Theoretical study of the intensity of chemically induce dynamic electron polarization of radical-triplet pairs

被引:2
|
作者
XU Xinsheng ZHANG Xianyi ZHANG Weijun CUI Zhifeng LU Tongxing Laboratory of Spectroscopy and Materials Anhui Normal University Wuhu AnhuiP R China Anhui Institute of Optics and Fine Mechanics Academia Sinica Hefei Anhui P R China [1 ,2 ,1 ,2 ,2 ,1 ,1 ,1 ,241000 ,2 ,230031 ]
机构
关键词
Chemically induced dynamic electron polarization; RTPM; Density Matrix;
D O I
暂无
中图分类号
O562 [原子物理学];
学科分类号
摘要
Considering the interaction between excited triplet molecule and doublet radical, based on the second-order perturbation theory and the motion equation of density matrix, the polarization intensity of RTPM were theoretically calculated with the overpopulated doublet spin states and quartet spin states of radical-triplet pairs as initial conditions respectively. The results of calculation indicate that the net emissive polarization and the net absorptive polarization on the radical result from the zero-field-splitting (zfs) and the multiplet A/E and E/A polarization result from hyperfine (hf) interactions of the triplet molecule. The hyperfine related A+A/E or E+E/A CIDEP on the radical were the overpopulation of the net absorptive or emissive polarization and multiplet A/E or E/A polarization..
引用
收藏
页码:561 / 566+590 +590
页数:7
相关论文
共 2 条
  • [1] First observation of a radical-triplet pair mechanism (RTPM) with doublet precursor. Kawai A, Obi K. The Journal of Physical Chemistry . 1992
  • [2] The relaxatinal mechanism of net CIDEP generation in triplet-radical quenching. Shushin A I. Chemical Physics Letters . 1993