ABSTRACT
Nanoparticle (NP) self-assembly from suspension evaporation has been a topic of interest in recent times to fabricate a solid-state structure with diverse functions. We present a simple and facile evaporation-induced strategy for the formation of NP arrays on a flat substrate utilizing a template-directed sandwich system. The lithographic features assist the assembly of the typical nanoparticles (NPs), including SiO2, QDs@PS FMs, and QDs, on the top into circle, stripe, triangle, or square geometries with a fixed width of 2 µm. Additionally, an anionic surfactant, sodium dodecyl sulfonate (SDS), is incorporated into a negatively charged, hydrophilic SiO2 dispersion to govern the aggregation and self-assembly of NPs, fine tuning the morphologies of the residual structures on the substrate. SDS is attributed to modify the nature of SiO2 NPs to be hydrophobic, increase the hydrophobic attraction, dominating particle-particle and particle-interface interactions, and strengthen the particle-particle repulsive electrostatic force that results in the reduction of SiO2 NPs trapped in the separated colloidal suspension drop. Thus, using the SDS surfactant with the concentration ranging from 0 to 1 wt %, the obtained well-ordered SiO2 NP pattern packing on the substrate varies from six layers to one layer.
ABSTRACT
A microfluidic system was created to fabricate polydimethylsiloxane (PDMS) microspheres, whose shape, surface smoothness, and size were controlled. Resulting from their excellent optical properties and elasticity prepared by the apparatus, each PDMS microsphere could act as a microlens and separate imaging unit. The focal length of the microlens was simply tuned by the forces posed on the beads. For the microlens array (MLA) application, it was constructed simply through the assembly of the monodisperse PDMS beads.
Subject(s)
Dimethylpolysiloxanes , Microfluidics , MicrospheresABSTRACT
Orientation control of ordered materials would not only produce new physical phenomenon but also facilitate the development of fancy devices. Discotic liquid crystals (DLCs) form 1D charge transport pathway by self-organizing into columnar nanostructures via π-π stacking. However, controlling the electrical properties in such nanostructures with some direct and instant way is a formidable task for their high viscosity and insensitivity to external stimuli. Herein, the arbitrary control over electrical conductivity of such columnar nanostructures is achieved with UV light by incorporating DLCs with molecular motors. Highly ordered DLC microstripe arrays are generated on desired substrate through a capillary bridge dewetting strategy. The conductivity of the microstripes could be continuously modulated by 365 nm light due to the influence of molecular motion under UV irradiation on the electron orbital overlap of columnar nanostructures. This is so because the disorder degree of the DLC molecules is associated with the intensity of UV light and the doping concentration of molecular motors. Moreover, the device shows memory effect and reversible conductivity change. The DLC microstripe arrays are very promising for the applications in UV detectors, memory devices, optical switches, and so on.
ABSTRACT
The large-area formation of functional micropatterns with liquid crystals is of great significance for diversified applications in interdisciplinary fields. Meanwhile, the control of molecular alignment in the patterns is fundamental and prerequisite for the adequate exploitation of their photoelectric properties. However, it would be extremely complicated and challenging for discotic liquid crystals (DLCs) to achieve the goal, because they are insensitive to external fields and surface chemistry. Herein, a simple method of patterning and aligning DLCs on flat substrates is disclosed through precise control of the formation and dewetting of the capillary liquid bridges, within which the DLC molecules are confined. Large-area uniform alignment occurs spontaneously due to directional shearing force when the solvent is slowly evaporated and programmable patterns could be directly generated on desired substrates. Moreover, the in-plane column direction of DLCs is tunable by slightly tailoring their chemical structures which changes their self-assembly behaviors in liquid bridges. The patterned DLCs show molecular orientation-dependent charge transport properties and are promising for templating self-assembly of other materials. The study provides a facile method for manipulation of the macroscopic patterns and microscopic molecular orientation which opens up new opportunities for electronic applications of DLCs.
