We studied the correlation between the molecular structure and the formation of helical nanofilaments (HNFs) of bent-core dimeric molecules with varying linkage lengths. To obtain precise structural data, a single domain of HNFs was prepared under physical confinement using porous 1D nanochannels, made up of anodic aluminium oxide films. Electron microscopy and grazing incidence X-ray diffraction were used to elucidate the linkage length-dependent formation of HNFs.
Photonic crystals (PCs) have recently attracted considerable attention, with much effort devoted to photonic bandgap (PBG) control for varying the reflected color. Here, fabrication of a modulated one-dimensional (1D) anodic aluminum oxide (AAO) PC with a periodic porous structure is reported. The PBG of the fabricated PC can be reversibly changed by switching the ultraviolet (UV) light on/off. The AAO nanopores contain a mixture of photoresponsive liquid crystals (LCs) with irradiation-activated cis/trans photoisomerizable azobenzene. The resultant mixture of LCs in the porous AAO film exhibits a reversible PBG, depending on the cis/trans configuration of azobenzene molecules. The PBG switching is reliable over many cycles, suggesting that the fabricated device can be used in optical and photonic applications such as light modulators, smart windows, and sensors.
The orientation control of soft matter to create a large area single domain is one of the most exciting research topics in materials science. Recently, this effort has been extended to fabricate two- or three-dimensional structures for electro-optical applications. Here, we create periodic zigzag structures in liquid crystals (LCs) using a combination of surface treatment and thermal annealing. The LC molecules in the nematic (N) phase were initially guided by the alignment layer of rubbed polymers, which were quenched and subsequently annealed in the smectic A (SmA) phase to create periodic zigzag structures that represent modulated layer structures. Direct investigation of the zigzags was performed using microscopy and diffraction techniques, showing the alternately arranged focal conic domains (FCDs) formed. The resulting macroscopic periodic structures will be of interest in further studies of the physical properties of soft matters.
Structural coloration using plasmonic particles has received substantial attention due to its robust, permanent, and scalable characteristics across the full color range. In this study, a plasmonic structure based on a porous anodic aluminum oxide (AAO) film coated with a metallic film was fabricated. Colors were varied by changing the refractive index, which was achieved with a convolution with nanopores of AAO film and an infiltrated liquid crystal (LC) material. LC molecules confined in the porous AAO film were uniformly aligned, and they exhibited pore-size-dependent colors because of the specific refractive index. The thermal phase transition of the LC material in the nanopores changed the effective refractive index, switching the reflected colors, and the LC-infiltrated AAO remained stable over a month. We believe LC materials can extend the use of rigid conventional plasmonic structures from simple sensor applications to multifunctional uses such as color printing, writing pens, and displays.
Controlling the orientation of building blocks in soft matter on the substrate has been a big challenge in material sciences. We have controlled the molecular orientation of liquid crystal (LC) materials on the porous anodic aluminum oxide (AAO) film having hexagonal pore arrays on the top surface. In our method, anchoring conditions can be varied by changing the pore size (Dp) and the porosity (P). As a proof-of-concept, the orientation of smectic A (SmA) structure at different anchoring conditions was successfully controlled in a sandwich cell consisting of AAO and a glass substrate, which has not been successfully controlled by conventional methods.
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