Organic molecules interact strongly with confined electromagnetic fields in plasmonic arrays or optical microcavities owing to their bright transition dipole moments. This interaction gives rise to molecular polaritons, hybrid light-matter quasiparticles. Molecular polaritonics opens doors for new room-temperature opportunities for the nontrivial control of physico-chemical properties of molecular assemblies . In this talk, I’ll showcase some of these opportunities that we have been theoretically (and, together with our experimental collaborators) exploring in the past few years. I will briefly discuss the relevant time and energy scales associated with molecular polaritons [1,2] and strategies to exploit them to control photoexcited processes including singlet fission , triplet harvesting , remote and topologically-protected energy transfer [5-7], and anomalous nonlinear optical effects [8,9,10]. Finally, I will conclude by explaining how vibrational polaritons can steer ground-state chemical reactions even in the absence of optical pumping , or be used to realize exotic processes such as remote control of chemical reactions .
Speaker: Joel Yuen-Zhou, UC San Diego
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