発表者名 |
齊藤 孝太朗 |
指導教員名 |
吉岡 孝高 准教授 |
発表題目(英語) |
Giant Rydberg excitons in the copper oxide Cu_2O |
要旨(英語) |
In bulk semiconductors, excitons are quasiparticles composed of an electron and a hole bound by the Coulomb interaction. They possess hydrogen-like energy levels. Rydberg excitons, characterized by high principal quantum numbers, have attracted significant attention as solid-state analogies to Rydberg atoms, which are promising platforms for quantum computing and quantum simulation in atomic physics.
In this talk, I will present experimental results, which reported the first observation of Rydberg excitons with principal quantum numbers ranging from n = 2 to 25 [1]. In this study, a natural Cu_2O crystal was cooled to 1.2 K and its exciton absorption spectrum was probed by a narrow-linewidth monochromatic laser, while the transmitted intensity was recorded with high spectral resolution. As a result, excitons with principal quantum number up to n = 25 were observed; their wavefunctions extended beyond a 2 μm diameter. From their data, the authors estimated that exciton lifetimes are on the order of nanosecond timescale. Furthermore, they interpreted the experimental results as evidence of a dipole-blockade effect, in which Rydberg excitons with high principal quantum numbers prevent the excitation of neighboring excitons.
In this study, they suggested that positions where Rydberg excitons are generated can be controlled with high precision by applying spatially modulated strain fields to the crystal. In our current research, we are investigating a spin‐flip dynamics of excitons in a Cu_2O crystal under spatially inhomogeneous strain. By understanding exciton behavior under spatially inhomogeneous strain, we consider our research can provide a basis for developing techniques to precisely control the positions where Rydberg excitons are generated.
[1] T. Kazimierczuk, D. Fröhlich, S. Scheel, H. Stolz, and M. Bayer, Nature 514, 343–347 (2014). |
発表言語 |
日本語 |