Two-dimensional IR–Raman spectroscopy of vibrational polaritons: Role of dipole surfaces

Abstract

Nonlinear spectroscopy provides a unique perspective to understand time-resolved molecular dynamics under vibrational strong coupling (VSC). Herein, equilibrium–nonequilibrium cavity molecular dynamics simulations are performed to compute the two-dimensional (2D) infrared–infrared–Raman (IIR) spectroscopy of liquid water under VSC. In conventional computational chemistry practices, accurate molecular spectra are often constructed by using an advanced molecular dipole or polarizability model to post-process molecular dynamics trajectories evolved under a computationally efficient potential. By contrast, this work highlights the necessity of employing a consistent dipole surface model in both cavity molecular dynamics (CavMD) simulations and spectroscopic post-processing. While utilizing inconsistent dipole models only mildly influences the linear polariton spectrum, it severely distorts 2D spectra in wide frequency regions. With a consistent dipole–induced-dipole model, compared to the outside-cavity molecular 2D-IIR spectrum, the cavity 2D-IIR spectrum splits the OH stretch band to a pair of polariton branches only along the IR (not Raman) axis, while fading molecular signals at other frequency regions. This work provides the foundation for employing direct CavMD simulations to construct 2D spectra of realistic molecules under VSC.