ABSTRACT
Plasmonic color filters are expected to be candidates for application to complementary metal-oxide-semiconductor (CMOS) image sensor arrays with reduced pixel size, owing to the subwavelength mode volume of plasmons. Designs of metallic gratings based on the guided-mode resonance effect suffer from the sideband transmission issue due to high-order diffraction. Here, we propose a plasmonic color filter structure based on a hetero-metal-insulator-metal grating. The guided mode, in resonance with the second-order diffraction, is highly attenuated by the forbidden band, such that the sideband transmission can be suppressed. As calculated by using the transfer matrix method and the finite-difference time-domain method, the Al-ZnO-Ag waveguide-based structure presents a color filter characteristic with the peak transmittance greater than 70% and the peak wavelength tunable in the visible light band. It may find application in displays, image sensors, and biomedical imaging technologies.
ABSTRACT
Branchlike nano-electrode structures were found to improve the THz emission intensity of a photomixer by approximately one order of magnitude higher than that of a photomixer with one row of nano-electrodes separated by the same 100 nm gap. The enhancement is attributed to a more efficient collection of generated carriers, which is in turn due to a more intense electric field under the branchlike nano-electrodes' structures. This is coupled with an increased number of effective areas where strong tip-to-tip THz field enhancements were observed. The optical-to-THz conversion efficiency of the photomixers with the new branchlike nano-electrodes was found to be 10 times higher. The more efficient THz photomixer will greatly benefit the development of continuous-wave THz imaging and spectroscopy systems.
ABSTRACT
A homologous series of polyhydroxylated poly(p-phenylene)s with different alkoxy groups (C6PPPOH, C12PPPOH, and C18PPPOH) were synthesized with use of the Suzuki polycondensation reaction. Comparative studies of the structure correlation between their photophysical properties and film morphology is described. The absorption and emission spectra of polymers in solution and thin films showed similar features indicating that the electronic properties in solution were retained in the film state. Compared to the polymer with the short alkoxy chains (C6PPPOH), the polymers with long alkoxy groups (C12PPPOH and C18PPPOH) showed improved film forming properties with continuous and smooth film morphology. The absorption properties of the C12PPPOH showed an enhanced effective conjugation length and high quantum yield implying planarization of the backbone through alkoxy chain packing (C12H25O-) and potential hydrogen bonds. No overlap in the absorption and emission spectra was observed, which indicated minimized excimer formation or excitation energy transfer in the films. Time-resolved fluorescence measurements showed that the decay times increased from 43 ps (C6PPPOH) to 78 ps (C12PPPOH) and 99 ps (C18PPPOH). Electrochemical studies were performed for all polymers and the observed oxidation potential for C6PPPOH was higher than that of C12PPPOH and C18PPPOH. In addition, the C12PPPOH has the lowest band gap of DeltaE = 2.59 eV when compared to the 3.1 (C6PPPOH) and 2.61 eV (C18PPPOH) gaps. The optical band gaps estimated from the absorption onset of the polymers are significantly higher than those obtained from electrochemical data. C12PPPOH was chosen for investigating the charge carrier mobility by the time-of-flight (TOF) technique. The observed results also showed negative field dependent values of the drift mobility for the polymer C12PPPOH.
