4.8 Article

Revealing Intermolecular Electronic and Vibronic Coherence with Polarization-Dependent Two-Dimensional Beating Maps

Journal

JOURNAL OF PHYSICAL CHEMISTRY LETTERS
Volume -, Issue -, Pages 838-845

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpclett.2c03413

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Two-dimensional electronic spectroscopy (2DES) is commonly used to study intermolecular electronic and vibronic coherence in light-harvesting complexes. However, intramolecular vibrational coherence can also contribute to the spectra, making it difficult to distinguish the different coherences. This study explores the possibility of selectively screening vibrational coherence using polarization-dependent 2DES, and demonstrates that population and vibrational coherence signals can be largely suppressed, allowing for clearer observation of intermolecular coherence.
Two-dimensional electronic spectroscopy (2DES) has been widely employed as an efficient tool to reveal the impact of intermolecular electronic and/ or vibronic quantum coherence on excitation energy transfer in light-harvesting complexes. However, intramolecular vibrational coherence would also contribute to oscillating signals in 2D spectra, along with the intermolecular coherence signals that are directly related to energy transfer. In this work, the possibility of screening the vibrational coherence signals is explored through polarization-dependent 2DES. The all-parallel (AP) and double-crossed (DC) polarization-dependent two-dimensional rephasing spectra (2DRS) are simulated for a minimalist heterodimer model with vibrational coupling. By combining the DC-2DRS and the 2D beating maps, we demonstrate that the population and vibrational coherence signals can be largely suppressed, resulting in highlighted intermolecular electronic and vibronic coherence signals. Moreover, the AP-and DC-2DBMs show rather different patterns at the vibrational frequency, indicating a possible way to identify pure vibrational coherence.

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