Room-Temperature CsPbBr3 Mixed Polariton States

Light-matter interactions are known to lead to the formation of polariton states through what is called strong coupling, allowing the formation of two hybrid states usually tagged as Upper and Lower Polaritons. Here, we consider a similar interaction between excitons and photons in the realm of strong interactions, with the difference that it enables us to obtain a mixed-polariton state. In this case, the energy of this mixed state is found between the energies of the exciton state and the cavity mode, resulting in an imaginary coupling coefficient related to a specific class of singular points. These mixed states are often considered unobservable, although they are predicted well when the dressed states of a two-level atom are considered. However, intense light confinement can be obtained by using a Bound State in the Continuum, reducing the damping rates, and enabling the observation of mixed states resulting from the correct kind of exceptional point giving place to strong coupling. In this study, using the Transfer Matrix Method, we simulated cavities made of porous silicon coupled with CsPbBr3 perovskite quantum dots to numerically observe the mixed states as well as experimentally, by fabricating appropriate samples. The dispersion relation of the mixed states is fitted using the same equation as that used for strong coupling but considering a complex coupling coefficient, which can be directly related to the appropriate type of exceptional point

Ultrafast Heat Transfer at the Nanoscale: Controlling Heat Anisotropy

Thermoplasmonics has benefited from increasing attention in recent years by exploiting the photothermal effects within plasmonic nanoparticles to generate nanoscale heat sources. Recently, it has been demonstrated that exciting gold nanoparticles with ultrashort light pulses could be used to achieve high-speed light management and nanoscale heat-sensitive chemical reaction control. In this work, we study non-uniform thermal energy transient distribution inside cross-shaped nanostructures with femtosecond transient spectroscopy coupled to a thermo-optical numerical model, free of fitting parameters. We show experimentally and numerically that the polarization of the excitation light can control the heat distribution in the nanostructures. We also demonstrate the necessity of considering nonthermal electron ballistic displacement in fast transient heat dynamics models

Ultrafast Heat Transfer at the Nanoscale: Controlling Heat Anisotropy

Thermoplasmonics has benefited from increasing attention in recent years by exploiting the photothermal effects within plasmonic nanoparticles to generate nanoscale heat sources. Recently, it has been demonstrated that exciting gold nanoparticles with ultrashort light pulses could be used to achieve high-speed light management and nanoscale heat-sensitive chemical reaction control. In this work, we study non-uniform thermal energy transient distribution inside cross-shaped nanostructures with femtosecond transient spectroscopy coupled to a thermo-optical numerical model, free of fitting parameters. We show experimentally and numerically that the polarization of the excitation light can control the heat distribution in the nanostructures. We also demonstrate the necessity of considering nonthermal electron ballistic displacement in fast transient heat dynamics models

Ultrafast Heat Transfer at the Nanoscale: Controlling Heat Anisotropy

Thermoplasmonics has benefited from increasing attention in recent years by exploiting the photothermal effects within plasmonic nanoparticles to generate nanoscale heat sources. Recently, it has been demonstrated that exciting gold nanoparticles with ultrashort light pulses could be used to achieve high-speed light management and nanoscale heat-sensitive chemical reaction control. In this work, we study non-uniform thermal energy transient distribution inside cross-shaped nanostructures with femtosecond transient spectroscopy coupled to a thermo-optical numerical model, free of fitting parameters. We show experimentally and numerically that the polarization of the excitation light can control the heat distribution in the nanostructures. We also demonstrate the necessity of considering nonthermal electron ballistic displacement in fast transient heat dynamics models