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D. G. Lidzey

Publications and source records attributed to D. G. Lidzey.

3 recordsLinked to original sources

Superabsorption in an organic microcavity: towards a quantum battery

The rate at which matter emits or absorbs light can be modified by its environment, as dramatically exemplified by the widely-studied phenomenon of superradiance. The reverse process, superabsorption, is harder to demonstrate due to the challenges of probing ultrafast processes, and has only been seen for small numbers of atoms. Its central idea - superextensive scaling of absorption meaning larger systems absorb faster - is also the key idea underpinning quantum batteries. Here we implement experimentally a paradigmatic model of a quantum battery, constructed of a microcavity enclosing a molecular dye. Ultrafast optical spectroscopy allows us to observe charging dynamics at femtosecond resolution to demonstrate superextensive charging rates and storage capacity, in agreement with our theoretical modelling. We find that decoherence plays an important role in stabilising energy storage. Our work opens new opportunities for harnessing collective effects in light-matter coupling for nanoscale energy capture, storage, and transport technologies.

quant-ph↗

Nano-second exciton-polariton lasing in organic microcavities

Organic semiconductors are a promising platform for ambient polaritonics. Several applications, such as polariton routers, and many-body condensed matter phenomena are currently hindered due to the ultra-short polariton lifetimes in organics. Here, we employ a single-shot dispersion imaging technique, using 4 nanosecond long non-resonant excitation pulses, to study polariton lasing in a $λ/2$ planar organic microcavity filled with BODIPY-Br dye molecules. At a power threshold density of $1.5 MW/cm^{2}$, we observe the transition to a quasi-steady state, 1.2 ns long-lived, single-mode polariton lasing and the concomitant superlinear increase of photoluminescence, spectral line-narrowing, and energy blueshift

physics.app-ph↗

Non-radiative exciton energy transfer in hybrid organic-inorganic heterostructures

Non-radiative optical energy transfer from a GaAs quantum well to a thin overlayer of an infrared organic semiconductor dye is unambiguously demonstrated. The dynamics of exciton transfer are studied in the time-domain using pump-probe spectroscopy at the donor site and fluorescence spectroscopy at the acceptor site. The effect is observed as simultaneous increase of the population decay rate at the donor and of the rise time of optical emission at the acceptor sites. The hybrid configuration under investigation provides an alternative non-radiative, non-contact pumping route to electrical carrier injection that overcomes the losses imposed by the associated low carrier mobility of organic emitters.

cond-mat.other↗