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中国科学院上海光学精密机械研究所
收稿日期:1985-01-05,
纸质出版日期:1985-08-30
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何迪洁, 倪忠强. 若丹明6G溶液体系的荧光量子效率[J]. 发光学报, 1985,6(3): 222-229
He Dijie, Ni Zhongqiang. SOLVENT EFFECT ON THE FLUORESCENCE QUANTUM YIELD FOR Rh6G SOLUTIONS[J]. Chinese Journal of Luminescence, 1985,6(3): 222-229
本文对八种若丹明6G溶液的荧光量子效率进行了测量
并着重讨论了染料若丹明6G溶液体系的量子效率的溶剂效应.在研究中发现:若丹明6G溶渡的荧光量子效率与溶液极性(ε-1)/(2ε+1)之间存在线性关系
体系的荧光量子效率随溶剂极性的增加而下降.由于染料分子与成氢键溶剂作用愈强
能量散逸愈快将是导致这一结果的主要原因.这一规律也适用于ANS染料溶液体系中.
Solvent effect on the absorption spectra
fluorescence spectra and fluorescence quantum yield were studied.In particular
the fluorescence quantum yields for Rh6G in hydrogen bond solvents were discussed.By using variation excited methods the fluorescence quantum yields were approximate.The linear variation between the fluorescence quantum yield of Rh6Gsolutions and the polarity(ε-1)/(2ε+1)of the solvents was found.It was alsofound that the same relationship between the fluorescence quantum yields
lifetimes and the polarity(ε-1)/(2ε+1)in ANS.Fluorescence quantum yields forRh6G and ANS in hydrogen bond solvents decreased with increase of solvent polarity(ε-1)/(2ε+1).The solvent effect on fluorescence quantum yield for Rh6G in hydrogen bond solvents could be interpreted by the energy dissipation.In the case of strong interaction between the molecules Rh6G and the hydrogenbond solvent molecules with high(ε-1)/(2ε+1)
the energy dissipated quickly.Whereas in those low(ε-1)/(2ε+1)solvents
the energy dissipated less rapidly.This paper's results show that the η
2/3
(η-viscosity)dependence
which was first proposed by Forster and was experimentally verified for the quantum yield and fluorescence lifetimes of several triphenyl methane dyes
did not coincide with Rh6G in hydrogen bond solvents as well as ANS solution.
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