RESUMEN
Localized surface plasmons exhibit promising capabilities in optoelectronic devices. In most cases, the metal nanoparticle arrays are located on interfaces or inside optical cavities. Fano interferences have been observed and explained via the interference between the waves generated by the localized surface plasmon and dielectric interfaces. Conventionally, these Fano interferences are modeled using the modified Fresnel equation. However, certain issues persist in the fundamental physics or in the numerical calculation process. Here, we adopt the equivalent medium theory (Maxwell-Garnett theory, MGT) to calculate and elucidate Fano interferences in different structures, in the region comprising nanoparticle arrays and dielectrics equivalent to a homogeneous layer of media via the mean field theory. Using this method, the Fano interference can be modeled by mixing different materials, i.e., metals and dielectrics in these cases. Furthermore, a multiple-layered equivalent medium theory is proposed to significantly improve the scalability of this simplified numerical method. In other words, this method can be easily extended to nanoparticles with different shapes, sizes, and materials; in addition, it exhibits robust practicability. Compared with the modified Fresnel equation and finite-difference time-domain methods, this MGT-based method can effectively minimize the calculation process, which is beneficial to the prospective application of plasmon photonics.
RESUMEN
The polarization properties of asymmetric plasmonic nanostructures originating from optical anisotropy show great application prospects in many fields, such as display, sensing, filtering, and detection. Here, we report the realization of polarization control in the deep ultraviolet (UV) region using Al nano-dimer structures. The simulation results indicated that the polarization effect was generated by the modulation of inter-coupling between the quadrupole plasmon resonances of the asymmetric dimer. By further optimizing the size and gap of the dimer, the extinction in the 200-nm deep UV region obtained a polarization ratio of 18%. This research is helpful for understanding the resonance hybridization of high-order surface plasmons in UV region and is of great significance to the emerging polarized micro-nano photonics fields, such as spin optoelectronics and deep UV optoelectronic devices.
RESUMEN
Solar-blind photodetectors (PDs) are widely applicable in special, military, medical, environmental, and commercial fields. However, high performance and flexible PD for deep ultraviolet (UV) range is still a challenge. Here, it is demonstrated that an upconversion of photon absorption beyond the energy bandgap is achieved in the ZnO nanoarray/h-BN heterostructure, which enables the ultrahigh responsivity of a solar-blind photodetecting paper. The direct growth of ultralong ZnO nanoarray on polycrystalline copper paper induced by h-BN 2D interlayer is obtained. Meanwhile, strong photon trapping takes place within the ZnO nanoarray forest through the cyclic state transition of surface oxygen ions, resulting in an extremely high absorption efficiency (> 99.5%). A flexible photodetecting paper is fabricated for switchable detections between near UV and deep UV signals by critical external bias. The device shows robust reliability, ultrahigh responsivity up to 700 A W-1 @ 265-276 nm, and high photoconductive gain of ≈2 × 103 . A negative differential resistance effect is revealed for driving the rapid transfer of up-converted electrons between adjacent energy valleys (Γ to A) above the critical bias (3.9 V). The discovered rationale and device structure are expected to bring high-efficiency deep UV detecting and future wearable applications.