Cavity-enhanced magnetic dipole resonance induced hot luminescence from hundred-nanometer-sized silicon spheres

腔增强磁偶极共振诱导百纳米级硅球产生热发光

阅读:1

Abstract

In this paper, we demonstrate the first example of phonon-assisted hot luminescence (PAHL) emission from silicon (Si) spheres (diameter > 100nm) without using the plasmonic effect or quantum confinement effect. Instead, we excite the hot luminescence of Si by a strong thin-film-cavity-enhanced magnetic dipole resonance. The thin-film cavity (80 nm SiO(2)/Ag) shows a strong co-enhancement with the magnetic dipole resonance of Si sphere (diameter = 120 nm). The concentrated electromagnetic fields induce significant light-matter interaction. Our Si sphere coupled with a thin-film cavity achieves a 10-fold field enhancement relative to the Si sphere without an enhancement substrate. Furthermore, we experimentally use cavity-enhanced magnetic dipole resonance to a 50-fold enhancement in PAHL. The measured internal quantum efficiency for the visible light emitted from the Si spheres was approximately 2.4%. Furthermore, we demonstrate the tunability of emission peaks merely by adjusting the sizes of Si spheres using thermal oxidation and etching processes. For comparison, we calculated the peak wavelength (λ (peak)) sensitivities (Δλ (peak)/ΔDiameter) of Si spheres and Si QDs through Mie theory and effective mass approximation, respectively. The predicated peak sensitivities of the Si spheres ranged from 1.3 to 3.2; they were much more controllable than those of the Si QDs (200-400). Thus, the peak wavelengths of the PAHL of the Si spheres could be modulated and controlled much more precisely and readily than that of the Si QDs. With the tunability and strong electromagnetic field confinement, the cavity-enhanced magnetic dipole resonance appears to have great potential in the development of all-optical processing based on Si photonics.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。