Ultrafast thermal-free photoluminescence of coherently extended single quantum states
Abstract The coherent volume of single quantum states of matter is typically smaller than that of photons by several orders of magnitude, and hence, interactions between photons and single quantum states are normally very weak. This limits the speed of radiative decay of matter states in free space....
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| Autores principales: | , , , |
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| Formato: | article |
| Lenguaje: | EN |
| Publicado: |
Nature Portfolio
2019
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| Materias: | |
| Acceso en línea: | https://doaj.org/article/d99ad904aa4847789d1e2e0dfae974a0 |
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| Sumario: | Abstract The coherent volume of single quantum states of matter is typically smaller than that of photons by several orders of magnitude, and hence, interactions between photons and single quantum states are normally very weak. This limits the speed of radiative decay of matter states in free space. Recent efforts to speed-up radiative processes have been focused on creating a small mode volume of photons using cavity systems, or on realizing spontaneous synchronization among quantum emitters to create a dipole at the macroscopic scale, which accelerates photon emission up to a couple of hundred femtoseconds. Here, we demonstrate the 10-fs class of photoluminescence (PL) of a single quantum state in solid thin films without the use of a photo-cavity system or the spontaneous synchronization effect. Significantly, this speed can beat thermal dephasing of relevant excited states at room temperature, which is typically a couple of tens of femtoseconds. The process occurs due to the giant interaction volume between light waves and the multipole excitonic waves. This result indicates the possibility to realize photoemission processes that complete before the thermal dephasing process activates, which opens up the hidden potential of ubiquitous solids as thermal-free or extremely low-energy-loss photonic materials. |
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