在AlN-on-sapphire平台上的高效,冷兼容的网格合器通过底侧合器通过底侧合器
Optics letters
|January 31, 2025
概括
我们通过在蓝宝石基板上使用底侧合提高了格子合器传输效率. 这种方法在化光子设备中实现了42%的效率,即使在冷温度下也是如此.
科学领域:
- 光子学 是一个光子学.
- 材料科学 材料科学 材料科学
- 光电学是指光电子产品.
背景情况:
- 蓝宝石基板被广泛用于宽带间隙III-化物光子设备.
- 蓝宝石的高折射率导致传统网格合器的传输效率较低.
- 高效的光合对于集成光子应用至关重要.
研究的目的:
- 在蓝宝石基板上的网格合器中显著提高传输效率.
- 为了研究一种新的底侧合技术.
- 为了评估网合器在低温温度下的性能.
主要方法:
- 提出并演示了一个底侧合方法.
- 在基板的顶部使用金属反射器,在基板的底部使用纤维阵列.
- 在电信波长的蓝宝石网格合器上实验测试了化 (AlN).
主要成果:
- 每个合器的最大传输效率达到了42%.
- 在低至3K的冷温度下表现出强大的性能.
- 对横向电 (TE) 和横向磁 (TM) 两种模式的经过验证的性能.
结论:
- 底侧合有效地提高了蓝宝石上的格子合器的传输效率.
- 开发的网格合器在冷条件下表现出色的性能.
- 这种技术有利于基于蓝宝石的光子应用,需要低合损失和低温操作.
相关概念视频
Spin–Spin Coupling: Two-Bond Coupling (Geminal Coupling)
Two NMR-active nuclei bonded to a central atom can be involved in geminal or two-bond coupling. Geminal coupling is commonly seen between diastereotopic protons in chiral molecules and unsymmetrical alkenes, among others.
The central atom need not be NMR-active because its electrons are affected by the electron polarization of the spin-active atoms. However, spin information is transmitted less effectively than in one-bond coupling, and 2J values are usually weaker than 1J values. The energy of...
The central atom need not be NMR-active because its electrons are affected by the electron polarization of the spin-active atoms. However, spin information is transmitted less effectively than in one-bond coupling, and 2J values are usually weaker than 1J values. The energy of...
¹H NMR: Long-Range Coupling
The coupling interactions of nuclei across four or more bonds are usually weak, with J values less than 1 Hz. While these are usually not observed in spectra, the presence of multiple bonds along the coupling pathway can result in observable long-range coupling.
In alkenes, spin information is communicated via σ–π overlap, as seen in allylic (four-bond) and homoallylic (five-bond) couplings. These coupling interactions are stronger when the σ bond is parallel to the alkene π orbitals.
In alkenes, spin information is communicated via σ–π overlap, as seen in allylic (four-bond) and homoallylic (five-bond) couplings. These coupling interactions are stronger when the σ bond is parallel to the alkene π orbitals.


