By Dalian Institute of Chemical Physics, Chinese Academy Sciences September 15, 2024
Collected at: https://scitechdaily.com/scientists-capture-elusive-quantum-floquet-states-with-visible-light/
Researchers have directly observed Floquet states in semiconductors using all-optical spectroscopy under ambient conditions, revealing new possibilities for controlling chemical reactions with light.
Solution-processed semiconductor nanocrystals, known as colloidal quantum dots (QDs), are an example of size-dependent quantum effects that physicists had long understood in theory. However, it wasn’t until the discovery of QDs that these effects could be realized in actual nanoscale materials.
The size-dependent colors of QDs are essentially naked-eye, ambient-condition visualization of the quantum size effect. In recent years, researchers across the world have been searching for fascinating quantum effects or phenomena using the material platform of QDs, such as single-photon emission and quantum coherence manipulation.
Floquet States and Quantum Phenomena
Floquet states (i.e., the photon-dressed states) are ubiquitously invoked to explain quantum phenomena in relation to coherent interaction between light field and matter. However, direct observation of these Floquet states has been an experimental challenge. For example, only until very recently did researchers report experimental signatures of Floquet-Bloch bands in black phosphorus (a narrow-gap model semiconductor) interacting with mid-infrared pulses by using complex time- and angle-resolved photoemission spectroscopy.
In such studies, the samples were almost exclusively housed in low-temperature, high-vacuum environments, and the driving fields were tuned to the infrared, terahertz, or even microwave regions to avoid sample damage.
Breakthrough Observation of Floquet States
In a study published in Nature Photonics, Prof. Kaifeng Wu and his colleagues from the Dalian Institute of Chemical Physics of the Chinese Academy of Sciences reported the first direct observation of Floquet states in semiconductors by using all-optical spectroscopy in the visible to near-infrared region under ambient conditions.
The researchers adopted the quasi-two-dimensional colloidal nanoplatelets developed in the past decade. The strong, atomically-precise quantum confinement in the thickness dimension results in interband and intersubband transitions in the visible and near-infrared regions, respectively. The levels involved in such transitions naturally form a three-level system. A sub-bandgap visible photon dresses a heavy-hole state (|hh1⟩) to a Floquet state of the same parity as the first quantized electron state (|e1⟩), allowing this Floquet state to be probed by a near-infrared photon through its transition to the second quantized electron state (|e2⟩).
Moreover, while the transiently populated Floquet states were often assumed to fade away outside the temporal overlap of pump and probe pulses, the researchers directly observed dephasing of the Floquet state into real population of |e1⟩ in hundreds of femtoseconds. All the experimental observations in this study are substantiated by quantum mechanical simulations.
“Not only does this study provide an all-optical direct observation of Floquet states in semiconductor materials, but it also uncovers the rich spectral and dynamic physics of Floquet states that can be harnessed to dynamically control the optical responses and coherent evolution in condensed-matter systems,” said Prof. Wu.
Since the current demonstration is attained for colloidal materials under ambient conditions, it will expand the reach of Floquet engineering, which currently focuses on tailoring the quantum and topological properties of solid-state materials, to coherently controlling surface/interfacial chemical reactions through nonresonant light field.
Reference: “Observation of Floquet states and their dephasing in colloidal nanoplatelets driven by visible pulses” by Yuxuan Li, Yupeng Yang, Yuan Liu, Jingyi Zhu and Kaifeng Wu, 13 August 2024, Nature Photonics.
DOI: 10.1038/s41566-024-01505-z
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