Browsing by Author "Yu, Min-Wen"
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Item type:Item, Absorption avoided resonance crossing of hybridization of silicon nanoparticles and gold nanoantennas(2019-08-13) ;Yang, Jhen-Hong ;Yu, Min-Wen ;Chen, Kuo-Ping ;光電系統研究所照明與能源光電研究所The near-field coupling between a high-refractive-index nanoparticle and gold nanoantennas is investigated theoretically. The absorption enhancement and also avoided resonance crossing in the absorption cross section spectra were observed with the hybridization system due to the coupling between the localized surface plasmon resonance of the gold nanoantennas and the magnetic dipole resonance of the silicon nanoparticle. By controlling the nanoparticle size or the separation distance, the near-field coupling can be tuned from the weak to the strong regime.Item type:Item, Graphene-Loaded Plasmonic Zirconium Nitride and Gold Nanogroove Arrays for Surface-Charge Modifications(2020-06-26) ;Yu, Min-Wen ;Ishii, Satoshi ;Ku, Ji-Ren ;Yang, Jhen-HongHuang, Chih-HsiangGraphene-on-metal (G/M) heterostructures have gained considerable attention in recent years owing to their outstanding optical and electrical properties. In this study, the polarity of graphene doping to different metallic materials underneath graphene is analyzed for applications in surface-charge modifications. Kelvin probe force microscopy clearly reveals the charge-transfer effects of plasmonic zirconium nitride (ZrN) and gold (Au) on the formation of G/M heterostructures. In addition, both ZrN and Au nanogroove arrays are fabricated by focused ion beam to generate surface plasmon resonances. The charge-transfer effects influence the effective permittivities of ZrN and Au surfaces such that opposite plasmonic resonance shifts are demonstrated for the ZrN and Au nanogroove arrays. Our results show that the choice of metallic material is important for achieving a desired charge transfer in the loading of graphene onto metallic materials.Item type:Item, Marimo-Bead-Supported Core-Shell Nanocomposites of Titanium Nitride and Chromium-Doped Titanium Dioxide as a Highly Efficient Water-Floatable Green Photocatalyst(2020-07-15) ;Kaur, Manpreet ;Shinde, Satish Laxman ;Ishii, Satoshi ;Jevasuwan, WipakornFukata, NaokiThe release of untreated industrial wastewater creates a hazardous impact on the environment. In this regard, the development of an environmentally friendly catalyst is of paramount importance. Here, we report a highly efficient and reusable core-shell TiN/SiO2/Cr-TiO2 (TSCT) photocatalyst that is composed of SiO2-cladded titanium nitride (TiN) nanoparticles (NPs) decorated with Cr-doped TiO2 NPs for the removal of organic contaminants from water. The TiN NPs serve as the main light absorber component with excellent visible-light absorption along with Cr-TiO2 NPs. The TSCT shows remarkable improvement in the photodecomposition of methylene blue (MB) over Cr-TiO2 and TiO2 NPs. An efficient structural design is proposed by adopting calcium alginate beads (P-Marimo beads) as a transparent scaffold for supporting our TSCT, which floats nature on the water surface and realizes easy handling as well as excellent reusability for multipurpose water purification. Surprisingly, our TSCT is found to keep its catalytic activity even after the illumination is turned off. Our proposed P-Marimo-encapsulated TSCT can be utilized as an excellent green photocatalyst with high photocatalytic performance, good recyclability, and easy handling.Item type:Item, Photocatalytic uphill conversion of natural gas beyond the limitation of thermal reaction systems(1970-01-01) ;Shoji, Shusaku ;Peng, Xiaobo ;Yamaguchi, Akira ;Watanabe, RyoFukuhara, ChojiDry reforming of methane is one of the key reactions to exploit natural gas feedstocks by their catalytic conversion to synthesis gas (CH4 + CO2 -> 2H(2) + 2CO), which is used in the production of transportable liquid fuel. However, this reaction suffers from thermodynamic conversion limits and high thermal energy requirements. Herein we report that a SrTiO3-supported rhodium (Rh/STO) catalyst efficiently promotes methane reforming under ultraviolet light irradiation without heat supply at low temperatures, which cannot be achieved by conventional thermal catalysis. The photoexcited holes and electrons are used for CH4 oxidation over STO and CO2 reduction over rhodium, respectively. Isotope analysis clarified that the lattice oxygens (O2-) act as mediator to drive dry reforming of methane. The materials design of Rh/STO can be extended in principle to diverse uphill reactions that utilize photon energy to obtain valued products from different carbon resources.Item type:Item, Plasmonic Nanolasers Enhanced by Hybrid Graphene-Insulator-Metal Structures(2019-08-01) ;Li, Heng ;Li, Jhu-Hong ;Hong, Kuo-Bin ;Yu, Min-WenChun, Yi-ChengGraphene is a two-dimensional (2D) structure that creates a linear relationship between energy and momentum that not only forms massless Dirac fermions with extremely high group velocity but also exhibits a broadband transmission from 300 to 2500 nm that can be applied to many optoelectronic applications, such as solar cells, light-emitting devices, touchscreens, ultrafast photodetectors, and lasers. Although the plasmonic resonance of graphene occurs in the terahertz band, graphene can be combined with a noble metal to provide a versatile platform for supporting surface plasmon waves. In this study, we propose a hybrid graphene-insulator-metal (GIM) structure that can modulate the surface plasmon polariton (SPP) dispersion characteristics and thus influence the performance of plasmonic nanolasers. Compared with values obtained when graphene is not used on an Al template, the propagation length of SPP waves can be increased 2-fold, and the threshold of nanolasers is reduced by 50% when graphene is incorporated on the template. The GIM structure can be further applied in the future to realize electrical control or electrical injection of plasmonic devices through graphene.Item type:Item, Structural Colors Enabled by Lattice Resonance on Silicon Nitride Metasurfaces(2020-05-26) ;Yang, Jhen-Hong ;Babicheva, Viktoriia E. ;Yu, Min-Wen ;Lu, Tien-ChangLin, Tzy-RongArtificial color pixels based on dielectric Mie resonators are appealing for scientific research as well as practical design. Vivid colors are imperative for displays and imaging. Dielectric metasurface-based artificial pixels are promising candidates for developing flat, flexible, and/or wearable displays. Considering the application feasibility of artificial color pixels, wide color gamuts are crucial for contemporary display technology. To achieve a wide color gamut, ensuring the purity and efficiency of nanostructure resonance peaks in the visible spectrum is necessary for structural color design. Low-loss dielectric materials are suitable for achieving vivid colors with structural color pixels. However, high-order Mie resonances prevent color pixels based on dielectric metasurfaces from efficiently generating highly saturated colors. In particular, fundamental Mie resonances (electric/magnetic dipole) for red can result in not only a strong resonance peak at 650 nm but also high-order Mie resonances at shorter wavelengths, which reduces the saturation of the target color. To address these problems, we fabricated silicon nitride metasurfaces on quartz substrates and applied Rayleigh anomalies at relatively short wavelengths to successfully suppress high-order Mie resonances, thus creating vivid color pixels. We performed numerical design, semianalytic considerations, and experimental proof-of-concept examinations to demonstrate the performance of the silicon nitride metasurfaces. Apart from traditional metasurface designs that involve transmission and reflection modes, we determined that lateral light incidence on silicon nitride metasurfaces can provide vivid colors through long-range dipole interactions; this can thus extend the applications of such surfaces to eyewear displays and guided-wave illumination techniques.