Excitonic-Vibrational Interaction at 2D Material/Organic Molecule Interfaces Studied by Time-Resolved Sum Frequency Generation

Abstract

The hybrid heterostructures formed between two-dimensional (2D) materials and organic molecules have gained great interest for their potential applications in advanced photonic and optoelectronic devices, such as solar cells and biosensors. Characterizing the interfacial structure and dynamic properties at the molecular level is essential for realizing such applications. Here, we report a time-resolved sum-frequency generation (TR-SFG) approach to investigate the hybrid structure of polymethyl methacrylate (PMMA) molecules and 2D transition metal dichalcogenides (TMDCs). By utilizing both infrared and visible light, TR-SFG can provide surface-specific information about both molecular vibrations and electronic transitions simultaneously. Our setup employed a Bragg grating for generating both a narrowband probe and an ultrafast pump pulse, along with a synchronized beam chopper and Galvo mirror combination for real-time spectral normalization, which can be readily incorporated into standard SFG setups. Applying this technique to the TMDC/PMMA interfaces yielded structural information regarding PMMA side chains and dynamic responses of both PMMA vibrational modes and TMDC excitonic transitions. We further observed a prominent enhancement effect of the PMMA vibrational SF amplitude for about 10 times upon the resonance with TMDC excitonic transition. These findings lay a foundation for further investigation into interactions at the 2D material/organic molecule interfaces.

Keywords

• 2D hybrid heterostructure
• TMDC/organic interface
• sum-frequency generation
• ultrafast dynamics
• surface field enhancement
• excitonic–vibronic coupling