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The Japan Society of Applied Physics

Observation of ultrafast luminescence at room temperature due to long-range coupling between excitons and light

Takuya Matsuda, Takuya Takahashi, Masayoshi Ichimiya, Masaaki Ashida, Hajime Ishihara

Published Jul 21, 2017• 0 citations
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We demonstrate ultrafast superradiance showing 10-fs decay due to the nonlocal interaction between light waves and exciton waves in CuCl mesoscopic thin films. This time constant is comparable with the thermal dephasing even at room temperature. Actually, we observed photoluminescence signal from one confined mode of translational motion of the exciton surviving at room temperature. In addition, temperature dependence of the photoluminescence spectra with multiple peaks was reproduced well by theoretical calculation. This finding opens a new avenue of “thermal free photonics”, where the exciton coherence is utilized at higher temperature.
Superfluorescence (SF) is a unique quantum mechanical behavior arising from the self-organization between emitters, thus forming a cooperatively coupled assembly. In contrast to isotropic spontaneous emission or normal fluorescence, SF produces a short but intense burst of light, which makes it ideal for a wide variety of applications in photonics, electronics, and optical computing. Due to the prerequisite of cooperative emitter coupling, SF has been conventionally observed under cryogenic conditions in limited systems, such as atomic gases, and a few bulk material systems. Here we show lanthanide-doped upconversion nanoparticles (UCNPs) as a medium to achieve antiStokes shift SF at room temperature. We observe such room temperature upconverted SF in a few nanoparticles assembly, and in a single nanoparticle, the latter of which is the smallest-ever SF media. In particular, we found that under near-infrared light (800 nm) excitation, each lanthanide ion in a single UCNP nanocrystal can be considered as an individual emitter that interact with each other to establish coherence and to enable anti-Stokes shift SF emission. More importantly, when compared to the microsecond scale slow lifetime of typical upconversion luminescence, the upconverted SF has a 10,000-fold accelerated lifetime (τ = 46 ns of SF v.s. τ = 455.8 μs of normal upconversion luminescence). When taken together, the observed ultrafast upconverted SF in both UCNP assembly and single nanocrystals under NIR light excitations, is uniquely well-positioned for applications in on-chip optical computing, and biophotonics, especially in deep tissue ultra-fast dynamic sensing.