Mapping electronic decoherence pathways in molecules

Abstract

Establishing the fundamental chemical principles that govern molecular electronic quantum decoherence has remained an outstanding challenge. Fundamental questions such as how solvent and intramolecular vibrations or chemical functionalization contribute to the decoherence remain unanswered and are beyond the reach of state-of-the-art theoretical and experimental approaches. Here we address this challenge by developing a strategy to isolate electronic decoherence pathways for molecular chromophores immersed in condensed phase environments that enables elucidating how electronic quantum coherence is lost. For this, we first identify resonance Raman spectroscopy as a general experimental method to reconstruct molecular spectral densities with full chemical complexity at room temperature, in solvent, and for fluorescent and non-fluorescent molecules. We then show how to quantitatively capture the decoherence dynamics from the spectral density and identify decoherence pathways by decomposing the overall coherence loss into contributions due to individual molecular vibrations and solvent modes. We illustrate the utility of the strategy by analyzing the electronic decoherence pathways of the DNA base thymine in water. Its electronic coherences decay in ∼ 30 fs. The early-time decoherence is determined by intramolecular vibrations while the overall decay by solvent. Chemical substitution of thymine modulates the decoherence with hydrogen-bond interactions of the thymine ring with water leading to the fastest decoherence. Increasing temperature leads to faster decoherence as it enhances the importance of solvent contributions but leaves the early-time decoherence dynamics intact. The developed strategy opens key opportunities to establish the connection between molecular structure and quantum decoherence as needed to develop chemical strategies to rationally modulate it.

Progress towards on-chip entangled photon spectroscopy and bioimaging

“…Moreover, atoms generally have classical TPA cross sections in the range of 10 −40 − 10 −35 cm 4 s, which are 7-15 orders of magnitude larger than those of organic molecules (10 −50 − 10 −47 cm 4 s). 113,[123][124][125][126][127] Atoms also have longer-lived excited state coherences than molecules [128][129][130][131][132][133] which could facilitate coherent biphoton processes. To date, experimental studies in organic molecules have only focused on virtual state-mediated ETPA (v-ETPA) instead of r-ETPA processes.…”