Femtosecond time resolved excited Raman spectrum system
A technology of stimulated Raman and spectroscopy systems, applied in the field of Raman spectroscopy, can solve problems such as complex data processing, and achieve the effects of improving signal intensity, avoiding fluorescence interference, and high time resolution.
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Embodiment 1
[0091] Using the femtosecond time-resolved stimulated Raman spectroscopy system described in the present invention, the structural evolution dynamics of charge-transfer (CT) complexes without covalent bonds were studied, revealing that the dynamics of charge-transfer (CT) complexes that occur during charge separation (CS) (by Franck-Condon Ultrafast process of structural change during excited state complexes to tightly bound ion pairs) and subsequent charge redistribution (CR). Since the vibrational spectrum of the Franck-Condon excited state is similar to that of ion pairs, it can give very important CS properties. figure 2 It is to apply the femtosecond time-resolved stimulated Raman spectroscopy system of the present invention to detect and analyze the excited state dynamics process of all-trans β-carotene, and observe the excited state dark process of β-carotene (S *) generation mechanism and dynamics.
Embodiment 2
[0093] The femtosecond time-resolved stimulated Raman spectroscopy system of the present invention is used to study the relationship between the aggregate structure and its excited state properties, revealing the influence of aggregate structure parameter changes on molecular aggregate spectra. When the influence of molecular vibration is not considered, the spectral shape and unimodal or multimodal characteristics of the aggregates are mainly determined by the spatial packing structure of the aggregates, which can better highlight the aggregation of molecular aggregates. However, in actual situations, some molecules often have a complex multi-peak structure in the spectrum of a single molecule due to the vibration energy level. After the molecular aggregate is formed, only by considering its vibration effect can the simulated calculation of the spectrum coincide with the experimental results. And analyze which spectral features are caused by unimolecular vibration and which sp...
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