In this work, a near-perfect broadband absorber, consisting of Fe, MgF2, Fe, TiO2 and MgF2 planar film, is proposed and investigated through simulations and experiments. The Fe material is first applied in the multilayer film structure, and it is proved to be more favorable for achieving broadband absorption. MgF2 and TiO2 are chosen as anti-reflection coatings to decrease unwanted reflections. The proposed absorber is optimized by employing a hybrid numerical method combining the transfer matrix method (TMM) and the genetic algorithm (GA). Under normal incidence conditions, the average absorption of the absorber is 97.6% in the range of 400 to 1400 nm. The finite difference time domain (FDTD) method and phase analysis reveal that the anti-reflection property and the Fabry-Perot resonance result in broadband absorption performance. Furthermore, when an additional Fe-MgF2 layer is inserted on the bottom Fe layer, an average absorption of 97.9% in the range of 400 to 2000 nm can be achieved. Our approach could be of vital significance for numerous applications involving solar energy.

We investigate a high-sensitivity surface plasmon resonance (SPR) biosensor consisting of a Au layer, four-layer MoS2, and monolayer graphene. The numerical simulations, by the transfer matrix method (TMM), demonstrate the sensor has a maximum sensitivity of 282°/RIU, which is approximately 2 times greater than the conventional Au-based SPR sensor. The finite difference time domain (FDTD) indicates that the presence of MoS2 film generates a strong surface electric field and enhances the sensitivity of the proposed SPR sensor. In addition, the influence of the number of MoS2 layers on the sensitivity of the proposed sensor is investigated by simulations and experiments. In the experiment, MoS2 and graphene films are transferred on the Au-based substrate by the PMMA-based wet transfer method, and the fabricated samples are characterized by Raman spectroscopy. Furthermore, the fabricated sensors with the Kretschmann configuration are used to detect okadaic acid (OA). The okadaic acid–bovine serum albumin bioconjugate (OA-BSA) is immobilized on the graphene layer of the sensors to develop a competitive inhibition immunoassay. The results show that the sensor has a very low limit of detection (LOD) of 1.18 ng/mL for OA, which is about 22.6 times lower than that of a conventional Au biosensor. We believe that such a high-sensitivity SPR biosensor has potential applications for clinical diagnosis and immunoassays.