Affiliation:
1. Department of Chemistry, Purdue University , West Lafayette, Indiana 47907, USA
Abstract
Two-dimensional (2D) infrared (IR) spectra are commonly interpreted using a quantum diagrammatic expansion that describes the changes to the density matrix of quantum systems in response to light–matter interactions. Although classical response functions (based on Newtonian dynamics) have shown promise in computational 2D IR modeling studies, a simple diagrammatic description has so far been lacking. Recently, we introduced a diagrammatic representation for the 2D IR response functions of a single, weakly anharmonic oscillator and showed that the classical and quantum 2D IR response functions for this system are identical. Here, we extend this result to systems with an arbitrary number of bilinearly coupled, weakly anharmonic oscillators. As in the single-oscillator case, quantum and classical response functions are found to be identical in the weakly anharmonic limit or, in experimental terms, when the anharmonicity is small relative to the optical linewidth. The final form of the weakly anharmonic response function is surprisingly simple and offers potential computational advantages for application to large, multi-oscillator systems.
Subject
Physical and Theoretical Chemistry,General Physics and Astronomy
Cited by
1 articles.
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1. Celebrating 25 years of 2D IR spectroscopy;The Journal of Chemical Physics;2024-01-02