photon excitation followed with a 398nm dumping laser pulseThe decay rate was measured as 15ps for BuPcFor ZnBuPc and ZnPrPc,decay rate of 134ps and 76ps were also observed respectively

【基金】 国家自然基金
  • 【文献出处】 化学物理学报 ,CHINESE JOURNAL OF CHEMICAL PHYSICS , 编辑部邮箱 ,1998年01期
  • 【分类号】O561.4
  • 【被引频次】42
  • 【下载频次】146
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