Studying ultrafast spectral diffusion and correlation dynamics using two-dimensional electronic spectroscopy

• Main Authors: Do, Thanh Nhut, Nguyen, Hoang Long, Sim, Jamie H. N., Leng, Xuan, Le, Duc Viet, Khyasudeen, M. Faisal, Nowakowski, Paweł J., Tan, Howe-Siang
• Other Authors: Asian Spectroscopy Conference 2020
• Format: Conference or Workshop Item
• Language: English
• Published: 2020
• Subjects: Science::Chemistry; Ultrafast Spectroscopy; Two-dimensional Electronic Spectroscopy
• Online Access: https://hdl.handle.net/10356/144271
• Institution: Nanyang Technological University

The Frequency Fluctuation Correlation Function (FFCF) is a measure of the spectral diffusion dynamics of an electronic transition and details the interaction between the chromophore and its environment. The Frequency Fluctuation Cross-Correlation Function (FXCF) allows us to study how correlated, the transitions between different electronic transitions, are. These quantities contain a wealth of information on how the electronic transitions in chromophores and excitonic states interact and couple with their environment, and with each other. We summarize the experimental implementations and theoretical considerations of using ultrafast coherent two-dimensional electronic spectroscopy (2DES) to characterize FFCFs and FXCFs. In 2DES, the measured peakshapes of the electronic transitions are highly sensitive to the spectral diffusion and correlation dynamics [1]. One method that allows us to analyse these peakshapes is the Centre Line Slope (CLS) method [2]. We describe applications to systems such as the chlorophyll (Chl) molecules which are the major pigment molecules in the plant photosynthetic light harvesting machinery. We characterize the FFCFs of the Qy transition of Chl a and Chl b in various solvent environment [3,4]. The solvent dependence of the FFCF values and the relation of these values to the molecule's interaction with the solvent environment, will be discussed. Using similar methods, the FXCF between the Qx and Qy transitions of Chl a are measured. The results indicate that the Qx and Qy transitions have only minimal initial correlation, which decays to zero in a timescale of about 2 ps [5]. We also characterize the FFCFs of CdSe quantum dots (QD) and nanoplatelet (NPL) [6]. We found that no spectral diffusion dynamics occurs for the CdSe QDs. On the other hand, spectral diffusion was observed in the CdSe 5 mono-layers NPLs heavy-hole transition. The normalized Frequency Fluctuation Correlation Function (FFCF) of the CdSe NPLs heavy-hole transition was measured to have a major fast decay component at < 200 fs.