Designing multifunctional surfaces that have user-specified interactions with impacting liquids and with incident light is a topic of both fundamental and practical significance. Taking cues from nature, we use tapered conical nanotextures to fabricate the multifunctional surfaces; the slender conical features result in large topographic roughness, while the axial gradient in the effective refractive index minimizes reflection through adiabatic index-matching between air and the substrate. Precise geometric control of the conical shape and slenderness of the features as well as periodicity at the nanoscale are all keys to optimizing the multifunctionality of the textured surface, but at the same time, these demands pose the toughest fabrication challenges. Here we report a systematic approach to concurrent design of optimal structures in the fluidic and optical domains and a fabrication procedure that achieves the desired aspect ratios and periodicities with few defects and large pattern area. Our fabricated nanostructures demonstrate structural superhydrophilicity or, in combination with a suitable chemical coating, robust superhydrophobicity. Enhanced polarization-independent optical transmission exceeding 98% has also been achieved over a broad range of bandwidth and incident angles. These nanotextured surfaces are also robustly antifogging or self-cleaning, offering potential benefits for applications such as photovoltaic solar cells.

A number of "top-down" lithographic and "bottom-up" self-assembly methods have been developed to fabricate three-dimensional (3D) nanostructures to support the recent advances in nanotechnology. But they are limited by a number of factors such as fabrication cost, pattern resolution, and/or flexibility of geometry. Here we present a 3D nanolithography process that utilizes self-assembled nanospheres to create a periodic array of focal spots, which are then replicated across multiple depth in a transparent medium according to the Talbot effect. The Talbot field then exposes a pattern onto the underlying photoresist, recording the 3D intensity distribution. We have demonstrated designable complex 3D periodic structures with 80 nm minimum feature size, roughly one-fourth of the operating wavelength. This approach combines 2D colloidal self-assembly and 3D phase lithography, is robust, cost-effective, and widely applicable to nanoscale research and manufacturing.

Thermally activated delayed fluorescence (TADF) properties of a dicarbazole-triazine compound, 9-(4,6-diphenyl-1,3,5-triazin-2-yl)-9'-phenyl-3,3'-bicarbazole (CzT), and its OLED characteristics were investigated. An estimated small energy gap of about 90 meV between the singlet and triplet energy states of CzT made the up-conversion of triplet excitons back to a singlet state possible. The origin of the observed delayed fluorescence has been shown to be thermally activated delayed fluorescence. An organic light emitting diode (OLED) with CzT as an emitter showed the maximum external quantum efficiency (EQE) of 6%. For comparison, another carbazole-triazine derivative of 3-(2'-(4,6-diphenyl-1,3,5-triazin-2-yl)-[1,1'-biphenyl]-2-yl)-9-phenyl-9H-carbazole (PhCzTAZ) with a similar structure was also studied. PhCzTAZ showed a low fluorescence quantum yield with no TADF.

Inspired by the tropical fish neon tetra, we report a mechanism to achieve dynamic iridescence that can be magnetically tuned. This approach is based on the tilting of periodic photonic nanostructures, as opposed to the more common strain-induced color tuning. In this method, a periodic array of magnetic nanopillars serves as a template to guide the assembly of iron oxide nanoparticles when magnetized in a liquid environment. The periodic local fields induced by the magnetic template anchor the assembled particle columns, allowing the structure to tilt about the base when the angle of the applied field is changed. This effect emulates a microscopic “Venetian blind” and results in dynamic optical properties through structural coloration that is tunable in real time. The fabricated prototype demonstrates tunable reflectance spectra with peak wavelength shift from 528 to 720 nm. The magnetic actuation mechanism is reversible and has a fast response time around 0.3 s. This structure can be implemented on an arbitrary surface as dynamic camouflage, iridescent display, and tunable photonic elements, as well as in other applications such as active fluidic devices and particle manipulation.

Wicking, the absorption of liquid into narrow spaces without the assistance of external forces, has drawn much attention due to its potential applications in many engineering fields. Increasing surface roughness using micro/nanostructures can improve capillary action to enhance wicking. However, reducing the structure length scale can also result in significant viscous forces to impede wicking. In this work, we demonstrate enhanced wicking dynamics by using nanostructures with three-dimensional (3D) hierarchical features to increase the surface area while mitigating the obstruction of liquid flow. The proposed structures were engineered using a combination of interference lithography and hydrothermal synthesis of ZnO nanowires, where structures at two length scales were independently designed to control wicking behavior. The fabricated hierarchical 3D structures were tested for water and ethanol wicking properties, demonstrating improved wicking dynamics with intermediate nanowire lengths. The experimental data agree with the derived fluid model based on the balance of capillary and vicious forces. The hierarchical wicking structures can be potentially used in applications in water harvesting surfaces, microfluidics, and integrated heat exchangers.

The interaction between light and colloidal elements can result in a wealth of interesting near-field optical patterns. By examining the optical and colloidal properties, the intensity distribution can be tailored and harnessed for three-dimensional nanolithography. Here, we examine the use of light scattering from colloidal particles to fabricate complex hollow nanostructures. In this approach, a single colloidal sphere is illuminated to create a scattering pattern, which is captured by a photoresist in close proximity. No external optical elements are required, and the colloidal elements alone provide the modulation of the optical intensity pattern. The fabricated nanostructures can be designed to have multiple shells, confined volumes, and single top openings, resembling "nano-volcanoes." The geometry of such structures is dependent on the scattered light distribution and can be accurately modeled by examining the light-particle interaction. The hollow nanostructures can be used to trap nanomaterial, and we demonstrate their ability to trap 50 nm silica nanoparticles. These well-defined surface hollow structures can be further functionalized for applications in controlled drug delivery and biotrapping. Colloidal elements with different geometries and material compositions can also be incorporated to examine other light-colloid interactions.

We demonstrated that oligo(9,9-diarylfluorene) derivatives have high potential for optoelectronic applications such as organic lasers and light-emitting organic field-effect transistors (LE-OFETs). The oligo(9,9diarylfluorene) derivatives have high photoluminescence quantum efficiencies up to Φ PL ≈ 70-75% and very low amplified spontaneous emission thresholds (E th ) down to 0.5 µJ/cm 2 in their vacuum-deposited neat films. In particular, the trimer derivatives (B3 and T3) show higher Φ PL and lower E th than those of the dimers (B2 and T2). Efficient deep-blue LE-OFETs with the electroluminescence (EL) peaking at λ peak ) 429 nm were demonstrated using the ter(9,9-diarylfluorene) as the active layer. Rather high luminance up to L ≈ 150 cd/m 2 and EL quantum efficiency up to η ext ≈ 0.60% were achieved with the optimum source-drain channel length, indicating bipolar carrier injection in the terfluorene layer under the FET operation.

We describe the fabrication and characterization of a nanostructured diffractive element with near-zero reflection losses. In this element, subwavelength nanostructures emulating adiabatic index matching are integrated on the surface of a diffractive microstructure to suppress reflected diffraction orders. The fabricated silicon grating exhibits reflected efficiencies that are suppressed by 2 orders of magnitude over broad wavelength bands and wide incident angles. Theoretical models of the fabricated structure based on rigorous coupled-wave analysis and effective medium theory are in agreement with the experimental data. The proposed principles can be applied to improve the performance of any diffractive structures, potentially leading to more efficient Fresnel lenses, holographic elements, and integrated optical systems.