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Theoretical study of the intensity of chemically induce dynamic electron polarization of radical-triplet pairs 被引量:4
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作者 XUXin-sheng ZHANGXiao-yi +2 位作者 ZHANGWei-Jun CUIZhi-feng LUTong-xing 《原子与分子物理学报》 CAS CSCD 北大核心 2003年第4期561-566,590,共7页
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 theore... 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.. 展开更多
关键词 化学诱导力学电子极化 密度矩阵 RTPM 电子自旋 三重态分子 基本三重态对波函数
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