Ultrafast dynamics in plasmon-exciton core-shell systems: the role of heat.

Strong coupling between plasmons and excitons gives rise to new hybrid polariton states with potential applications in various fields. Despite a plethora of research on plasmon-exciton systems, their transient behaviour is not yet fully understood. Besides Rabi oscillations in the first few femtoseconds after optical excitation, coupled systems show interesting non-linear features on the picosecond time scale. Here, we conclusively show that the source of these features is heat that is generated inside the particles. Until now, this hypothesis was only based on phenomenological arguments. We investigate the role of heat by recording the transient spectra of plasmon-exciton core-shell nanoparticles with excitation off the polariton resonance. We present analytical simulations that precisely recreate the measurements solely by assuming an initial temperature rise of the electron gas inside the particles. The simulations combine established strategies for describing uncoupled plasmonic particles with a recently published model for static spectra. The simulations are consistent for various excitation powers, confirming that heating of the particles is indeed the root of the changes in the transient signals.

Decoding the kinetic limitations of plasmon catalysis: the case of 4-nitrothiophenol dimerization.

Plasmon-mediated chemistry presents an intriguing new approach to photocatalysis. However, the reaction enhancement mechanism is not well understood. In particular, the relative importance of plasmon-generated hot charges and photoheating is strongly debated. In this article, we evaluate the influence of microscopic photoheating on the kinetics of a model plasmon-catalyzed reaction: the light-induced 4-nitrothiophenol (4NTP) to 4,4'-dimercaptoazobenzene (DMAB) dimerization. Direct measurement of the reaction temperature by nanoparticle Raman-thermometry demonstrated that the thermal effect plays a dominant role in the kinetic limitations of this multistep reaction. At the same time, no reaction is possible by dark heating to the same temperature. This shows that plasmon nanoparticles have the unique ability to enhance several steps of complex tandem reactions simultaneously. These results provide insight into the role of hot electron and thermal effects in plasmonic catalysis of complex organic reactions, which is highly important for the ongoing development of plasmon based photosynthesis.