Tuning quantum coherence time scales in molecules via light-matter hybridization
ORAL
Abstract
Protecting quantum coherences in matter from the detrimental effects introduced by its environment is essential to employ molecules and materials in quantum technologies and develop enhanced spectroscopies. Here, we show how dressing molecular chromophores with quantum light in the context of optical cavities can be used to generate quantum superposition states with tunable coherence time scales that are longer than those of the bare molecule, even at room temperature and for molecules immersed in solvent.
For this, we develop a theory of decoherence rates for molecular polaritonic states and demonstrate that quantum superpositions that involve such hybrid light-matter states can survive for times that are orders of magnitude longer than those of the bare molecule while remaining optically controllable. Further, by studying these tunable coherence enhancements in the presence of lossy cavities we demonstrate that they can be enacted using present-day optical cavities. The analysis offers a viable strategy to engineer and increase quantum coherence lifetimes in molecules.
For this, we develop a theory of decoherence rates for molecular polaritonic states and demonstrate that quantum superpositions that involve such hybrid light-matter states can survive for times that are orders of magnitude longer than those of the bare molecule while remaining optically controllable. Further, by studying these tunable coherence enhancements in the presence of lossy cavities we demonstrate that they can be enacted using present-day optical cavities. The analysis offers a viable strategy to engineer and increase quantum coherence lifetimes in molecules.
–
Presenters
-
Wenxiang Hu
University of Rochester
Authors
-
Ignacio Franco
University of Rochester
-
Todd Krauss
University of Rochester
-
Wenxiang Hu
University of Rochester