Pixelated Microsized Quantum Dot Arrays Using Surface-Tension-Induced Flow.

Quantum dots (QDs) are semiconducting nanoparticles that exhibit unique fluorescent characteristics when excited by an ultraviolet light source. Owing to their highly saturated emissions, display panels using QDs as pixels have been presented. However, the complications of the nanofabrication procedure limit the industrial application of QDs. This study suggests a method to arrange high-aspect-ratio QD pixels by inducing both Laplace-pressure-driven capillary flow and thermally driven Marangoni flow. The evaporation of colloidal QDs induces a capillary flow that drives the QDs toward the inner tips of V-shaped structures. Additionally, the Marangoni flow arranges the gathered QDs at the tip; thus, they could form a high dune, overcoming the limitations of the existing capillary assembly method using evaporation. Using these phenomena, clover-shaped (assembly of V-shaped edges) templates were made to gather numerous QDs, and the clover with a 30° angle afforded the highest brightness among all the angle structures. Finally, by demonstrating a 100-cm2-sized QD microarray with high uniformity (98.6%), our method shows the feasibility of large-area fabrication, which has extensive application in manufacturing QD displays, anti-counterfeiting labels, and other QD-based optical devices.

Evaporation-Crystallization Method to Promote Coalescence-Induced Jumping on Superhydrophobic Surfaces.

Biphilic surfaces exhibit outstanding condensation efficiency compared to surfaces having homogeneous wettability. Especially, hydrophilic patterns on a superhydrophobic substrate significantly promote the coalescence-induced jumping of condensed droplets by increasing the nucleation rate of condensation, thus enhancing the condensation efficiency drastically. However, the application of biphilic surfaces in practical industries remains challenging because controlling the size and spacing of the hydrophilic spots on large and complex surfaces is difficult. In this study, we have achieved heterogeneous wettability using the evaporation-crystallization method, which can be applied to various surfaces as required by industries. The crystals generated using the evaporation-crystallization process drastically increased the number density of condensed droplets on a superhydrophobic surface (SHS), so the developed biphilic surface increased the cumulative volume of jumping droplets by up to 63% compared to that on a conventional superhydrophobic surface. Furthermore, the condensation dynamics on the biphilic surface were analyzed with the classical nucleation theory and the Ohnesorge number. The analysis results indicated that the generated hydrophilic crystals can reduce the nucleation energy barrier and decrease the available excessive surface energy of coalesced droplets on the biphilic surface; this implies that the size distribution of the crystals determines the condensation dynamics. In sum, this study not only introduced an effective surface tailoring approach for enhancing condensation but also provided insights into the design of optimum biphilic surfaces for various conditions, creating new opportunities to widen the applicability of biphilic surfaces in practical industries that exploit condensation.

Nanograssed Zigzag Structures To Promote Coalescence-Induced Droplet Jumping.

To increase the efficiency of jumping-droplet condensation, this study proposes a hierarchical superhydrophobic surface that promotes coalescence-induced jumping. Inspired by the phenomenon in which a growing droplet moves spontaneously within a superhydrophobic V structure, we fabricated nanograssed zigzag structures on the surface to induce the spontaneous motion of condensed droplets. The direction of the motion was parallel to the surface, so the condensed droplets easily coalesced on it. Compared with a conventional nanograssed superhydrophobic surface, the proposed surface increased the frequency of coalescence-induced jumping by ≥17 times and increased the cumulative volume of jumping droplets by ∼1.8 times. The proposed surface has great potential to increase the efficiency of applications such as water- and energy-harvesting and cooling systems that exploit jumping-droplet condensation.

Reduction of magnetic resonance image artifacts of NiTi implant by carbon coating.

A paramagnetic NiTi substrate was coated with diamagnetic carbon materials, i.e., graphene, graphene oxide (GO), and carbon nanotubes (CNTs), in order to reduce magnetic resonance (MR) image artifacts of NiTi implants. The present study focused on the effect of magnetic susceptibility variations in NiTi caused by the carbon coating on MR image artifacts. In the case of the graphene and GO coatings, the reduction of the magnetic susceptibility was greater along the perpendicular direction than the parallel direction. In contrast, the CNT coating exhibited a larger reduction along the parallel direction. The reduction of magnetic susceptibility measured in CNT-coated NiTi (CNT/NiTi) was smaller than the theoretical prediction especially when measured along the parallel direction, because CNTs on the NiTi surface were randomly arranged, rather than in a single direction. MR image artifacts were substantially reduced in all carbon-coated NiTi specimens, which is due to the reduction of magnetic susceptibility in NiTi by the carbon coating. This method can also be applied to other paramagnetic bio-metallic materials such as Co-Cr.

Effects of wettability on droplet movement in a V-shaped groove.

As basic research to understand the behavior of droplets on structured surfaces, we investigated droplet movement in a V-shaped groove while the volume of the droplet changes. We developed a model to explain the mechanism of the droplet movement and the effects of the wettability of the inner walls of the groove on the droplet movement. Furthermore, the model predicted new phenomena and explains the effect of the nonhomogeneous wettability on droplet movement. The predictions of the model match the experimental results well. This research can provide the basic knowledge for manipulating droplets with structured surfaces for various applications.

Design of Reduction Process of SnO2 by CH4 for Efficient Sn Recovery.

We design a novel method for the CH4 reduction of SnO2 for the efficient recovery of Sn from SnO2 through a study combining theory and experiment. The atomic-level process of CH4-SnO2 interaction and temperature-dependent reduction behavior of SnO2 were studied with a combination of a multi-scale computational method of thermodynamic simulations and density functional theory (DFT) calculations. We found that CH4 was a highly efficient and a versatile reducing agent, as the total reducing power of CH4 originates from the carbon and hydrogen of CH4, which sequentially reduce SnO2. Moreover, as a result of the CH4 reduction of SnO2, a mixture of CO and H2 was produced as a gas-phase product (syngas). The relative molar ratio of the produced gas-phase product was controllable by the reduction temperature and the amount of supplied CH4. The laboratory-scale experimental study confirmed that CH4 actively reduces SnO2, producing 99.34% high-purity Sn and H2 and CO. Our results present a novel method for an efficient, green, and economical recycling strategy for Sn with economic value added that is held by the co-produced clean energy source (syngas).